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Evidence reviews for the effectiveness and acceptability of intravitreal steroids, macular laser and anti-vascular endothelial growth factor agents for treating diabetic macular oedema

Diabetic retinopathy: management and monitoring

Evidence review G

NICE Guideline, No. 242

London: National Institute for Health and Care Excellence (NICE); .
ISBN-13: 978-1-4731-6435-2
Copyright © NICE 2024.

1. Effectiveness and acceptability of intravitreal steroids, macular laser and anti-vascular endothelial growth factor agents for treating diabetic macular oedema

1.1. Review question

What is the effectiveness and acceptability of intravitreal steroids, macular laser and anti-vascular endothelial growth factor agents for treating diabetic macular oedema?

1.1.1. Introduction

People with diabetic retinopathy can develop macular oedema, a swelling or thickening of the macula. Diabetic macular oedema is a common complication of diabetic retinopathy and can lead to moderate to severe visual loss. Currently there are several treatment options for people with diabetic macular oedema including macular laser (standard threshold or subthreshold laser), anti-vascular endothelial growth factor agents (anti-VEGFs), intravitreal steroids, or combinations of these treatments. This review aims to compare all treatments to identify the most effective treatment strategy for people with diabetic macular oedema.

This evidence review informed recommendations in the NICE guideline on the management and treatment of diabetic retinopathy, which is a new NICE guideline in this area.

1.1.2. Summary of the protocol

1.1.3. Methods and process

This evidence review was developed using the methods and process described in Developing NICE guidelines: the manual. Methods specific to this review question are described in the review protocol in (Appendix A) and the methods document.

Results were separated into two populations (people with central-involving macular oedema and people with non-central-involving macular oedema) and were reported at short-term and longer-term time points (12 months and 24 months or longer). As not all studies reported outcomes at these exact time points, it was decided that the 12-month data would include any results from 6 months to 18 months from the beginning of treatment, and 24 months would represent any results reported from 24 months onwards. Results for the primary outcomes of change in visual acuity from baseline and change in central retinal thickness were analysed using network meta-analyses (NMAs) where sufficient data was available. NMAs were therefore used to analyse:

  • change in visual acuity from baseline for people with central-involving macular oedema at 12 months and at 24 months.
  • change in central retinal thickness for people with central-involving macular oedema at 12 and at 24 months.

Insufficient data was available for an NMA for the other population groups of the primary outcomes, and so results were presented as pairwise meta-analysis for:

  • change in visual acuity from baseline for people with non-central-involving macular oedema at 12 months. No data was available for this comparison at 24 months.

Subgroup analysis of the primary NMAs were used to assess the different effects of treatment for people with central retinal thickness greater, or less than, 400 micrometres at baseline. Sufficient data was available for NMAs for:

  • change in visual acuity from baseline for people with central-involving macular oedema and central retinal thickness of 400 micrometres or more at 12 months and at 24 months
  • change in central retinal thickness from baseline for people with central-involving macular oedema and central retinal thickness of 400 micrometres or more at 12 months.

Insufficient data was available for a network analysis for subgroup analysis of the other population groups, and so results were presented as meta-analysis for:

  • change in central retinal thickness at 24 months for people with central-involving macular oedema and central retinal thickness of 400 micrometres or more
  • all change in visual acuity and central retinal thickness outcomes for people with central-involving macular oedema and central retinal thickness less than 400 micrometres

All secondary outcomes were presented using meta-analysis as stated in the review protocol. These were performed according to the NICE methods stated in the methods document.

Declarations of interest were recorded according to NICE’s conflicts of interest policy.

1.1.4. Effectiveness evidence

1.1.4.1. Included studies

Four Cochrane reviews (Jorge et al. 2018, Mehta et al. 2018, Rittiphairoj et al. 2020, Virgili et al. 2022) were identified which assessed the effects of monotherapy using macular laser, anti-VEGFs or intravitreal steroids for people with diabetic macular oedema. Each review was judged to be high quality and directly applicable to the review (see Appendix D) and so information about these interventions were taken directly from the reviews, rather than undertaking a new literature search (see Table 2 in the methods document).The results of these reviews were combined, and an additional search was conducted for combinations of different treatments that were not included in the Cochrane reviews, plus any studies published after the search dates of the Cochrane reviews. The studies in the Cochrane reviews were assessed to ensure that they met the inclusion criteria for this review.

Sixty studies were included from the Cochrane reviews (one study was included in both the Mehta et al. 2018 and Rittiphairoi et al. 2020 reviews). The number of primary studies included from each Cochrane review were:

In the NICE additional search, a total of 3139 records were screened at title and abstract stage. Following title and abstract screening, 129 studies were included for full text screening. These studies were reviewed against the inclusion criteria as described in the review protocol (Appendix A) and 8 additional RCTs were included. An additional 80 studies were found in the re-run search, of which 1 matched the review protocol and was included in the review. One further study was identified during consultation. The comparisons from each of the studies identified in the NICE search were for:

  • Anti-VEGFs vs macular laser: 1 study
  • Anti-VEGFs vs steroids: 2 studies
  • Anti-VEGFs vs anti-VEGFs: 3 studies
  • Steroids vs sham: 1 study
  • Steroids vs macular laser: 1 study
  • Steroids with macular laser vs macular laser: 2 studies
  • Steroids with macular laser vs steroids: 1 study
  • Subthreshold laser vs standard threshold laser: 1 study

This included one study with three arms which compared steroids, macular laser, and steroids with macular laser.

1.1.4.2. Excluded studies

117 studies were excluded following examination of the full text articles. See Appendix I for the list of excluded studies with reasons for their exclusion.

1.1.5. Summary of studies included in the effectiveness evidence

See Appendix D for full evidence tables.

Summary of included primary studies from Cochrane systematic review

1.1.6. Summary of the effectiveness evidence

Network meta-analysis

People with centre-involving macular oedema

Visual acuity
Whole population
Subgroup analysis: People with baseline central retinal thickness >400 micrometres
Central retinal thickness
Whole population
Subgroup analysis: People with baseline central retinal thickness >400 micrometres
Pairwise Meta-analysis
People with centre-involving macular oedema (whole population)
Anti-VEGFs vs standard threshold laser
Anti-VEGF vs Anti-VEGF
Anti-VEGF plus standard threshold laser vs Anti-VEGF
Anti-VEGF vs sham
Anti-VEGFs + steroids vs Anti-VEGF
Steroids vs sham
Steroids vs Anti-VEGFs
Steroids vs Macular Laser
Subthreshold laser vs standard threshold laser
People with non-centre-involving macular oedema
Comparisons vs standard threshold laser
Anti-VEGFs vs sham
Subgroup analysis: People with centre-involving diabetic macular oedema with a baseline central retinal thickness of less than 400 micrometres
Subthreshold vs standard threshold laser
Anti-VEGFs vs Anti-VEGFs with standard threshold laser
Anti-VEGFs vs standard threshold laser
Steroids vs sham
Anti-VEGF vs Anti-VEGF
Steroids vs Anti-VEGFs
Steroids vs standard threshold laser
Combination treatments vs standard threshold laser
Combination treatments vs Anti-VEGFs
Anti-VEGFs vs standard threshold laser
Steroids vs standard threshold laser
Combination treatments vs standard threshold laser
Subgroup analysis: People with centre-involving diabetic macular oedema with a baseline central retinal thickness of 400 micrometres or more
Subgroup analysis: People with non-centre-involving diabetic macular oedema and baseline central retinal thickness of less than 400 micrometres
Subgroup analysis: People with non-centre-involving diabetic macular oedema and baseline central retinal thickness of 400 micrometres or more

See Appendix G for full GRADE tables.

1.1.7. Economic evidence

A literature search was conducted to identify published economic evaluations to answer this question. Additionally, any relevant economic analyses conducted for published technology appraisals were reviewed for use in discussion around model conceptualisation and validation for the de novo economic model developed for this review question. The following technology appraisals in treatments for DMO were reviewed: TA824, TA820, TA799, TA346, TA953, TA274.

1.1.7.1. Included studies

A single search was performed to identify published economic evaluations of relevance to any of the questions in this guideline update (see Appendix B). This search retrieved 672 studies. Based on title and abstract screening, 638 studies could confidently be excluded for this review question and a further 24 studies excluded following the full-text review. Thus, 10 studies were included in the review (see Appendix G).

See the health economic study selection flow chart presented in Appendix G.

1.1.7.2. Excluded studies

Twenty-four studies were excluded at full text review. Some studies were selectively excluded based on limitations of the study, given there were similar studies with fewer limitations already included in the review.

See Appendix J for excluded studies and reasons for exclusion.

1.1.8. Summary of included economic evidence

1.1.9. Economic model

A de novo Markov economic model was conducted from the perspective of UK NHS and personal social services (PSS) for this review question.

Due to the heterogeneity of the population and associated treatments for diabetic macular oedema (DMO), the model results have been separated by the following populations:

  • All centre involving DMO
  • Centre involving DMO with a central retinal thickness (CRT) ≥400µm

Due to a lack of data to be able to form an NMA, it was not possible to generate model results for the subpopulations of “centre involving DMO with a CRT<400µm” and “non-centre involving DMO”.

The model was a lifetime cost-utility analysis comparing nine treatments along with no treatment for DMO: standard threshold laser; subthreshold laser; aflibercept; ranibizumab (Lucentis); ranibizumab plus standard threshold laser; bevacizumab; bevacizumab plus standard threshold laser; brolucizumab; and faricimab. In addition, ranibizumab biosimilar (Ongavia) was considered as a scenario assuming the same efficacy, safety and resource use as ranibizumab.

Intravitreal steroids are also treatments of interest in DMO, namely: dexamethasone (TA824) and fluocinolone (TA953). Intravitreal steroids are predominantly used as second line therapies and are only considered as first line treatments for patients in whom other first line treatments are not suitable or who had not responded to previous treatments (mainly laser), which would be a different population to that considered in this economic analysis. Therefore, intravitreal steroids were not included in the economic model. Consequently, the focus of this economic analysis was first line therapies only. Combination treatment of intravitreal steroids plus anti-VEGF agents was also not considered a comparator of interest as the committee felt it was unlikely that the combination would be used over either type of treatment alone.

Clinical inputs in the model were based on the literature, while the results of an NMA informed the mean difference in visual acuity. Main outputs were costs, health outcomes (in quality-adjusted life-years; QALYs), incremental cost-effectiveness ratios (ICERs) and net monetary benefits (NMBs).

All centre involving diabetic macular oedema

In the base-case probabilistic analysis using list prices for the anti-VEGF therapies, subthreshold laser had the lowest ICER of £1,248 compared with no treatment. The probabilistic base-case fully incremental results are presented in Table 68. Macular laser treatments are not suitable for all people with centre involving macular oedema, for example people with thicker retinas, and for this reason the probabilistic base-case results compared with no treatment are also presented in Table 69. Whilst subthreshold laser treatment still had the lowest ICER compared with no treatment (and standard threshold laser had the second lowest ICER), bevacizumab monotherapy also had an ICER below £20,000 which is the opportunity cost used by NICE for decision making. It should be noted that these results were not used by the committee when drafting recommendations for this review question, as they do not take into account the confidential discounts associated with each of the anti-VEGF treatments.

The committee was also presented with the results of the probabilistic base-case and scenario analyses when the confidential Patient Access Scheme (PAS) discounts were applied in the model and these results were used as the basis for their recommendations. These results cannot be presented here because they are commercially sensitive. When these discounts were applied, subthreshold laser remained the treatment with the lowest ICER, and standard threshold laser had the second lowest ICER. Subthreshold laser was the treatment with the lowest ICER in most scenario analyses, but the difference was very small between the two macular laser types. Both bevacizumab and brolucizumab had ICERs below £20,000 per QALY in people for whom laser treatments are not suitable. In the scenario where the confidential prices and the ranibizumab biosimilar (Ongavia) were considered, all treatments had ICERs below £25,000 per QALY. It should be noted that the NICE reference case uses an opportunity cost of £20,000 per QALY gained, but consideration can be given to therapies with an ICER between £20,000 and £30,000, for example when there are few other treatments available for a population or if the strategy is likely to reduce health inequalities.

Centre involving diabetic macular oedema with a CRT≥400µm

In the base-case probabilistic analysis using list prices for the anti-VEGF therapies, subthreshold laser had the lowest ICER of £1,442 compared with no treatment. The probabilistic base-case fully incremental results are presented in Table 70 and the results compared with no treatment are presented in Table 71. Whilst subthreshold laser treatment still had the lowest ICER compared with no treatment (and standard threshold laser had the second lowest ICER), for people in whom laser therapy is not suitable bevacizumab monotherapy also had an ICER below £20,000 which is the opportunity cost used by NICE for decision making. It should be noted that these results were not used by the committee when drafting recommendations for this review question, as they do not take into account the confidential discounts associated with each of the anti-VEGF treatments.

The committee was also presented with the results of the probabilistic base-case and scenario analyses when the confidential PAS discounts were applied in the model and these results were used as the basis for their recommendations comparing anti-VEGFs with macular laser therapies. These results cannot be presented here because they are commercially sensitive. When these discounts were applied, subthreshold laser remained treatment with the lowest ICER, while standard threshold laser remained the treatment with the second lowest ICER. The difference was very small between the two macular laser types, and it should be noted that the efficacy for subthreshold laser was assumed equivalent to standard threshold laser due to a lack of data for this population which would explain the very small differences. When the confidential prices were considered, all treatments had ICERs below £25,000 per QALY.

Non-centre involving diabetic macular oedema

As described above there was insufficient evidence to form an NMA. However, a pairwise comparison was available for the treatment of non-centre involving DMO with bevacizumab compared with sham treatment. After exploring the impact this mean difference would have on results, no change in conclusion was found compared to the centre involving population. Bevacizumab could still be considered a cost-effective treatment compared with no treatment in people for whom laser treatment is unsuitable.

1.1.10. Unit costs

The list prices of the drugs for this review question are presented in Table 72. It should be noted that aflibercept, ranibizumab, brolucizumab, faricimab and bevacizumab are recommended by NICE only if the manufacturer provides them with the agreed confidential patient access scheme discount.

1.1.11. Economic evidence statements

Ten published cost-utility analyses were identified:

  • Regnier et al (2015) compared intravitreal ranibizumab treatment (as needed and treat and extend regimens) with intravitreal aflibercept for the treatment of DMO. This study found that over a lifetime horizon both of the intravitreal ranibizumab treatment regimens were more effective and less costly compared with aflibercept. This analysis was from an NHS perspective and was informed by the RESTORE clinical trial.
  • Mitchell et al (2012) compared intravitreal ranibizumab monotherapy, intravitreal ranibizumab in combination with laser therapy and laser monotherapy for the treatment of DMO from an NHS perspective. This study found over a 15-year time horizon ranibizumab monotherapy could be considered cost effective assuming a willingness-to-pay threshold of £30,000 per QALY.
  • Pochopien et al (2019) compared the cost effectiveness of fluocinolone acetonide (FAc) implant with dexamethasone and usual care (mixture of laser treatment and anti-VEGF treatments ranibizumab, bevacizumab and aflibercept) for the treatment of vision impairment in people with DMO which has not responded to previous treatment and who have Pseudophakic lens. The authors also compared the cost effectiveness of FAc compared with usual care for eyes with phakic lens. This study found that over 15 years FAc could be considered cost effective for the population with Pseudophakic lens based on an ICER of £14,070 for FAc compared with dexamethasone and an ICER of £16,609 for FAc compared with usual care.
  • Haig et al (2016) compared the cost effectiveness of intravitreal ranibizumab monotherapy and intravitreal ranibizumab in combination with laser therapy with laser monotherapy for the treatment of DMO from a Canadian healthcare system perspective. The authors considered both ranibizumab monotherapy and ranibizumab in combination with laser to be cost effective over a period of 36 months compared with laser monotherapy for the treatment of visual impairment in people with DMO assuming QALYs are valued at CA$50,000. However, this study was only considered partially applicable due to the Canadian study setting and the different ICER thresholds.
  • Holekamp et al (2020) compared the cost effectiveness of intravitreal ranibizumab and intravitreal aflibercept for the treatment of DMO. This study found over 10 years aflibercept could not be considered cost effective compared to ranibizumab for the treatment of DMO. However, this study was only partially applicable due to the US study setting which is very different to the NHS, and the study had serious limitations with how the analysis was conducted and reported.
  • Brown et al (2015) compared the cost effectiveness of intravitreal ranibizumab compared with the sham arm from RIDE and RISE clinical trials for the treatment of DMO. This study found over 14 years that the ICER incorporating all direct costs from a third-party insurer perspective was $4,587 (£3,186) per QALY. However, this study was only partially applicable due to the US study setting, which is very different to the NHS and the study had serious limitations with how the analysis was conducted and reported.
  • Stein et al (2013) compared the cost-effectiveness of immediate laser treatment plus ranibizumab, delayed laser treatment plus ranibizumab, immediate laser treatment plus bevacizumab, and delayed laser treatment plus bevacizumab with laser monotherapy for the treatment of DMO. This study found that over 25 years delayed laser treatment was considered cost effective compared to laser treatment with an ICER of $11,138 (£7,774) per QALY and dominated immediate laser plus bevacizumab because deferred laser plus bevacizumab both increased QALYs and had lower costs. Neither immediate laser plus ranibizumab or delayed laser plus ranibizumab would not be considered cost effective with an ICER of $89,903 (£62,752) and $71,271 (£49,747) respectively per QALY. However, this study was only partially applicable due to the US study setting, which is very different to the NHS.
  • Sharma et al (2000) compared the cost-effectiveness of laser photocoagulation with no treatment in people with DMO. The study estimated over a 40-year life expectancy laser treatment could be considered cost effective compared to no treatment for improving vision in DMO based on a QALY being valued at $20,000. However, this study was only partially applicable due to the US study setting, which is very different to the NHS and the study had serious limitations with how the analysis was conducted and reported.
  • Lois et al (2022) compared the cost-effectiveness of subthreshold micro pulse laser compared with standard threshold laser treatment in adults with centre involving DMO with either a CRT between 300µm and 400µm or CRT<300µm and subretinal fluid was present in the central subfield. Over the two-year DIAMOND clinical trial duration, the study estimated that subthreshold laser could be considered equivalent to standard threshold laser in terms of both costs and clinical benefits and considered both treatments to be cost-effective treatments in people for whom laser treatment is suitable and have a CRT<400µm.
  • Hutton et al (2023) compared the cost-effectiveness of aflibercept monotherapy with bevacizumab as first line treatment followed by aflibercept if needed. The study estimated bevacizumab as first line treatment followed by aflibercept if needed to be a cost saving treatment without any changes in visual acuity gains across the two-year clinical trial duration. Aflibercept monotherapy was not considered to be cost effective compared with bevacizumab as first line treatment.

1.1.12. The committee’s discussion and interpretation of the evidence

1.1.12.1. The outcomes that matter most

The committee agreed that change in visual acuity as well as change in central (subfield) retinal thickness are very important outcomes in decision-making. These are the outcomes that determine how a person’s diabetic macular oedema can be treated and managed, and improvements in vision are a crucial outcome for people who have diabetic macular oedema.

The committee were also interested in other outcomes, such as visual acuity gain of three lines or more and the complications associated with treatment (adverse events). While improving or maintaining vision is a crucial aim of treatments for people with diabetic macular oedema, some of the adverse events associated with some treatments can have a considerable impact on a person’s quality of life. As such the committee thought it was important to consider these when deciding on recommendations.

1.1.12.2. The quality of the evidence
People with centre-involving diabetic macular oedema

There was sufficient evidence that was representative of current practice in the NHS and from similar population groups to combine the data into a network meta-analysis (NMA) for the outcomes of change of best corrected visual acuity and central retinal thickness at 12 months and 24 months for people with centre-involving diabetic macular oedema. NMA outcomes were moderate- to high-quality and directly applicable to the review.

The evidence for individual anti-VEGFs used a range of doses, time between doses and treatment durations. However, the committee stated that these were all within an acceptable range for clinical practice and so the data for each of anti-VEGFs was grouped for analysis.

It is important to note the aim of this review was to support the committee decision making in recommending treatment options for people with diabetic macular oedema (macular laser, anti-vascular endothelial growth factor agents (anti-VEGFs), intravitreal steroids, or combinations of these treatments). When discussing the approach for combining the evidence the committee noted that some of the treatments varied in their administration and should be considered separately in the analysis rather than grouped by class or type of treatment. The committee noted that the different anti-VEGFs have different recommended dosing regimens and there are different types of macular laser treatment thresholds . It was therefore decided that each treatment (anti-VEGFs, types of macular laser and steroids) should be considered separately in the analysis, rather than grouped by class or type of treatment. This separation aimed to minimise the heterogeneity in the analysis, which could otherwise affect the results of the NMA and their interpretation by the committee.

Studies reported visual acuity using a range of outcomes, as either logMAR, the number of ETDRS letters or using the Snellen ratio. To ensure these could be compared, all visual acuity results were converted into logMAR which the committee agreed was a suitable way to interpret the results.

There was considerably more data for the NMAs at 12 months than at 24 months. Fewer studies for the 24-month analysis, and therefore wider credible intervals, made it difficult to be confident in the longer-term effects of different treatment options on visual acuity. The effects for change in central retinal thickness were more apparent, but there were fewer treatments in the evidence base, making it difficult to determine whether treatments that were most effective at 12 months were also most effective longer-term. However, the committee thought that the results from the 12-month analysis were of high enough quality on which to base decision making, agreeing that at 12 months, any improvements in visual acuity are important to people who have diabetic macular oedema.

Data for outcomes other than visual acuity and central retinal thickness were much less widely reported and ranged from high- to very low-quality. For this reason, most of the decisions on recommendations were based on the visual acuity and central retinal thickness data, with the committee using their clinical knowledge and experience of other outcomes, such as adverse events.

A number of subgroups were listed in the protocol. However, data was only available for one of these subgroups (central retinal thickness of 400 micrometres or more, and central retinal thickness of less than 400 micrometres at baseline). Where studies reported data separated into these categories, the relevant data was included in each subgroup. However, many of the studies only reported pooled results for all people in the trial and did not separate the results by subgroups based on central retinal thickness. In this instance, studies were assigned to a subgroup based on whether the mean central retinal thickness at baseline was above or below 400 micrometres. A limitation to this subgroup analysis is that some people who had central retinal thickness of below 400 micrometres will have been included in the over 400 micrometres subgroup if the mean central retinal thickness for the whole study was above 400 micrometres (and vice versa). However, limited reporting in the studies meant that it was not possible to differentiate these populations further. Most of the studies had a mean baseline central retinal thickness of 400 micrometres or more and so there was limited information to determine whether the effects of treatment were different for these groups. While there was enough data to compare the effectiveness of different treatments using an NMA for the subgroup of 400 micrometres or more, the limited number of studies in the less than 400 micrometres subgroup meant that pairwise meta-analysis had to be used. As the studies reported on a range of different interventions and comparators, some of the outcomes were based on the result of a single study. Quality of the evidence for the outcomes for people in the less than 400 micrometres subgroup ranged from high- to low-quality, with most being high-quality.

The committee also discussed the use of rescue treatments in the studies. Rescue treatments may make the treatment used in the study arms appear more effective. However, this was not clearly reported in many of the studies, making it difficult to be sure whether the effect was purely a result of the treatment used in the intervention arm, or whether the results also represented the effect of any rescue treatments.

People with non-centre-involving diabetic macular oedema

There were very few studies for people with non-centre-involving diabetic macular oedema, and evidence for each of the outcomes was fully applicable to the review and ranged from low- to high-quality. Most of the studies had small sample sizes, and each reported on different interventions. This meant that the evidence was based on results from single studies, rather than pooled pairwise meta-analysis. Neither of the primary outcomes (change in visual acuity and change in central retinal thickness from baseline) were widely reported in these studies. There was very limited evidence for other outcomes, for example ocular adverse events were rare and poorly reported, which limited the comparisons that the committee could make between different treatments.

1.1.12.3. Imprecision and clinical importance of effects
People with centre-involving diabetic macular oedema

At 12 months in the overall NMA analysis and in the NMA analysis for the subgroup with central retinal thickness of 400 micrometres or more, the majority of anti-VEGFs as well as intravitreal dexamethasone implant were more effective at improving visual acuity than standard threshold laser for people with centre-involving macular oedema. The credible intervals did not cross the line of no effect and the committee were satisfied that this reflected a genuine effect that was large enough to be clinically meaningful. Most anti-VEGFs were also more effective at reducing central retinal thickness at 12 months than standard threshold laser, although results for bevacizumab crossed the line of no effect.

Combination treatments such as Ranibizumab with Dexamethasone, Ranibizumab with standard threshold laser, Triamcinolone with Bevacizumab and Bevacizumab with standard threshold laser were also more effective at improving visual acuity at 12 months than standard threshold laser alone. Some combination treatments (Ranibizumab with Dexamethasone, Ranibizumab with standard threshold laser) were more effective than standard threshold laser at reducing central retinal thickness at 12 months. This indicates that where anti-VEGF treatment alone is not effective, the addition of macular laser may be beneficial.

Results varied for the subgroup of people with central retinal thickness less than 400 micrometres. Many of the outcomes were based on single study analysis and some had wide confidence intervals, making it more difficult to be certain of the effects of different treatments for those outcomes. The evidence indicated there were some benefits in improving visual acuity and reducing central retinal thickness with anti-VEGFs compared to standard threshold laser. However, the limited number of studies and the range of different comparisons made it more difficult for the committee to be certain of the effectiveness of different treatments than it was for the subgroup with central retinal thickness of 400 micrometres or more.

There was considerably less data available to assess longer-term effectiveness of each treatment for the overall analysis and the subgroups. For change in visual acuity, the NMA effect estimates at 24 months favoured anti-VEGF treatments and anti-VEGF combined with standard threshold laser in comparison to standard threshold laser alone. However, the limited data meant there were wide credible intervals making it difficult to be sure of the longer-term effects of each treatment. Results for change in central retinal thickness at 24 months were more precise, and the committee thought that these indicated a clinically meaningful effect. The committee were confident that, while there was less evidence and fewer treatments for the 24-month analysis, the short-term results were enough to make recommendations on the most effective treatments for people with centre-involving macular oedema.

People with non-central-involving diabetic macular oedema

The limited number of studies, small sample sizes and reliance on outcomes from single studies meant that it was difficult to be certain of the effects of different treatments. These limitations also meant that many of the outcomes had wide confidence intervals, which made decision making about the most effective treatment options for this group more difficult. Therefore, the committee relied on their clinical knowledge and experience as well as information from the treatment thresholds review when discussing recommendations (see evidence review B).

1.1.12.4. Benefits and harms
People with centre-involving and non-centre-involving diabetic macular oedema

The committee highlighted the importance of all people who have clinically significant diabetic macular oedema being offered treatment, whether this is centre-involving or non-centre-involving oedema. Without treatment all people with clinically significant diabetic macular oedema are at risk of vision loss and of needing further treatments. They also discussed the importance of ensuring that people with diabetic macular oedema are aware of their diagnosis, including whether they have centre-involving or non-centre-involving macular oedema. They should also be made aware of the benefits and side-effects of each treatment option. It was highlighted that many people with macular oedema are offered treatment without being provided with a clear explanation of what the treatment involves and why it is being offered to them. This can be very stressful, particularly at a time when people are already concerned about further loss of vision. People are unlikely to be familiar with macular laser and anti-VEGF treatments and are therefore often concerned about what the treatments may involve. Shared decision making is therefore an important part of the treatment pathway for macular oedema and will help patients to understand why a particular treatment may be best for them. It will also ensure that treatment fits their personal needs and circumstances.

People with non-centre-involving diabetic macular oedema

Given the limited evidence for people with non-centre-involving diabetic macular oedema, the committee used their clinical knowledge and experience, as well as evidence from the thresholds for starting treatment review (see evidence review B) to decide on the recommendations for this group.

The committee highlighted the importance of the use of macular laser for people with non-centre-involving macular oedema, as this can delay the need for anti-VEGF treatment that is more commonly needed once a person’s macular oedema progresses to the point where it is centre-involving. Although there was limited evidence to compare the effectiveness of macular laser to other treatments for people with non-centre involving macular oedema, the committee were confident that this is an effective treatment for this group, and something that already happens in clinical practice. They thought a recommendation was important for this group because, without treatment, these people will progress to centre-involving macular oedema and be at higher risk of its associated complications, such as vision loss. They also noted that the review on treatment thresholds (see Tables 12 and 13 and section 1.1.11.4 in evidence review B) included high- to moderate-quality evidence from a large study that indicated that when macular laser is provided when someone is at an early stage of diabetic macular oedema, it can slow the worsening of visual acuity compared to when it is provided later. Slowing the worsening of visual acuity is an important outcome for people who have diabetic retinopathy, and so it was recommended that macular laser should be offered to all people who have non-centre-involving diabetic macular oedema as this is an early stage of diabetic macular oedema.

People with centre-involving diabetic macular oedema

The committee were aware of the NICE technology appraisals relating to the use of anti-VEGFs and steroids for people with centre-involving diabetic macular oedema. Their discussion therefore centred around the effectiveness of anti-VEGFs, steroids and combinations of treatments in comparison to standard threshold laser. They did not consider the relative effectiveness of different anti-VEGFs, or of different steroids. The committee concluded that the NMAs showed that, anti-VEGFs, either alone or combined with standard threshold laser, are more effective at improving visual acuity and reducing central retinal thickness at 12 months than standard threshold laser alone. Pairwise meta-analysis indicated that anti-VEGF treatments resulted in more people achieving a gain in visual acuity of three lines or more than standard threshold laser, although it did have a higher mean number of treatments. The number of adverse events reported for both treatments were very small and could not differentiate between treatments. The committee noted that, in their experience, anti-VEGFs are not commonly associated with a high number of ocular adverse events and are generally well tolerated.

For steroids, in comparison to standard threshold laser, visual acuity was improved with the use of dexamethasone alone or in combination with ranibizumab at 12 months. However, pairwise meta-analysis results showed a higher number of ocular adverse events (development of cataract, increased intraocular pressure and vitreous haemorrhage) associated with intravitreal steroids. The committee also emphasised that there is no way to predict who is more likely develop adverse events which makes decision making difficult, particularly as some of the adverse events could have a big impact on someone’s quality of life. The pairwise meta-analysis also showed greater improvements in visual acuity (three or more lines improvement) for anti-VEGFs than steroids at 12 months.

Based on the evidence of effectiveness from the NMA and adverse events from pairwise meta-analysis, the committee decided to recommend that anti-VEGFs should be offered as first line treatment for people with centre-involving diabetic macular oedema and central retinal thickness of 400 micrometres or more. The benefits of greater improvements in vision compared to other treatment options was considered important, as this will have a considerable impact on the lives of people who have diabetic macular oedema. Macular laser is often less effective for this group of people and therefore the committee thought that, although anti-VEGFs can require a greater number of treatments than macular laser, this is outweighed by the benefits of improvements in vision and the relatively small risks of adverse events. The committee added an extra criterion that these recommendations are for people with visual impairment, as they were aware that the most effective treatment varies between those who have good and poor vision. The criteria to distinguish between people who are considered to have good or poor vision was based on the inclusion criteria that are reported in many of the studies. The recommendations for the use of anti-VEGFs included reference to the NICE technology appraisals for the use of ranibizumab, aflibercept, faricimab and brolucizumab. Each of these anti-VEGFs was shown to be effective in the NMA and so the committee were satisfied that there were no contradictions in the evidence base.

While the overall NMA and economic model in this review indicated that anti-VEGFs are both clinically and cost-effective for the full diabetic macular oedema population, they are only considered to be cost-effective for people with central retinal thickness of 400 micrometres or more in the technology appraisals. The committee discussed how some people, such as women and people of South Asian or Afro-Caribbean descent tend to have thinner retinas. This means that even if they have retinal thickening, they may not reach, or will take longer to reach, the 400 micrometre threshold, and may therefore miss out on important treatment, which could lead to greater loss of vision. Given that the NMAs and economic model in this review showed anti-VEGFs to be clinically and cost-effective for a wider population, and the meta-analysis indicated that there may be some benefits to the use of anti-VEGFs in this group, the committee decided to recommend that anti-VEGFs are considered for people with central retinal thickness of less than 400 micrometres. With more limited evidence for people with thinner retinas, and an awareness that macular laser can have benefits, they did not think they could make as strong a recommendation in favour of anti-VEGFs as for those in the subgroup with greater central retinal thickness. Macular laser was recommended as the alternative option for this group. Although the analysis suggests that some anti-VEGFs may be most effective, macular laser can also be effective and is current practice for many people in this group because of the 400 micrometre threshold in the NICE technology appraisal guidance. It also has the benefit of delaying the need for anti-VEGF treatment for some people.

The committee were aware that some people who have anti-VEGF treatments will not respond as well as others and may need additional treatment. For this reason, they recommended that clinicians should consider macular laser as adjuvant treatment if a person’s vision does not improve or stabilise after the anti-VEGF loading dose. They also highlighted how some people have a delayed response to treatment, and so a further review should take place to identify if someone still has a suboptimal response to treatment. When discussing the timing of this additional review, the committee noted that the evidence for the technology appraisal for ranibizumab showed improvements in visually acuity in the first 12 months after treatment. They were also concerned that switching treatment before this point could result in people experiencing the additional adverse events associated with intravitreal steroids, when they could still respond to anti-VEGF treatment if they are given more time. They therefore decided that 12 months is an appropriate time for this additional review for most people. If someone still shows a suboptimal response at this point then an intravitreal steroid implant should be considered.

When discussing a change in treatment following a suboptimal response, the committee decided to recommend the use of intravitreal steroids. The committee reviewed the NMA evidence and acknowledged the limitations of the NMA with regards to the limited data for inclusion in the NMA for fluocinolone acetonide. The committee was aware of NICE technology appraisal guidance for the use of a dexamethasone intravitreal implant or fluocinolone acetonide intravitreal implant as second line therapies for DMO. The NMA showed that an intravitreal dexamethasone implant is an effective treatment option, even if associated with a higher number of adverse events which is in line with the NICE technology appraisal guidance. While the committee considered the limitations of the NMA applied for both corticosteroid therapies, evidence for fluocinolone acetonide was limited, with no evidence for visual acuity at 12 months, and a similar effect to dexamethasone at 24 months. Evidence for reduction in central retinal thickness showed a greater effect for dexamethasone than fluocinolone at 12 months and there was no evidence for fluocinolone at 24 months. With this limited data for fluocinolone, there was insufficient evidence to widen the population beyond that included in the NICE technology appraisal guidance. The committee acknowledged that NICE Technology Appraisal (TA953) demonstrated comparable safety and efficacy between fluocinolone acetonide and dexamethasone intravitreal therapies. They agreed that the recommendation doesn’t specify which intravitreal corticosteroid therapy should be used, leaving the choice open. Therefore, links were provided to each of the technology appraisal recommendations for people who have shown a suboptimal response to anti-VEGF treatment. The committee noted that there are also some people who may not be able to regularly attend a clinic to have anti-VEGF injections, such as those who have work or carer commitments that make it difficult to attend, or people who have limited access to transport. There are also people who may not want to continue with regular injections for other reasons, such as anxiety about injections. They therefore recommended the use of intravitreal steroids is also considered for these people to ensure that they don’t miss out on the benefits of treatment. The committee discussed how a person can decide that they do not want anti-VEGF treatment at any time, from when they are first being considered as a treatment option, or at any point after they have been prescribed. Finally, the committee highlighted how some people may not be able to have non-corticosteroid therapy, such as people who are pregnant at the time of diagnosis or who become pregnant during treatment, and so this was also included in the recommendation. Current NICE technology appraisal guidance supports the use of dexamethasone for these groups of people.

Most of the recommendations are based on people who have central-involving diabetic macular oedema and poor vision, as this is the group who will benefit most from treatment and reflects most of the evidence base. However, some people with diabetic macular oedema will have good vision. These people may gain fewer benefits from the use of anti-VEGFs, steroids or macular laser, but could still be considered for treatment. In the review on thresholds for starting treatment (see evidence review B), one study with high quality outcomes (ETDRS 1985) reported that early laser can reduce the worsening of visual acuity and the incidence of clinically significant macular oedema compared to delayed macular laser treatment. The committee thought this was important to consider because, in their clinical experience, macular laser can be useful for people with diabetic macular oedema and good vision as a way to delay the need for anti-VEGF treatment, which will be needed once their vision becomes worse. However, given that this evidence was based on a single study, the committee decided to recommend that either observation or macular laser should be considered for this group of people. The decision over which to use should be based on a discussion with the patient about the benefits and risks of each option. The committee were aware that while the two types of macular laser (standard threshold and subthreshold) show similar levels of effectiveness, subthreshold laser is associated with fewer adverse events, and so may be a more beneficial option for this group of people. However, there are currently no studies that compare the effectiveness of subthreshold laser to observation, and so the committee thought that the decision over macular laser or observation should be a choice between a patient and their clinician and should involve careful consideration of the best option to reduce the patients’ chance of progression.

1.1.12.5. Cost-effectiveness and resource use

The committee considered the ten cost-effectiveness studies identified in the literature for the treatment of diabetic macular oedema (DMO). Although some studies were directly applicable, the committee felt that not all relevant comparators were included in the studies to suitably aid the decision making. The de novo economic model allowed all treatment options to be considered together using inputs and assumptions relevant to NHS clinical practice based on both the literature and committee expertise.

The committee considered the de novo economic model results alongside the clinical evidence for centre involving DMO. The economic model results for all people with centre involving DMO found subthreshold laser treatment had the lowest ICER and was considered to be the most cost-effective therapy compared with no treatment. When the PAS prices were considered, all treatments had ICERs below £25,000 per QALY. The committee considered these results to be reasonable given anti-VEGFs are only reimbursed by NICE for the population of people with centre-involving DMO with a CRT≥400µm. The committee did discuss that in general subthreshold laser would be expected to be used predominantly in those with a CRT<400µm and laser-based therapies may not be suitable for those with a CRT≥400µm. The results were found to be sensitive to changes in assumptions around the source of utility mapping from visual acuity to evaluate quality of life and the number of treatment and monitoring visits anticipated over time. In the base-case analysis, the committee felt the utility values from Czoski-Murray et al (2009) were most appropriate as it has been widely accepted within the technology appraisals in DMO despite the limitation of this being a simulated study. The use of other utility sources were explored in scenario analyses. The economic model results for people with centre involving DMO and a CRT≥400µm found subthreshold laser treatment to be the most cost-effective therapy compared to no treatment. When the PAS prices were considered, all treatments had ICERs below £25,000 per QALY. The committee highlighted that the restriction to treatment using anti-VEGFs for those with a CRT≥400µm could increase health inequalities. The committee explained that some populations such as some ethnic minority populations and females commonly have thinner retinas, meaning they may miss out on treatment options for the anti-VEGFs restricted to the treatment of people with a CRT≥400µm.

The committee discussed that given the potential health inequalities associated with limiting recommending anti-VEGFs based on central retinal thickness threshold they should be at least considered as treatment for everyone with centre involving DMO with reduced visual acuity. This recommendation is supported by the economic evidence given the similarity in the results across both the all centre involving DMO population and the subgroup of those with a CRT≥400µm.

The committee discussed the key differences in the assumptions and data used within the technology appraisal guidance and of the de novo cost-effectiveness analysis presented to the committee. The clinical data used to inform the economic model was different to that used in the technology appraisals, in that this model utilised outcomes of NMAs on mean difference in BCVA with aggregate data from many RCTs, whereas technology appraisals generally use patient level data from RCTs that include the technology being appraised. The NMA results found anti-VEGFs to be clinically effective compared with macular laser therapy or no treatment; however, it is possible this effect may be different than in the individual technology appraisals because of the wider population and evidence base considered. Although anti-VEGFs were more clinically effective than either type of laser, both lasers came out as most cost-effective options since they were very cheap even when the confidential prices for anti-VEGFs were used. This may explain any differences in conclusions of cost-effectiveness of treatments, where the anti-VEGFs are recommended currently by NICE for those with a CRT≥400µm.

The results were sensitive to changes in the utility source, the proportion of patients remaining on treatment after five years and the number of monitoring and treatment visits. Many of the previous technology appraisals restricted treatment duration to five years, which the committee discussed is not realistic in current clinical practice. When this scenario was explored most anti-VEGFs became cost effective below an ICER threshold of £20,000 per QALY. However, people can remain on anti-VEGFs for much longer than this which is why this assumption was not used within the base-case analysis.

After accounting for patient costs, the other anti-VEGFs could also be considered cost effective; however, it should be noted that these are only community related costs outside of the NHS and PSS perspective for people with low vision, which refers to BCVA of less than 35 letters. The committee discussed the substantial burden of transport related costs for attending the frequent appointments associated with anti-VEGFs. It is possible the results of this scenario could be different should data on transport costs for patients become available.

The committee recommended the use of anti-VEGFs as a first line treatment for those with centre-involving DMO. The committee discussed anti-VEGFs can be resource intensive in terms of clinical time as patients may be required to attend appointments as regularly as every four weeks, which can have pressure on demand for services. Likewise, attending clinics can be burdensome for the patient particularly for those of working age. The committee discussed that the benefits of treatment with anti-VEGF outweighs the costs, in terms of preventing sight loss which can reduce the high long-term costs associated with support for people with low vision and has a greater impact on quality of life. Overall, the committee did not anticipate this would have a resource impact as this is currently in line with current clinical practice. However, it should be noted that the long-term usage of an anti-VEGF can represent a large cost burden to both the NHS and the patient in terms of transport costs for frequent clinic visits. The introduction of biosimilars is anticipated to reduce some of this financial burden to the NHS.

In the absence of economic evidence comparing dexamethasone and fluocinolone acetonide, the committee made recommendations on intravitreal steroids that aligned with the existing technology appraisals of those treatments.

No economic analyses were presented alongside the clinical evidence for non-centre involving DMO. The committee discussed that by offering a macular laser this can delay regression of disease and reduce the need and quantity of costly anti-VEGF treatments. Overall, the committee anticipated that by treating people with non-centre involving DMO with a macular laser treatment, this would have a positive resource impact by delaying the need for more resource intensive treatment.

1.1.13. Other factors the committee took into account

The committee were aware of other recommendations about when to assess response to anti-VEGFs. They highlighted how the NHS Framework Agreement for the supply of Medical Retinal Vascular Treatments states that one approach to this is to assess response after 6 months of anti-VEGF treatment. However, they noted that these decisions were based primarily on the effectiveness of anti-VEGF treatments and steroids, and not the additional adverse events associated with steroids. As such, they thought that their decision to recommend a review of response to anti-VEGF treatment after 12 months was appropriate for most people.

The committee discussed how people may have different pathologies in each eye. They stressed the importance of treating diabetic retinopathy on a per-eye basis. This will ensure that individuals receive the most effective treatment which addresses the specific active issues in each eye, rather than focusing solely on one eye with more severe disease. Treating both eyes individually is essential because it reduces the risk of progression in either eye, ultimately lowering the chances of severe consequences like vision loss.

1.1.14. Recommendations supported by this evidence review

This evidence review supports recommendations 1.3.1 and 1.6.1 to 1.6.11.

1.1.15. References – included studies

    1.1.14.1. Effectiveness
      Included studies from NICE search
      • Callanan, David G, Gupta, Sunil, Boyer, David S et al. (2013) Dexamethasone intravitreal implant in combination with laser photocoagulation for the treatment of diffuse diabetic macular edema. Ophthalmology 120(9): 1843–51 [PubMed: 23706947]
      • Chen, Y.-X., Li, X.-X., Yoon, Y.H. et al. (2020) Intravitreal aflibercept versus laser photocoagulation in asian patients with diabetic macular edema: The VIVID-east study. Clinical Ophthalmology 14: 741–750 [PMC free article: PMC7069586] [PubMed: 32210527]
      • Faghihi, H, Esfahani, MR, Harandi, ZA et al. (2010) Intravitreal bevacizumab vs. combination of intravitreal bevacizumab plus macular photocoagulation in clinically significant diabetic macular edema: 6 months results of a randomized clinical trial. Iranian journal of ophthalmology 22(1): 21–26
      • Fouda, S.M. and Bahgat, A.M. (2017) Intravitreal aflibercept versus intravitreal ranibizumab for the treatment of diabetic macular edema. Clinical Ophthalmology 11: 567–571 [PMC free article: PMC5367610] [PubMed: 28356711]
      • Gillies, Mark C, Simpson, Judy M, Gaston, Christine et al. (2009) Five-year results of a randomized trial with open-label extension of triamcinolone acetonide for refractory diabetic macular edema. Ophthalmology 116(11): 2182–7 [PubMed: 19796823]
      • Lam, Dennis S C, Chan, Carmen K M, Mohamed, Shaheeda et al. (2007) Intravitreal triamcinolone plus sequential grid laser versus triamcinolone or laser alone for treating diabetic macular edema: six-month outcomes. Ophthalmology 114(12): 2162–7 [PubMed: 17459479]
      • Shaggily, Cemal and Duru, Necati (2020) COMPARISON OF INTRAVITREAL DEXAMETHASONE IMPLANT AND AFLIBERCEPT IN PATIENTS WITH TREATMENT-NAIVE DIABETIC MACULAR EDEMA WITH SEROUS RETINAL DETACHMENT. Retina (Philadelphia, Pa.) 40(6): 1044–1052 [PubMed: 30950970]
      • Vader, Maartje J C, Schauwvlieghe, Ann-Sofie M E, Verbraak, Frank D et al. (2020) Comparing the Efficacy of Bevacizumab and Ranibizumab in Patients with Diabetic Macular Edema (BRDME): The BRDME Study, a Randomized Trial. Ophthalmology. Retina 4(8): 777–788 [PubMed: 32362552]
      • Included studies from Cochrane review: Virgili et al-2022
        • Azad 2012

          Azad R, Sain S, Sharma YR, Mahajan D. Comparison of intravitreal bevacizumab, intravitreal triamcinolone acetonide, and macular grid augmentation in refractory diJuse diabetic macular edema: A prospective, randomized study. Oman Journal of Ophthalmology 2012;5(3):166–70. [PMC free article: PMC3574512] [PubMed: 23439853]
        • Baker 2019 Baker 2019 {published data only}

          Baker CW, Glassman AR, Beaulieu WT, Antoszyk AN, Browning DJ, Chalam KV, et al. EJect of initial management with aflibercept vs laser photocoagulation vs observation on vision loss among patients with diabetic macular edema involving the center of the macula and good visual acuity: a randomized clinical trial. JAMA 2019;321(19):1880–94. [PMC free article: PMC6537845] [PubMed: 31037289]
        • BOLT 2010 (Michaelides 2010)

          Michaelides M, Kaines A, Hamilton RD, Fraser-Bell S, Rajendram R, Quhill F, et al. A prospective randomized trial of intravitreal bevacizumab or laser therapy in the management of diabetic macular edema (BOLT study) 12-month data: report 2. Ophthalmology 2010;117(6):1078–86. [PubMed: 20416952]
          Rajendram R, Fraser-Bell S, Kaines A, Michaelides M, Hamilton RD, Esposti SD, et al. A 2-year prospective randomized controlled trial of intravitreal bevacizumab or laser therapy (BOLT) in the management of diabetic macular edema: 24-month data: report 3. Archives of Ophthalmology 2012;130(8):972–9. [PubMed: 22491395]
          Sivaprasad S, Crosby-Nwaobi R, Esposti S, Peto T, Rajendram R, Michaelides M, et al. Structural and functional measures of eJicacy in response to bevacizumab monotherapy in diabetic macular oedema: exploratory analyses of the BOLT Study (Report 4). PloS ONE 2013;8(8):e72755 [PMC free article: PMC3754932] [PubMed: 24013651]
        • Brown 2015

          Brown DM, Schmidt-Erfurth U, Do DV, Holz FG, Boyer DS, Midena E, Heier JS, Terasaki H, Kaiser PK, Marcus DM, Nguyen QD, JaJe GJ, Slakter JS, Simader C, Soo Y, Schmelter T, Yancopoulos GD, Stahl N, Vitti R, Berliner AJ, Zeitz O, Metzig C, Korobelnik JF. Intravitreal Aflibercept for Diabetic Macular Edema: 100-Week Results From the VISTA and VIVID Studies. Ophthalmology 2015;122(10):2044–52. [PubMed: 26198808]
        • Brown 2020

          Brown DM, Emanuelli A, Bandello F, Barranco JJ, Figueira J, Souied E, et al. KESTREL and KITE: 52-week results from two Phase III pivotal trials of brolucizumab for diabetic macular edema. American Journal of Ophthalmology 2022;238:157–72 [PubMed: 35038415]
        • Chatzirallis 2020

          Chatzirallis A, Theodossiadis P, Droutsas K, Koutsandrea C, Ladas I, Moschos MM. Ranibizumab versus aflibercept for diabetic macular edema: 18-month results of a comparative, prospective, randomized study and multivariate analysis of visual outcome predictors. Cutaneous and Ocular Toxicology 2020;39:317–22 [PubMed: 32722955]
        • DA VINCI 2011 (Do 2012)

          Do DV, Nguyen QD, Boyer D, Schmidt-Erfurth U, Brown DM, Vitti R, et al. One-year outcomes of the DA VINCI Study of VEGF Trap-Eye in eyes with diabetic macular edema. Ophthalmology 2012;119(8):1658–65. [PubMed: 22537617]
          Do DV, Schmidt-Erfurth U, Gonzalez VH, Gordon CM, Tolentino M, Berliner AJ, et al. The DAVINCI Study: phase 2 primary results of VEGF Trap-Eye in patients with diabetic macular edema. Ophthalmology 2011;118(9):1819–26 [PubMed: 21546089]
        • DRCRnet 2010

          Anonymous. Erratum: Patient-reported visual function outcomes improve aGer ranibizumab treatment in patients with vision impairment due to diabetic macular edema: Randomized clinical trial (JAMA Ophthalmology (2013) 131:10 (1339-1347) DOI: 10.1001/jamaophthalmol.2013.4592). JAMA Ophthalmology 2013;131(12):1652. [PubMed: 23974915]
          Bressler SB, Qin H, Beck RW, Chalam KV, Kim JE, Melia M, et al. Factors associated with changes in visual acuity and central subfield thickness at 1 year aGer treatment for diabetic [PMC free article: PMC3543147] [PubMed: 22965591]
          Bressler SB, Qin H, Melia M, Bressler NM, Beck RW, Chan CK, et al. Exploratory analysis of the eJect of intravitreal ranibizumab or triamcinolone on worsening of diabetic retinopathy in a randomized clinical trial. JAMA Ophthalmology 2013;131(8):1033–40. [PMC free article: PMC4162127] [PubMed: 23807371]
          Dewan V, Lambert D, Edler J, Kymes S, Apte RS. CosteJectiveness analysis of ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema. Ophthalmology 2012;119(8):1679–84. Diabetic Retinopathy Clinical Research Network, [PMC free article: PMC3612959] [PubMed: 22503301]
          Elman MJ, Aiello LP, Beck RW, Bressler NM, Bressler SB, et al. Randomized trial evaluating ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema. Ophthalmology 2010;117(6):1064–77. [PMC free article: PMC2937272] [PubMed: 20427088]
          Elman MJ, Bressler NM, Qin H, Beck RW, Ferris FL 3rd, Friedman SM, et al. Expanded 2-year follow-up of ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema. Ophthalmology 2011;118(4):609–14. [PMC free article: PMC3096445] [PubMed: 21459214]
          Elman MJ, Qin H, Aiello LP, Beck RW, Bressler NM, Ferris FL, et al. Intravitreal ranibizumab for diabetic macular edema with prompt versus deferred laser treatment: three-year randomized trial results. Ophthalmology 2012;119(11):2312–8. [PMC free article: PMC3490003] [PubMed: 22999634]
        • DRCRnet 2015

          Diabetic Retinopathy Clinical Research Network, Wells JA, Glassman AR, Ayala AR, Jampol LM, Aiello LP, et al. Aflibercept, bevacizumab, or ranibizumab for diabetic macular edema. New England Journal of Medicine 2015;372(13):1193–203. [PMC free article: PMC4422053] [PubMed: 25692915]
          Wells JA, Glassman AR, Ayala AR, Jampol LM, Bressler NM, et al. Aflibercept, bevacizumab, or ranibizumab for diabetic macular edema: two-year results from a comparative eJectiveness randomized clinical trial. Ophthalmology 2016;123(6):1351–9. [PMC free article: PMC4877252] [PubMed: 26935357]
        • Ekinci 2014

          Ekinci M, Ceylan E, Cakici O, Tanyildiz B, Olcaysu O, Cagatay HH. Treatment of macular edema in diabetic retinopathy: Comparison of the eJicacy of intravitreal bevacizumab and ranibizumab injections. Expert Review of Ophthalmology 2014;9(2):139–43
        • Ishibashi 2014

          Ishibashi T, Yuzawa M, Yoshimura N, Ohji M, Ishida S, Isogawa N, et al. Japan phase 3 study of pegaptanib sodium in patients Anti-vascular endothelial growth factor for diabetic macular oedema: a network meta-analysis (Review) Copyright © 2018 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd. 38 For Preview Only Cochrane Library Trusted evidence. Informed decisions. Better health. Cochrane Database of Systematic Reviews with diabetic macular edema. Nippon Ganka Gakkai Zasshi 2014;118(9):773–82. [PubMed: 25318186]
        • Korobelnik 2014 (1)

          Korobelnik JF, Do DV, Schmidt-Erfurth U, Boyer DS, Holz FG, Heier JS, et al. Intravitreal aflibercept for diabetic macular edema. Ophthalmology 2014;121(11):2247–54. [PubMed: 25012934]
        • Li 2019

          Li X, Dai H, Li X, Han M, Li J, Suhner A, et al. EJicacy and safety of ranibizumab 0.5 mg in Chinese patients with visual impairment due to diabetic macular edema: results from the 12-month REFINE study. Graefe’s Archive for Clinical and Experimental Ophthalmology 2019;257(3):529–41. [PubMed: 30645696]
        • Liu 2022

          Liu K, Wang H, He W, Ye J, Song Y, Wang Y, et al. Intravitreal conbercept for diabetic macular oedema: 2-year results from a randomised controlled trial and open-label extension study. British Journal of Ophthalmology 2021 17 May [Epub Ahead of Print]. [DOI: 10.1136/bjophthalmol-2020-318690 [PMC free article: PMC9510409] [PubMed: 34001667] [CrossRef]
        • Prunte 2016

          Prünte C, Fajnkuchen F, Mahmood S, Ricci F, Hatz K, Studnička J, et al. Ranibizumab 0.5 mg treat-and-extend regimen for diabetic macular oedema: the RETAIN study. British Journal of Ophthalmology 2016;100(6):787–95. [PMC free article: PMC4893084] [PubMed: 26453639]
        • LUCIDATE 2014 (Comyn 2014)

          Comyn O, Sivaprasad S, Peto T, Neveu MM, Holder GE, Xing W, et al. A randomized trial to assess functional and structural eJects of ranibizumab versus laser in diabetic macular edema (the LUCIDATE study). American Journal of Ophthalmology 2014;157(5):960–70. [PubMed: 24531025]
        • Macugen 2005

          Cunningham ET Jr, Adamis AP, Altaweel M, Aiello LP, Bressler NM, D’Amico DJ, et al. A phase II randomized doublemasked trial of pegaptanib, an anti-vascular endothelial growth factor aptamer, for diabetic macular edema. Ophthalmology 2005;112(10):1747–57. [PubMed: 16154196]
        • Macugen 2011 (Sultan 2011)

          LoGus JV, Sultan MB, Pleil AM, Macugen 1013 Study Group. Changes in vision and health-related quality of life in patients with diabetic macular edema treated with pegaptanib sodium or sham. Investigative Ophthalmology and Visual Science 2011;52(10):7498–505. [PubMed: 21896838]
          * Sultan MB, Zhou D, LoGus J, Dombi T, Ice KS, Macugen 1013 Study Group. A phase 2/3, multicenter, randomized, doublemasked, 2-year trial of pegaptanib sodium for the treatment of diabetic macular edema. Ophthalmology 2011;118(6):1107–18 [PubMed: 21529957]
        • Nepomuceno 2013

          Nepomuceno AB, Takaki E, Paes de Almeida FP, Peroni R, Cardillo JA, Siqueira RC, et al. A prospective randomized trial of intravitreal bevacizumab versus ranibizumab for the management of diabetic macular edema. American Journal of Ophthalmology 2013;156(3):502–10 [PubMed: 23795985]
        • READ2 2009 (Nguyen 2009)

          Do DV, Nguyen QD, Khwaja AA, Channa R, Sepah YJ, Sophie R, et al. Ranibizumab for edema of the macula in diabetes study: 3- year outcomes and the need for prolonged frequent treatment. JAMA Ophthalmology 2013;131(2):139–45. [PubMed: 23544200]
          Nguyen QD, Shah SM, Heier JS, Do DV, Lim J, Boyer D, et al. Primary end point (six months) results of the ranibizumab for edema of the mAcula in diabetes (READ-2) study. Ophthalmology 2009;116(11):2175–81. [PubMed: 19700194]
          Nguyen QD, Shah SM, Khwaja AA, Channa R, Hatef E, Do DV, et al. Two-year outcomes of the ranibizumab for edema of the mAcula in diabetes (READ-2) study. Ophthalmology 2010;117(11):2146–51. [PubMed: 20855114]
        • RELATION 2012

          CRFB002DD13. A 12-month, two-armed, randomized, doublemasked, multicenter, phase IIIb study assessing the eJicacy and safety of laser photocoagulation as adjunctive to ranibizumab intravitreal injections vs. laser photocoagulation monotherapy in patients with visual impairment due to diabetic macular edema followed by a 12 month follow up period. Novartis clinical trial results database www​.novctrd.com/ctrdWebApp​/clinicaltrialrepository​/public/login.jsp (accessed 2 June 2014).
          NCT01131585. A 12-month, two-armed, randomized, doublemasked, multicenter, phase IIIb study assessing the eJicacy and safety of laser photocoagulation as adjunctive to ranibizumab intravitreal injections vs. laser photocoagulation monotherapy in patients with visual impairment due to diabetic macular edema followed by a 12 month follow up period. clinicaltrials.gov/show/NCT01131585 (first received 25 May 2010).
        • RESOLVE 2010 (Massin 2010)

          CRFB002D2201. A randomized, double-masked, multicenter, phase II study assessing the safety and eJicacy of two concentrations of ranibizumab (intravitreal injections) compared with non-treatment control for the treatment of diabetic macular edema with center involvement. Novartis clinical trial results database www​.novctrd.com/ctrdWebApp​/clinicaltrialrepository​/public/login.jsp (accessed 2 June 2014).
          Massin P, Bandello F, Garweg JG, Hansen LL, Harding SP, Larsen M, et al. Safety and eJicacy of ranibizumab in diabetic macular edema (RESOLVE Study): a 12-month, randomized, controlled, double-masked, multicenter phase II study. Diabetes Care 2010;33(11):2399–405 [PMC free article: PMC2963502] [PubMed: 20980427]
        • RESPOND 2013

          Berger A, Sheidow T, Li R, Rehel B, De Takacsy F, Courseau AS. A Canadian 12-month, phase IIIb study of ranibizumab combination or monotherapy in visual impairment due to diabetic macular edema: Preliminary analysis (“RESPOND”). In: 16th Annual Canadian Diabetes Association/Canadian Society of Endocrinology and Metabolism Professional Conference and Annual Meetings; 2013 Oct 17-19; Montreal. 2013. CRFB002DCA05.
          A Canadian 12-month, prospective, randomized, open-label, multicenter, phase IIIb study assessing the eJicacy, safety and cost of ranibizumab as combination and monotherapy in patients with visual impairment due to diabetic macular edema. Novartis clinical trial results database www​.novctrd.com/ctrdWebApp​/clinicaltrialrepository​/public/login.jsp (accessed 2 June 2014).
        • RESTORE 2011 (Mitchell 2011)

          Anonymous. Erratum: Intravitreal ranibizumab for diabetic macular edema with prompt versus deferred laser treatment: Three year randomized trial results (Ophthalmology 2012;119:2312-8). Ophthalmology 2014;121(3):805. [PMC free article: PMC3490003] [PubMed: 22999634]
          Lang GE, Berta A, Eldem BM, Simader C, Sharp D, Holz FG, et al. Two-year safety and eJicacy of ranibizumab 0.5 mg in diabetic macular edema: interim analysis of the RESTORE extension study. Ophthalmology 2013;120(10):2004–12. [PubMed: 23725735]
          Mitchell P, Annemans L, Gallagher M, Hasan R, Thomas S, Gairy K, et al. Cost-eJectiveness of ranibizumab in treatment of diabetic macular oedema (DME) causing visual impairment: evidence from the RESTORE trial. British Journal of Opthalmology 2012;96(5):688–93. [PMC free article: PMC3329632] [PubMed: 22399690]
          Mitchell P, Bandello F, Schmidt-Erfurth U, Lang GE, Massin P, Schlingemann RO, et al. The RESTORE study: ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema. Ophthalmology 2011;118(4):615–62. [PubMed: 21459215]
          Mitchell P, Bressler N, Tolley K, Gallagher M, Petrillo J, Ferreira A, et al. Patient-reported visual function outcomes improve aGer ranibizumab treatment in patients with vision impairment due to diabetic macular edema: randomized clinical trial. JAMA Ophthalmology 2013;131(10):1339–47. [PubMed: 23974915]
          Schmidt-Erfurth U, Lang GE, Holz FG, Schlingemann RO, Lanzetta P, Massin P, et al. Three-year outcomes of individualized ranibizumab treatment in patients with diabeticmacular edema: the RESTORE extension study. Ophthalmology2014;121(5):1045–53 [PubMed: 24491642]
        • REVEAL 2015 (Ishibashi 2015)

          Ishibashi T, Li X, Koh A, Lai TY, Lee FL, Lee WK, et al. The REVEAL Study: ranibizumab monotherapy or combined with laser versus laser monotherapy in asian patients with diabetic macular edema. Ophthalmology 2015;122(7):1402–15 [PubMed: 25983216]
        • RISE-RIDE (Nguyen 2012)

          Bressler NM, Varma R, Suñer IJ, Dolan CM, Ward J, Ehrlich JS, et al. Vision-related function aGer ranibizumab treatment for diabetic macular edema: results from RIDE and RISE. Ophthalmology 2014;121(12):2461–72. [PubMed: 25148789]
          Brown DM, Nguyen QD, Marcus DM, Boyer DS, Patel S, Feiner L, et al. Long-term outcomes of ranibizumab therapy for diabetic macular edema: the 36-month results from two phase III trials: RISE and RIDE. Ophthalmology 2013;120(10):2013–22. [PubMed: 23706949]
          Ip MS, Domalpally A, Hopkins JJ, Wong P, Ehrlich JS. Long-term eJects of ranibizumab on diabetic retinopathy severity and progression. Archives of Ophthalmology 2012;130(9):1145–52. [PubMed: 22965590]
          Mieler WF, Kim JE, Yau L, Ehrlich JS. Earlier treatment is important in diabetic macular edema: Outcomes from phase III trials of intravitreal ranibizumab. In: 73rd Scientific sessions of the American Diabetes Association; 2013 Jun 21-25; Chicago. 2013.
          Nguyen QD, Brown DM, Marcus DM, Boyer DS, Patel S, Feiner L, et al. Ranibizumab for diabetic macular edema: results from 2 phase III randomized trials: RISE and RIDE. Ophthalmology 2012;119(4):789–801 [PubMed: 22330964]
        • Soheilian 2007

          Soheilian M, Garfami KH, Ramezani A, Yaseri M, Peyman GA. Two-year results of a randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus laser in diabetic macular edema. Retina 2012;32(2):314–21. [PubMed: 22234244]
          Soheilian M, Ramezani A, Bijanzadeh B, Yaseri M, Ahmadieh H, Dehghan MH, et al. Intravitreal bevacizumab (avastin) injection alone or combined with triamcinolone versus macular photocoagulation as primary treatment of diabetic macular edema. Retina 2007;27(9):1187–95. [PubMed: 18046223]
          * Soheilian M, Ramezani A, Obudi A, Bijanzadeh B, Salehipour M, Yaseri M, et al. Randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus macular photocoagulation in diabetic macular edema. Ophthalmology 2009;116(6):1142–50 [PubMed: 19376585]
        • Turkoglu 2015

          Turkoglu EB, Celık E, Aksoy N, Bursalı O, Ucak T, Alagoz G. Changes in vision related quality of life in patients with diabetic macular edema: ranibizumab or laser treatment? Journal of Diabetes and its Complications 2015;29(4):540–3. [PubMed: 25817172]
        • Wykoff 2022

          WykoJ CC, Abreu F, Adamis AP, Basu K, Eichenbaum DA, Haskova Z, et al. EJicacy, durability, and safety of intravitreal faricimab withextended dosing up to every 16 weeks in patients withdiabetic macular oedema (YOSEMITE and RHINE):two randomised, double-masked, phase 3 trials. Lancet 2022;399(10326):741–55 [PubMed: 35085503]
        Included studies from Cochrane review: Rittiphairoj et al-2020
        • BEVORDEX 2014 {published data only}

          Alessandrello EM, Hodgson LA, McAuley AK, Fraser-Bell S, Gillies MC, Lim LL, et al. Retinal vascular calibre changes in the bevordex randomised clinical trial of intravitreal bevacizumab versus intravitreal dexamethasone for diabetic macular oedema. Clinical and Experimental Ophthalmology 2015;43:117–8.
          Cornish, E E, Teo, K Y C, Gillies, M C, Lim, L L, McAllister, I, Sanmugasundram, S, Nguyen, V, Wickremasinghe, S, Mehta, H, Fraser-Bell, S. Five year outcomes of the bevordex study (a multicenter randomized clinical trial of intravitreal bevacizumab versus intravitreal dexamethasone). Investigative Ophthalmology and Visual Science 2018;59(9).
          Gillies MC, Lim Ll, Campain A, Quin G, Salem W, Li J, et al. A randomized clinical trial of intravitreal bevacizumab versus intravitreal dexamethasone for diabetic macular edema: the BEVORDEX study. Ophthalmology 2014;121(12):2473–81. [PubMed: 25155371]
          Gillies MC, Lim Ll, Campain A, Quin G, Salem W, Li J, et al. BEVORDEX—a multicentre randomized clinical trial of intravitreal bevacizumab versus intravitreal dexamethasone for persistent diabetic macular oedema. Investigative Ophthalmology and Visual Science 2014;55(13):ARVO E-abstract 5053. [PubMed: 25155371]
        • Callanan 2017 {published data only}

          Callanan DG, Loewenstein A, Patel SS, Massin P, Corcóstegui B, Li XY, et al. A multicenter, 12-month randomized study comparing dexamethasone intravitreal implant with ranibizumab in patients with diabetic macular edema. Graefe’s Archive for Clinical and Experimental Ophthalmology 2017;255(3):463–73. [PubMed: 27632215]
        • DRCR​.net 2008 {published data only}

          Aiello LP, Edwards AR, Beck RW, Bressler NM, Davis MD, Ferris F, et al. Factors associated with improvement and worsening of visual acuity 2 years aQer focal/grid photocoagulation for diabetic macular edema. Ophthalmology 2010;117(5):946–53. [PMC free article: PMC2864322] [PubMed: 20122739]
          Bressler NM, Edwards AR, Beck RW, Flaxel CJ, Glassman AR, Ip MS, et al. Exploratory analysis of diabetic retinopathy progression through 3 years in a randomized clinical trial that compares intravitreal triamcinolone acetonide with focal/grid photocoagulation. Archives of Ophthalmology 2009;127(12):1566–71. [PMC free article: PMC2872985] [PubMed: 20008708]
          Diabetic Retinopathy Clinical Research Network. A randomized trial comparing intravitreal triamcinolone acetonide and focal/grid photocoagulation for diabetic macular edema. Ophthalmology 2008;115(9):1447–9. [PMC free article: PMC2748264] [PubMed: 18662829]
          Diabetic Retinopathy Clinical Research Network (DRCRnet), Beck RW, Edwards AR, Aiello LP, Bressler NM, Ferris F, Glassman AR, et al. Three-year follow-up of a randomized trial comparing focal/grid photocoagulation and intravitreal triamcinolone for diabetic macular edema. Archives of Ophthalmology 2009;127(3):245–51. [PMC free article: PMC2754047] [PubMed: 19273785]
          Ip MS, Bressler SB, Antoszyk AN, Flaxel CJ, Kim JE, Friedman SM, et al. A randomized trial comparing intravitreal triamcinolone and focal/grid photocoagulation for diabetic macular edema: baseline features. Retina 2008;28(7):919–30. [PMC free article: PMC2796075] [PubMed: 18698292]
          Ip MS. A randomized trial comparing intravitreal triamcinolone acetonide and laser photocoagulation for diabetic macular edema (DME): study design and baseline characteristics. Investigative Ophthalmology and Visual Science 2008:ARVO Eabstract 3468.
          Lauer AK, Bressler NM, Edwards AR, Diabetic Retinopathy Clinical Research Network. Frequency of intraocular pressure increase within days aQer intravitreal triamcinolone injections in the Diabetic Retinopathy Clinical Research Network. Archives of Ophthalmology 2011;129(8):1097–9. [PMC free article: PMC4164019] [PubMed: 21825200]
          WykoJ CC, Hariprasad SM. DRCR protocol-T: reconciling 1- and 2-year data for managing diabetic macular edema. Ophthalmic Surgery Lasers and Imaging Retina 2016;47(4):308–12. [PubMed: 27065368]
        • FAME 2011 {published data only}

          Campochiaro PA, Brown DM, Pearson A, Ciulla T, Boyer D, Holz FG, et al. Long-term benefit of sustained-delivery fluocinolone acetonide vitreous inserts for diabetic macular edema. Ophthalmology 2011;118(4):626–35. [PubMed: 21459216]
          Dempe C, Scholl S, Augustin A. Fluocinolone acetonide (FAc) intravitreal implants improve visual acuity in chronic diabetic macular edema (DME) for up to 36 months. In: Acta Ophthalmologica. Conference: 40th Nordic Congress of Ophthalmology, Helsinki, Finland. 2012.
        • Kriechbaum 2014 {published data only}

          Deak GG, Lammer J, Prager S, Mylonas G, Bolz M, Schmidt-Erfurth U. Refractive changes aQer pharmacologic resolution of diabetic macular edema. Ophthalmology 2014;121:1054–8. [PubMed: 24439462]
          Kriechbaum K, Prager S, Mylonas G, Scholda C, Rainer G, Funk M, et al. Intravitreal bevacizumab (Avastin) versus triamcinolone (Volon A) for treatment of diabetic macular edema: one-year results. Eye 2014;28(1):9–15. [PMC free article: PMC3890767] [PubMed: 24336297]
          Prager SG, Lammer J, Mitsch C, Hafner J, Pemp B, Scholda C, et al. Analysis of retinal layer thickness in diabetic macular oedema treated with ranibizumab or triamcinolone. Acta Ophthalmologica 2018;96:e195–200. [PubMed: 29063703]
        • Lim 2012 {published data only}

          Lim JW, Lee HK, Shin MC. Comparison of intravitreal bevacizumab alone or combined with triamcinolone versus triamcinolone in diabetic macular edema: a randomized clinical trial. Ophthalmologica 2012;227(2):100–6. [PubMed: 21997197]
        Included studies from Cochrane review: Mehta et al-2018
        • DRCRnet U 2018 {published data only}

          Maturi RK, Glassman AR, Liu D, Beck RW, Bhavsar AR, Bressler NM, et al. EFect of adding dexamethasone to continued ranibizumab treatment in patients with persistent diabetic macular edema: a DRCR network phase 2 randomized clinical trial. JAMA Ophthalmology 2018;136(1):29–38. [PMC free article: PMC5833605] [PubMed: 29127949]
          NCT01945866. Phase II combination steroid and anti-VEGF for persistent DME [Short-term evaluation of combination corticosteroid+anti-VEGF treatment for persistent central involved diabetic macular edema following anti-VEGF therapy]. clinicaltrials.gov/ct2/show/NCT01945866 (first received 19 September 2013).
        • Lim 2012 {published data only}

          Lim JW, Lee HK, Shin MC. Comparison of intravitreal bevacizumab alone or combined with triamcinolone versus triamcinolone in diabetic macular edema: a randomized clinical trial. Ophthalmologica 2012;227(2):100–6. [PubMed: 21997197]
        • Maturi 2015 {published and unpublished data}

          Maturi RK, Bleau L, Saunders J, Mubasher M, Stewart MW. A 12- month, single-masked, randomized controlled study of eyes with persistent diabetic macular edema aKer multiple anti-VEGF Injections to assess the Efficacy of the dexamethasone delayed delivery system as an adjunct to bevacizumab compared with continued bevacizumab monotherapy. Retina 2015;35(8):1604–14. [PubMed: 25829346]
        • Neto 2017 {published data only}

          NCT00737971. Efficacy study of triamcinolone and bevacizumab intravitreal for treatment of diabetic macular edema (ATEMD) [Multicenter, randomized clinical trial to assess the Effectiveness of intravitreal Injections of bevacizumab, triamcinolone, or their combination in the treatment of diabetic macular edema]. clinicaltrials.gov/ct2/show/NCT00737971 (first received 20 August 2008).
          Neto HO, Regatieri CV, Nobrega MJ, Muccioli C, Casella AM, Andrade RE, et al. Multicenter, randomized clinical trial to assess the eFectiveness of intravitreal injections of bevacizumab, triamcinolone, or their combination in the treatment of diabetic macular edema. Ophthalmic Surgery, Lasers and Imaging Retina 2017;48(9):734–40. [PubMed: 28902334]
        • Riazi-Esfahani 2017 {published data only}

          Riazi-Esfahani M, Riazi-Esfahani H, Ahmadraji A, Karkhaneh R, Mahmoudi A, Roohipoor R, et al. Intravitreal bevacizumab alone or combined with 1 mg triamcinolone in diabetic macular edema: a randomized clinical trial. International Ophthalmology 2017;37:1–14. [PubMed: 28349504]
        • Shoeibi 2013 {published data only}

          Ahmadieh H, Ramezani A, Shoeibi N, Bijanzadeh B, Tabatabaei A, Azarmina M, et al. Intravitreal bevacizumab with or without triamcinolone for refractory diabetic macular edema; a placebo-controlled, randomized clinical trial. Graefe’s Archive for Clinical and Experimental Ophthalmology 2008;246(4):483–9. [PubMed: 17917738]
          Shoeibi N, Ahmadieh H, Entezari M, Yaseri M. Intravitreal bevacizumab with or without triamcinolone for refractory diabetic macular edema: long-term results of a clinical trial. Journal of Ophthalmic and Vision Research 2013;8(2):99–106. [PMC free article: PMC3740475] [PubMed: 23943683]
        • Soheilian 2012 {published data only}

          Soheilian M, Garfami KH, Ramezani A, Yaseri M, Peyman GA. Two-year results of a randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus laser in diabetic macular edema. Retina 2012;32(2):314–21. [PubMed: 22234244]
          Soheilian M, Ramezani A, Obudi A, Bijanzadeh B, Salehipour M, Yaseri M, et al. Randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus macular photocoagulation in diabetic macular edema. Ophthalmology 2009;116(6):1142–50. [PubMed: 19376585]
          Yaseri M, Zeraati H, Mohammad K, Soheilian M, Ramezani A, Eslani M, et al. Intravitreal bevacizumab injection alone or combined with triamcinolone versus macular photocoagulation in bilateral diabetic macular edema; application of bivariate generalized linear mixed model with asymmetric random Effects in a subgroup of a clinical trial. Journal of Ophthalmic and Vision Research 2014;9(4):453–60. [PMC free article: PMC4329706] [PubMed: 25709771]
        • Synek 2011 {published data only}

          Synek S, Vesely P. Intravitreal Bevacizumab with or without triamcinolone for refractory diabetic macular oedema. Collegium Antropologicum 2011;35(3):841–5. [PubMed: 22053565]
        Included studies from Cochrane review: Jorge et al-2018
        • B Bandello 2005 {published data only}

          Bandello F, Polito A, Del Borrello M, Zemella N, Isola M. “Light” versus “classic” laser treatment for clinically significant diabetic macular oedema. British Journal of Ophthalmology 2005;89(7):864–70. [PMC free article: PMC1772712] [PubMed: 15965168]
        • Blankenship 1979 {published data only}

          Blankenship GW. Diabetic macular edema and argon laser photocoagulation: a prospective randomized study. Ophthalmology 1979;86(1):69–78. [PubMed: 530565]
        • Casson 2012 {published data only}

          Casson RJ, Raymond G, Newland HS, Gilhotra JS, Gray TL. Pilot randomized trial of a nanopulse retinal laser versus conventional photocoagulation for the treatment of diabetic macular oedema. Clinical and Experimental Ophthalmology 2012;40(6):604–10. [PubMed: 22300292]
        • Casswell 1990 {published data only}

          Casswell AG, Canning CR, Gregor ZJ. Treatment of diNuse diabetic macular oedema: a comparison between argon and krypton lasers. Eye 1990;4(Pt 5):668–72. [PubMed: 2282940]
        • DRCRNET 2007 {published data only}

          Browning DJ, Apte RS, Bressler SB, Chalam KV, Danis RP, Davis MD, et al. Association of the extent of diabetic macular edema as assessed by optical coherence tomography with visual acuity and retinal outcome variables. Retina 2009;29(3):300–5. [PMC free article: PMC2657814] [PubMed: 19174719]
          Writing Committee for the Diabetic Retinopathy Clinical Research Network, Fong DS, Strauber SF, Aiello LP, Beck RW, Callanan DG, et al. Comparison of the modified Early Treatment Diabetic Retinopathy Study and mild macular grid laser photocoagulation strategies for diabetic macular edema. Archives of Ophthalmology 2007;125(4):469–80. [PMC free article: PMC2536574] [PubMed: 17420366]
        • ETDRS 1985 {published data only}

          Anonymous. Early photocoagulation for diabetic retinopathy. ETDRS report number 9. Early Treatment Diabetic Retinopathy Study Research group. Ophthalmology 1991;98(5 Suppl):766–85. [PubMed: 2062512]
          Anonymous. Focal photocoagulation treatment of diabetic macular edema. Relationship of treatment eNect to fluorescein angiographic and other retinal characteristics at baseline: ETDRS report no. 19. Early Treatment Diabetic Retinopathy Study Research Group. Archives of Ophthalmology 1995;113(9):1144–55. [PubMed: 7661748]
          Anonymous. Photocoagulation for diabetic macular edema. Early Treatment Diabetic Retinopathy Study Report No. 4. Early Treatment Diabetic Retinopathy Research group. International Ophthalmology Clinics 1987;27(4):265–72. [PubMed: 3692708]
          Anonymous. Photocoagulation for diabetic macular edema. Early Treatment Diabetic Retinopathy Study report number 1. Early Treatment Diabetic Retinopathy Study research group. Archives of Ophthalmology 1985;103(12):1796–806. [PubMed: 2866759]
        • Figueira 2009 {published data only}

          Figueira J, Khan J, Nunes S, Sivaprasad S, Rosa A, de Abreu JF, et al. Prospective randomised controlled trial comparing sub-threshold micropulse diode laser photocoagulation and conventional green laser for clinically significant diabetic macular oedema. British Journal of Ophthalmology 2009;93(10):1341–4. [PubMed: 19054831]
        • Freyler 1990 {published data only}

          Freyler H. Laser therapy of diabetic maculopathy. A comparative study of the argon green laser and dye red laser. Klinische Monatsblätter für Augenheilkunde 1990;197(2):176–81. [PubMed: 2243481]
        • Ladas 1993 {published data only}

          Ladas ID, Theodossiadis GP. Long-term eNectiveness of modified grid laser photocoagulation for diNuse diabetic macular edema. Acta Ophthalmologica 1993;71(3):393–7. [PubMed: 8362641]
        • Laursen 2004 {published data only}

          Laursen ML, Moeller F, Sander B, Sjoelie AK. Subthreshold micropulse diode laser treatment in diabetic macular oedema. British Journal of Ophthalmology 2004;88(9):1173–9. [PMC free article: PMC1772323] [PubMed: 15317711]
        • Lavinsky 2011 {published data only}

          Lavinsky D, Cardillo JA, Melo LA Jr, Dare A, Farah ME, Belfort R Jr. Randomized clinical trial evaluating mETDRS versus normal or high-density micropulse photocoagulation for diabetic macular edema. Investigative Ophthalmology and Visual Science 2011;52(7):4314–23. [PubMed: 21345996]
        • Olk 1986 {published data only}

          Olk RJ. Modified grid argon (blue-green) laser photocoagulation for diNuse diabetic macular edema. Ophthalmology 1986;93(7):938–50. [PubMed: 3763140]
        • Olk 1990 {published data only}

          Olk, RJ. Argon green (514 nm) versus krypton red (647 nm) modified grid laser photocoagulation for diNuse diabetic macular edema. Ophthalmology 1990;97(9):1101–12. [PubMed: 2234840]
        • Pei-Pei 2015 {published data only}

          Pei-Pei W, Shi-Zhou H, Zhen T, Lin L, Ying L, Jiexiong O. Randomised clinical trial evaluating best-corrected visual acuityandello 2005 [PMC free article: PMC4366477] [PubMed: 25697457]
        • Tewari 1998 {published data only}

          Tewari HK, Gupta V, Kumar A, Verma L. ENicacy of diode laser for managing diabetic macular oedema. Acta Ophthalmologica Scandinavica 1998;76(3):363–6. [PubMed: 9686856]
        • Venkatesh 2011 {published data only}

          Venkatesh P, Ramanjulu R, Azad R, Vohra R, Garg S. Subthreshold micropulse diode laser and double frequency neodymium: YAG laser in treatment of diabetic macular edema: a prospective, randomized study using multifocal electroretinography. Photomedicine and Laser Surgery 2011;29(11):727–33. [PubMed: 21612513]
        • Vujosevic 2010 {published data only}

          Vujosevic S, Bottega E, Casciano M, Pilotto E, Convento E, Midena E. Microperimetry and fundus autofluorescence in diabetic macular edema: subthreshold micropulse diode laser versus modified early treatment diabetic retinopathy study laser photocoagulation. Retina 2010;30(6):908–16. [PubMed: 20168272]
        • Xie 2013 {published data only}

          Xie TY, Guo QQ, Wang Y, Wang Q, Chen XY. Randomized, controlled clinical trial comparison of SDM laser versus argon ion laser in diabetic macular edema [阈下微脉冲激光与氩离 ⼦激光治疗糖尿病性⻩斑⽔肿的临床随机对照研究(英⽂)]. International Eye Science 2013;13(12):2370–2.
    1.1.14.2. Economic
    • Brown, Gary C, Brown, Melissa M, Turpcu, Adam et al. (2015) The Cost-Effectiveness of Ranibizumab for the Treatment of Diabetic Macular Edema. Ophthalmology 122(7): 1416–25 [PubMed: 25935787]
    • Haig, Jennifer; Barbeau, Martin; Ferreira, Alberto (2016) Cost-effectiveness of ranibizumab in the treatment of visual impairment due to diabetic macular edema. Journal of medical economics 19(7): 663–71 [PubMed: 26882365]
    • Holekamp, Nancy, Duff, Steven B, Rajput, Yamina et al. (2020) Cost-effectiveness of ranibizumab and aflibercept to treat diabetic macular edema from a US perspective: analysis of 2-year Protocol T data. Journal of medical economics 23(3): 287–296 [PubMed: 31502893]
    • Hutton, D.W., Glassman, A.R., Liu, D. et al. (2023) Cost-effectiveness of Aflibercept Monotherapy vs Bevacizumab First Followed by Aflibercept If Needed for Diabetic Macular Edema. JAMA ophthalmology [PMC free article: PMC9896372] [PubMed: 36729431]
    • Lois, Noemi, Campbell, Christina, Waugh, Norman et al. (2022) Standard threshold laser versus subthreshold micropulse laser for adults with diabetic macular oedema: the DIAMONDS non-inferiority RCT. Health technology assessment (Winchester, England) 26(50): 1–86 [PMC free article: PMC9791463] [PubMed: 36541393]
    • Mitchell, Paul, Annemans, Lieven, Gallagher, Meghan et al. (2012) Cost-effectiveness of ranibizumab in treatment of diabetic macular oedema (DME) causing visual impairment: evidence from the RESTORE trial. The British journal of ophthalmology 96(5): 688–93 [PMC free article: PMC3329632] [PubMed: 22399690]
    • Pochopien, Michal, Beiderbeck, Annette, McEwan, Phil et al. (2019) Cost-effectiveness of fluocinolone acetonide implant (ILUVIEN R) in UK patients with chronic diabetic macular oedema considered insufficiently responsive to available therapies. BMC health services research 19(1): 22 [PMC free article: PMC6327492] [PubMed: 30626376]
    • Regnier, S.A., Malcolm, W., Haig, J. et al. (2015) Cost-effectiveness of ranibizumab versus aflibercept in the treatment of visual impairment due to diabetic macular edema: A UK healthcare perspective. ClinicoEconomics and Outcomes Research 7: 235–247 [PMC free article: PMC4427067] [PubMed: 25999748]
    • Sharma, S, Brown, G C, Brown, M et al. (2000) The cost-effectiveness of grid laser photocoagulation for the treatment of diabetic macular edema: results of a patient-based cost-utility analysis. Current opinion in ophthalmology 11(3): 175–9 [PubMed: 10977223]
    • Stein, Joshua D, Newman-Casey, Paula Anne, Kim, David D et al. (2013) Cost-effectiveness of various interventions for newly diagnosed diabetic macular edema. Ophthalmology 120(9): 1835–42 [PMC free article: PMC3737388] [PubMed: 23642372]
    1.1.14.3. Other
    • National Institute for Health and care Excellence (NICE). British National Formulary (BNF). Published 2023. Accessed February, 2023. https://bnf​.nice.org.uk/
    • National Institute for Health and Care Excellence (NICE). TA824: Dexamethasone intravitreal implant for treating diabetic macular oedema. 2022. Available from: https://www​.nice.org.uk/guidance/ta824
    • Czoski-Murray, C., Carlton, J., Brazier, J., Young, T., Papo, N. L., & Kang, H. K. (2009). Valuing condition-specific health states using simulation contact lenses. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research, 12(5), 793–799. 10.1111/j.1524-4733.2009.00527.x [PubMed: 19490557] [CrossRef]

Appendices

Appendix B. Literature search strategies

Search design and peer review

NICE information specialists conducted the literature searches for the evidence review. The searches were run in October 2022. Update searches were run in Feb 2023. This search report is compliant with the requirements of PRISMA-S.

The MEDLINE strategy below was quality assured (QA) by a trained NICE information specialist. All translated search strategies were peer reviewed to ensure their accuracy. Both procedures were adapted from the 2016 PRESS Checklist.

The principal search strategy was developed in MEDLINE (Ovid interface) and adapted, as appropriate, for use in the other sources listed in the protocol, taking into account their size, search functionality and subject coverage.

Review Management

The search results were managed in EPPI-Reviewer v5. Duplicates were removed in EPPI-R5 using a two-step process. First, automated deduplication is performed using a high-value algorithm. Second, manual deduplication is used to assess ‘low-probability’ matches. All decisions made for the review can be accessed via the deduplication history.

Limits and restrictions

English language limits were applied in adherence to standard NICE practice and the review protocol.

Limits to exclude, conference abstract or conference paper or “conference review” were applied in adherence to standard NICE practice and the review protocol. The limit to remove animal studies in the searches was the standard NICE practice, which has been adapted from: Dickersin, K., Scherer, R., & Lefebvre, C. (1994). Systematic Reviews: Identifying relevant studies for systematic reviews. BMJ, 309(6964), 1286. [PMC free article: PMC2541778] [PubMed: 7718048]

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Limits and restrictions

English language limits were applied in adherence to standard NICE practice and the review protocol.

Limits to exclude, comment or letter or editorial or historical articles or conference abstract or conference paper or “conference review” or letter or case report were applied in adherence to standard NICE practice and the review protocol.

The limit to remove animal studies in the searches was the standard NICE practice, which has been adapted from: Dickersin, K., Scherer, R., & Lefebvre, C. (1994). Systematic Reviews: Identifying relevant studies for systematic reviews. BMJ, 309(6964), 1286. [PMC free article: PMC2541778] [PubMed: 7718048]

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Appendix C. Effectiveness evidence study selection

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Appendix D. Effectiveness evidence

D.1. NICE additional studies (PDF, 337K)

D.2. Cochrane Systematic Reviews (PDF, 181K)

Appendix F. GRADE Tables

F.1. Network meta-analyses (PDF, 157K)

F.2. Pairwise meta-analysis (PDF, 436K)

Appendix G. Economic evidence study selection

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Appendix H. Economic evidence tables

Table 128. Economic evidence table (PDF, 342K)

Table 129. Economic evaluation checklist (PDF, 360K)

Appendix I. Health economic model

A de novo economic analysis was conducted for this review question and is detailed in the economic model report for review G.

Appendix J. Excluded studies

Clinical evidence

StudyReason for exclusion
Ahmadieh, H, Shoeibi, N, Entezari, S et al. (2008) Intravitreal Bevacizumab With or Without Triamcinolone for Refractory Diabetic Macular Edema: long-term Results of a Clinical Trial. American academy of ophthalmology: 262 [PMC free article: PMC3740475] [PubMed: 23943683] - people with Refractory Diabetic Macular Edema
Ahmadieh, Hamid, Ramezani, Alireza, Shoeibi, Nasser et al. (2008) Intravitreal bevacizumab with or without triamcinolone for refractory diabetic macular edema; a placebo-controlled, randomized clinical trial. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 246(4): 483–9 [PubMed: 17917738] - study included in cochrane review
Anonymous. (2018) Erratum: Persistent macular thickening following intravitreous aflibercept, bevacizumab, or ranibizumab for central-involved diabetic macular edema with vision impairment: A secondary analysis of a randomized clinical trial (JAMA Ophthalmology (2018) 136:3 (257-269) DOI: 10.1001/jamaophthalmol.2017.6565). JAMA Ophthalmology 136(5): 601 [PMC free article: PMC5885906] [PubMed: 29392288] - Secondary publication of an included study that does not provide any additional relevant information
Arevalo, J Fernando, Fromow-Guerra, Jans, Quiroz-Mercado, Hugo et al. (2007) Primary intravitreal bevacizumab (Avastin) for diabetic macular edema: results from the Pan-American Collaborative Retina Study Group at 6-month follow-up. Ophthalmology 114(4): 743–50 [PubMed: 17398322] - study included in cochrane review
Aroney, Christine, Fraser-Bell, Samantha, Lamoureux, Ecosse L et al. (2016) Vision-Related Quality of Life Outcomes in the BEVORDEX Study: A Clinical Trial Comparing Ozurdex Sustained Release Dexamethasone Intravitreal Implant and Bevacizumab Treatment for Diabetic Macular Edema. Investigative ophthalmology & visual science 57(13): 5541–5546 [PubMed: 27768792] - study included in cochrane review
Augustin, Albert J, Kuppermann, Baruch D, Lanzetta, Paolo et al. (2015) Dexamethasone intravitreal implant in previously treated patients with diabetic macular edema: subgroup analysis of the MEAD study. BMC ophthalmology 15: 150 [PMC free article: PMC4628378] [PubMed: 26519345] - Secondary publication of an included study that does not provide any additional relevant information
Bahrami, Bobak, Hong, Thomas, Zhu, Meidong et al. (2017) Switching therapy from bevacizumab to aflibercept for the management of persistent diabetic macular edema. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 255(6): 1133–1140 [PubMed: 28238195] - Comparator in study does not match that specified in protocol
Baker, Carl W, Glassman, Adam R, Beaulieu, Wesley T et al. (2019) Effect of Initial Management With Aflibercept vs Laser Photocoagulation vs Observation on Vision Loss Among Patients With Diabetic Macular Edema Involving the Center of the Macula and Good Visual Acuity: A Randomized Clinical Trial. JAMA 321(19): 1880–1894 [PMC free article: PMC6537845] [PubMed: 31037289] - study included in cochrane review
Bandello, F, Polito, A, Dimastrogiovanni, A et al. (2005) Intravitreal Triamcinolone Associated with Grid Laser Photocoagulation for Diffuse Diabetic Macular Edema. The macula society: 196 - study included in cochrane review
Bertelmann, Thomas, Feltgen, Nicolas, Scheffler, Martin et al. (2016) Vision-related quality of life in patients receiving intravitreal ranibizumab injections in routine clinical practice: baseline data from the German OCEAN study. Health and quality of life outcomes 14(1): 132 [PMC free article: PMC5029004] [PubMed: 27644469] - Secondary publication of an included study that does not provide any additional relevant information
Bodla, A.A. and Bodla, M.A. (2017) A prospective, randomized, interventional study comparing treatment modalities for diffuse diabetic macular oedema: Bevacizumab and bevacizumab combined with macular grid - A prospective single centre study. Medical Forum Monthly 28(2): 103–107 - people with Refractory Diabetic Macular Edema
Bordon, AF, Kuczmainski, JF, Gelmini, A et al. (2006) Photocoagulation versus 8 mg Intravitreous Trimcinolone Acetate (TAAC) for Diabetic Clinical Significant Macular Edema (CSME): a Prospective Study. IOVS 47: ARVO E-abstract 3844 - Comparator in study does not match that specified in protocol
Bressler, Neil M, Beaulieu, Wesley T, Glassman, Adam R et al. (2018) Persistent Macular Thickening Following Intravitreous Aflibercept, Bevacizumab, or Ranibizumab for Central-Involved Diabetic Macular Edema With Vision Impairment: A Secondary Analysis of a Randomized Clinical Trial. JAMA ophthalmology 136(3): 257–269 [PMC free article: PMC5885906] [PubMed: 29392288] - study included in cochrane review
Brown, David M, Boyer, David S, Csaky, Karl et al. (2022) INTRAVITREAL NESVACUMAB (ANTIANGIOPOIETIN 2) PLUS AFLIBERCEPT IN DIABETIC MACULAR EDEMA: Phase 2 RUBY Randomized Trial. Retina (Philadelphia, Pa.) 42(6): 1111–1120 [PMC free article: PMC9112959] [PubMed: 35234673] - study included in cochrane review
Brown, David M, Emanuelli, Andres, Bandello, Francesco et al. (2022) KESTREL and KITE: 52-Week Results From Two Phase III Pivotal Trials of Brolucizumab for Diabetic Macular Edema. American journal of ophthalmology 238: 157–172 [PubMed: 35038415] - Secondary publication of an included study that does not provide any additional relevant information
Brown, David M, Nguyen, Quan Dong, Marcus, Dennis M et al. (2013) Long-term outcomes of ranibizumab therapy for diabetic macular edema: the 36-month results from two phase III trials: RISE and RIDE. Ophthalmology 120(10): 2013–22 [PubMed: 23706949] - Secondary publication of an included study that does not provide any additional relevant information
Brown, David M, Schmidt-Erfurth, Ursula, Do, Diana V et al. (2015) Intravitreal Aflibercept for Diabetic Macular Edema: 100-Week Results From the VISTA and VIVID Studies. Ophthalmology 122(10): 2044–52 [PubMed: 26198808] - study included in cochrane review
Callanan, David G, Loewenstein, Anat, Patel, Sunil S et al. (2017) A multicenter, 12-month randomized study comparing dexamethasone intravitreal implant with ranibizumab in patients with diabetic macular edema. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 255(3): 463–473 [PubMed: 27632215] - study included in cochrane review
Chakrabarti, M, Chakrabarti, A, Stephen, V et al. (2008) Intravitreal Monotherapy With Bevacizumab and Triamcinolone Acetonide vs. Combination Therapy for Recalcitrant Diabetic Macular Edema. American academy of ophthalmology: 263 - Secondary publication of an included study that does not provide any additional relevant information
Chatzirallis, Alexandros, Theodossiadis, Panagiotis, Droutsas, Konstantinos et al. (2020) Ranibizumab versus aflibercept for diabetic macular edema: 18-month results of a comparative, prospective, randomized study and multivariate analysis of visual outcome predictors. Cutaneous and ocular toxicology 39(4): 317–322 [PubMed: 32722955] - Secondary publication of an included study that does not provide any additional relevant information
Chen, Guohai, Li, Wensheng, Tzekov, Radouil et al. (2014) Ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema: a meta-analysis of randomized controlled trials. PloS one 9(12): e115797 [PMC free article: PMC4277392] [PubMed: 25541937] - Secondary publication of an included study that does not provide any additional relevant information
Cheung, Ning; Wong, Ian Y; Wong, Tien Y (2014) Ocular anti-VEGF therapy for diabetic retinopathy: overview of clinical efficacy and evolving applications. Diabetes care 37(4): 900–5 [PubMed: 24652721] - population with age-related macular degeneration
Cho, Hee Yoon, Kang, Se Woong, Kim, Yun Taek et al. (2012) A three-year follow-up of intravitreal triamcinolone acetonide injection and macular laser photocoagulation for diffuse diabetic macular edema. Korean journal of ophthalmology : KJO 26(5): 362–8 [PMC free article: PMC3464320] [PubMed: 23060723] - Comparator in study does not match that specified in protocol
CRFB002DCA05 (2014) A Canadian 12-month, prospective, randomized, open-label, multicenter, phase IIIb study assessing the efficacy, safety and cost of ranibizumab as combination and monotherapy in patients with visual impairment due to diabetic macular edema. Novartis clinical trial results database www​.novctrd.com/ctrdwebapp​/clinicaltrialrepository​/public/login.jsp - Secondary publication of an included study that does not provide any additional relevant information
CRFB002DD13 (2014) A 12-month, two-armed, randomized, double-masked, multicenter, phase IIIb study assessing the efficacy and safety of laser photocoagulation as adjunctive to ranibizumab intravitreal injections vs. laser photocoagulation monotherapy in patients with visual impairment due to diabetic macular edema followed by a 12 month follow up period. Novartis clinical trial results database www​.novctrd.com/ctrdwebapp​/clinicaltrialrepository​/public/login.jsp - study included in cochrane review
Cunningham, Emmett T Jr, Adamis, Anthony P, Altaweel, Michael et al. (2005) A phase II randomized double-masked trial of pegaptanib, an anti-vascular endothelial growth factor aptamer, for diabetic macular edema. Ophthalmology 112(10): 1747–57 [PubMed: 16154196] - Secondary publication of an included study that does not provide any additional relevant information
Dehghan, Mohammad H, Ahmadieh, Hamid, Ramezani, Alireza et al. (2008) A randomized, placebo-controlled clinical trial of intravitreal triamcinolone for refractory diabetic macular edema. International ophthalmology 28(1): 7–17 [PubMed: 17589809] - Secondary publication of an included study that does not provide any additional relevant information
Diabetic Retinopathy Clinical Research Network, (DRCR​.net), Beck, Roy W, Edwards, Allison R et al. (2009) Three-year follow-up of a randomized trial comparing focal/grid photocoagulation and intravitreal triamcinolone for diabetic macular edema. Archives of ophthalmology (Chicago, Ill. : 1960) 127(3): 245–51 [PMC free article: PMC2754047] [PubMed: 19273785] - study included in cochrane review
Diabetic Retinopathy Clinical Research, Network (2008) A randomized trial comparing intravitreal triamcinolone acetonide and focal/grid photocoagulation for diabetic macular edema. Ophthalmology 115(9): 1447–10 [PMC free article: PMC2748264] [PubMed: 18662829] - study included in cochrane review
Diabetic Retinopathy Clinical Research, Network, Googe, Joseph, Brucker, Alexander J et al. (2011) Randomized trial evaluating short-term effects of intravitreal ranibizumab or triamcinolone acetonide on macular edema after focal/grid laser for diabetic macular edema in eyes also receiving panretinal photocoagulation. Retina (Philadelphia, Pa.) 31(6): 1009–27 [PMC free article: PMC3489032] [PubMed: 21394052] - study included in cochrane review
Diabetic Retinopathy Clinical Research, Network, Scott, Ingrid U, Edwards, Allison R et al. (2007) A phase II randomized clinical trial of intravitreal bevacizumab for diabetic macular edema. Ophthalmology 114(10): 1860–7 [PMC free article: PMC2245885] [PubMed: 17698196] - Secondary publication of an included study that does not provide any additional relevant information
Diabetic Retinopathy Clinical Research, Network, Wells, John A, Glassman, Adam R et al. (2015) Aflibercept, bevacizumab, or ranibizumab for diabetic macular edema. The New England journal of medicine 372(13): 1193–203 [PMC free article: PMC4422053] [PubMed: 25692915] - study included in cochrane review
Do, Diana V, Nguyen, Quan Dong, Vitti, Robert et al. (2016) Intravitreal Aflibercept Injection in Diabetic Macular Edema Patients with and without Prior Anti-Vascular Endothelial Growth Factor Treatment: Outcomes from the Phase 3 Program. Ophthalmology 123(4): 850–7 [PubMed: 26832658] - Secondary publication of an included study that does not provide any additional relevant information
Dugel, P.U., Hillenkamp, J., Sivaprasad, S. et al. (2016) Baseline visual acuity strongly predicts visual acuity gain in patients with diabetic macular edema following anti-vascular endothelial growth factor treatment across trials. Clinical Ophthalmology 10: 1103–1110 [PMC free article: PMC4913960] [PubMed: 27366049] - Retrospective cohort
Ehlers, J.P., Wang, K., Singh, R.P. et al. (2018) A Prospective Randomized Comparative Dosing Trial of Ranibizumab in Bevacizumab-Resistant Diabetic Macular Edema: The REACT Study. Ophthalmology Retina 2(3): 217–224 [PMC free article: PMC5839652] [PubMed: 29527585] - Comparator in study does not match that specified in protocol
Ertan, Elif; Duman, Rahmi; Duman, Resat (2020) Comparison of pain during intravitreal dexamethasone, ranibizumab and aflibercept injection. Clinical & experimental optometry 103(5): 630–633 [PubMed: 31691370] - study included in cochrane review
Escobar-Barranco, JJ; Pina-Marin, B; Fernandez-Bonet, M (2015) Dexamethasone implants in patients with naive or refractory diffuse diabetic macular edema. Ophthalmologica. Journal international d’ophtalmologie [International journal of ophthalmology] 233: 176–185 [PubMed: 25661239] - people with Refractory Diabetic Macular Edema
Faghihi, H, Roohipoor, R, Mohammadi, S-F et al. (2008) Intravitreal bevacizumab versus combined bevacizumab-triamcinolone versus macular laser photocoagulation in diabetic macular edema. European journal of ophthalmology 18(6): 941–8 [PubMed: 18988166] - study included in cochrane review
Fazel, F., Oliya, B., Mirmohammadkhani, M. et al. (2020) Intravitreal injections of bevacizumab plus methotrexate versus bevacizumab alone for the treatment of diabetic macular edema: A randomized, sham-controlled trial. Journal of Current Ophthalmology 32(2): 164–169 [PMC free article: PMC7337024] [PubMed: 32671300] - Secondary publication of an included study that does not provide any additional relevant information
Fortin P, Mintzes B, Innes M (2012) A systematic review of intravitreal bevacizumab for the treatment of diabetic macular edema. Ottawa: Canadian Agency for Drugs and Technologies in Health (CADTH) [PubMed: 24279000] - Secondary publication of an included study that does not provide any additional relevant information
Gardner, TW (2011) The restore study: ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema. Evidence-based ophthalmology 12(4): 206–207 [PubMed: 21459215] - Secondary publication of an included study that does not provide any additional relevant information
Garweg, Justus G, Stefanickova, Jana, Hoyng, Carel et al. (2019) Vision-Related Quality of Life in Patients with Diabetic Macular Edema Treated with Intravitreal Aflibercept: The AQUA Study. Ophthalmology. Retina 3(7): 567–575 [PubMed: 31080168] - Secondary publication of an included study that does not provide any additional relevant information
Gillies, Mark C, McAllister, Ian L, Zhu, Meidong et al. (2011) Intravitreal triamcinolone prior to laser treatment of diabetic macular edema: 24-month results of a randomized controlled trial. Ophthalmology 118(5): 866–72 [PubMed: 21232801] - study included in cochrane review
Gillies, Mark C, Sutter, Florian K P, Simpson, Judy M et al. (2006) Intravitreal triamcinolone for refractory diabetic macular edema: two-year results of a double-masked, placebo-controlled, randomized clinical trial. Ophthalmology 113(9): 1533–8 [PubMed: 16828501] - Secondary publication of an included study that does not provide any additional relevant information
Gillies, MC (2008) Intravitreal Triamcinolone for Refractory Diabetic Macular Oedema: 5-Year Results of a Double-Masked, Placebo-Controlled, Randomised Clinical Trial With Open Label Extension. IOVS: ARVO E- abstract 1565 [PubMed: 16828501] - Does not contain correct population
Giocanti-Auregan, A., Hrarat, L., Qu, L.M. et al. (2017) Functional and anatomical outcomes in patients with serous retinal detachment in diabetic macular edema treated with ranibizumab. Investigative Ophthalmology and Visual Science 58(2): 797–800 [PubMed: 28152140] - Retrospective cohort
Glassman, Adam R, Wells, John A 3rd, Josic, Kristin et al. (2020) Five-Year Outcomes after Initial Aflibercept, Bevacizumab, or Ranibizumab Treatment for Diabetic Macular Edema (Protocol T Extension Study). Ophthalmology 127(9): 1201–1210 [PMC free article: PMC7483366] [PubMed: 32402554] - study included in cochrane review
Goodart, RA, Faber, DW, Mehr, DS et al. (2007) Lucentis in the Treatment of Macular Edema (LIME): a Phase II Study Evaluating the Safety and Efficacy of Ranibizumab versus Focal Laser Treatment in Patients With Diabetic Macular Edema. IOVS 48: ARVO E-Abstract 1431 - More recent systematic review included that covers the same topic
Granstam, Elisabet, Rosenblad, Andreas, Modher Raghib, Aseel et al. (2020) Long-term follow-up of antivascular endothelial growth factor treatment for diabetic macular oedema: a four-year real-world study. Acta ophthalmologica 98(4): 360–367 [PubMed: 31656056] - Retrospective cohort
Granstrom, Therese, Forsman, Henrietta, Lindholm Olinder, Anna et al. (2016) Patient-reported outcomes and visual acuity after 12months of anti-VEGF-treatment for sight-threatening diabetic macular edema in a real world setting. Diabetes research and clinical practice 121: 157–165 [PubMed: 27718374] - Retrospective cohort
Greigorian, R A, Zarbin, M A, Brimacombe, M et al. (2004) Comparison of subthreshold micropulse diode laser photocoagulation with conventional laser photocoagulation for clinically significant macular edema in diabetic patients. IOVS 45: ARVO E-abstract 4067 - Comparator in study does not match that specified in protocol
Habib, Ahmed E, Abdel-Kader, Ahmed A, Eissa, Iman M et al. (2019) Adherence to Intravitreal Anti-Vascular Endothelial Growth Factor (Anti-VEGF) Drugs in Diabetic Macular Edema in an Egyptian Population: A Health Belief Model. Current eye research 44(3): 303–310 [PubMed: 30383436] - Retrospective cohort
Heier, Jeffrey S, Bressler, Neil M, Avery, Robert L et al. (2016) Comparison of Aflibercept, Bevacizumab, and Ranibizumab for Treatment of Diabetic Macular Edema: Extrapolation of Data to Clinical Practice. JAMA ophthalmology 134(1): 95–9 [PubMed: 26512939] - study included in cochrane review
Heier, Jeffrey S, Korobelnik, Jean-Francois, Brown, David M et al. (2016) Intravitreal Aflibercept for Diabetic Macular Edema: 148-Week Results from the VISTA and VIVID Studies. Ophthalmology 123(11): 2376–2385 [PubMed: 27651226] - Secondary publication of an included study that does not provide any additional relevant information
Hernandez-Bel, Laura, Cervera-Taulet, Enrique, Navarro-Palop, Catalina et al. (2019) Sequential Dexamethasone and Aflibercept Treatment in Patients with Diabetic Macular Edema: Structural and Functional Outcomes at 52 Weeks. Ophthalmologica. Journal international d’ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 241(2): 98–104 [PubMed: 29996128] - Retrospective cohort
Hu, X.-Y., Cao, L., Gao, Y. et al. (2023) Comparative Efficacy of Subthreshold Micropulse Laser Photocoagulation vs. Conventional Laser Photocoagulation for Diabetic Macular Edema: A Meta-analysis. Ophthalmic research [PubMed: 36682350] - Systematic review used as source of primary studies
Hykin, P, Ockrim, Z, Falk, S et al. (2006) A Randomized Trial of Intravitreal Triamcinolone vs. Macular Laser Therapy for Persistent Clinically Significant Diabetic Macular Edema. The macula society: 174 - study included in cochrane review
Ip, Michael S, Bressler, Susan B, Antoszyk, Andrew N et al. (2008) A randomized trial comparing intravitreal triamcinolone and focal/grid photocoagulation for diabetic macular edema: baseline features. Retina (Philadelphia, Pa.) 28(7): 919–30 [PMC free article: PMC2796075] [PubMed: 18698292] - study included in cochrane review
Jampol, Lee M, Glassman, Adam R, Bressler, Neil M et al. (2016) Anti-Vascular Endothelial Growth Factor Comparative Effectiveness Trial for Diabetic Macular Edema: Additional Efficacy Post Hoc Analyses of a Randomized Clinical Trial. JAMA ophthalmology 134(12) [PMC free article: PMC5567802] [PubMed: 27711918] - study included in cochrane review
Javanovic, Sandra, Canadanovic, Vladimir, Sabo, Ana et al. (2015) Intravitreal bevacizumab injection alone or combined with macular photocoagulation compared to macular photocoagulation as primary treatment of diabetic macular edema. Vojnosanitetski pregled 72(10): 876–82 [PubMed: 26665553] - study included in cochrane review
Kaldirim, Havva, Yazgan, Serpil, Kirgiz, Ahmet et al. (2019) A Comparison Study of Ranibizumab and Aflibercept in Patients with Naive Diabetic Macular Edema in Presence of Serous Retinal Detachment. Current eye research 44(9): 987–993 [PubMed: 30983426] - Comparator in study does not match that specified in protocol
Kaya, M., Atas, F., Kocak, N. et al. (2023) Intravitreal Ranibizumab and Dexamethasone Implant Injections as Primary Treatment of Diabetic Macular Edema: The Month 24 Results from Simultaneously Double Protocol. Current Eye Research [PubMed: 36629472] - Study does not contain a relevant intervention
Kim, HD, Kang, KD, Choi, KS et al. (2014) Combined therapy with intravitreal bevacizumab and posterior subtenon triamcinolone acetonide injection in diabetic macular oedema. Acta ophthalmologica 92(7): e589–e590 [PubMed: 24866832] - study included in cochrane review
Kim, Judy E, Pollack, John S, Miller, David G et al. (2008) ISIS-DME: a prospective, randomized, dose-escalation intravitreal steroid injection study for refractory diabetic macular edema. Retina (Philadelphia, Pa.) 28(5): 735–40 [PubMed: 18463518] - study included in cochrane review
Kriechbaum, K, Prager, S, Mylonas, G et al. (2014) Intravitreal bevacizumab (Avastin) versus triamcinolone (Volon A) for treatment of diabetic macular edema: one-year results. Eye (London, England) 28(1): 9–16 [PMC free article: PMC3890767] [PubMed: 24336297] - study included in cochrane review
Lee, C M and Olk, R J (1991) Modified grid laser photocoagulation for diffuse diabetic macular edema. Long-term visual results. Ophthalmology 98(10): 1594–602 [PubMed: 1961650] - study included in cochrane review
Lee, Ho Young; Lee, Seung Yong; Park, Jong Seok (2009) Comparison of photocoagulation with combined intravitreal triamcinolone for diabetic macular edema. Korean journal of ophthalmology : KJO 23(3): 153–8 [PMC free article: PMC2739972] [PubMed: 19794940] - study included in cochrane review
Li, Xiaoxin, Dai, Hong, Li, Xiaorong et al. (2019) Efficacy and safety of ranibizumab 0.5 mg in Chinese patients with visual impairment due to diabetic macular edema: results from the 12-month REFINE study. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 257(3): 529–541 [PubMed: 30645696] - Secondary publication of an included study that does not provide any additional relevant information
Limon, U (2021) Early effect of simultaneous intravitreal dexamethasone and bevacizumab combination treatment in patients with persistent diabetic macular edema. Journal francais d’ophtalmologie 44(6): 849–854 [PubMed: 33840497] - study included in cochrane review
Liu, Kun, Wang, Hanying, He, Wei et al. (2022) Intravitreal conbercept for diabetic macular oedema: 2-year results from a randomised controlled trial and open-label extension study. The British journal of ophthalmology 106(10): 1436–1443 [PMC free article: PMC9510409] [PubMed: 34001667] - Secondary publication of an included study that does not provide any additional relevant information
Liu, Xiangdong, Zhou, Xiaodong, Wang, Zhi et al. (2014) Intravitreal bevacizumab with or without triamcinolone acetonide for diabetic macular edema: a meta-analysis of randomized controlled trials. Chinese medical journal 127(19): 3471–6 [PubMed: 25269916] - study included in cochrane review
Marey, HM and Ellakwa, AF (2011) Intravitreal bevacizumab alone or combined with triamcinolone acetonide as the primary treatment for diabetic macular edema. Clinical ophthalmology (Auckland, N.Z.) 5(1): 1011–1016 [PMC free article: PMC3151562] [PubMed: 21845026] - study included in cochrane review
Martel, A, Nahon-Esteve, S, Martini, K et al. (2020) Feelings, preoperative anxiety, and need for information in patients undergoing intravitreal injections. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 258(7): 1395–1403 [PubMed: 32346786] - study included in cochrane review
Massin, Pascale, Bandello, Francesco, Garweg, Justus G et al. (2010) Safety and efficacy of ranibizumab in diabetic macular edema (RESOLVE Study): a 12-month, randomized, controlled, double-masked, multicenter phase II study. Diabetes care 33(11): 2399–405 [PMC free article: PMC2963502] [PubMed: 20980427] - study included in cochrane review
Massin, PG (2008) Phase 2 RESOLVE Trial: twelve-Month Analysis of Ranibizumab in Diabetic Macular Edema. American academy of ophthalmology: 180 - study included in cochrane review
Maturi, Raj K, Glassman, Adam R, Liu, Danni et al. (2018) Effect of Adding Dexamethasone to Continued Ranibizumab Treatment in Patients With Persistent Diabetic Macular Edema: A DRCR Network Phase 2 Randomized Clinical Trial. JAMA ophthalmology 136(1): 29–38 [PMC free article: PMC5833605] [PubMed: 29127949] - study included in cochrane review
Michaelides, Michel, Kaines, Andrew, Hamilton, Robin D et al. (2010) A prospective randomized trial of intravitreal bevacizumab or laser therapy in the management of diabetic macular edema (BOLT study) 12-month data: report 2. Ophthalmology 117(6): 1078–1086e2 [PubMed: 20416952] - study included in cochrane review
Mitchell, Paul, Sheidow, Tom G, Farah, Michel E et al. (2020) Effectiveness and safety of ranibizumab 0.5 mg in treatment-naive patients with diabetic macular edema: Results from the real-world global LUMINOUS study. PloS one 15(6): e0233595 [PMC free article: PMC7269267] [PubMed: 32492069] - study included in cochrane review
Nepomuceno, Antonio Brunno, Takaki, Erika, Paes de Almeida, Felipe Piacentini et al. (2013) A prospective randomized trial of intravitreal bevacizumab versus ranibizumab for the management of diabetic macular edema. American journal of ophthalmology 156(3): 502–510e2 [PubMed: 23795985] - study included in cochrane review
Neto, Hermelino O, Regatieri, Caio V, Nobrega, Mario J et al. (2017) Multicenter, Randomized Clinical Trial to Assess the Effectiveness of Intravitreal Injections of Bevacizumab, Triamcinolone, or Their Combination in the Treatment of Diabetic Macular Edema. Ophthalmic surgery, lasers & imaging retina 48(9): 734–740 [PubMed: 28902334] - Secondary publication of an included study that does not provide any additional relevant information
Nguyen, QD (2012) Randomized, Multi-center, Phase 2 Study of the Safety, Tolerability and Bioactivity of Repeated Intravitreal Injections of iCo-007 as Monotherapy or in Combination with Ranibizumab or Laser Photocoagulation in the Treatment of Diabetic Macular Edema with Involvement of the FoveAL Center (the iDEAL Study). Ocular surgery news 30(6): 9–8 - Secondary publication of an included study that does not provide any additional relevant information
Ockrim, ZK, Senswathi, S, Falk, S et al. (2006) A Randomised Trial of Intravitreal Triamcinolone verses Macular Laser Therapy for Persistent Clinically Significant Diabetic Macular Oedema. IOVS 47: ARVO E-abstract 5438 - study included in cochrane review
Pappas, GD, Adam, CI, Papageorgioy, E et al. (2008) Triamcinolone and Grid Laser versus Bevacizumab Alone for the Treatment of Diabetic Macular Edema. IOVS: ARVO E- abstract 3483 - Comparator in study does not match that specified in protocol
Patil, N.S., Mihalache, A., Hatamnejad, A. et al. (2022) Intravitreal Steroids Compared with Anti-VEGF Treatment for Diabetic Macular Edema: A Meta-Analysis. Ophthalmology Retina [PubMed: 36272716] - Data not reported in an extractable format
Pearson, P.A., Comstock, T.L., Ip, M. et al. (2011) Fluocinolone acetonide intravitreal implant for diabetic macular edema: A 3-year multicenter, randomized, controlled clinical trial. Ophthalmology 118(8): 1580–1587 [PubMed: 21813090] - Secondary publication of an included study that does not provide any additional relevant information
Pearson, P, Baker, C, Eliott, D et al. (2004) Fluocinolone Acetonide Intravitreal Implant for Diabetic Macular Edema: 2 Year Results. IOVS 45: ARVO E-abstract 1111 - study included in cochrane review
Pearson, P, Baker, CW, Eliott, D et al. (2003) Fluocinolone Acetonide Intravitreal Implant in Patients with Diabetic Macular Edema: 12 Month Results. IOVS: ARVO E-abstract 4288 - Secondary publication of an included study that does not provide any additional relevant information
Pearson, P; Levy, B; Cornstock, T (2006) Fluocinolone Acetonide Intravitreal Implant to Treat Diabetic Macular Edema: 3-Year Results of a Multi-Center Clinical Trial. IOVS 47: ARVO E-abstract 5442 - study included in cochrane review
Pei-Pei, W, Shi-Zhou, H, Zhen, T et al. (2015) Randomised clinical trial evaluating best-corrected visual acuity and central macular thickness after 532-nm subthreshold laser grid photocoagulation treatment in diabetic macular oedema. Eye (London, England) 29(3): 313–322 [PMC free article: PMC4366477] [PubMed: 25697457] - study included in cochrane review
Pennington, Becky M, Hernandez-Alava, Monica, Hykin, Philip et al. (2020) Mapping From Visual Acuity to EQ-5D, EQ-5D With Vision Bolt-On, and VFQ-UI in Patients With Macular Edema in the LEAVO Trial. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 23(7): 928–935 [PMC free article: PMC7427317] [PubMed: 32762995] - study included in cochrane review
Prunte, Christian, Fajnkuchen, Franck, Mahmood, Sajjad et al. (2016) Ranibizumab 0.5 mg treat-and-extend regimen for diabetic macular oedema: the RETAIN study. The British journal of ophthalmology 100(6): 787–95 [PMC free article: PMC4893084] [PubMed: 26453639] - study included in cochrane review
Rajendram, Ranjan, Fraser-Bell, Samantha, Kaines, Andrew et al. (2012) A 2-year prospective randomized controlled trial of intravitreal bevacizumab or laser therapy (BOLT) in the management of diabetic macular edema: 24-month data: report 3. Archives of ophthalmology (Chicago, Ill. : 1960) 130(8): 972–9 [PubMed: 22491395] - Secondary publication of an included study that does not provide any additional relevant information
Rodrigues, Murilo W, Cardillo, Jose A, Messias, Andre et al. (2020) Bevacizumab versus triamcinolone for persistent diabetic macular edema: a randomized clinical trial. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 258(3): 479–490 [PubMed: 31873786] - Secondary publication of an included study that does not provide any additional relevant information
Schmidt-Erfurth, Ursula, Lang, Gabriele E, Holz, Frank G et al. (2014) Three-year outcomes of individualized ranibizumab treatment in patients with diabetic macular edema: the RESTORE extension study. Ophthalmology 121(5): 1045–53 [PubMed: 24491642] - Secondary publication of an included study that does not provide any additional relevant information
Scott, Ingrid U, Danis, Ronald P, Bressler, Susan B et al. (2009) Effect of focal/grid photocoagulation on visual acuity and retinal thickening in eyes with non-center-involved diabetic macular edema. Retina (Philadelphia, Pa.) 29(5): 613–7 [PMC free article: PMC2735881] [PubMed: 19373126] - study included in cochrane review
Shah, Chirag P and Heier, Jeffrey S (2016) Aflibercept for Diabetic Macular Edema in Eyes Previously Treated With Ranibizumab and/or Bevacizumab May Further Improve Macular Thickness. Ophthalmic surgery, lasers & imaging retina 47(9): 836–9 [PubMed: 27631479] - Retrospective cohort
Shah, SM, Nguyen, QD, Sy, JP et al. (2008) The RIDE and RISE Studies of the Efficacy and Safety of Intravitreal Ranibizumab (LUCENTIS®) in Clinically Significant Macular Edema With Center Involvement Secondary to Diabetes Mellitus. IOVS: ARVO E- abstract 1562 - population with age-related macular degeneration
Sharma, Ashish, Bellala, Keerthi, Dongre, Pankaj et al. (2020) Anti-VEGF versus dexamethasone implant (Ozurdex) for the management of Centre involved Diabetic Macular Edema (CiDME): a randomized study. International ophthalmology 40(1): 67–72 [PubMed: 31377905] - study included in cochrane review
Singer, Michael A; Wykoff, Charles C; Grewal, Dilraj S (2020) Effects of Long-Term DME Control With 0.2 microg/Day Fluocinolone Acetonide Implant on Quality of Life: An Exploratory Analysis From the FAME Trial. Ophthalmic surgery, lasers & imaging retina 51(11): 658–667 [PubMed: 33231701] - study included in cochrane review
Soheilian, Masoud, Garfami, Kiumars Heidari, Ramezani, Alireza et al. (2012) Two-year results of a randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus laser in diabetic macular edema. Retina (Philadelphia, Pa.) 32(2): 314–21 [PubMed: 22234244] - study included in cochrane review
Soheilian, Masoud, Ramezani, Alireza, Bijanzadeh, Bijan et al. (2007) Intravitreal bevacizumab (avastin) injection alone or combined with triamcinolone versus macular photocoagulation as primary treatment of diabetic macular edema. Retina (Philadelphia, Pa.) 27(9): 1187–95 [PubMed: 18046223] - study included in cochrane review
Soheilian, Masoud, Ramezani, Alireza, Obudi, Arash et al. (2009) Randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus macular photocoagulation in diabetic macular edema. Ophthalmology 116(6): 1142–50 [PubMed: 19376585] - study included in cochrane review
Solaiman, Kamal A M; Diab, Mohammad M; Abo-Elenin, Mostafa (2010) Intravitreal bevacizumab and/or macular photocoagulation as a primary treatment for diffuse diabetic macular edema. Retina (Philadelphia, Pa.) 30(10): 1638–45 [PubMed: 20838357] - study included in cochrane review
Sutter, FK; Simpson, JM; Gillies, MC (2004) Intravitreal triamcinolone for diabetic macular edema that persists after laser treatment: three-month efficacy and safety results of a prospective, randomized, double-masked, placebo-controlled clinical trial. Ophthalmology 111(11): 2044–2049 [PubMed: 15522370] - study included in cochrane review
Tornambe, Paul (2017) Re: Wells et al.: Aflibercept, Bevacizumab, or Ranibizumab for diabetic macular edema: Two-year results from a comparative effectiveness randomized clinical trial (Ophthalmology 2016;123:1351-1358). Ophthalmology 124(3): e25–e26 [PMC free article: PMC4877252] [PubMed: 26935357] - Secondary publication of an included study that does not provide any additional relevant information
Tranos, P G, Topouzis, F, Stangos, N T et al. (2004) Effect of laser photocoagulation treatment for diabetic macular oedema on patient’s vision-related quality of life. Current eye research 29(1): 41–9 [PubMed: 15370366] - study included in cochrane review
Turkoglu, Elif Betul, Celik, Erkan, Aksoy, Nilgun et al. (2015) Changes in vision related quality of life in patients with diabetic macular edema: ranibizumab or laser treatment?. Journal of diabetes and its complications 29(4): 540–3 [PubMed: 25817172] - study included in cochrane review
Virgili, G, Parravano, M, Evans, JR et al. (2018) Anti-vascular endothelial growth factor for diabetic macular oedema: a network meta-analysis. Cochrane Database of Systematic Reviews [PMC free article: PMC6517135] [PubMed: 30325017] - Secondary publication of an included study that does not provide any additional relevant information
Wang, Jia-Kang, Huang, Tzu-Lun, Su, Pei-Yuan et al. (2015) An updated review of long-term outcomes from randomized controlled trials in approved pharmaceuticals for diabetic macular edema. Eye science 30(4): 176–83 [PubMed: 27215008] - study included in cochrane review
Wang, X-X, Zhang, P-C, Xie, J et al. (2021) Efficacy of Aflibercept versus Ranibizumab in the treatment of diabetic macular edema. International eye science 21(12): 2183–2186 - study included in cochrane review
Wang, Yu-Sheng, Li, Xiao, Wang, Hai-Yan et al. (2011) Intravitreal bevacizumab combined with/without triamcinolone acetonide in single injection for treatment of diabetic macular edema. Chinese medical journal 124(3): 352–8 [PubMed: 21362332] - study included in cochrane review
Weingessel, B, Miháltz, K, Gleiss, A et al. (2018) Treatment of Diabetic Macular Edema with Intravitreal Antivascular Endothelial Growth Factor and Prompt versus Deferred Focal Laser during Long-Term Follow-Up and Identification of Prognostic Retinal Markers. Journal of ophthalmology: 1–11 [PMC free article: PMC6188720] [PubMed: 30364034]

- Study does not contain a relevant intervention

- Full text paper not available

Wells, John A, Glassman, Adam R, Ayala, Allison R et al. (2016) Aflibercept, Bevacizumab, or Ranibizumab for Diabetic Macular Edema: Two-Year Results from a Comparative Effectiveness Randomized Clinical Trial. Ophthalmology 123(6): 1351–9 [PMC free article: PMC4877252] [PubMed: 26935357] - study included in cochrane review
Wells, John A, Glassman, Adam R, Jampol, Lee M et al. (2016) Association of Baseline Visual Acuity and Retinal Thickness With 1-Year Efficacy of Aflibercept, Bevacizumab, and Ranibizumab for Diabetic Macular Edema. JAMA ophthalmology 134(2): 127–34 [PMC free article: PMC5567793] [PubMed: 26605836] - study included in cochrane review
Wykoff, C.C., Marcus, D.M., Midena, E. et al. (2017) Intravitreal aflibercept injection in eyes with substantial vision loss after laser photocoagulation for diabetic macular edema subanalysis of the vista and vivid randomized clinical trials. JAMA Ophthalmology 135(2): 107–114 [PubMed: 28006063] - Secondary publication of an included study that does not provide any additional relevant information
Wykoff, Charles C, Abreu, Francis, Adamis, Anthony P et al. (2022) Efficacy, durability, and safety of intravitreal faricimab with extended dosing up to every 16 weeks in patients with diabetic macular oedema (YOSEMITE and RHINE): two randomised, double-masked, phase 3 trials. Lancet (London, England) 399(10326): 741–755 [PubMed: 35085503] - study included in cochrane review
Yahia, SB, Attia, S, Hmidi, K et al. (2008) Intravitreal Bevacizumab vs. Intravitreal Triamcinolone for Diabetic Macular Edema With Severe Hard Exudates. American academy of ophthalmology: 181 - study included in cochrane review
Yaseri, M, Zeraati, H, Mohammad, K et al. (2014) Intravitreal bevacizumab injection alone or combined with triamcinolone versus macular photocoagulation in bilateral diabetic macular edema; application of bivariate generalized linear mixed model with asymmetric random effects in a subgroup of a clinical trial. Journal of ophthalmic and vision research 9(4): 453–460 [PMC free article: PMC4329706] [PubMed: 25709771] - Secondary publication of an included study that does not provide any additional relevant information
Ziemssen, F., Cruess, A., Dunger-Baldauf, C. et al. (2017) Ranibizumab in diabetic macular oedema - A benefit-risk analysis of ranibizumab 0.5 mg PRN versus laser treatment. European Endocrinology 13(2): 91–98 [PMC free article: PMC5813472] [PubMed: 29632615] - study included in cochrane review
Ziemssen, Focke and Agostini, Hansjurgen (2015) Re: Boyer et al.: Three-year, randomized, sham-controlled trial of dexamethasone intravitreal implant in patients with diabetic macular edema (Ophthalmology 2014;121:1904-14). Ophthalmology 122(3): e20–1 [PubMed: 25703473] - Secondary publication of an included study that does not provide any additional relevant information

Economic evidence

StudyReason for exclusion
Anonymous (2018) Pharmacoeconomic Review Report: Dexamethasone (Ozurdex): (Allergan Inc.): Indication: For the treatment of adult patients with diabetic macular edema who are pseudophakic. [PubMed: 30933447]
  • Pharmacoeconomic review report
Anonymous (2019) Pharmacoeconomic Review Report: Fluocinolone acetonide intravitreal implant (Iluvien): (Knight Therapeutics Inc.): Indication: For the treatment of diabetic macular edema (DME) in patients who have been previously treated with a course of corticosteroids and did not have a clinically significant rise in intraocular pressure. [PubMed: 31876997]
  • Pharmacoeconomic review report
Crijns, H; Casparie, A F; Hendrikse, F (1999) Continuous computer simulation analysis of the cost-effectiveness of screening and treating diabetic retinopathy. International journal of technology assessment in health care 15(1): 198–206 [PubMed: 10407606]
  • Population - diabetes NOT diabetic macular oedema
  • Costs only no outcome data
Cutino, Antonio, Green, Kenneth, Kendall, Robyn et al. (2015) Economic evaluation of a fluocinolone acetonide intravitreal implant for patients with DME based on the FAME study. The American journal of managed care 21(4suppl): 63–72 [PubMed: 25734663]
  • Includes productivity costs which is outside NICE reference case
Dewan, Vinay, Lambert, Dennis, Edler, Joshua et al. (2012) Cost-effectiveness analysis of ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema. Ophthalmology 119(8): 1679–84 [PMC free article: PMC3612959] [PubMed: 22503301]
  • Not applicable – interventions
  • The only interventions which it is possible to estimate an ICER based on the cost per QALY is relative to triamcinolone which is not a relevant comparator for this review question
Foglia, Emanuela, Ferrario, Lucrezia, Bandello, Francesco et al. (2018) Diabetic macular edema, innovative technologies and economic impact: New opportunities for the Lombardy Region healthcare system?. Acta ophthalmologica 96(4): e468–e474 [PubMed: 29240298]
  • Costs only no outcome data
Holden, Sarah E; Currie, Craig J; Owens, David R (2017) Health-economic evaluation of fluocinolone acetonide 190 microg implant in people with diabetic macular edema. Current medical research and opinion 33(sup2): 45–52 [PubMed: 28881146]
  • Costs only no outcome data
Javitt J C, Aiello L P (1996) Cost-effectiveness of detecting and treating diabetic retinopathy. Annals of Internal Medicine 124(1 Part 2): 164–169 [PubMed: 8554212]
  • Not applicable - US study, pre-1990 analysis different from current UK setting
  • Population - diabetes NOT diabetic macular oedema
  • Not applicable - inappropriate comparison of interventions
Javitt, J C; Canner, J K; Sommer, A (1989) Cost effectiveness of current approaches to the control of retinopathy in type I diabetics. Ophthalmology 96(2): 255–64 [PubMed: 2495499]
  • Not applicable - US study, pre-1990 analysis different from current UK setting
  • Population - diabetes NOT diabetic macular oedema
Kourlaba, G., Relakis, J., Mahon, R. et al. (2016) Cost-utility of ranibizumab versus aflibercept for treating Greek patients with visual impairment due to diabetic macular edema. Cost Effectiveness and Resource Allocation 14(1): 7 [PMC free article: PMC4831170] [PubMed: 27081372]
  • Not applicable Greek population
  • Adaption of the study by Regnier et al 2015, using exactly the same inputs other than Greek costs
Lois, Noemi, Campbell, Christina, Waugh, Norman et al. (2023) Diabetic Macular Edema and Diode Subthreshold Micropulse Laser: A Randomized Double-Masked Noninferiority Clinical Trial. Ophthalmology 130(1): 14–27 [PubMed: 35973593]
  • Duplication, summary paper of another include, the paper with the most detail has been selected for inclusion
Montes Rodriguez, P., Mateo Gabas, J., Esteban Floria, O. et al. (2022) Cost-effectiveness of dexamethasone compared with aflibercept in naive diabetic macular edema. Cost Effectiveness and Resource Allocation 20(1): 61 [PMC free article: PMC9713987] [PubMed: 36457024]
  • Not applicable – societal perspective
Mukkamala, Lekha; Bhagat, Neelakshi; Zarbin, Marco (2017) Practical Lessons from Protocol T for the Management of Diabetic Macular Edema. Developments in ophthalmology 60: 109–124 [PubMed: 28427070]
  • US study
  • Very serious limitations
Navarro-Navarro, A, Salom, D, Martinez-Toldos, J et al. (2017) The diabetic retinopathy clinical research network analysis of the cost-effectiveness of aflibercept, bevacizumab and ranibizumab for the treatment of diabetic macular oedema and its application in Spain. Archivos de la Sociedad Espanola de Oftalmologia 92(5): 245–246 [PubMed: 28215618]
  • Non-English language
Patel, N.A., Yannuzzi, N.A., Lin, J. et al. (2021) A Cost-Effectiveness Analysis of Intravitreal Aflibercept for the Prevention of Progressive Diabetic Retinopathy. Ophthalmology Retina [PubMed: 34547529]
  • Population for non-proliferative diabetic retinopathy not diabetic macular oedema
  • Not applicable - non-QALY outcomes
  • Not applicable - discounting not applied
Pershing, Suzann, Enns, Eva A, Matesic, Brian et al. (2014) Cost-effectiveness of treatment of diabetic macular edema. Annals of internal medicine 160(1): 18–29 [PMC free article: PMC4020006] [PubMed: 24573663]
  • Not applicable – unable to separate from the societal perspective
Pesonen, Mari; Kankaanpaa, Eila; Vottonen, Pasi (2021) Cost-effectiveness of dexamethasone and triamcinolone for the treatment of diabetic macular oedema in Finland: A Markov-model. Acta ophthalmologica 99(7): e1146–e1153 [PMC free article: PMC8597173] [PubMed: 33421332]
  • Not applicable - irrelevant comparator
  • Triamcinolone is not included as an intervention within the protocol
Ramsey, D.J., Poulin, S.J., Lamonica, L.C. et al. (2021) Early conversion to aflibercept for persistent diabetic macular edema results in better visual outcomes and lower treatment costs. Clinical Ophthalmology 15: 31–39 [PMC free article: PMC7802895] [PubMed: 33447009]
  • US population
  • Very serious limitations, unclear modelling methods
Romero-Aroca, Pedro, de la Riva-Fernandez, Sofia, Valls-Mateu, Aida et al. (2016) Cost of diabetic retinopathy and macular oedema in a population, an eight year follow up. BMC ophthalmology 16: 136 [PMC free article: PMC4973531] [PubMed: 27491545]
  • Population – people with diabetes rather than diabetic macular oedema
Ross, Eric L, Hutton, David W, Stein, Joshua D et al. (2016) Cost-effectiveness of Aflibercept, Bevacizumab, and Ranibizumab for Diabetic Macular Edema Treatment: Analysis From the Diabetic Retinopathy Clinical Research Network Comparative Effectiveness Trial. JAMA ophthalmology 134(8): 888–96 [PMC free article: PMC6648661] [PubMed: 27280850]
  • Partially applicable US population
  • Very serious limitations with model structure
Ruiz-Moreno, J M; de Andres-Nogales, F; Oyaguez, I (2020) Cost-consequence analysis of extended loading dose of anti-VEGF treatment in diabetic macular edema patients. BMC ophthalmology 20(1): 37 [PMC free article: PMC7500029] [PubMed: 32943041]
  • Interventions not relevant to question
  • Severe limitations – only considers 6 months
  • Cost consequence not cost utility
Schauwvlieghe, A M E, Dijkman, G, Hooymans, J M et al. (2015) Comparing the effectiveness and costs of Bevacizumab to Ranibizumab in patients with Diabetic Macular Edema: a randomized clinical trial (the BRDME study). BMC ophthalmology 15: 71 [PMC free article: PMC4491889] [PubMed: 26149170]
  • Protocol study – no results
Smiddy, William E (2011) Economic considerations of macular edema therapies. Ophthalmology 118(9): 1827–33 [PMC free article: PMC3483086] [PubMed: 21507488]
  • Not applicable – one year duration with no modelling and unclear methods
Vondeling, H (1993) Evaluation of argon laser treatment of diabetic retinopathy and its diffusion in The Netherlands. Health policy (Amsterdam, Netherlands) 23(12): 97–111 [PubMed: 10123418]
  • Not applicable - US study, pre-1990 analysis different from current UK setting

Appendix K. Network meta-analysis

Network meta-analyses were conducted for the outcomes ‘change in visual acuity’ and ‘change in central retinal thickness’ to allow the evidence across comparisons to be combined into a single internally consistent model. Seven network meta-analyses were conducted, all for people with centre-involving macular oedema. The populations and outcomes where there was sufficient data for network meta-analyses were:

  • Whole centre-involving population
    • Change in visual acuity at 12 months
    • Change in visual acuity at 24 months
    • Change in central retinal thickness at 12 months
    • Change in central retinal thickness at 24 months
  • Subgroup analysis: People with central retinal thickness >400 µm at baseline
    • Change in visual acuity at 12 months
    • Change in visual acuity at 24 months
    • Change in central retinal thickness at 12 months

K.1. Implementation (PDF, 169K)

K.2. WinBUGS code (PDF, 1.9M)

Tables

Table 1Effectiveness and acceptability of intravitreal steroids, macular laser and anti-vascular endothelial growth factor agents for treating diabetic macular oedema

Population

Inclusion: People diagnosed with diabetic macular oedema

Exclusion: People who are about to undergo or have undergone cataract surgery

Interventions
  • Intravitreal steroid therapy (intravitreal injection or surgical implantation).
  • Macular laser, subclassified as:
    • Standard threshold laser
    • Subthreshold laser
  • Anti-vascular endothelial growth factor agents
  • Anti-vascular endothelial growth factor agents plus intravitreal steroid therapy
  • Anti-vascular endothelial growth factor agents plus macular laser
  • Intravitreal steroid therapy plus macular laser
Comparator
  • Another intervention listed above.
  • Placebo, sham treatment, or no treatment
-

Trials comparing standard threshold and subthreshold laser will be included. Trials comparing types of standard threshold laser or types of subthreshold laser will not be included.

-

Trials comparing different Anti-VEGF agents or different intravitreal steroids will be included.

Outcomes

Primary outcomes:

  • Best corrected visual acuity
    • (1) the change from baseline of best-corrected visual acuity (BCVA) as continuous data (converted into logMAR); and
    • (2) three or more lines improvement from baseline (ETDRS, Snellen, or logMAR equivalent; one line improvement analysed if three lines not available).
Outcomes will be assessed at 12 months (plus or minus 6 months) and at the longest timepoint available in the study if 24 months or greater.

Secondary outcomes:

  • Mean change in retinal thickness from baseline.
  • Quality of life (assessed using a validated tool)
  • Adverse events (development of cataract, Intraocular inflammation, raised intraocular pressure, need for glaucoma drainage surgery)
  • Acceptability (additional outcome not assessed in Cochrane reviews). Qualitative or quantitative data on acceptability collected alongside included randomised controlled trials will be included.
  • Driving vision (dichotomous outcome, number of participants with vision sufficient to allow driving)
  • Number of treatments

Table 2Table of included studies

Studies from NICE additional searches

Study

Country

Study type and follow-up (FU) timePopulationInterventionComparatorOutcomes
Callanan, 2013

Parallel-group RCT

1 year FU

Inclusion criteria
  • At least 18 years of age
  • Diagnosis of type 1 or type 2 diabetes mellitus
  • Mean retinal thickness 275 mm by OCT in the 1-mm central macular subfield due to diffuse DME not amenable to laser at
  • stand-alone treatment (at screening)
  • Diffuse macular capillary bed leakage evident on FA
  • BCVA >34 and <70 letters (approximately 20/200 and 20/40Snellen) using the ETDRS method at screening and baseline)
Key exclusion criteria
  • Uncontrolled systemic disease
  • Use of systemic corticosteroid within 12 weeks prior to baseline or anticipated use during the study
  • Active ocular infection (either eye)
  • Glaucoma (either eye)
  • History of an IOP increase
  • 10 mm Hg or to 25 mm Hg in response to corticosteroid treatment that required multiple IOP-lowering medications or laser or surgical treatment (either eye)
  • History or presence of venous occlusive disease, uveitis, Irvine-Gass syndrome, or any condition other than diabetic retinopathy that could contribute to macular oedema
  • Epiretinal membrane or vitreomacular traction macular oedema
  • History of pars plana vitrectomy
  • Active optic disc or retinal neovascularization
  • History of intravitreal corticosteroid use except dexamethasone

DEX implant plus laser (N = 126)

Dexamethasone Intravitreal Implant Plus Laser

Sham implant and laser (N = 127)

Laser Alone

  • Mean of best corrected visual acuity in logMAR
  • Mean of central macular thickness
  • Mean number of treatments

Chen, 2020

The VIVID-East study

Parallel-group RCT

1 year FU

Inclusion criteria
  • Age 18 years or over
  • Type 1 or type 2 diabetes
  • Clinically significant DME involving the centre of the macula
Exclusion criteria
  • Patients with an ocular condition with a poorer prognosis in the fellow eye than in the study eye
  • any surgical interventions or laser photocoagulation in the study eye within 120 and 90 days of day 1
  • any treatments with corticosteroids or anti-angiogenic drugs in either eye within 90 days of day 1
  • active proliferative diabetic retinopathy in the study eye
  • a history of idiopathic or autoimmune uveitis in the study eye

IVT-AFL every 4 weeks (N = 127)

or

IVT-AFL every 8 weeks (N = 127)

macular laser

(N = 127)

  • mean change in BCVA in ETDRS letter score from baseline
  • eyes that gained ≥10 ETDRS letters
  • proportion of eyes that gained ≥15 ETDRS letters
  • proportion of eyes with a ≥2-step improvement from baseline in the Diabetic Retinopathy Severity Scale (DRSS)
  • change in central retinal thickness
  • mean number of treatments
Faghihi, 2010

Parallel-group RCT

6 month FU

Inclusion criteria

  • Bilateral non-tractional CSME
  • 10/10> V.A < 1/10
Controlled blood pressure.

Key exclusion criteria

  • HRC PDR
  • Advanced or advanced active PDR
  • Significant cataract
  • Glaucoma
  • History of recent vascular accident (e.g, MI, CVA, )
  • Previous treatment of CSME or PDR, or pharmacotherapy for CSME.
  • Macular ischemia
  • Uncontrolled hypertension

IVB plus MPC (N = 40)IVB (N = 40)
  • Best corrected visual acuity in logMAR
  • Central macular thickness
  • Mean number of treatments
Fouda, 2017

Parallel-group RCT

1 year FU

Inclusion criteria
  • Patients with type I or II diabetes,
  • DME in eyes as diagnosed clinically and with OCT
  • patients with best corrected visual acuity (BCVA) ranged from 0.1 to 0.25 (moderate visual loss)
  • oedema affecting the central 1 mm of the macula
Key exclusion criteria
  • Eyes with vascular retinal disorders other than diabetic retinopathy (eg, choroidal neovascularization)
  • eyes that received previous intravitreal injection of any agents

IVT-AFL (N = 35)

All eyes in group I received an injection of 2 mg/0.05 mL aflibercept (Eylea; Regeneron Pharmaceuticals, NY, USA) and those in

(IVT-RAN (N = 35)

group II received an injection of 0.5 mg/0.1 mL ranibizumab (Lucentis; Genentech, USA, Inc., San Francisco, CA, USA)

  • Best corrected visual acuity
  • Central macular thickness
  • Mean number of treatments
Gillies, 2009

Parallel-group RCT

5 year FU

Inclusion criteria
  • Diabetes mellitus (type 1 or 2)
  • Diabetic macular oedema in study eye associated to diabetic retinopathy
  • Diffuse macular oedema defined as macular thickening determined by biomicroscopy and fluorescein angiography.
  • Best corrected visual acuity between 34 (20/200) and 68 letters (20/50).
  • Macular thickness greater than 300 mcm on OCT.
Key exclusion criteria
  • Uncontrolled systemic disease
  • Start of medical therapy for diabetes or change in treatment from oral to insulin four months before initial visit.
  • HbA1c levels greater than 10%
  • Presence of retinal venous occlusion, cystoid macular oedema, or other condition that would contribute to macular oedema.
  • Presence of epiretinal membrane
  • Presence of vitreomacular traction in the study eye.
  • Aphakic or anterior chamber intraocular lens in the study eye.
  • Neovascularization of disc or elsewhere in the study eye.
  • History or presence of choroidal neovascularization in the study eye.
  • Presence of rubeosis irides in the study eye.
  • Eye opacity that interfere with clinical documentation and photography.
  • Intra-ocular surgery 90 days before initial visit.
  • Previous vitrectomy in study eye.
  • Previous history of intravitreal or periocular corticoid or any other intravitreal drug in study eye.
  • Scheduled surgery for study eye.
  • Patients with known allergies to fluorescein, iodo-povidone or any component of study drug.
Initial Triamcinolone (N = 23)Initial Placebo (N = 21)
  • best corrected visual acuity in logMAR
Lam, 2007

Parallel-group RCT

6 monthFU

Inclusion criteria
  • Patients 18 years or older with type I or II diabetes mellitus
  • Eyes had DME involving the fovea, as defined by clinically significant macular oedema according to ETDRS guidelines.
  • central foveal thickness (CFT) >250 um,
Exclusion criteria
  • macular oedema secondary to causes other than diabetic maculopathy
  • signs of vitreomacular traction
  • proliferative diabetic retinopathy
  • Patients who had phakia
  • history of glaucoma or ocular hypertension
  • macular ischemia (1-disc diameters of capillary closure at the macula on fluorescein angiography).
  • Patients who had any laser procedure within 3 months

4 mg of intravitreal TA (N = 38)

OR

4 mg of intravitreal TA + grid laser (N = 36)

grid laser (N = 37)
  • Central foveal thickness
  • (logMAR) best-corrected visual acuity
Lois,2023

RCT

24 months follow up

Inclusion criteria
  • centre-involving DMO, as determined by slit-lamp biomicroscopy and SD-OCT
  • in one or both eyes, with either:
  • a CRT of > 300 µm but < 400 µm in the central subfield (central 1 mm) owing to DMO as determined by SD-OCT
  • a CRT of < 300 µm provided that intra-retinal and/or subretinal fluid was present in the central subfield (central 1 mm) owing to DMO.
  • The following conditions also had to be met:
  • visual acuity of > 24 Early Treatment Diabetic Retinopathy Study (ETDRS) letters (Snellen equivalent > 20/320)
  • amenable to laser treatment, as judged by the treating ophthalmologist
  • aged ≥ 18 years.
Exclusion criteria
  • A patient’s eyes were not eligible for the study if their macular oedema was owing to causes other than DMO o
  • ineligible for macular laser, as judged by the treating ophthalmologist
  • DMO with a CRT of ≥ 400 µm
  • active PDR requiring treatment
  • received intravitreal anti-VEGF therapy within the previous 2 months
  • received macular laser treatment within the previous 12 months
  • received intravitreal injection of steroids
  • cataract surgery within the previous 6 weeks
panretinal photocoagulation (PRP) within the previous 3 months.

subthreshold micropulse laser 577 nm SML

(n = 133;

Standard threshold laser [e.g. argon, frequency doubled neodymium-doped yttrium aluminium garnet (Nd:YAG) 532 nm laser].

(n = 133)

  • Mean change in BCVA
  • Mean change in central retinal thickness
  • Number meeting driving standards
  • Number of laser treatments used
Ozsaygili, 2020

Parallel-group RCT

1 year FU

  • Patients older than 18 years of age diagnosed with Type 1 or Type 2 DM
  • Treatment-naïve DME with SRD and hyperreflective foci
  • BCVA letter score between 73 and 34 (Snellen equivalent 20/40–20/200);
  • The CRT obtained from the 1-mm central macular subfield greater than 450 mm by SD-OCT.
Key exclusion criteria
  • Previous history of intraocular anti-VEGF or steroid injection
  • macular ischemia defined by fundus fluorescein angiogram
  • any other ocular pathologies causing visual impairment
  • recent (within 3 months) serious cardiovascular or cerebrovascular events
  • IOP over 23mmHg without treatment or IOP over 21 mmHg with one antiglaucoma medication
  • presence of vitreomacular interface abnormalities
  • aphakia or an anterior chamber intraocular lens
  • active proliferative diabetic retinopathy.
3 monthly injections of 2 mg of aflibercept as a loading phase in the anti–vascular endothelial growth factor group0.7 mg of DEX implant in the DEX group and then pro re nata treatment.
  • Best corrected visual acuity
  • Mean number of treatments
  • Adverse events
Sahni,2019

Parallel-group RCT

6 months FU

  • Patients 18 years of age or older
  • Center-involving DMO
  • central subfield thickness (CST) of 325 mm or more measured with the Spectralis OCT device
  • Best corrected visual acuity (BCVA) of 73 to 24 Early Treatment Diabetic Retinopathy Study (ETDRS) letters (Snellen equivalent, 20/40/-20/320).
Key exclusion criteria
  • high-risk proliferative DR
  • prior panretinal photocoagulation, macular laser photocoagulation within 3 months of the start of the study
  • any history of Iluvien or Ozurdex implants, and any history of anti-VEGF treatment.
  • Per a protocol amendment, patients who previously received anti-VEGF treatment were enrolled as a separate population from anti-VEGF treatment-naïve patients to enable the exploratory evaluation of faricimab efficacy in this population.
6.0 mg faricimab or 1.5 mg faricimab0.3mg ranibizumab
  • Central subfield thickness reduction
  • BCVA change from baseline (ETDRS letters)
Vader, 2020

Parallel-group RCT

6 months FU

Inclusion criteria
  • patients were older than 18 years,
  • diagnosed with type 1 or type 2 diabetes mellitus and with a glycosylated haemoglobin of less than 12%,
  • central area thickness on (OCT) of more than 325 mm
  • visual impairment resulting from DME
  • best-corrected visual acuity (BCVA) outcome of at least 24 letters and less than 79 letters on standardized ETDRS
Key exclusion criteria
  • Untreated PDR was defined as leakage on
  • fluorescein angiogram resulting from a neovascularization
  • the presence of preretinal haemorrhages
  • vitreous haemorrhages,
  • Structural damage included the presence of laser scars, retinal pigment epithelium
  • Atrophy
  • organized hard exudate plaques close to the macula
1.25 mg bevacizumab (N = 86) 0.5 mg ranibizumab (N = 84)
  • Best corrected visual acuity in logMAR
  • Central macular thickness
  • Mean number of treatments

Notes: Abbreviations: BCVA, best corrected visual acuity; DME, diabetic macular oedema; ETDRS, Early Treatment Diabetic Retinopathy Study; FU, follow up;

Table 3Summary of Cochrane reviews used for clinical effectiveness evidence

StudyNumber of included studiesInclusion criteriaExclusion criteriaInterventionsComparisonOutcomes
Jorge et al-2018 15 studiesRandomised controlled trials (RCTs) comparing any type of focal/grid macular laser versus another type or technique of laser treatment and no interventionExcluded studies comparing laser with other interventionsDifferent macular laser as monotherapy in the treatment of diabetic macular oedema.another type or technique of laser treatment and no intervention
  • Gain or loss of 3 lines (0.3 logMAR or 15 ETDRS letters) of best-corrected visual acuity (BCVA) at one year of follow-up (plus or minus six months) after treatment initiation.
  • Mean change in BCVA
  • Resolution of macular oedema
  • Central retinal thickness
  • Quality of life
  • Adverse events, all at one year
Mehta et al-2018 8Randomised controlled trials (RCTs) comparing intravitreal anti-VEGF combined with intravitreal steroids versus intravitreal anti-VEGF alone, intravitreal steroids alone or macular laser alone for managing DMONRintravitreal anti-VEGF combined with intravitreal steroidsintravitreal anti-VEGF alone, intravitreal steroids alone or macular laser alone
  • Change in best corrected visual acuity (BCVA) between baseline and one year
  • Change in central macular thickness (CMT)
  • Quality of life
  • Adverse events including intraocular inflammation, raised intraocular pressure (IOP) and development of cataract
Rittiphairoj et al-2020 9Randomised controlled trials (RCTs) comparing intravitreal steroid therapies versus other treatments, including intravitreal anti-VEGF therapy, laser photocoagulation, and sham injectionNRany type of intravitreal steroids as monotherapy againstany other intervention (e.g., observation, laser, anti-vascular endothelial growth factor (anti-VEGF) for DMO
  • Change in best corrected visual acuity (BCVA) between baseline and one year
  • Change in central macular thickness
Virgili et al-2022 29Randomised controlled trials (RCTs) comparing any anti-angiogenic drug with an anti-VEGF mechanism of action versus another anti-VEGF drug, another treatment, sham or no treatment in people with DMOPeople with normal best corrected visual acuity (BCVA) were not includedany anti-angiogenic drug with an anti-VEGF mechanism of actionanother anti-VEGF drug, another treatment, sham, or no treatment
  • Change in best corrected visual acuity (BCVA) between baseline and one year
  • Change of BCVA at 24 months.
  • Improvement of three or more lines of visual acuity
  • Change in central macular thickness (CMT)

Table 4Randomised controlled trials (for full study details, see Virgili et al. 2022)

StudyFollow-up timePopulationInterventionComparatorOutcomes
Randomised controlled trials (from Virgili et al 2022 Cochrane systematic review)
Azad 2012 6 months

Inclusion:

  • Diffuse DMO with at least two prior sessions of macular laser photocoagulation
  • CRT > 250 μm
Exclusion:

History of having received prior intraocular, peribulbar, or systemic steroids or prior anti-VEGF therapy

Bevacizumab (1.25 mg)

[Triamcinolone acetonide arm – not reported in Virgili 2018]

Macular grid augmentation
  • best corrected visual acuity (BCVA)
  • Mean central macular thickness
Baker 2019 24 months and 5 yearsInclusion criteria:
  • Age ≥ 18 years.
  • Diagnosis of diabetes mellitus (type 1 or type 2).
Exclusion criteria:
  • History of chronic renal failure requiring dialysis or kidney transplant.
  • unstable medical status including blood pressure, cardiovascular disease, and glycaemic control).
  • Initiation of intensive insulin treatment (a pump or multiple daily injections) within 4 months prior to randomization

Aflibercept (n=236)

Macular laser (n=240

Observation (n=236)
  • mean change in visual acuity from baseline,
  • visual acuity of at least 84 letters (Snellen equivalent of 20/20), loss of at least 10
  • gain of at least 5 letters of visual acuity
  • mean change in central subfield thickness
  • proportion of eyes with at least 10% CST change from baseline
  • incidence of cataracts
  • adverse events (increased intraocular pressure, vitreous haemorrhage)
BOLT 2010 (Michaelides 2010) Inclusion criteria:
  • Centre-involving CSMO
  • CRT of ≥ 270 µm
  • BCVA in the study eye between 35 and 69 ETDRS letters at 4 m (Snellen equivalent 6/60 or 6/12)
  • At least 1 prior macular laser therapy
Exclusion criteria:
  • PDR except for tufts of new vessels elsewhere < 1 disc in area with no vitreous haemorrhage

Bevacizumab (1.25 mg)

n = 42 (42 eyes

Macular laser therapy

n = 38 (38 eyes)

  • change in central retinal thickness
  • gain and loss of 15 and 10 letters of ETDRS
  • loss of 30 ETDRS letters
  • VA 3 or more lines improvement
  • retinopathy severity (ETDRS grading)
  • number of treatments
  • adverse events (increased intraocular pressure, vitreous haemorrhage)
Brown 2015 12 months
  • Adult patients with type 1 or 2 diabetes mellitus
  • central-involved DME (defined as retinal thickening involving the 1-mm central [OCT]
  • subfield thickness [CST]) were if best-corrected visual acuity (BCVA) was between 73 and 24 letters (20/40 to 20/320 Snellen equivalent) in the study eye.
  • Only 1 eye per patient

VISTA: 154 IAI 2q4, or 151 IAI 2q8

VIVID: 136 IAI 2q4, or 135 IAI 2q8

VISTA: 154 Laser control

VIVID: 132 Laser control

  • mean change from baseline in best-corrected visual acuity (BCVA) at week 52.
  • change from baseline in central subfield thickness
  • number of treatments
Brown 2022 12 monthsInclusion criteria:
  • aged ≥18 years with type 1 or 2 diabetes mellitus
  • glycosylated haemoglobin (HbA1c) ≤ 10%
  • BCVA score between 78 and 23 letters
  • Snellen equivalent of 20/32 to 20/320) at screening
  • central-involved DME with CSFT of ≥320μm
Exclusion criteria:
  • active proliferative diabetic retinopathy in the study eye
  • received intraocular or periocular corticosteroids in the 6 months prior to baseline or prior anti-VEGF

Brolucizumab 3 mg, brolucizumab 6 mg, (KESTREL)

or brolucizumab 6 mg (KITE)

Aflibercept 2mg (KESTREL and KITE)
  • BCVA change from baseline
  • incidence of ocular and non-ocular adverse events.
  • mean number of treatments
Chatzirallis 2020 12- & 18-months FUInclusion criteria:
  • Type 2 diabetes mellitus
  • Central involved DME
  • Central retinal thickness (CRT) ≥320 μm
Exclusion criteria:
  • AMD
  • Retinal vein occlusion, vitreomacular traction, intraocular inflammation, cornea disorders
  • Media opacities
  • Uncontrolled glaucoma
  • High myopia >6D
  • Previous trauma
  • Intraocular surgery within the last 6 month
0.5 mg Ranibizumab n = 54 (54 eyes)Aflibercept 2 mg n = 58 (58 eyes)
  • change in BCVA and central retinal thickness at month 12 and 18
  • mean number of treatments
DA VINCI 2011 (Do 2012) 6 months and 12 months

Inclusion criteria:

  • DMO involving central macula
  • CRT ≥ 250 μm in central subfield
  • BCVA letter score at 4 m of 73-24 (Snellen equivalent: 20/40–20/320)
Exclusion criteria:

PDR (unless regressed and currently inactive)

VEGF Trap-Eye

n = 177 (177 eyes)

Standard threshold laser

n = 44 (44 eyes)

  • Change in central retinal thickness
  • safety and tolerability
  • change in BCVA from baseline at week 52
  • proportion of eyes that gained at least 15 ETDRS letters in BCVA compared with baseline at weeks 24 and 52
  • number of focal laser treatments given
  • incidence of cataracts
  • adverse events (increased intraocular pressure, vitreous haemorrhage)
DRCRnet 2010 12 monthsInclusion criteria:
  • Retinal thickness of ≥ 250 μm in the central subfield
  • Best-corrected ETDRS VA letter score 78-24 (20/32–20/320)
  • Retinal thickening due to DME involving the centre of the macula

Ranibizumab (0.5 mg) and standard threshold laser (macular laser) (375 eyes)

[Triamcinolone with prompt laser photocoagulation – not included in Virgili 2018]

Sham injection and standard threshold laser (macular laser) (293 eyes)
  • BCVA
  • Central retinal thickness
DRCRnet 2015 12 monthsInclusion criteria:
  • Definite retinal thickening due to DMO involving the centre of the macular
  • Retinal thickness of ≥ 250 μm in the central subfield
  • ETDRS BCVA 78-24 (20/32 - 20/320)
  • Aflibercept (2 mg)
224 eyes
  • Ranibizumab (0.3 mg)
218 Eyes
  • Bevacizumab (1.25 mg)
218 eyes
  • BCVA
  • Central retinal thickness
Ekinci 2014 12 monthsInclusion criteria:
  • CSMO
  • CRT>300 μm
[Unclear whether DMO is centre involving]

Bevacizumab (1.25 mg)

n = 50 (50 eyes)

Ranibizumab (0.05 mg)

n = 50 (50 eyes)

  • BCVA using the Snellen chart
  • Central retinal thickness
  • Intra-ocular pressure
Korobelnik 2014 (1) Inclusion criteria:
  • Central DMO involvement (defined as retinal thickening involving the 1 mm central (OCT) subfield thickness)
  • Retinal thickness ≥ 300 µm
  • BCVA ETDRS letter score of 73-24 (20/40-20/320) in the study eye
  • Type I or type II
Exclusion criteria:
  • Active PDR in the study eye with the exception of inactive, regressed PDR
  • aflibercept 2q4 n = 290 (290 eyes): aflibercept 2 mg every 4 weeks
  • aflibercept 2q8 n = 286 (286 eyes): aflibercept 2 mg monthly for 5 months, then every 8 weeks
Standard threshold laser and sham monthly injection = 286 (286 eyes)
  • proportion of eyes that gained at least 10 ETDRS letters in BCVA at week 52 compared with baselineproportion of eyes that gained at least 15 ETDRS letters in BCVA compared with baseline
  • change in central retinal thickness
  • proportion of eyes with a 2-step improvement in the ETDRS Diabetic Retinopathy Severity Scale (DRSS) score
  • change from baseline in the National Eye Institute Visual FunctionQuestionnaire-25 (NEI VFQ-25) near activities subscale score
  • change from baseline in the NEI VFQ-25 distance activities subscale score
  • Number of treatments
  • Incidence of cataracts
Li 2019 Follow-up: 12 months
  • Patients with visual impairment due to focal or diffuse DME in at least one eye.
  • BCVA score at both screening and baseline between 78 and 39 letters as measured by ETDRS-
(Approximately 20/32 to 20/160 Snellen equivalent).
ranibizumab 0.5mgMacular laser
  • Mean change in BCVA
  • Mean change in central subfield thickness
  • Proportion of patients with BCVA gain of ≥ 10 and ≥ 15 letters and loss of <10 and <15 letters
  • Proportion of patients with BCVA ≥ 73 letters (approximate20/40 Snellen chart equivalent)
  • treatment exposure, number of retreatments
  • ocular and non-ocular adverse events (AEs) and serious AEs (SAEs) over 12 months (increased intraocular pressure, vitreous haemorrhage)
Liu 2022 Follow-up: 12 months
  • >18 years of age.
  • type I or II diabetes mellitus.
  • haemoglobin A1c (HbA1c) 10%.
  • CRT 300 µm according to (OCT) imaging,
  • clear ocular media and adequate pupil dilation for examination
  • ETDRS BCVA of the subject’s non-target eye of ≥24 letters (equivalent to 20/320 of the Snellen vision).

Conbercept

(n=76)

Macular laser

(n=80)

  • mean change in BCVA
  • change in central retinal thickness
  • ocular and non-ocular adverse events (vitreous haemorrhage)
  • serious adverse events (SAEs)
  • number of treatments
Prunte 2016 24-month FU
  • 18 years with either type I or II diabetes mellitus
  • glycosylated haemoglobin (HbA1c) values of ≤12% at screening
  • (ETDRS) BCVA letter score ranging from 78 to 39, inclusive (approximate Snellen equivalent of 20/32–20/160)
  • those with visual impairment due to focal or diffuse DMO of any extent or thickness in at least one eye who were eligible for laser treatment
  • One eye was treated as the study eye.
Ranibizumab 0.5 mg with laserRanibizumab 0.5 mg
  • mean change in BCVA
  • treatment exposure
  • safety profile
LUCIDATE 2014 (Comyn 2014) 12 month follow upInclusion criteria:
  • Central subfield thickness of 300 μm or more
  • BCVA of 55-79 ETDRS (Snellen equivalent, 20/30-20/80)
  • Type I or type II diabetes
  • Centre-involving DMO
Exclusion criteria:
  • PDR either active or treatment within previous 3 months
  • Cataract precluding fundus photography

Ranibizumab (0.5 mg)

N= 25

Macular laser N=12
  • change in ETDRS BCVA
  • change in central macular thickness
  • change in ETDRS severity grade of diabetic retinopathy from fundus photographs
  • number of treatments
Macugen 2005 12 months FUInclusion criteria:
  • An area of retinal thickening of at least half a disc area involving the central macula
  • BCVA letter scores between 68-25 inclusive (approximate Snellen equivalent, 20/50–20/320)
  • MO involving the centre of the macula – demonstrated on OCT
Exclusion criteria:
  • History of PRP or focal photocoagulation
  • Cataract surgery within 12 months
Pegaptanib (0.3 mg, 1 mg, or 3 mg)Sham injection
  • BCVA
  • Central retinal thickness
Macugen 2011 (Sultan 2011)

12 months

24 months FU

Inclusion criteria:
  • Foveal thickness of ≥ 250 µm
  • BCVA with a letter score of 65-35 (20/50–20/200 Snellen equivalents)
  • DMO involving centre of macula

Pegaptanib sodium (0.3 mg)

n = 133

Sham injection

N = 127

  • BCVA (standardised ETDRS refraction protocol)
  • Central retinal thickness
Nepomuceno 2013 Inclusion criteria:
  • Central subfield thickness > 300 µm
  • BCVA ETDRS measurement between 0.3 logMAR (Snellen equivalent: 20/40) and 1.6 logMAR (Snellen equivalent: 20/800)
  • At least 1 session of macular laser photocoagulation performed at least 3 months previously
  • Centre-involved DMO
Exclusion criteria:
  • PDR needing PRP or anticipated to need PRP in the next 12 months

Bevacizumab (1.5 mg)

32 eyes

Ranibizumab (0.5 mg) 28 eyes
  • BCVA
  • Central retinal thickness
  • Mean number of treatments
READ2 2009 (Nguyen 2009)

12 months

24 months

Inclusion criteria:
  • Centre subfield thickness of ≥250 µm
  • VA between 20/40-20/320
  • Ranibizumab (0.5 mg)
    n = 42 (42 eyes)
  • Ranibizumab (0.5 mg) plus macular laser
    n = 42 (42 eyes)

Standard threshold laser

n = 42 (42 eyes)

  • Change in BCVA
  • 3 or more lines improvement
  • Change in foveal thickness
RELATION 2012 12 months FUInclusion criteria:
  • Focal or diffuse macular oedema
  • BCVA between 78-39 letters

Ranibizumab (0.5 mg) plus laser

n = 85 (85 eyes)

Laser plus sham injection

n = 85 (85 eyes)

  • mean change in BCVA
  • adverse events
RESOLVE 2010 (Massin 2010) 12 Month FUInclusion criteria:
  • CRT ≥ 300 µm
  • BCVA score between 73-39 letters (approximate Snellen equivalent of 20/40-20/160)
  • DMO with centre involvement
Exclusion criteria:
  • PDR in the study eye, with the exception of tufts of neovascularization < 1 disc area with no vitreous haemorrhage

Ranibizumab (0.3 mg or 0.5 mg)

n = 102 (102 eyes)

Sham injection

n = 49 (49 eyes)

  • Change in BCVA
  • Change in central retinal thickness
  • safety
RESPOND 2013 12 Month FUInclusion criteria:
  • Stable type I or type II diabetes
  • Focal or diffuse DMO
  • Ranibizumab (0.5 mg) n = 80 (80 eyes)
  • Ranibizumab (0.5 mg) plus laser n = 78 (78 eyes)

Laser

n = 81 (81 eyes)

  • mean change from baseline in Best Correct Visual Acuity (BCVA)
  • number of patients with improvement in BCVA
  • change in central retinal thickness
RESTORE 2011 (Mitchell 2011) 12 Month FUInclusion criteria:
  • Focal or diffuse MO
  • BCVA letter score between 78-39 (approximate Snellen equivalent 20/32-20/160)
  • Ranibizumab (0.5 mg) plus sham laser n = 116 (116 eyes)
  • Ranibizumab (0.5 mg) plus laser118 (118 eyes)
Laser treatment plus sham injections n = 111 (111 eyes
  • change in BCVA
  • VA improvement
  • BCVA letter score 73 (20/40 Snellen equivalent) at month 12
  • mean change in BCVA letter score
  • change in central retinal (subfield) thickness
  • number of treatments
  • incidence of cataracts
REVEAL 2015 (Ishibashi 2015) 12 monthsInclusion criteria:
  • Focal or diffuse macular oedema
  • BCVA letter score between 78-39 (approximate Snellen equivalent 20/32-20/160)
  • Ranibizumab sham laser (n = 133)
  • Ranibizumab + active laser (n =132)
Sham injection + active laser (n = 131).
  • change in BCVA
  • change in central retinal (subfield) thickness
  • safety
  • number of treatments
RISE-RIDE (Nguyen 2012) 24 monthsInclusion criteria:
  • Central subfield thickness ≥ 275 µm
  • BCVA, 20/40–20/320 Snellen equivalent using ETDRS testing
  • Ranibizumab (0.3 mg or 0.5 mg) n = 244 (244 eyes)
Sham injection (n = 122)
  • gain of 15 or more ETDRS letters in BCVA score from baseline at 24 months (corresponding to 3 lines on the eye chart)
  • change in BCVA
  • proportion of participants with BCVA Snellen equivalent of 20/40
  • change in BCVA score
  • proportion of participants losing 15 letters in BCVA score from baseline
  • mean change from baseline in CFT
  • proportion of participants with a 3-step progression from baseline in ETDRS retinopathy severity
  • mean number of treatments
Soheilian 2007 12 month FUInclusion criteria:
  • Clinically significant DMO
Exclusion criteria:
  • Previous PRP or focal laser photocoagulation
  • High-risk PDR
  • Significant media opacities
  • VA of 20/40 or better, or worse than 20/300
Bevacizumab (1.25 mg)Macular laser
  • mean change from baseline BCVA
  • proportion of participants with BCVA Snellen equivalent of 20/40
  • number of treatments
Turkoglu 2015 12-month FUInclusion criteria:
  • CSMO
Exclusion criteria:
  • History of intravitreal injection and laser photocoagulation for PDR or CSMO
Focal or grid laser treatmentInitial injection of ranibizumab 0.5 mg/0.05 mL
  • best corrected visual acuity (BCVA) between baseline and one year
  • central macular thickness
Wykoff 2022 12 Months FU
  • Age ≥18 years
  • DM type 1 or 2
  • Current regular use of insulin
  • Current regular use of oral anti-hyperglycaemic agents
  • HbA1c of ≤10% within 2 months before day

Intravitreal Faricimab 6·0 mg every 8 weeks,

intravitreal Faricimab 6·0 mg

Intravitreal aflibercept 2·0 mg every 8 weeks
  • BCVA outcomes
  • Central retinal thickness
  • DR severity outcomes

BCVA: best-corrected visual acuity; CMT: central macular thickness; CRT: central retinal thickness; CSMO: clinically significant macular oedema; CSRT: central subfield retinal thickness; DME: diabetic macular oedema; DMO: diabetic macular oedema; DR: diabetic retinopathy; ETDRS: Early Treatment Diabetic Retinopathy Study; FAZ: foveal avascular zone; IVS: intravitreal steroid; logMAR: log of the Minimum Angle of Resolution; mETDRS: modified Early Treatment of Diabetic Retinopathy Study; MMG: mild macular grid; MO: macular oedema; NPDR: non-proliferative diabetic retinopathy; NR: not reported; OCT: optical coherence tomography; PDR: proliferative diabetic retinopathy; PR: proliferative retinopathy; PRN: pro-re-nata (i.e. as needed); PRP: panretinal photocoagulation; SDM: subthreshold micropulse diode; VA: visual acuity; VEGF: vascular endothelial growth factor

Table 5Randomised controlled trials (for full study details, see Jorge et al. 2018)

StudyFollow-up timePopulationInterventionComparatorOutcomes
Randomised controlled trials (from Jorge et al. 2018 Cochrane systematic review)
Bandello 2005 12 Months FUInclusion criteria:
  • CSMO
  • NPDR
  • Foveal thickness exceeding 2 SD normal mean value
  • VA≥ 20/200 of ETDRS chart
  • Type I or type II diabetes
Exclusion criteria:
  • Cataract extraction within the past 12 months
  • PDR
  • Significant media opacities
  • Previous laser treatment

Standard threshold laser

“Classic” Nd:Yag 532 nm laser treatment

Subthreshold laser

“Light” Nd:Yag 532 nm laser treatment

  • significant decrease in FTH on OCT retina thickness
  • eyes that experienced a visual gain or loss of ≥ 5 letters (approximately 1 line) on the ETDRS chart
  • mean changes in VA
Blankenship 1979 12 Months FUInclusion criteria:
  • Diffuse and cystoid MO
  • BCVA ≥ 20/100 (0.7 logMAR)
Exclusion:
  • PDR
  • Previous photocoagulation
Argon laserNo treatment
  • Changes of VA
Casson 2012 6 Months FUInclusion criteria:
  • Focal or diffuse MO
  • CSRT ≥ 250 μm or ≥ 300 μm in ≥ 1 of the 4 inner subfields
  • Best-corrected ETDRS VA score ≥ 19 letters
  • Type I or type II diabetes

Subthreshold laser

Nanopulse (2RT) laser treatment

Standard threshold laser
  • Changes of VA
  • Changes of central retinal thickness
DRCNET 2007 12 Months FUInclusion criteria:
  • CSMO
  • Definite retinal thickening due to previously untreated DMO within 500μm of the macular centre
  • Retinal thickness ≥ 250μm in central subfield or ≥ 300μm in ≥ 1 of the 4 inner subfields
  • Best-corrected electronic ETDRS VA score ≥ 19 (approximately 20/400 or better)
  • Type I or type II diabetes
  • No prior laser or other treatment for DMO
Exclusion criteria:
  • Cataract surgery within prior 6 months

Standard threshold laser (mETDRS style focal laser)

(162 eyes)

Subthreshold laser (MMG laser)

(161 eyes)

  • change in retinal thickening in the central subfield on OCT.
  • Change in VA
  • adverse events
ETDRS 1985 12 Months FUInclusion criteria:
  • CSMO
  • Early PR and moderate-to-severe non-proliferative retinopathy
Exclusion criteria:
  • Right risk proliferative retinopathy
  • VA<20/200

Immediate standard threshold laser (argon laser)

754 eyes

Deferred standard threshold laser = (no intervention)

) (1490)

  • Outcomes VA and occurrence of retinal thickening
Figueira 2009 12 Months FUInclusion criteria:
  • CSMO
  • BCVA ≥ 55 letters on the modified ETDRS chart (equivalent to 20/80 or better)
  • Type II diabetes
Exclusion criteria:
  • Significant cataract
  • Previous laser treatment

Subthreshold laser (Micropulse diode)

44 Eyes

Standard threshold laser (argon green)

40 eyes

  • BCVA
  • Central macular thickness
Ishibashi 2014 12 Months FUInclusion criteria:
  • Macular oedema involving central fovea
  • Retinal thickening ≥ 250 µm
  • Corrected VA 35-68 letters by ETDRS charts
Pegaptanib sodiumSham injection
  • Change in visual acuity
  • Change in retinal thickness
Ladas 1993 12 Months FUInclusion criteria:
  • CSMO
  • Background DR
  • Diffuse MO [defined as having 2 or more-disc areas of diffuse fluorescein involving some portion of the FAZ – indicating that DMO is centre-involving]
Exclusion criteria:
  • Significant media opacities
  • Previous treatment with PRP or photocoagulation to within 2-disc diameters of the foveola
  • BCVA ≤ 0.1

Standard threshold laser (Blue-green argon laser)

(27 eyes)

control (23 eyes)
  • Change in VA defined as a difference of ≥ 2 lines on the standard Snellen’s VA charts
Laursen 2004 12 Months FUInclusion criteria:
  • CSMO
  • Type I or type II diabetes
Exclusion criteria:
  • Cataract extraction within past 12 months
  • PDR
  • Significant media opacities
  • Previous laser photocoagulation for DR
Subthreshold laser (MPDL) n=12Standard threshold laser (argon laser) n=11
  • Visual improvement/loss by > 2 lines on ETDRS chart and reduction/elimination of macular oedema evaluated by OCT
Lavinsky 2011 12 Months FUInclusion criteria:
  • CSMO
  • Retinal thickening within 500 µm of macular centre and CMT ≥ 250 µm
  • BCVA > 20/400 and < 20/40 by the ETDRS protocol
Exclusion criteria:
  • No prior laser or drug treatment for DMO
  • Standard threshold laser (mETDRS focal/grid)
(42 eyes)

Subthreshold laser

  • normal-density SDM laser
high-density SDM laser

(42 eyes)

  • changes from baseline in ETDRS BCVA and in CMT assessed by OCT;
Olk 1986 12 Months FUInclusion criteria:
  • Diffuse with or without cystoid macular oedema
  • ≥ 2-disc areas of retinal thickening
  • Retinal thickening that involved the centre of the macular
  • BCVA < 20/32+2 and better than 20/200-3
Exclusion criteria:
  • Cataract extraction within previous 12 months
  • Significant media opacities
  • Previous laser photocoagulation to within 2-disc diameters of the centre of the FAZ

Standard threshold laser

Grid with PRP

82 eyes

No treatment

78 eyes

  • improvement or worsening of visual acuity and reduction of macular oedema and/or cystoid macular oedema
Pei-Pei 2015 12 Months FUInclusion criteria:
  • Diffuse and cystoid MO
  • Newly diagnosed severe NPDR
  • Mean CRT > 300 µm
  • ETDRS VA > 19 letters (Snellen’s equivalent of 20/400 or better)
  • Type II diabetes
Exclusion criteria:
  • Previous retinal treatment: laser, drug, or surgery

Subthreshold laser

21 eyes

543 nm subthreshold laser (laser grid)

Standard threshold laser

21 eyes

  • VA as determined by the ETDRS vision chart
  • mean CMT as determined by OCT,
Tewari 1998 12 Months FUInclusion criteria:
  • CSMO
  • BCVA of 6/60 or better in each eye
Exclusion criteria:
  • Severe NPDR or PDR in either of the eyes
  • Significant media opacities
  • Previous laser photocoagulation

Subthreshold laser

Diode laser (40 eyes; 20 focal and 20 grid)

Standard threshold laser

Argon green (40 eyes; 20 focal and 20 grid)

  • VA (considering a 2-line change of Snellen’s).
  • Secondary outcome: complications such as submacular haemorrhage
Venkatesh 2011 12 Months FUInclusion criteria:
  • Focal and diffuse
  • NPDR
Exclusion criteria:
  • Significant media opacities
  • Prior medical treatment (intravitreal/peribulbar steroids or antiangiogenic drugs), or prior laser treatment

Subthreshold laser

Subthreshold micropause diode laser

(n = 23)

Standard threshold laser

Double-frequency neodymium YAG (Nd:YAG) laser

(n = 23)

  • Change in central macular thickness as measured by OCT
  • change in macular retinal sensitivity
  • measured using multifocal electroretinography
  • change in BCVA and contrast sensitivity
Vujosevic 2010 12-months FUInclusion criteria:
  • CSMO
  • Type II diabetes
Exclusion criteria:
  • Significant media opacities
  • Any type of previous macular treatment (macular laser photocoagulation, vitrectomy, intravitreal steroids, antiangiogenic drugs)

Subthreshold laser

Micropulse diode laser

(32 eyes)

Standard threshold laser

(30 eyes)

m-ETDRS with green laser

  • OCT changes and BCVA.
Xie 2013 12-months FUInclusion criteria:
  • Type 2 or type 1 diabetes.
  • DMO by ophthalmologist combined FFA, OCT
  • no significant refractive media turbidity.
  • no other ocular disease history including glaucoma or anti - glaucoma surgery history, congenital retinal disease history or acquired retinal surgery, retinal laser treatment history.
Argon ion laser groupsubthreshold micropulse diode laser ( SDM, 810nm)
  • mean best corrected visual acuity ( BCVA )
  • mean central macular thickness

BCVA: best-corrected visual acuity; CMT: central macular thickness; CRT: central retinal thickness; CSMO: clinically significant macular oedema; CSRT: central subfield retinal thickness; DME: diabetic macular oedema; DMO: diabetic macular oedema; DR: diabetic retinopathy; ETDRS: Early Treatment Diabetic Retinopathy Study; FAZ: foveal avascular zone; IVS: intravitreal steroid; logMAR: log of the Minimum Angle of Resolution; mETDRS: modified Early Treatment of Diabetic Retinopathy Study; MMG: mild macular grid; MO: macular oedema; NPDR: non-proliferative diabetic retinopathy; NR: not reported; OCT: optical coherence tomography; PDR: proliferative diabetic retinopathy; PR: proliferative retinopathy; PRN: pro-re-nata (i.e. as needed); PRP: panretinal photocoagulation; SDM: subthreshold micropulse diode; VA: visual acuity; VEGF: vascular endothelial growth factor

Table 6Randomised controlled trials (for full study details, see Mehta et al. 2018)

StudyFollow-up timePopulationInterventionComparatorOutcomes
Randomised controlled trials (from Mehta et al. 2018 Cochrane systematic review)
DRCRnet U 2018 (Maturi 2018)6 Months FUInclusion criteria:
  • Persistent DMO (previously received at least 3 injections of anti-VEGF within prior 20 weeks)
  • Retinal thickening involving the centre of the macular
  • CMT thickness greater than 300 µm
  • VA letter score in study eye ≤ 78 and ≥ 24 logMAR letters (approximate Snellen equivalent 20/32 to 20/320)
  • Type I or type II diabetes
Intravitreal ranibizumab (0.3 mg) and dexamethasone implant (0.7g)Intravitreal ranibizumab (0.3 mg) and sham injection
  • Mean change in visual acuity
  • Percentage of eyes with at leat 10 and 15 ETDRS letters gain
  • Mean change in central macular thickness
  • Adverse events
Lim 2012 12 Months FUInclusion criteria:
  • CSMO
  • CMT of at least 300 µm
Exclusion criteria:
  • Previous treatment for DMO
  • PDR with active neovascularisation
  • Previous panretinal photocoagulation
Intravitreal bevacizumab (1.25mg/0.05ml) and intravitreal triamcinolone acetonide (2mg/0.05ml)
  • Intravitreal bevacizumab (1.25mg/0.05ml)
Intravitreal triamcinolone acetonide (2mg/0.05ml)
  • Change in BCVA at 1 year (LogMAR chart)
  • Change in CMT at 1 year
Maturi 2015 12 Months FUInclusion criteria:
  • BCVA scores between 24 and 78, ETDRS letters (20/32–20/320 Snellen equivalent)
  • DMO because of type I or type II diabetes
  • CMT of greater than 250 µm
Intravitreal bevacizumab (1.25mg) and dexamethasone implant (0.7mg)Intravitreal bevacizumab (1.25mg)
  • Change in visual acuity (ETDRS letters) at 12 months
  • Change in central subfield thickness (OCT) at 12 months
  • Adverse events
Neto 2017 6 Months FUInclusion criteria:
  • CRT ≥ 275 µm
  • BCVA score between 20 letters (20/400 ETDRS) and 70 letters (20/40 ETDRS)
  • Type I or type II diabetes
  • No prior foveal treatment with laser therapy
Intravitreal bevacizumab (1.25mg/0.05ml) and intravitreal triamcinolone acetate (4mg/0.1ml)
  • Intravitreal bevacizumab (1.25mg/0.05ml)
  • Intravitreal triamcinolone acetate (4mg/0.1ml)
  • Change in BCVA (ETDRS)
  • Change in central retinal thickness
  • Adverse events
Riazi-Esfahani 2017 6 Months FUInclusion criteria:
  • Bilateral clinically significant DMO based on ETDRS criteria
  • CMT of > 320 µm
Exclusion criteria:
  • PDR
  • Significant media opacities
  • A history of any treatment for DMO (panretinal or focal laser photocoagulation and anti-VEGF or IVS)
  • VA ≤ 20/320
Intravitreal bevacizumab (1.25mg/0.05ml) and intravitreal triamcinolone acetonide (1mg/0.025ml)Intravitreal bevacizumab (1.25mg/0.05ml)
  • Mean change in BCVA
  • Mean change in CMT
  • Number of injections
  • Adverse events
Shoeibi 2013 6 Months FUInclusion criteria:
  • DMO refractory to laser treatment
  • Participants had refractory DMO that had not responded to macular laser treatment
Exclusion criteria:
  • Significant media opacities
Intravitreal bevacizumab (1.25mg/0.05ml) and triamcinolone acetonide (2mg/0.05ml)Intravitreal bevacizumab (1.25mg/0.05ml) and sham injection
  • Change in central macular thickness
  • Change in BCVA
  • Adverse events
Soheilian 2012

12 Months FU

24 months FU

Inclusion criteria:
  • CSMO based on ETDRS criteria
Exclusion criteria:
  • High-risk PDR
  • Significant media opacities
  • Panretinal or focal laser photocoagulation

Intravitreal bevacizumab (1.25mg/0.05ml) and triamcinolone acetonide (2mg/0.05ml)

n = 50 eyes

Intravitreal bevacizumab (1.25mg/0.05ml)

Standard threshold laser (Focal or modified grid laser)

n = 50 eyes

  • BCVA
  • Central macular thickness
  • Adverse events
Synek 2011 6 Months FUInclusion criteria:
  • CSMO unresponsive to previous macular photocoagulation
Exclusion criteria:
  • History of cataract surgery within past 6 months
  • PDR with high-risk characteristics
  • Significant media opacities
  • Prior intraocular injection or vitrectomy
Intravitreal bevacizumab (1.25mg/0.05ml) and triamcinolone acetonide (2mg/0.05ml)Intravitreal bevacizumab (1.25mg/0.05ml)
  • Change in central macular thickness
  • Change in BCVA
  • Ocular adverse events: IOP rise, cataract progression, intraocular inflammation

BCVA: best-corrected visual acuity; CMT: central macular thickness; CRT: central retinal thickness; CSMO: clinically significant macular oedema; CSRT: central subfield retinal thickness; DME: diabetic macular oedema; DMO: diabetic macular oedema; DR: diabetic retinopathy; ETDRS: Early Treatment Diabetic Retinopathy Study; FAZ: foveal avascular zone; IVS: intravitreal steroid; logMAR: log of the Minimum Angle of Resolution; mETDRS: modified Early Treatment of Diabetic Retinopathy Study; MMG: mild macular grid; MO: macular oedema; NPDR: non-proliferative diabetic retinopathy; NR: not reported; OCT: optical coherence tomography; PDR: proliferative diabetic retinopathy; PR: proliferative retinopathy; PRN: pro-re-nata (i.e. as needed); PRP: panretinal photocoagulation; SDM: subthreshold micropulse diode; VA: visual acuity; VEGF: vascular endothelial growth factor

Table 7Randomised controlled trials (for full study details, see Rittiphairoj et al. 2020)

StudyFollow-up timePopulationInterventionComparatorOutcomes
Randomised controlled trials (from Rittiphairoj et al. 2020 Cochrane systematic review)
BEVORDEX 2014 (Gillies 2014)12 Months FUInclusion criteria:
  • DME for whom the investigator believed that laser treatment would be unhelpful
  • BCVA 20/400 to 20/40
Intravitreal dexamethasone implant (Ozurdex 0.7 mg) every 16 weeks (PRN)Intravitreal bevacizumab (1.25 mg) every 4 weeks (PRN)
  • change in mean BCVA
  • mean change in central macular thickness
  • mean number of treatments
  • incidence of cataracts
  • adverse events
  • Patient-reported outcome: Impact of Vision Impairment questionnaire
Callanan 2017 12 Months FUInclusion criteria:
  • CRT by SD-OCT ≥ 300 μm with Spectralis (Heidelberg) or ≥ 275 μm with Cirrus (Zeiss)
  • BCVA > 34 and < 70
Intravitreal treatment with dexamethasone implant 0.7 mgRanibizumab 0.5 mg
  • Central retinal thickness
  • BCVA
  • Mean number of treatments
  • Incidence of cataracts
  • Adverse events
DRCR​.net 2008 24 Months FUInclusion criteria:
  • Definite retinal thickening resulting from DME involving the centre of the macular
  • CRT of ≥ 250 μm in the central subfield
  • Best-corrected electronic ETDRS VA letter score between 73 (approximately 20/40) and 24 (approximately 20/320)
  • Type I or type II diabetes
Exclusion criteria:
  • Prior treatment with intravitreal corticosteroids

Intravitreal triamcinolone (1 mg)

Intravitreal triamcinolone (4 mg)

Standard threshold laser (Focal/grid laser)
  • BCVA
  • central retinal thickness
  • adverse events
FAME 2011 (Campochiaro 2011)24 Months FUInclusion criteria:
  • Mean foveal thickness of at least 250 μm in the study eye
  • BCVA of ≥ 19 and ≤ 68 letters (20/50 or worse but at least 20/ 400) in the study eye by an ETDRS chart.
  • BCVA of the non-study eye must be no worse than 20/400.
  • Type I or type II diabetes
  • At least 1 macular laser treatment more than 12 weeks prior to the screening visit

0.2 μg/day fluocinolone (low dose insert)

0.5 μg/day fluocinolone (high dose insert)

Sham injection
  • improvement from baseline BCVA
  • adverse events
Kriechbaum 2014 12 Months FUInclusion criteria:
  • CSRT of at least 300 µm
  • BCVA of 20/25 to 20/400 Snellen equivalent in the study eye
Exclusion criteria:
  • Active proliferative DR with necessity of panretinal laser treatment
  • Previous macular laser photocoagulation or intravitreal injection therapy
3 injections of 2.5 mg bevacizumab, 2 sham injections after 4 and 8 weeks, then PRN regimen1 initial injection of 8 mg triamcinolone, 2 sham injections after 4 and 8 weeks, then PRN regimen
  • correlation BCVA
  • central subfield retinal thickness
Lim 2012 12 Months FUInclusion criteria:
  • eyes with clinically significant DME based on ETDRS criteria
  • macular oedema with central macular thickness of at least 300 µm by OCT
Exclusion criteria:
  • unstable medical status, including glycaemic control and blood pressure
  • any previous treatment for DME, including intravitreal, sub-Tenon injection or macular photocoagulation
  • history of vitreoretinal surgery
  • uncontrolled glaucoma
  • proliferative diabetic retinopathy with active neovascularization
  • previous panretinal photocoagulation
  • presence of vitreomacular traction

Treatment intervention 1: intravitreal injection of bevacizumab alone

Treatment intervention 2: intravitreal injection of bevacizumab 1.25 mg with triamcinolone 2 mg

Treatment intervention 3: intravitreal injection of triamcinolone 2 mg
  • logMAR BCVA.
  • central macular thickness.
  • Adverse events
MEAD 2014 (Boyer 2014)12 Months FUInclusion criteria:
  • Fovea-involved macular oedema that was associated with DR
  • CRT of 300 μm
  • BCVA between 34 and 68 letters (20/200 to 20/50)
  • Type I or type II diabetes
  • Previously treated with medical or laser therapy
  • Naïve patients who had refused laser treatment or would not benefit from laser therapy
  • Intravitreal dexamethasone implant 0.7 mg
Intravitreal dexamethasone implant 0.37 mg
Sham procedure
  • change in BCVA from baseline
  • percentage of participants with BCVA of 20/40 at each study visit,
  • change in CRT from baseline
  • adverse events
Ockrim 200812 Months FUInclusion criteria:
  • CSMO persisting 4 months or more
  • BCVA between 6/12 and 3/60
  • At least 1 prior laser treatment
Intravitreal triamcinolone 4 mgStandard threshold laser
  • proportion of participants who improved by 15 or more ETDRS letters at 12 months
  • mean ETDRS letter score at 12 months
  • mean CRT measured with OCT
  • adverse events
Sutter 2004 12 Months FUInclusion criteria:
  • Persistent DME, diffuse or focal, involving the central fovea persisting 3 months or more after adequate laser treatment. BCVA in the affected eye(s) of 6/9 or worse
Intravitreal triamcinolone (4 mg)Sham treatment (subconjunctival saline injection)
  • best corrected logMAR visual acuity
  • adverse events
  • change in macular thickness

BCVA: best-corrected visual acuity; CMT: central macular thickness; CRT: central retinal thickness; CSMO: clinically significant macular oedema; CSRT: central subfield retinal thickness; DME: diabetic macular oedema; DMO: diabetic macular oedema; DR: diabetic retinopathy; ETDRS: Early Treatment Diabetic Retinopathy Study; FAZ: foveal avascular zone; IVS: intravitreal steroid; logMAR: log of the Minimum Angle of Resolution; mETDRS: modified Early Treatment of Diabetic Retinopathy Study; MMG: mild macular grid; MO: macular oedema; NPDR: non-proliferative diabetic retinopathy; NR: not reported; OCT: optical coherence tomography; PDR: proliferative diabetic retinopathy; PR: proliferative retinopathy; PRN: pro-re-nata (i.e. as needed); PRP: panretinal photocoagulation; SDM: subthreshold micropulse diode; VA: visual acuity; VEGF: vascular endothelial growth factor

Table 8Visual acuity at 12 months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Subthreshold laser0.00 (−0.05, 0.06)ModerateCould not differentiate
Bevacizumab−0.12 (−0.16, −0.08)Favours Bevacizumab
Ranibizumab−0.13 (−0.16, −0.10)Favours Ranibizumab
Aflibercept−0.18 (−0.22, −0.15)Favours Aflibercept
Pegaptanib0.01 (−0.10, 0.13)Could not differentiate
Dexamethasone−0.10 (−0.15, −0.05)Favours Dexamethasone
Triamcinolone−0.03 (−0.08, 0.02)Could not differentiate
Ranibizumab + standard threshold laser−0.11 (−0.15, −0.08)Favours Ranibizumab + standard threshold laser
Triamcinolone + standard threshold laser−0.02 (−0.07, 0.03)Could not differentiate
Bevacizumab + standard threshold laser−0.16 (−0.31, −0.02)Favours Bevacizumab + standard threshold laser
Bevacizumab + triamcinolone−0.08 (−0.15, −0.01)Favours Bevacizumab + triamcinolone
Sham0.10 (−0.01, 0.21)Could not differentiate
Dexamethasone + ranibizumab−0.12 (−0.21, −0.04)Favours Dexamethasone + Ranibizumab
Dexamethasone + bevacizumab−0.13 (−0.30, 0.04)Could not differentiate
Conbercept−0.17 (−0.25, −0.09)Favours Conbercept
Faricimab−0.20 (−0.26, −0.14)Favours Faricimab
Brolucizumab−0.18 (−0.24, −0.12)Favours brolucizumab

Table 9Visual acuity at 24 months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Bevacizumab−0.12 (−0.36, 0.11)ModerateCould not differentiate
Ranibizumab−0.13 (−0.46, 0.20)Could not differentiate
Aflibercept−0.11 (−0.29, 0.07)Could not differentiate
Dexamethasone−0.06 (−0.38, 0.25)Could not differentiate
Triamcinolone0.08 (−0.25, 0.41)Could not differentiate
Ranibizumab + standard threshold laser−0.12 (−0.45, 0.21)Could not differentiate
Fluocinolone−0.08 (−0.51, 0.34)Could not differentiate
Sham−0.03 (−0.30, 0.24)Could not differentiate
Triamcinolone + standard threshold laser−0.02 (−0.36, 0.29)Could not differentiate

Table 10Visual acuity at 12 months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Bevacizumab−0.14 (−0.19, −0.09)HighFavours Bevacizumab
Ranibizumab−0.15 (−0.19, −0.11)Favours Ranibizumab
Aflibercept−0.19 (−0.24, −0.14)Favours Aflibercept
Pegaptanib0.00 (−0.15, 0.14)Could not differentiate
Dexamethasone−0.11 (−0.19, −0.04)Favours Dexamethasone
Triamcinolone−0.04 (−0.10, 0.02)Could not differentiate
Ranibizumab + standard threshold laser−0.14 (−0.19, −0.09)Favours Ranibizumab + standard threshold laser
Triamcinolone + standard threshold laser−0.04 (−0.13, 0.04)Could not differentiate
Bevacizumab + triamcinolone−0.08 (−0.17, 0.01)Could not differentiate
Sham0.08 (−0.04, 0.21)Could not differentiate
Conbercept−0.17 (−0.27, −0.07)Favours Conbercept
Faricimab−0.17 (−0.24, −0.10)Favours Faricimab
Brolucizumab−0.18 (−0.27, −0.10)Favours Brolucizumab

Table 11Visual acuity at 24

months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Bevacizumab−0.18 (−0.21, −0.15)ModerateFavours Bevacizumab
Ranibizumab−0.23 (−0.27, −0.18)Favours Ranibizumab
Aflibercept−0.24 (−0.27, −0.20)Favours Aflibercept
Dexamethasone−0.10 (−0.22, 0.02)Could not differentiate
Triamcinolone0.00 (−0.26, 0.26)Could not differentiate
Ranibizumab + standard threshold laser−0.12 (−0.17, −0.07)Favours Ranibizumab + standard threshold laser
Fluocinolone−0.11 (−0.24, 0.02)Could not differentiate
Sham−0.05 (−0.18, 0.07)Could not differentiate
Triamcinolone + standard threshold laser−0.02 (−0.07, 0.03)Could not differentiate

Table 12Central retinal thickness at 12 months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Subthreshold laser−1.91 (−42.49, 39.60)ModerateCould not differentiate
Bevacizumab−10.16 (−48.22, 29.93)Could not differentiate
Ranibizumab−57.29 (−82.28, −29.18)Favours ranibizumab
Aflibercept−75.46 (−105.60, −42.43)Favours aflibercept
Dexamethasone−99.51 (−144.00, −51.61)Favours dexamethasone
Triamcinolone−20.67 (−70.86, 27.70)Could not differentiate
Ranibizumab + standard threshold laser−76.03 (−111.70, −37.07)Favours ranibizumab + standard threshold laser
Bevacizumab + triamcinolone−10.65 (−65.13, 44.80)Could not differentiate
Dexamethasone + ranibizumab−93.82 (−159.20, −21.61)Favours dexamethasone + ranibizumab
Fluocinolone−1.67 (−89.06, 85.14)Could not differentiate
Conbercept−53.82 (−127.10, 20.39)Could not differentiate
Sham74.02 (2.90, 144.50)Favours standard threshold laser
Dexamethasone + bevacizumab−18.29 (−105.90, 70.61)Could not differentiate
Bevacizumab + standard threshold laser−9.74 (−82.00, 64.46)Could not differentiate
Brolucizumab−92.06 (−144.60, −34.13)Favours brolucizumab
Faricimab−88.27 (−136.70, −34.00)Favours faricimab

Table 13Central retinal thickness at 24 months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Bevacizumab−65.47 (−96.59, −34.19)ModerateFavours bevacizumab
Ranibizumab−92.13 (−123.70, −60.70)Favours ranibizumab
Aflibercept−109.70 (−132.90, −86.52)Favours aflibercept
Dexamethasone−44.67 (−87.87, −2.08)Favours dexamethasone
Triamcinolone66.54 (42.15, 91.00)Could not differentiate
Ranibizumab + standard threshold laser24.93 (−24.70, 73.77)Could not differentiate
Fluocinolone−23.15 (−66.75, 20.09)Could not differentiate
Sham35.27 (−4.62, 74.69)Could not differentiate
Subthreshold laser−0.59 (−13.95, 12.78)Could not differentiate

Table 14Central retinal thickness at 12 months relative to Standard threshold laser

TreatmentMD (95% CrI)QualityInterpretation of effect
Bevacizumab−19.86 (−58.85, 22.87)ModerateCould not differentiate
Ranibizumab−61.86 (−90.77, −29.01)Favours ranibizumab
Aflibercept−82.36 (−116.10, −42.93)Favours aflibercept
Dexamethasone−99.68 (−145.30, −48.09)Favours dexamethasone
Triamcinolone−34.29 (−106.90, 42.55)Could not differentiate
Ranibizumab + standard threshold laser−73.83 (−111.50, −32.27)Favours ranibizumab + standard threshold laser
Triamcinolone + standard threshold laser−70.44 (−135.10, −1.97)Favours triamcinolone + standard threshold laser
Bevacizumab + triamcinolone−29.34 (−101.60, 46.33)Could not differentiate
Fluocinolone−5.03 (−96.26, 86.60)Could not differentiate
Conbercept−53.25 (−129.80, 25.25)Could not differentiate
Sham70.01 (−4.07, 144.20)Could not differentiate
Subthreshold laser40.74 (−56.21, 136.70)Could not differentiate
Bevacizumab + standard threshold laser−18.28 (−94.00, 61.36)Could not differentiate
Dexamethasone + bevacizumab−26.41 (−117.30, 66.87)Could not differentiate
Brolucizumab−97.65 (−154.80, −32.70)Favours brolucizumab
Faricimab−110.60 (−166.60, −44.61)Favours faricimab

Table 15Anti-VEGF vs standard threshold laser: Visual Acuity: three or more lines improvement from baseline up to 12M

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF)
Overall
11Parallel RCTs2410RR: 2.30 [1.54, 3.45]Very LowFavours Anti-VEGF
Subgroup: Conbercept (RR greater than 1 favours anti-VEGF)
1Parallel RCTs199RR: 1.67 [0.92, 3.03]HighCould not differentiate
Subgroup aflibercept (RR greater than 1 favours anti-VEGF)
4Parallel RCT1098RR: 3.36 [2.15, 5.23]ModerateFavours aflibercept
Subgroup bevacizumab (RR greater than 1 favours anti-VEGF)
1Parallel RCT50RR: 2.26 [0.47, 10.98]HighCould not differentiate
Subgroup ranibizumab (RR greater than 1 favours anti-VEGF)
5Parallel RCT1033RR: 1.92 [0.87, 4.24]Very LowCould not differentiate

Table 16Anti-VEGF vs standard threshold laser: The mean number of treatments at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subgroup aflibercept (MD lower than 0 favours anti-VEGF)
4Parallel RCT905MD: 9.49 [8.76, 10.23]LowFavours standard threshold laser
Subgroup bevacizumab (MD lower than 0 favours anti-VEGF)
2Parallel RCT164MD: 2.10 [1.62, 2.58]ModerateFavours standard threshold laser
Subgroup ranibizumab (MD lower than 0 favours anti-VEGF)
4Parallel RCT903MD: 1.98 [−2.34, 6.29]Very LowFavours standard threshold laser
Subgroup: Conbercept (MD lower than 0 favours anti-VEGF)
1Parallel RCT157MD: −0.10 [−1.18, 0.98]HighCould not differentiate

Table 17Anti-VEGF vs standard threshold laser: The mean number of treatments at 24 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Aflibercept (MD lower than 0 favours anti-vegf)
2Parallel RCT578MD: 19.00 [16.64, 21.35]ModerateFavours standard threshold laser

Table 18Anti-VEGF vs standard threshold laser: Adverse Events at 24 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect

Adverse Event: Cataract progression

Subgroup aflibercept (RR lower than 1 favours anti-VEGF)

3Parallel RCTs1132RR: 0.92 [0.36, 2.35]HighFavours standard threshold laser
Subgroup: ranibizumab (RR lower than 1 favours anti-VEGF)
1Parallel RCTs227RR: 0.32 [0.01, 7.75]HighFavours standard threshold laser
Adverse Event: IOP increase
Subgroup aflibercept (RR lower than 1 favours anti-VEGF)
2Parallel RCT554RR: 1.75 [0.94, 3.26]ModerateFavours standard threshold laser
Subgroup bevacizumab (RR lower than 1 favours anti-VEGF)
1Parallel RCT80RR: 2.72 [0.11, 64.85]HighFavours standard threshold laser
Subgroup ranibizumab (RR lower than 1 favours anti-VEGF)
1Parallel RCT80RR: 8.14 [0.49, 134.21]HighFavours standard threshold laser
Adverse Event: Vitreous haemorrhage
Subgroup aflibercept (RR lower than 1 favours anti-VEGF)
3Parallel RCTs1132RR: 0.73 [0.35, 1.50]LowFavours standard threshold laser
Subgroup: Conbercept (RR lower than 1 favours anti-VEGF)
1Parallel RCTs156RR: 1.05 [0.27, 4.06]HighFavours standard threshold laser
Subgroup bevacizumab (RR lower than 1 favours anti-VEGF)
1Parallel RCT80RR: 0.30 [0.01, 7.21]HighFavours standard threshold laser
Subgroup ranibizumab (RR lower than 1 favours anti-VEGF)
1Parallel RCT382RR: 0.31 [0.08, 1.11]HighFavours standard threshold laser

Table 19Bevacizumab VS Ranibizumab

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR lower than 1 favours bevacizumab)
2Parallel RCTs636RR: 0.88 [0.68, 1.14]HighCould not differentiate
The mean number of treatments at 12 months (MD lower than 0 favours bevacizumab)
2Parallel RCT226MD: 1.06 [−1.09, 3.22]HighFavours bevacizumab

Table 20Aflibercept vs Ranibizumab

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
The mean number of treatments at 12 months (MD lower than 0 favours aflibercept)
2Parallel RCT182MD: −0.95 [−2.11, 0.21]LowCould not differentiate

Table 21Brolucizumab vs Aflibercept

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF)
2Parallel RCTs736RR: 1.14 [0.96, 1.37]HighCould not differentiate
The mean number of treatments at 12 months (MD lower than 0 favours brolucizumab)
2Parallel RCT736MD: −1.60 [−1.80, −1.39]HighFavours brolucizumab

Table 22Faricimab vs Aflibercept

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF)
2Parallel RCTs1094RR: 1.01 [0.85, 1.21]HighCould not differentiate

Table 23Ranibizumab vs Ranibizumab + standard threshold laser

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favour anti-VEGF plus laser)
3Parallel RCTs636RR: 1.05 [0.78, 1.42]ModerateCould not distinguish

Table 24Bevacizumab vs Bevacizumab + standard threshold laser

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
The mean number of treatments at 12 months (MD lower than 0 favours bevacizumab+ laser)
1Parallel RCT736MD: 0.26 [−0.25, 0.77]HighCould not differentiate

Table 25Ranibizumab vs sham

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF)
2Parallel RCTs5092.66 [1.94, 3.65]HighFavours ranibizumab

Table 26Anti-VEGF and steroid versus anti-VEGF alone

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Significant intraocular inflammation (RR less than 1 favour Anti-VEGF and steroid)
2Parallel RCTs189RR 0.99 [0.14, 6.95]HighCould not differentiate
Development of cataract (RR less than 1 favour Anti-VEGF and steroid)
3Parallel RCTs268RR: 9.30 [2.21, 39.02]HighFavours anti- VEGF alone
Raised intraocular pressure (RR less than 1 favour Anti-VEGF and steroid)
7Parallel RCT557RR: 12.07 [4.67, 31.25]ModerateFavours anti- VEGF alone

Table 27Intravitreal dexamethasone versus sham

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours intravitreal dexamethasone)
1Parallel RCTs701RR: 1.39 [0.91, 2.12]ModerateCould not differentiate
Visual Acuity: three or more lines improvement from baseline up to 24 M (RR greater than 1 favours intravitreal dexamethasone)
1Parallel RCTs701RR: 1.54 [1.04, 2.26]ModerateFavours intravitreal dexamethasone
Adverse events Cataract progression at 36 months (RR less than 1 favours intravitreal dexamethasone)
1Parallel RCT697RR 3.89 [2.75, 5.50]ModerateFavours sham
Adverse events IOP increase at 36 months (RR less than 1 favours intravitreal dexamethasone)
1Parallel RCT697RR: 8.99 [5.05, 16.03]ModerateFavours sham

Table 28Intravitreal fluocinolone acetonide implant versus sham

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favour Intravitreal fluocinolone acetonide implant)
1Parallel RCTs560RR: 1.79 [1.16, 2.78]HighFavours Intravitreal fluocinolone acetonide
Visual Acuity: three or more lines improvement from baseline up to 24 M (RR greater than 1 favour Intravitreal fluocinolone acetonide implant)
1Parallel RCTs560RR: 1.76 [1.22, 2.53]HighFavours Intravitreal fluocinolone acetonide
Adverse events Cataract progression at 24 M (RR less than 1 favours Intravitreal fluocinolone acetonide implant)
1Parallel RCT351RR: 1.63 [1.35, 1.97]HighFavours sham
Adverse events IOP increase at 24 M (RR less than 1 favours Intravitreal fluocinolone acetonide implant)
1Parallel RCT531RR: 3.35 [2.22, 5.06]HighFavours sham

Table 29Intravitreal triamcinolone acetonide injection versus sham

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement (RR greater than 1 favour Intravitreal triamcinolone acetonide
1Parallel RCTs69RR: 4.12 [0.48, 34.99]ModerateFavours Intravitreal triamcinolone acetonide injection
Adverse events Cataract progression at 24 M (RR less than 1 favours Intravitreal triamcinolone acetonide
1Parallel RCT69RR: 3.00 [0.97, 9.30]ModerateFavours Intravitreal triamcinolone acetonide injection
Adverse events IOP increase at 24 M (RR less than 1 favours Intravitreal triamcinolone acetonide
1Parallel RCT69RR: 10.29 [1.39, 76.12]ModerateFavours sham

Table 30Intravitreal dexamethasone versus intravitreal anti-VEGF

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect

Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours: Intravitreal dexamethasone

Subgroup bevacizumab

1Parallel RCT88RR: 0.99 [0.70, 1.40]ModerateCould not differentiate
Subgroup ranibizumab (RR greater than 1 favour: Intravitreal dexamethasone
1Parallel RCT363RR: 0.50 [0.32, 0.79]ModerateFavours ranibizumab

Table 31Intravitreal dexamethasone versus intravitreal anti-VEGF: The mean number of treatments at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subgroup aflibercept
1Parallel RCT98MD: Not estimableHighCould not differentiate
Subgroup bevacizumab
1Parallel RCT88MD:Not estimableHighCould not differentiate
Subgroup ranibizumab
1Parallel RCT363MD: Not estimableHighCould not differentiate

Table 32Intravitreal dexamethasone versus intravitreal anti-VEGF: Adverse Events at 12 and 24 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Adverse Event: Cataract progression at 12 to 24 months
Subgroup bevacizumab (RR less than 1 favours: Bevacizumab)
1Parallel RCTs88RR: 2.74 [0.58, 12.84]HighCould not differentiate
Subgroup: Ranibizumab (RR less than 1 favours: Ranibizumab)
1Parallel RCTs247RR: 4.54 [2.41, 8.55]HighFavours Ranibizumab
Adverse Event: IOP increase at 24 months
Subgroup aflibercept (RR less than 1 favours: Aflibercept)
1Parallel RCT98RR: 11.45 [0.65, 201.60]HighCould not differentiate
Subgroup bevacizumab (RR less than 1 favours: Bevacizumab)
1Parallel RCT88RR: 2.40 [1.19, 4.82]HighFavours bevacizumab
Subgroup ranibizumab (RR less than 1 favours: Ranibizumab)
1Parallel RCT363RR: 5.03 [1.12, 22.63]HighFavours Ranibizumab

Table 33Intravitreal triamcinolone acetonide versus macular laser

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Visual Acuity: three or more lines improvement from baseline up to 12M
1Parallel RCTs584RR: 0.85[0.55,1.35]HighCould not differentiate
Visual Acuity: three or more lines improvement from baseline up to 24 M
1Parallel RCTs584RR: 0.95 [0.66, 1.35]HighCould not differentiate
Adverse events Cataract progression at 24 M
1Parallel RCT459RR: 2.68 [2.21, 3.24]HighFavours standard threshold laser
Adverse events IOP increase at 24 M
1Parallel RCT584RR: 9.20 [5.14, 16.47]HighFavours standard threshold laser

Table 34Number of patients meeting driving standards at month 24, n (%)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Number of patients meeting driving standards at month 24, n (%)
Lois 2023 Pragmatic RCT217OR: 0.74 [0.16, 3.37]HighFavours standard threshold laser

Table 35Number of laser treatments used from baseline to month 24 in study eye, mean (SD)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Number of laser treatments used from baseline to month 24 in study eye, mean (SD)
Lois 2023 Pragmatic RCT231−1.96 [−3.89, −0.03]HighFavours standard threshold laser

Table 36Comparisons vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subthreshold laser MD less than 0 favours comparison
1 Figueira 2009Parallel RCTs84MD −0.04 [−018,0.08]HighCould not differentiate
Bevacizumab MD less than 0 favours comparison
1 Soheilian 2007Parallel RCTs85MD −0.19 [−0.32.−0.08]ModerateFavours Bevacizumab
Ranibizumab MD less than 0 favours comparison
1 Turkoglu 2015Parallel RCT70MD −0.10 [−0.19.−0.02]HighFavours ranibizumab
Triamcinolone MD less than 0 favours comparison
1 Ockrim 2008Parallel RCT83MD 0.04 [−0.57.0.64]LowCould not differentiate
Ranibizumab + standard threshold laser MD less than 0 favours comparison
1 RELATION 2012Parallel RCT128MD −0.10 [−0.16.−0.04]LowFavours Triamcinolone

Table 37Change in central retinal thickness from baseline (mean difference) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subthreshold laser MD less than 0 favours comparison
1 Figueira 2009Parallel RCTs84MD 13.20 [−31.58 , 57.98]HighCould not differentiate
Bevacizumab MD less than 0 favours comparison
1 Soheilian 2007Parallel RCTs85MD −42.00 [−95.60, −11.60]ModerateCould not differentiate
Ranibizumab MD less than 0 favours comparison
1 Turkoglu 2015Parallel RCT70MD −66.00 [−78.59, −55.41]HighFavours ranibizumab

Table 38Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab MD less than 0 favours comparison
1 Soheilian 2012Parallel RCTs78MD −0.07 [−0.23,0.09]HighCould not differentiate
Bevacizumab + triamcinolone MD less than 0 favours comparison
1 Soheilian 2012Parallel RCTs75MD −0.06 [−0.21,0.09]HighCould not differentiate

Table 39Change in central retinal thickness at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab MD less than 0 favours comparison
1 Soheilian 2012Parallel RCTs75MD −4.00 [−66.81,58.81]HighCould not differentiate
Bevacizumab + triamcinolone MD less than 0 favours comparison
1 Soheilian 2012Parallel RCTs78MD −26.00 [−81.03, 29.03]HighCould not differentiate

Table 40Anti-VEGF vs sham: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab (MD less than 0 favours anti-vegf)
1 Ahmadieh 2008Parallel RCTs78MD −0.15 [−0.26, −0.04]HighFavours Bevacizumab

Table 41Subthreshold vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subthreshold laser vs standard threshold laser (MD less than 0 favours subthreshold laser)
4Parallel RCT213MD −0.01 [−0.12, 0.09]LowCould not differentiate

Table 42bevacizumab vs bevacizumab + standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab vs bevacizumab + standard threshold laser (MD less than 0 favours vs bevacizumab + standard threshold laser)
1 (Faghihi,2010)Parallel RCT80

MD:

−0.04 [−0.17, 0.08]

HighCould not differentiate

Table 43Anti-VEGF vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab Vs Standard threshold laser (MD less than 0 favours anti-VEGF)
2Parallel RCTMD −0.17 [−0.21, −0.13]ModerateFavours bevacizumab
Aflibercept Vs Standard threshold laser (MD less than 0 favours anti-VEGF)
3Parallel RCTMD −0.09 [−0.19, 0.02]LowCould not differentiate

Table 44Steroids vs sham: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Fluocinolone Vs Sham (MD less than 0 favours steroid)
1 FAME 2011 (Campochiaro 2011)Parallel RCT560MD −0.06 [−0.08, −0.03]HighFavours Fluocinolone
Dexamethasone Vs Sham (MD less than 0 favours steroid)
1 MEAD 2014 (Boyer 2014)Parallel RCT701MD −0.05 [−0.09, 0.00]HighFavour Dexamethasone

Table 45Brolucizumab vs aflibercept: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Brolucizumab Vs Aflibercept (MD less than 0 favours Brolucizumab)
1 (Brown 2022)Parallel RCT360MD 0.02 [−0.02, 0.07]HighCould not differentiate

Table 46Anti VEGF vs Anti VEGF: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Aflibercept vs. Bevacizumab (MD less than 0 favours Aflibercept)
1 DRCRnet 2015Parallel RCT386MD−0.06 [−0.10, −0.01]HighFavours Aflibercept
Aflibercept vs Ranibizumab (MD less than 0 favours Aflibercept)
1 DRCRnet 2015Parallel RCT392MD −0.01 [−0.06, 0.04]HighCould not differentiate
Ranibizumab vs Bevacizumab (MD less than 0 favours Ranibizumab)
1 DRCRnet 2015Parallel RCT376MD −0.05 [−0.09, −0.00]HighFavour Ranibizumab

Table 47Dexamethasone vs bevacizumab: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Dexamethasone Vs Bevacizumab (MD less than 0 favours Dexamethasone)
1 BEVORDEX 2014 (Gillies 2014)Parallel RCT88MD 0.08 [−0.03, 0.19]HighCould not differentiate

Table 48Triamcinolone vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Triamcinolone Vs Standard threshold laser (MD less than 0 favours Triamcinolone)
1 DRCRnet 2008Parallel RCT584MD 0.08 [0.01, 0.15]HighFavours Standard threshold laser

Table 49Combination treatment vs sham + standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Ranibizumab + standard threshold laser (MD less than 0 favours ranibizumab + standard threshold laser
1 DRCRnet 2010Parallel RCT480MD −0.12 [−0.17, −0.07]HighFavours ranibizumab + standard threshold laser
Ttriamcinolone + standard threshold laser (MD less than 0 favours triamcinolone + standard threshold laser)
1 DRCRnet 2010Parallel RCT479MD −0.02 [−0.07, 0.03]HighCould not differentiate

Table 50Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab Vs Triamcinolone + Bevacizumab (MD less than 0 favours Triamcinolone + Bevacizumab)
1 Soheilian 2012Parallel RCT75MD 0.01 [−0.15, 0.17]HighCould not differentiate

Table 51Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Ranibizumab + standard threshold laser vs standard threshold laser: (MD less than 0 favours Ranibizumab + standard threshold laser)
1 DRCRnet 2010Parallel RCT253MD −0.08 [−0.13, −0.03]HighFavours Ranibizumab + standard threshold laser
Triamcinolone + standard threshold laser vs standard threshold laser: (MD less than 0 favours triamcinolone + standard threshold laser)
1 DRCRnet 2010Parallel RCT256MD 0.00 [−0.06, 0.06]HighFavours triamcinolone + standard threshold laser

Table 52Aflibercept vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Aflibercept vs standard threshold Laser (MD less than 0 favours Aflibercept)
1 VISTA & VIVID (Korobelnik 2014)Parallel RCT168MD −0.15 [−0.15, −0.14]HighFavours Aflibercept

Table 53Aflibercept vs standard threshold laser: Change in visual acuity (logMAR) at 24 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Aflibercept vs standard threshold laser: (MD less than 0 favours Aflibercept)
1 VISTA & VIVID (Korobelnik 2014)Parallel RCT168MD −0.15 [−0.16, −0.14]HighFavours Aflibercept

Table 54Aflibercept vs standard threshold laser: Change in central retinal thickness at 12 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Aflibercept vs standard threshold laser: (MD less than 0 favours Aflibercept)
1 VISTA & VIVID (Midena 2018)Parallel RCT168MD −69.30 [−73.28, −65.32]HighFavours Aflibercept

Table 55Aflibercept vs standard threshold laser: Change in central retinal thickness at 24 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Laser vs aflibercept: change in central retinal thickness at 24 months. (MD less than 0 favours aflibercept)
1 VISTA & VIVID (Midena 2018Parallel RCT168MD 67.80 [63.42, 72.18]HighFavours standard threshold laser

Table 56Triamcinolone vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)Quality
Triamcinolone vs standard threshold laser: (MD less than 0 favours Triamcinolone)
1 DRCRnet 2008Parallel RCT296MD 0.08 [0.01, 0.15]HighFavours standard threshold laser

Table 57Combination treatment vs standard threshold laser: Change in central retinal thickness from baseline (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Ranibizumab + standard threshold laser (MD less than 0 favours Ranibizumab + standard threshold laser)
1 DRCRnet 2010Parallel RCT227MD −44.00 [−65.63, −22.37HighFavours Ranibizumab + standard threshold laser
triamcinolone + standard threshold laser (MD less than 0 favours triamcinolone + standard threshold laser
1 DRCRnet 2010Parallel RCT231MD −32.00 [−54.39, −9.61]HighFavours triamcinolone + standard threshold laser

Table 58Aflibercept vs standard threshold laser

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Aflibercept vs standard threshold laser: Change in central retinal thickness from baseline to 24 months (MD less than 0 favours aflibercept)
1 VISTA & VIVID (Midena 2018)Parallel RCT168MD −151.70 [−154.35, −149.05]HighFavours standard threshold laser

Table 59Comparisons vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subthreshold laser vs standard threshold laser (MD less than 0 favours Subthreshold laser)
1 Figueira 2009Parallel RCT84MD −0.04 [−0.16, 0.08]HighCould not differentiate
Bevacizumab vs standard threshold laser (MD less than 0 favours Bevacizumab)
1 Soheilian 2007Parallel RCT85MD −0.19 [−0.32, −0.06]HighFavours Bevacizumab

Table 60Comparisons vs standard threshold laser: Change in central retinal thickness from baseline (mean difference) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Subthreshold laser vs standard threshold laser (MD less than 0 favours Subthreshold laser)
1 Figueira 2009Parallel RCT84MD 13.20 [−31.58, 57.98]HighCould not differentiate
Bevacizumab vs standard threshold laser (MD less than 0 favours Bevacizumab
1 Soheilian 2007Parallel RCT85MD −42.00 [−95.60, 11.60]HighCould not differentiate

Table 61Comparisons vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Ranibizumab vs standard threshold laser
Turkoglu 2015 Parallel RCT70MD −0.10 [−0.19, −0.02]HighFavours Ranibizumab
Triamcinolone vs standard threshold laser
Ockrim 2008Parallel RCT83MD 0.04 [−0.57, 0.64]HighCould not differentiate

Table 62Ranibizumab vs standard threshold laser: Change in central retinal thickness from baseline (mean difference) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Ranibizumab + standard threshold laser vs standard threshold laser
RELATION 2012 Parallel RCT128MD −0.10 [−0.16, −0.04]HighFavours Ranibizumab + standard threshold laser

Table 63Bevacizumab vs sham

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab vs sham
Ahmadieh 2008 Parallel RCT78MD −0.15 [−0.26, −0.04]HighFavours Bevacizumab

Table 64Ranibizumab vs standard threshold laser: Change in central retinal thickness from baseline (mean difference) at 12 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Ranibizumab vs standard threshold laser
Turkoglu 2015 Parallel RCT70MD −66.00 [−76.59, −55.41]HighFavours Ranibizumab

Table 65Comparisons vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab
Soheilian 2012 Parallel RCT77MD −0.07 [−0.23, 0.09]HighCould not differentiate
Bevacizumab + triamcinolone
Soheilian 2012 Parallel RCT74MD −0.06 [−0.21, 0.09]HighCould not differentiate

Table 66Comparisons vs standard threshold laser: Change in central retinal thickness from baseline to 24 months

No. of studiesStudy designSample sizeEffect size (95% CI)QualityInterpretation of effect
Bevacizumab
Soheilian 2012 Parallel RCT77MD −4.00 [−66.81, 58.81]HighCould not differentiate
Bevacizumab + triamcinolone
Soheilian 2012 Parallel RCT74MD −26.00 [−81.03, 29.03]HighCould not differentiate

Table 67Economic evidence profile

StudyApplicabilityLimitationsOther commentsIncrementalUncertainty
Cost (£)Effects (QALYs)ICER (£/QALY)
Regnier et al (2015) Cost-effectiveness of ranibizumab versus aflibercept in the treatment of visual impairment due to diabetic macular edema: a UK healthcare perspectiveDirectly applicable; NHS perspectiveMinor limitations, assumes treatment limited to 3 years

Markov cohort model with 8 health states based on visual acuity plus death health state

Aflibercept compared with ranibizumab treat and extend (T&E) vs. ranibizumab treatment as needed (PRN)

Population included patients with any central retinal thickness

Aflibercept compared with ranibizumab PRN: £5,841 and ranibizumab T&E: £2,930Aflibercept compared with ranibizumab PRN: 0.05 and ranibizumab T&E: 0.05

ICER

Aflibercept compared with ranibizumab PRN: £116,820 and ranibizumab T&E: £58,600

NMB at £20K

Ranibizumab PRN: £6,768

Ranibizumab T&E: £3,934

Deterministic: The results were most sensitive to changes in the odds ratio of ranibizumab PRN compared with aflibercept, followed by the price discount assumed to apply to aflibercept (20%) and assumptions made for the number of injections and monitoring assumptions for ranibizumab and aflibercept. The net monetary benefit (NMB) for ranibizumab PRN remained positive in all scenarios explored.

Probabilistic: Ranibizumab PRN had a 79% probability and ranibizumab (T&E) had a 67% probability of being cost effective compared with aflibercept assuming QALYs are valued at £20,000 each.

Mitchell et al (2012) Cost-effectiveness of ranibizumab in treatment of diabetic macular oedema (DME) causing visual impairment: evidence from the RESTORE trialDirectly applicable; NHS perspectiveMinor limitations, EQ-5D used as utility source in the base-case which is not sensitive to changes in eye conditions

Based on RESTORE and RETAIN clinical trials

The study did not mention whether the population was separated by central retinal thickness

Ranibizumab monotherapy compared with laser mono: £4,191

Ranibizumab combo compared with laser mono: £4,695

Ranibizumab mono compared with laser: 0.17

Ranibizumab combo compared with laser mono: 0.13

Ranibizumab mono compared with laser mono: £24,028

Ranibizumab combo compared with laser mono: £36,106

Deterministic: Model most sensitive to changes in the number of injections and reducing the time horizon to 10 years. Changing the source of utilities increased the QALY gains and reduced the ICER.

Probabilistic: 64% probability ranibizumab monotherapy would be cost effective compared to laser and 42% probability combination therapy would be cost effective compared to laser therapy based on a willingness to pay threshold of £30,000 per QALY.

Pochopien et al (2019) Cost-effectiveness of fluocinolone acetonide implant (ILUVIEN R) in UK patients with chronic diabetic macular oedema considered insufficiently responsive to available therapiesDirectly applicable; NHS perspectiveMinor limitations, disutility applied to anti-VEGF injections only and not for insertion of implants

The text refers to the use of dexamethasone in the Pseudophakic population however the table reports the results for dexamethasone under the phakic lens population

Analysis was not separated by central retinal thickness

Disutility applied to injections for anti-VEGFs however not applied to the implant

Pseudophakic lens at baseline:

Fluocinolone acetonide implant (FAc) compared with usual care: £3,066

FAc compared with dexamethasone: £1,777

Phakic lens at baseline:

FAc compared with usual care: £3,170

Pseudophakic lens at baseline:

FAc compared with usual care: 0.185

FAc compared with dexamethasone 0.126

Phakic lens at baseline:

FAc compared with usual care: 0.11

Pseudophakic lens at baseline:

FAc compared with usual care: £16,609

FAc compared with dexamethasone: £14,070

Phakic lens at baseline:

FAc compared with usual care: £28,751

Incremental costs and QALYs are rounded so calculating the ICER from above gives a different result

Deterministic: Main drivers of the ICER for FAc compared with usual care were utility decrements per health state, distribution of treatment within usual care, transition probabilities for sham baseline for the pseudo phakic population.

Main drivers of the ICER for FAc compared with dexamethasone were the cost of dexamethasone and the number of outpatient visits for patients treated with FAc in the pseudo phakic population.

Phakic population: Main driver of the ICER for FAc compared with usual care in the phakic population was the transition probabilities.

Probabilistic: Pseudophakic population

The FAc implant was found to have a 73.4% probability of being cost effective compared to usual care based on a willingness to pay threshold of £30,000.

No probabilistic results presented for dexamethasone.

Phakic population: The FAc implant was found to have a 59.2% probability of being cost effective compared to usual care based on a willingness to pay threshold of £30,000.

Haig et al (2016) Cost-effectiveness of ranibizumab in the treatment of visual impairment due to diabetic macular edemaPartially applicable; Canada study setting with 5% discount rateMinor limitations, due to a lack of data, clinical expertise was used to populate resource use for treatment monitoring

Analysis for both societal and health care system were presented in the analysis, only results for the healthcare perspective are presented to align with NICE reference case

The analysis was not separated by central retinal thickness

Ranibizumab mono compared with laser mono: CA$9,849 (£5,555)

Ranibizumab combo compared with laser mono: CA$ 11,471 (£6,470)

Ranibizumab mono compared with laser mono: 0.4

Ranibizumab combo compared with laser mono: 0.32

Ranibizumab mono compared with laser mono: CA$24,494 (£13,815)

Ranibizumab combo compared with laser mono: CA$ 36,414 (£20,538)

Deterministic: Ranibizumab monotherapy and combination remained cost effective compared with laser monotherapy. Model most sensitive to removing the assumption patients stopped treatment if BCVA above 75 letters this increased the ICER to CA$72,989 (£41,167) for ranibizumab monotherapy.

Probabilistic: Ranibizumab monotherapy and ranibizumab combination therapy had a 74% and 60% probability of being cost effective at the ICER threshold of CA$50,000 (£28,201)

Holekamp et al (2020) Cost-effectiveness of ranibizumab and aflibercept to treat diabetic macular edema from a US perspective: analysis of 2-year Protocol T dataPartially applicable; US study; 3% discount rate from 2 years onwardsPotentially serious limitations, base-case only 2 years based on trial data, natural history source is unclear

Based on the Protocol T clinical trial, uses ranibizumab 0.3mg rather than 0.5mg

Accounted for treatment in one or two eyes, assumptions made for starting treatment for the second eye to be mid study if not at baseline

The analysis was not separated by central retinal thickness

Aflibercept compared with ranibizumab:

2 years:

Full cohort: $9,894 (£6,896)

VA 20/40 or better at baseline: $8,597 (£5,992)

VA 20/50 or worse: $10,967 (£7,644)

Aflibercept compared with ranibizumab:

10 years:

Full cohort: $20,608 (£14,364)

VA 20/40 or better at baseline: $19,721 (£13,746)

VA 20/50 or worse: $21,633 (£15,078)

Aflibercept compared with ranibizumab (2 years):

Full cohort: 0.010

VA 20/40 or better at baseline: −0.002

VA 20/50 or worse: 0.021

Aflibercept compared with ranibizumab (10 years):

Full cohort: 0.029

VA 20/40 or better at baseline: −0.032

VA 20/50 or worse: 0.088

Aflibercept compared with ranibizumab (2 years):

Full cohort: $986,159 (£687,353)

VA 20/40 or better at baseline: ranibizumab dominates

VA 20/50 or worse: $523,377 (£364,794)

Aflibercept compared with ranibizumab (10 years):

Full cohort: $711,301 (£495,777)

VA 20/40 or better at baseline: Ranibizumab dominates

VA 20/50 or worse: $246,978 (£172,144)

Deterministic: Model most sensitive to drug costs and the number of injections. Aflibercept only became cost effective for the full cohort based on an ICER of $19,930 (£13,891) when the number of injections for aflibercept over 2 years reduced from 15 to 11 whilst ranibizumab remained the same. Ranibizumab remained dominant in all scenarios in the 20/40 or better VA subgroup.

Probabilistic: Assuming QALYs were valued at $150,000 ((£104,550) aflibercept had a 0.1% probability of being cost effective for the full cohort and 2.5% probability for the 20/50 or worse VA subgroup.

Brown et al (2015) The Cost-effectiveness of ranibizumab for the treatment of diabetic macular edemaPartially applicable; US study (includes societal costs); 3% discount ratePotentially serious limitations, assumes last observation from 24 months is carried forward for the remainder of the model which may overestimate benefits, no deterministic or probabilistic sensitivity analysis

RIDE and RISE clinical trials with vision loss from 20/40 to 20/320 from DMO. Laser treatment could be given in addition to all treatment arms. 0.3mg ranibizumab cohort received average 0.8 laser treatments and the sham arm received 1.8 laser treatments over 24 months.

Societal perspective was used in the base-case only the payer perspective results are presented here

Assumes vision similar in both eyes, treatment in both eyes considered in the base-case, adverse events were included

The analysis was not separated by central retinal thickness

Ranibizumab compared with sham (all direct medical costs considering both eyes): $4,578 (£3,186)Ranibizumab compared with sham 0.9981Ranibizumab compared with sham considering both eyes $4,587 (£3,193)/QALYNo full deterministic or probabilistic sensitivity analysis was presented, only scenarios around the frequency of injections over 3 years. ICERS range from $37,693 (£26,234)/QALY for first eye to $107,784 (£75,018) when four annual injections administered bilaterally through 36 months. Assuming monthly injections for ranibizumab up to 36 months the ICER is $33,029 (£22,988)/QALY
Stein et al (2013) Cost-effectiveness of various interventions for newly diagnosed diabetic macular edemaPartially applicable; US study; 3% discount ratesMinor limitations, time horizon may not cover all patients lifetime and equal efficacy assumed between bevacizumab and ranibizumab and no data available for the rates of cerebrovascular accident (CVA) for bevacizumab

Includes focal laser plus triamcinolone as a comparator which is not an included comparator within this guideline as the intraocular formulation is not available in the UK

The analysis was not separated by central retinal thickness

Laser compared with:

Laser plus ranibizumab $58,257 (£40,663)

Delayed laser plus ranibizumab $61,424 (£42,874)

Laser plus bevacizumab $27,200 (£18,986)

Delayed laser plus bevacizumab $26,485 (£18,487)

Laser compared with:

Laser plus ranibizumab: 10.83

Delayed laser plus ranibizumab: 10.99

Laser plus bevacizumab: 10.83

Delayed laser plus bevacizumab: 10.99

Laser compared with:

Laser plus ranibizumab: $89,903 (£62,752)

Delayed laser plus ranibizumab: $71,271 (£49,747)

Laser plus bevacizumab Dominated by delayed laser plus bevacizumab

Delayed laser plus bevacizumab: $11,138 (£7,774)

Scenarios including the side effects of adverse events were included, which increased costs and reduced HRQOL for laser which had high rates of 6%. Due to the uncertainty around the rates of CVA for bevacizumab scenarios were run to identify if bevacizumab would not be considered cost effective based on a QALY valued at $50,000 if the probability of CVA is more than 4%.

Probabilistic: In the analysis with ranibizumab based on a willingness to pay threshold of $50,000 per QALY there is a 70% probability laser would be the preferred treatment, when the threshold is increased to $100,000/QALY there is a 90% probability that ranibizumab with laser (either immediate or delayed) would be the preferred treatment.

In the scenario with bevacizumab, at a value of $14,000 (£9,772) /QALY bevacizumab is very likely to be the preferred treatment compared with laser with over 90% probability.

Sharma et al (2000) The cost-effectiveness of grid laser photocoagulation for the treatment of diabetic macular edema: results of a patient-based cost-utility analysisPartially applicable; US study; 0 or 5% discount rate usedPotentially serious limitations, not all costs considered only direct treatment costs, no probabilistic sensitivity analysis

Data based on ETDRS clinical trial. Utility valuations for adverse events based on physician opinion

The analysis was not separated by central retinal thickness

Laser photocoagulation compared with no treatment $733 (£509)Laser photocoagulation compared with no treatment: 0.236

Laser photocoagulation compared with no treatment:

No discounting

$3,101 (£2,152)

5% discount rate based on an additional 40-year life expected $3,655 (£2,537)

Deterministic: Efficacy values were varied within the 95% confidence limits, the results remained robust with laser photocoagulation remained the preferred treatment.

No probabilistic sensitivity analysis was undertaken.

Lois et al (2022) Standard threshold laser versus subthreshold micro pulse laser for adults with diabetic macular oedema: the DIAMONDS non-inferiority RCTDirectly applicable; NHS and PSS perspectiveMinor limitations, short 2-year time horizon

Data based on the DIAMOND clinical trial

The population was people with central retinal thickness <400µm

Subthreshold micro pulse laser compared with standard threshold laser: −£365Subthreshold micro pulse laser compared with standard threshold laser: 0.008Subthreshold micro pulse laser compared with standard threshold laser: Subthreshold micro pulse laser dominates

Large confidence intervals for the cost difference of subthreshold micro pulse laser compared with standard threshold laser 95% confidence interval (−£822 to £93).

Subthreshold micro pulse laser had 80% probability of being cost effective at a threshold of £15,000 per QALY and 76% probability of being cost effective at £20,000 per QALY.

Hutton et al (2023) Cost-effectiveness of aflibercept monotherapy vs bevacizumab first followed by aflibercept if needed for diabetic macular edemaPartially applicable; US healthcare settingMinor limitations, 3% discount rate, short 2-year time horizon

Data based on the DRCR retina network protocol AC clinical trial

The mean retinal thickness of the population was 504µm, with a 95% CI of 487 to 521µm

Aflibercept monotherapy compared with bevacizumab first followed by aflibercept if needed: $12,575 (£8,740)Aflibercept monotherapy compared with bevacizumab first followed by aflibercept if needed: 0.015Aflibercept monotherapy compared with bevacizumab first followed by aflibercept if needed: $837,077 (£581,769)

Deterministic: Changing utility source from Brown et al 1999 to RESTORE clinical trial and assumptions around costs will likely change the results, however the ICER would remain above $100,000 (£69,500).

Probabilistic sensitivity analysis: 0% probability aflibercept monotherapy would be considered cost effective at a willingness to pay below $200,000 (£139,000) per QALY gained.

Abbreviations: BCVA: Best corrected visual acuity; BSE: Best seeing eye; CI-DME, centre involving diabetic macular oedema; Combo: combination therapy; CVA: cerebrovascular accident; CRT: central retinal thickness; FAc: Fluocinolone acetonide implant; Mono: Monotherapy; NMB: Net monetary benefit; PRN: Pro re nata – treatment as needed; PRP, pan retinal photocoagulation; PSS: Personal social services; T & E: treat and extend dosage schedule; WSE: Worst seeing eye. *Costs have been converted from dollars to pounds using EPPI-Centre Cost Converter https://eppi.ioe.ac.uk/costconversion/default.aspx

Table 68Economic model results (list price) fully incremental analysis

StrategyAbsolute costsAbsolute QALYsInc. costsInc. QALYsICERNMB at £20K/QALY (95% CI)
No treatment£3,8438.485---£165,850 (£152,520 to £179,419)
Subthreshold laser£4,4318.956£5880.471£1,248£174,682 (£160,969 to £188,956)
Standard threshold laser£4,8238.976£3920.020£19,272£174,697 (£161,500 to £188,126)
Bevacizumab£9,3859.201£4,5620.225£20,318£174,625 (£161,698 to £188,032)
Bevacizumab plus standard laser£11,4089.216£2,0230.015£133,549£172,905 (£159,025 to £186,478)
Ranibizumab£23,9209.220£12,5110.004Extendedly dominated£160,471 (£147,567 to £173,477)
Brolucizumab£24,3609.266£12,9520.051£256,445£160,963 (£147,392 to £174,636)
Ranibizumab plus standard laser£24,6939.199£333−0.067Dominated£159,295 (£146,028 to £173,040)
Faricimab£33,9479.266£9,5870.000Dominated£151,368 (£137,455 to £166,067)
Aflibercept£34,3889.258£10,028−0.008Dominated£150,771 (£136,228 to £165,577)

Table 69Economic model results (list price) compared with no treatment

StrategyAbsolute costsAbsolute QALYsInc. costsInc. QALYsICER
No treatment£3,8438.485---
Subthreshold laser£4,4318.956£5880.471£1,248
Standard threshold laser£4,8238.976£9800.491£1,994
Bevacizumab£9,3859.201£5,5420.716£7,741
Bevacizumab plus standard laser£11,4089.216£7,5650.731£10,349
Ranibizumab£23,9209.220£20,0760.735£27,319
Brolucizumab£24,3609.266£20,5170.781£26,253
Ranibizumab plus standard laser£24,6939.199£20,8490.715£29,172
Faricimab£33,9479.266£30,1040.781£38,541
Aflibercept£34,3889.258£30,5450.773£39,500

Table 70Economic model results (list price) fully incremental analysis

StrategyAbsolute costsAbsolut QALYsInc. costsInc. QALYsICERNMB at £20K/QALY (95% CI)
No treatment£3,8228.503£00.000£0£166,238 (£152,957 to £180,234)
Subthreshold laser£4,4588.944£6350.441£1,442£174,414 (£160,952 to £187,227)
Standard threshold laser£4,9198.928£462−0.015Dominated£173,646 (£159,605 to £187,244)
Bevacizumab£9,3089.211£4,8500.268£18,125£174,916 (£161,429 to £187,533)
Bevacizumab plus standard laser£11,3259.211£2,0170.000Extendedly dominated£172,899 (£159,168 to £186,269)
Ranibizumab£24,0399.224£14,7310.012Extendedly dominated£160,434 (£146,828 to £174,059)
Brolucizumab£24,3489.268£15,0400.057£263,607£161,016 (£147,669 to £173,755)
Ranibizumab plus standard laser£24,9049.209£556−0.060Dominated£159,268 (£145,571 to £172,882)
Faricimab£33,9799.271£9,6300.003£3,116,792£151,448 (£137,073 to £164,968)
Aflibercept£34,5229.267£544−0.005Dominated£150,813 (£136,809 to £164,845)

Table 71Economic model results (list price) compared with no treatment

StrategyAbsolute costsAbsolute QALYsInc. costsInc. QALYsICER
No treatment£3,8228.503---
Subthreshold laser£4,4588.944£6350.441£1,442
Standard threshold laser£4,9198.928£1,0970.425£2,579
Bevacizumab£9,3089.211£5,4850.708£7,746
Bevacizumab plus standard laser£11,3259.211£7,5020.708£10,593
Ranibizumab£24,0399.224£20,2160.721£28,054
Brolucizumab£24,3489.268£20,5260.765£26,824
Ranibizumab plus standard laser£24,9049.209£21,0810.706£29,878
Faricimab£33,9799.271£30,1560.768£39,250
Aflibercept£34,5229.267£30,7000.764£40,196

Table 72List prices for treatments included in the recommendations

ResourceUnit costsSource
Aflibercept 4.0mg/0.1ml£816.00BNF (accessed 13/02/2023)
Ranibizumab (Lucentis) 2.3mg/0.23ml£551.00BNF (accessed 13/02/2023)
Ranibizumab biosimilar (Ongavia) 2.3mg/0.23ml£523.45BNF (accessed 28/04/2023)
Bevacizumab* 1.25mg£50.00Poku et al (2012) cited in NICE TA824
Brolucizumab 19.8mg/0.165ml£816.00BNF (accessed 13/02/2023)
Faricimab 28.8mg/0.24ml£857.00BNF (accessed 13/02/2023)
Standard threshold laser£41.16 Lois et al (2022)
Subthreshold laser£47.11 Lois et al (2022)
*

Bevacizumab is only available in a 100mg per 4ml vial at a list price of £242.66, and for intravitreal use must be reconstituted into a 1.25mg dose in an aseptic pharmacy.

Final

Evidence reviews underpinning recommendations 1.3.1 and 1.6.1 to 1.6.11 in the NICE guideline

These evidence reviews were developed by NICE

Disclaimer: The recommendations in this guideline represent the view of NICE, arrived at after careful consideration of the evidence available. When exercising their judgement, professionals are expected to take this guideline fully into account, alongside the individual needs, preferences and values of their patients or service users. The recommendations in this guideline are not mandatory and the guideline does not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of the individual patient, in consultation with the patient and/or their carer or guardian.

Local commissioners and/or providers have a responsibility to enable the guideline to be applied when individual health professionals and their patients or service users wish to use it. They should do so in the context of local and national priorities for funding and developing services, and in light of their duties to have due regard to the need to eliminate unlawful discrimination, to advance equality of opportunity and to reduce health inequalities. Nothing in this guideline should be interpreted in a way that would be inconsistent with compliance with those duties.

NICE guidelines cover health and care in England. Decisions on how they apply in other UK countries are made by ministers in the Welsh Government, Scottish Government, and Northern Ireland Executive. All NICE guidance is subject to regular review and may be updated or withdrawn.

Copyright © NICE 2024.
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