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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:
- Jorge et al. 2018 (Monotherapy laser photocoagulation): 16 studies
- Mehta et al. 2018 (Anti-VEGFs with intravitreal steroids): 8 studies
- Rittiphairoj et al. 2020 (Intravitreal steroids): 9 studies
- Virgili et al. 2022 (Anti-VEGFs): 28 studies
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
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Azad 2012
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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]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
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].net 2008 {published data only}
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]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]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.- 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]
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- 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]
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1.1.14.1. Effectiveness
Included studies from NICE search
Included studies from Cochrane review: Virgili et al-2022
Included studies from Cochrane review: Rittiphairoj et al-2020
Included studies from Cochrane review: Mehta et al-2018
Included studies from Cochrane review: Jorge et al-2018
1.1.14.2. Economic
1.1.14.3. Other
Appendices
Appendix A. Review protocols
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]
Search filters
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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 E. Forest plots
E.1. People with centre-involving macular oedema (whole population) (PDF, 343K)
E.2. People with non-centre-involving macular oedema (PDF, 163K)
Appendix F. GRADE Tables
F.1. Network meta-analyses (PDF, 157K)
F.2. Pairwise meta-analysis (PDF, 436K)
Appendix G. Economic evidence study selection
Download PDF (118K)
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
Study | Reason 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 | - 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 | - 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 | - 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
Study | Reason 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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
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] |
|
Smiddy, William E (2011) Economic considerations of macular edema therapies. Ophthalmology 118(9): 1827–33 [PMC free article: PMC3483086] [PubMed: 21507488] |
|
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] |
|
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 |
|
Comparator |
|
Outcomes |
Primary outcomes:
Secondary outcomes:
|
Table 2Table of included studies
Studies from NICE additional searches
Study Country | Study type and follow-up (FU) time | Population | Intervention | Comparator | Outcomes |
---|---|---|---|---|---|
Callanan, 2013 |
Parallel-group RCT 1 year FU | Inclusion criteria
|
DEX implant plus laser (N = 126) Dexamethasone Intravitreal Implant Plus Laser |
Sham implant and laser (N = 127) Laser Alone |
|
The VIVID-East study |
Parallel-group RCT 1 year FU | Inclusion criteria
|
IVT-AFL every 4 weeks (N = 127) or IVT-AFL every 8 weeks (N = 127) |
macular laser (N = 127) |
|
Faghihi, 2010 |
Parallel-group RCT 6 month FU |
Inclusion criteria
Key exclusion criteria
| IVB plus MPC (N = 40) | IVB (N = 40) |
|
Fouda, 2017 |
Parallel-group RCT 1 year FU | Inclusion criteria
|
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) |
|
Gillies, 2009 |
Parallel-group RCT 5 year FU | Inclusion criteria
| Initial Triamcinolone (N = 23) | Initial Placebo (N = 21) |
|
Lam, 2007 |
Parallel-group RCT 6 monthFU | Inclusion criteria
|
4 mg of intravitreal TA (N = 38) OR 4 mg of intravitreal TA + grid laser (N = 36) | grid laser (N = 37) |
|
Lois,2023 |
RCT 24 months follow up | Inclusion criteria
|
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) |
|
Ozsaygili, 2020 |
Parallel-group RCT 1 year FU |
| 3 monthly injections of 2 mg of aflibercept as a loading phase in the anti–vascular endothelial growth factor group | 0.7 mg of DEX implant in the DEX group and then pro re nata treatment. |
|
Sahni,2019 |
Parallel-group RCT 6 months FU |
| 6.0 mg faricimab or 1.5 mg faricimab | 0.3mg ranibizumab |
|
Vader, 2020 |
Parallel-group RCT 6 months FU | Inclusion criteria
| 1.25 mg bevacizumab (N = 86) | 0.5 mg ranibizumab (N = 84) |
|
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
Study | Number of included studies | Inclusion criteria | Exclusion criteria | Interventions | Comparison | Outcomes |
---|---|---|---|---|---|---|
Jorge et al-2018 | 15 studies | Randomised controlled trials (RCTs) comparing any type of focal/grid macular laser versus another type or technique of laser treatment and no intervention | Excluded studies comparing laser with other interventions | Different macular laser as monotherapy in the treatment of diabetic macular oedema. | another type or technique of laser treatment and no intervention |
|
Mehta et al-2018 | 8 | Randomised 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 DMO | NR | intravitreal anti-VEGF combined with intravitreal steroids | intravitreal anti-VEGF alone, intravitreal steroids alone or macular laser alone |
|
Rittiphairoj et al-2020 | 9 | Randomised controlled trials (RCTs) comparing intravitreal steroid therapies versus other treatments, including intravitreal anti-VEGF therapy, laser photocoagulation, and sham injection | NR | any type of intravitreal steroids as monotherapy against | any other intervention (e.g., observation, laser, anti-vascular endothelial growth factor (anti-VEGF) for DMO |
|
Virgili et al-2022 | 29 | Randomised 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 DMO | People with normal best corrected visual acuity (BCVA) were not included | any anti-angiogenic drug with an anti-VEGF mechanism of action | another anti-VEGF drug, another treatment, sham, or no treatment |
|
Table 4Randomised controlled trials (for full study details, see Virgili et al. 2022)
Study | Follow-up time | Population | Intervention | Comparator | Outcomes |
---|---|---|---|---|---|
Randomised controlled trials (from Virgili et al 2022 Cochrane systematic review) | |||||
Azad 2012 | 6 months |
Inclusion:
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 |
|
Baker 2019 | 24 months and 5 years | Inclusion criteria:
|
Aflibercept (n=236) Macular laser (n=240 | Observation (n=236) |
|
BOLT 2010 (Michaelides 2010) | Inclusion criteria:
|
Bevacizumab (1.25 mg) n = 42 (42 eyes |
Macular laser therapy n = 38 (38 eyes) |
| |
Brown 2015 | 12 months |
|
VISTA: 154 IAI 2q4, or 151 IAI 2q8 VIVID: 136 IAI 2q4, or 135 IAI 2q8 |
VISTA: 154 Laser control VIVID: 132 Laser control |
|
Brown 2022 | 12 months | Inclusion criteria:
|
Brolucizumab 3 mg, brolucizumab 6 mg, (KESTREL) or brolucizumab 6 mg (KITE) | Aflibercept 2mg (KESTREL and KITE) |
|
Chatzirallis 2020 | 12- & 18-months FU | Inclusion criteria:
| 0.5 mg Ranibizumab n = 54 (54 eyes) | Aflibercept 2 mg n = 58 (58 eyes) |
|
DA VINCI 2011 (Do 2012) | 6 months and 12 months |
Inclusion criteria:
PDR (unless regressed and currently inactive) |
VEGF Trap-Eye n = 177 (177 eyes) |
Standard threshold laser n = 44 (44 eyes) |
|
DRCRnet 2010 | 12 months | Inclusion criteria:
|
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) |
|
DRCRnet 2015 | 12 months | Inclusion criteria:
|
|
|
|
Ekinci 2014 | 12 months | Inclusion criteria:
|
Bevacizumab (1.25 mg) n = 50 (50 eyes) |
Ranibizumab (0.05 mg) n = 50 (50 eyes) |
|
Korobelnik 2014 (1) | Inclusion criteria:
|
| Standard threshold laser and sham monthly injection = 286 (286 eyes) |
| |
Li 2019 | Follow-up: 12 months |
| ranibizumab 0.5mg | Macular laser |
|
Liu 2022 | Follow-up: 12 months |
|
Conbercept (n=76) |
Macular laser (n=80) |
|
Prunte 2016 | 24-month FU |
| Ranibizumab 0.5 mg with laser | Ranibizumab 0.5 mg |
|
LUCIDATE 2014 (Comyn 2014) | 12 month follow up | Inclusion criteria:
|
Ranibizumab (0.5 mg) N= 25 | Macular laser N=12 |
|
Macugen 2005 | 12 months FU | Inclusion criteria:
| Pegaptanib (0.3 mg, 1 mg, or 3 mg) | Sham injection |
|
Macugen 2011 (Sultan 2011) |
12 months 24 months FU | Inclusion criteria:
|
Pegaptanib sodium (0.3 mg) n = 133 |
Sham injection N = 127 |
|
Nepomuceno 2013 | Inclusion criteria:
|
Bevacizumab (1.5 mg) 32 eyes | Ranibizumab (0.5 mg) 28 eyes |
| |
READ2 2009 (Nguyen 2009) |
12 months 24 months | Inclusion criteria:
|
|
Standard threshold laser n = 42 (42 eyes) |
|
RELATION 2012 | 12 months FU | Inclusion criteria:
|
Ranibizumab (0.5 mg) plus laser n = 85 (85 eyes) |
Laser plus sham injection n = 85 (85 eyes) |
|
RESOLVE 2010 (Massin 2010) | 12 Month FU | Inclusion criteria:
|
Ranibizumab (0.3 mg or 0.5 mg) n = 102 (102 eyes) |
Sham injection n = 49 (49 eyes) |
|
RESPOND 2013 | 12 Month FU | Inclusion criteria:
|
|
Laser n = 81 (81 eyes) |
|
RESTORE 2011 (Mitchell 2011) | 12 Month FU | Inclusion criteria:
|
| Laser treatment plus sham injections n = 111 (111 eyes |
|
REVEAL 2015 (Ishibashi 2015) | 12 months | Inclusion criteria:
|
| Sham injection + active laser (n = 131). |
|
RISE-RIDE (Nguyen 2012) | 24 months | Inclusion criteria:
|
| Sham injection (n = 122) |
|
Soheilian 2007 | 12 month FU | Inclusion criteria:
| Bevacizumab (1.25 mg) | Macular laser |
|
Turkoglu 2015 | 12-month FU | Inclusion criteria:
| Focal or grid laser treatment | Initial injection of ranibizumab 0.5 mg/0.05 mL |
|
Wykoff 2022 | 12 Months FU |
|
Intravitreal Faricimab 6·0 mg every 8 weeks, intravitreal Faricimab 6·0 mg | Intravitreal aflibercept 2·0 mg every 8 weeks |
|
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)
Study | Follow-up time | Population | Intervention | Comparator | Outcomes |
---|---|---|---|---|---|
Randomised controlled trials (from Jorge et al. 2018 Cochrane systematic review) | |||||
Bandello 2005 | 12 Months FU | Inclusion criteria:
|
Standard threshold laser “Classic” Nd:Yag 532 nm laser treatment |
Subthreshold laser “Light” Nd:Yag 532 nm laser treatment |
|
Blankenship 1979 | 12 Months FU | Inclusion criteria:
| Argon laser | No treatment |
|
Casson 2012 | 6 Months FU | Inclusion criteria:
|
Subthreshold laser Nanopulse (2RT) laser treatment | Standard threshold laser |
|
DRCNET 2007 | 12 Months FU | Inclusion criteria:
|
Standard threshold laser (mETDRS style focal laser) (162 eyes) |
Subthreshold laser (MMG laser) (161 eyes) |
|
ETDRS 1985 | 12 Months FU | Inclusion criteria:
|
Immediate standard threshold laser (argon laser) 754 eyes |
Deferred standard threshold laser = (no intervention) ) (1490) |
|
Figueira 2009 | 12 Months FU | Inclusion criteria:
|
Subthreshold laser (Micropulse diode) 44 Eyes |
Standard threshold laser (argon green) 40 eyes |
|
Ishibashi 2014 | 12 Months FU | Inclusion criteria:
| Pegaptanib sodium | Sham injection |
|
Ladas 1993 | 12 Months FU | Inclusion criteria:
|
Standard threshold laser (Blue-green argon laser) (27 eyes) | control (23 eyes) |
|
Laursen 2004 | 12 Months FU | Inclusion criteria:
| Subthreshold laser (MPDL) n=12 | Standard threshold laser (argon laser) n=11 |
|
Lavinsky 2011 | 12 Months FU | Inclusion criteria:
|
|
Subthreshold laser
(42 eyes) |
|
Olk 1986 | 12 Months FU | Inclusion criteria:
|
Standard threshold laser Grid with PRP 82 eyes |
No treatment 78 eyes |
|
Pei-Pei 2015 | 12 Months FU | Inclusion criteria:
|
Subthreshold laser 21 eyes 543 nm subthreshold laser (laser grid) |
Standard threshold laser 21 eyes |
|
Tewari 1998 | 12 Months FU | Inclusion criteria:
|
Subthreshold laser Diode laser (40 eyes; 20 focal and 20 grid) |
Standard threshold laser Argon green (40 eyes; 20 focal and 20 grid) |
|
Venkatesh 2011 | 12 Months FU | Inclusion criteria:
|
Subthreshold laser Subthreshold micropause diode laser (n = 23) |
Standard threshold laser Double-frequency neodymium YAG (Nd:YAG) laser (n = 23) |
|
Vujosevic 2010 | 12-months FU | Inclusion criteria:
|
Subthreshold laser Micropulse diode laser (32 eyes) |
Standard threshold laser (30 eyes) m-ETDRS with green laser |
|
Xie 2013 | 12-months FU | Inclusion criteria:
| Argon ion laser group | subthreshold micropulse diode laser ( SDM, 810nm) |
|
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)
Study | Follow-up time | Population | Intervention | Comparator | Outcomes |
---|---|---|---|---|---|
Randomised controlled trials (from Mehta et al. 2018 Cochrane systematic review) | |||||
DRCRnet U 2018 (Maturi 2018) | 6 Months FU | Inclusion criteria:
| Intravitreal ranibizumab (0.3 mg) and dexamethasone implant (0.7g) | Intravitreal ranibizumab (0.3 mg) and sham injection |
|
Lim 2012 | 12 Months FU | Inclusion criteria:
| Intravitreal bevacizumab (1.25mg/0.05ml) and intravitreal triamcinolone acetonide (2mg/0.05ml) |
|
|
Maturi 2015 | 12 Months FU | Inclusion criteria:
| Intravitreal bevacizumab (1.25mg) and dexamethasone implant (0.7mg) | Intravitreal bevacizumab (1.25mg) |
|
Neto 2017 | 6 Months FU | Inclusion criteria:
| Intravitreal bevacizumab (1.25mg/0.05ml) and intravitreal triamcinolone acetate (4mg/0.1ml) |
|
|
Riazi-Esfahani 2017 | 6 Months FU | Inclusion criteria:
| Intravitreal bevacizumab (1.25mg/0.05ml) and intravitreal triamcinolone acetonide (1mg/0.025ml) | Intravitreal bevacizumab (1.25mg/0.05ml) |
|
Shoeibi 2013 | 6 Months FU | Inclusion criteria:
| Intravitreal bevacizumab (1.25mg/0.05ml) and triamcinolone acetonide (2mg/0.05ml) | Intravitreal bevacizumab (1.25mg/0.05ml) and sham injection |
|
Soheilian 2012 |
12 Months FU 24 months FU | Inclusion criteria:
|
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 |
|
Synek 2011 | 6 Months FU | Inclusion criteria:
| Intravitreal bevacizumab (1.25mg/0.05ml) and triamcinolone acetonide (2mg/0.05ml) | Intravitreal bevacizumab (1.25mg/0.05ml) |
|
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)
Study | Follow-up time | Population | Intervention | Comparator | Outcomes |
---|---|---|---|---|---|
Randomised controlled trials (from Rittiphairoj et al. 2020 Cochrane systematic review) | |||||
BEVORDEX 2014 (Gillies 2014) | 12 Months FU | Inclusion criteria:
| Intravitreal dexamethasone implant (Ozurdex 0.7 mg) every 16 weeks (PRN) | Intravitreal bevacizumab (1.25 mg) every 4 weeks (PRN) |
|
Callanan 2017 | 12 Months FU | Inclusion criteria:
| Intravitreal treatment with dexamethasone implant 0.7 mg | Ranibizumab 0.5 mg |
|
DRCR | 24 Months FU | Inclusion criteria:
|
Intravitreal triamcinolone (1 mg) Intravitreal triamcinolone (4 mg) | Standard threshold laser (Focal/grid laser) |
|
FAME 2011 (Campochiaro 2011) | 24 Months FU | Inclusion criteria:
|
0.2 μg/day fluocinolone (low dose insert) 0.5 μg/day fluocinolone (high dose insert) | Sham injection |
|
Kriechbaum 2014 | 12 Months FU | Inclusion criteria:
| 3 injections of 2.5 mg bevacizumab, 2 sham injections after 4 and 8 weeks, then PRN regimen | 1 initial injection of 8 mg triamcinolone, 2 sham injections after 4 and 8 weeks, then PRN regimen |
|
Lim 2012 | 12 Months FU | Inclusion criteria:
|
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 |
|
MEAD 2014 (Boyer 2014) | 12 Months FU | Inclusion criteria:
|
| Sham procedure |
|
Ockrim 2008 | 12 Months FU | Inclusion criteria:
| Intravitreal triamcinolone 4 mg | Standard threshold laser |
|
Sutter 2004 | 12 Months FU | Inclusion criteria:
| Intravitreal triamcinolone (4 mg) | Sham treatment (subconjunctival saline injection) |
|
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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Subthreshold laser | 0.00 (−0.05, 0.06) | Moderate | Could 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 | |
Pegaptanib | 0.01 (−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 | |
Sham | 0.10 (−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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Bevacizumab | −0.12 (−0.36, 0.11) | Moderate | Could 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 | |
Triamcinolone | 0.08 (−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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Bevacizumab | −0.14 (−0.19, −0.09) | High | Favours Bevacizumab |
Ranibizumab | −0.15 (−0.19, −0.11) | Favours Ranibizumab | |
Aflibercept | −0.19 (−0.24, −0.14) | Favours Aflibercept | |
Pegaptanib | 0.00 (−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 | |
Sham | 0.08 (−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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Bevacizumab | −0.18 (−0.21, −0.15) | Moderate | Favours 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 | |
Triamcinolone | 0.00 (−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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Subthreshold laser | −1.91 (−42.49, 39.60) | Moderate | Could 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 | |
Sham | 74.02 (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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Bevacizumab | −65.47 (−96.59, −34.19) | Moderate | Favours 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 | |
Triamcinolone | 66.54 (42.15, 91.00) | Could not differentiate | |
Ranibizumab + standard threshold laser | 24.93 (−24.70, 73.77) | Could not differentiate | |
Fluocinolone | −23.15 (−66.75, 20.09) | Could not differentiate | |
Sham | 35.27 (−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
Treatment | MD (95% CrI) | Quality | Interpretation of effect |
---|---|---|---|
Bevacizumab | −19.86 (−58.85, 22.87) | Moderate | Could 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 | |
Sham | 70.01 (−4.07, 144.20) | Could not differentiate | |
Subthreshold laser | 40.74 (−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 studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF) | |||||
Overall | |||||
11 | Parallel RCTs | 2410 | RR: 2.30 [1.54, 3.45] | Very Low | Favours Anti-VEGF |
Subgroup: Conbercept (RR greater than 1 favours anti-VEGF) | |||||
1 | Parallel RCTs | 199 | RR: 1.67 [0.92, 3.03] | High | Could not differentiate |
Subgroup aflibercept (RR greater than 1 favours anti-VEGF) | |||||
4 | Parallel RCT | 1098 | RR: 3.36 [2.15, 5.23] | Moderate | Favours aflibercept |
Subgroup bevacizumab (RR greater than 1 favours anti-VEGF) | |||||
1 | Parallel RCT | 50 | RR: 2.26 [0.47, 10.98] | High | Could not differentiate |
Subgroup ranibizumab (RR greater than 1 favours anti-VEGF) | |||||
5 | Parallel RCT | 1033 | RR: 1.92 [0.87, 4.24] | Very Low | Could not differentiate |
Table 16Anti-VEGF vs standard threshold laser: The mean number of treatments at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subgroup aflibercept (MD lower than 0 favours anti-VEGF) | |||||
4 | Parallel RCT | 905 | MD: 9.49 [8.76, 10.23] | Low | Favours standard threshold laser |
Subgroup bevacizumab (MD lower than 0 favours anti-VEGF) | |||||
2 | Parallel RCT | 164 | MD: 2.10 [1.62, 2.58] | Moderate | Favours standard threshold laser |
Subgroup ranibizumab (MD lower than 0 favours anti-VEGF) | |||||
4 | Parallel RCT | 903 | MD: 1.98 [−2.34, 6.29] | Very Low | Favours standard threshold laser |
Subgroup: Conbercept (MD lower than 0 favours anti-VEGF) | |||||
1 | Parallel RCT | 157 | MD: −0.10 [−1.18, 0.98] | High | Could not differentiate |
Table 17Anti-VEGF vs standard threshold laser: The mean number of treatments at 24 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Aflibercept (MD lower than 0 favours anti-vegf) | |||||
2 | Parallel RCT | 578 | MD: 19.00 [16.64, 21.35] | Moderate | Favours standard threshold laser |
Table 18Anti-VEGF vs standard threshold laser: Adverse Events at 24 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Adverse Event: Cataract progression Subgroup aflibercept (RR lower than 1 favours anti-VEGF) | |||||
3 | Parallel RCTs | 1132 | RR: 0.92 [0.36, 2.35] | High | Favours standard threshold laser |
Subgroup: ranibizumab (RR lower than 1 favours anti-VEGF) | |||||
1 | Parallel RCTs | 227 | RR: 0.32 [0.01, 7.75] | High | Favours standard threshold laser |
Adverse Event: IOP increase | |||||
Subgroup aflibercept (RR lower than 1 favours anti-VEGF) | |||||
2 | Parallel RCT | 554 | RR: 1.75 [0.94, 3.26] | Moderate | Favours standard threshold laser |
Subgroup bevacizumab (RR lower than 1 favours anti-VEGF) | |||||
1 | Parallel RCT | 80 | RR: 2.72 [0.11, 64.85] | High | Favours standard threshold laser |
Subgroup ranibizumab (RR lower than 1 favours anti-VEGF) | |||||
1 | Parallel RCT | 80 | RR: 8.14 [0.49, 134.21] | High | Favours standard threshold laser |
Adverse Event: Vitreous haemorrhage | |||||
Subgroup aflibercept (RR lower than 1 favours anti-VEGF) | |||||
3 | Parallel RCTs | 1132 | RR: 0.73 [0.35, 1.50] | Low | Favours standard threshold laser |
Subgroup: Conbercept (RR lower than 1 favours anti-VEGF) | |||||
1 | Parallel RCTs | 156 | RR: 1.05 [0.27, 4.06] | High | Favours standard threshold laser |
Subgroup bevacizumab (RR lower than 1 favours anti-VEGF) | |||||
1 | Parallel RCT | 80 | RR: 0.30 [0.01, 7.21] | High | Favours standard threshold laser |
Subgroup ranibizumab (RR lower than 1 favours anti-VEGF) | |||||
1 | Parallel RCT | 382 | RR: 0.31 [0.08, 1.11] | High | Favours standard threshold laser |
Table 19Bevacizumab VS Ranibizumab
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR lower than 1 favours bevacizumab) | |||||
2 | Parallel RCTs | 636 | RR: 0.88 [0.68, 1.14] | High | Could not differentiate |
The mean number of treatments at 12 months (MD lower than 0 favours bevacizumab) | |||||
2 | Parallel RCT | 226 | MD: 1.06 [−1.09, 3.22] | High | Favours bevacizumab |
Table 20Aflibercept vs Ranibizumab
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
The mean number of treatments at 12 months (MD lower than 0 favours aflibercept) | |||||
2 | Parallel RCT | 182 | MD: −0.95 [−2.11, 0.21] | Low | Could not differentiate |
Table 21Brolucizumab vs Aflibercept
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF) | |||||
2 | Parallel RCTs | 736 | RR: 1.14 [0.96, 1.37] | High | Could not differentiate |
The mean number of treatments at 12 months (MD lower than 0 favours brolucizumab) | |||||
2 | Parallel RCT | 736 | MD: −1.60 [−1.80, −1.39] | High | Favours brolucizumab |
Table 22Faricimab vs Aflibercept
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF) | |||||
2 | Parallel RCTs | 1094 | RR: 1.01 [0.85, 1.21] | High | Could not differentiate |
Table 23Ranibizumab vs Ranibizumab + standard threshold laser
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favour anti-VEGF plus laser) | |||||
3 | Parallel RCTs | 636 | RR: 1.05 [0.78, 1.42] | Moderate | Could not distinguish |
Table 24Bevacizumab vs Bevacizumab + standard threshold laser
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
The mean number of treatments at 12 months (MD lower than 0 favours bevacizumab+ laser) | |||||
1 | Parallel RCT | 736 | MD: 0.26 [−0.25, 0.77] | High | Could not differentiate |
Table 25Ranibizumab vs sham
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours anti-VEGF) | |||||
2 | Parallel RCTs | 509 | 2.66 [1.94, 3.65] | High | Favours ranibizumab |
Table 26Anti-VEGF and steroid versus anti-VEGF alone
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Significant intraocular inflammation (RR less than 1 favour Anti-VEGF and steroid) | |||||
2 | Parallel RCTs | 189 | RR 0.99 [0.14, 6.95] | High | Could not differentiate |
Development of cataract (RR less than 1 favour Anti-VEGF and steroid) | |||||
3 | Parallel RCTs | 268 | RR: 9.30 [2.21, 39.02] | High | Favours anti- VEGF alone |
Raised intraocular pressure (RR less than 1 favour Anti-VEGF and steroid) | |||||
7 | Parallel RCT | 557 | RR: 12.07 [4.67, 31.25] | Moderate | Favours anti- VEGF alone |
Table 27Intravitreal dexamethasone versus sham
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours intravitreal dexamethasone) | |||||
1 | Parallel RCTs | 701 | RR: 1.39 [0.91, 2.12] | Moderate | Could not differentiate |
Visual Acuity: three or more lines improvement from baseline up to 24 M (RR greater than 1 favours intravitreal dexamethasone) | |||||
1 | Parallel RCTs | 701 | RR: 1.54 [1.04, 2.26] | Moderate | Favours intravitreal dexamethasone |
Adverse events Cataract progression at 36 months (RR less than 1 favours intravitreal dexamethasone) | |||||
1 | Parallel RCT | 697 | RR 3.89 [2.75, 5.50] | Moderate | Favours sham |
Adverse events IOP increase at 36 months (RR less than 1 favours intravitreal dexamethasone) | |||||
1 | Parallel RCT | 697 | RR: 8.99 [5.05, 16.03] | Moderate | Favours sham |
Table 28Intravitreal fluocinolone acetonide implant versus sham
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favour Intravitreal fluocinolone acetonide implant) | |||||
1 | Parallel RCTs | 560 | RR: 1.79 [1.16, 2.78] | High | Favours 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) | |||||
1 | Parallel RCTs | 560 | RR: 1.76 [1.22, 2.53] | High | Favours Intravitreal fluocinolone acetonide |
Adverse events Cataract progression at 24 M (RR less than 1 favours Intravitreal fluocinolone acetonide implant) | |||||
1 | Parallel RCT | 351 | RR: 1.63 [1.35, 1.97] | High | Favours sham |
Adverse events IOP increase at 24 M (RR less than 1 favours Intravitreal fluocinolone acetonide implant) | |||||
1 | Parallel RCT | 531 | RR: 3.35 [2.22, 5.06] | High | Favours sham |
Table 29Intravitreal triamcinolone acetonide injection versus sham
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement (RR greater than 1 favour Intravitreal triamcinolone acetonide | |||||
1 | Parallel RCTs | 69 | RR: 4.12 [0.48, 34.99] | Moderate | Favours Intravitreal triamcinolone acetonide injection |
Adverse events Cataract progression at 24 M (RR less than 1 favours Intravitreal triamcinolone acetonide | |||||
1 | Parallel RCT | 69 | RR: 3.00 [0.97, 9.30] | Moderate | Favours Intravitreal triamcinolone acetonide injection |
Adverse events IOP increase at 24 M (RR less than 1 favours Intravitreal triamcinolone acetonide | |||||
1 | Parallel RCT | 69 | RR: 10.29 [1.39, 76.12] | Moderate | Favours sham |
Table 30Intravitreal dexamethasone versus intravitreal anti-VEGF
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M (RR greater than 1 favours: Intravitreal dexamethasone Subgroup bevacizumab | |||||
1 | Parallel RCT | 88 | RR: 0.99 [0.70, 1.40] | Moderate | Could not differentiate |
Subgroup ranibizumab (RR greater than 1 favour: Intravitreal dexamethasone | |||||
1 | Parallel RCT | 363 | RR: 0.50 [0.32, 0.79] | Moderate | Favours ranibizumab |
Table 31Intravitreal dexamethasone versus intravitreal anti-VEGF: The mean number of treatments at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subgroup aflibercept | |||||
1 | Parallel RCT | 98 | MD: Not estimable | High | Could not differentiate |
Subgroup bevacizumab | |||||
1 | Parallel RCT | 88 | MD:Not estimable | High | Could not differentiate |
Subgroup ranibizumab | |||||
1 | Parallel RCT | 363 | MD: Not estimable | High | Could not differentiate |
Table 32Intravitreal dexamethasone versus intravitreal anti-VEGF: Adverse Events at 12 and 24 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Adverse Event: Cataract progression at 12 to 24 months | |||||
Subgroup bevacizumab (RR less than 1 favours: Bevacizumab) | |||||
1 | Parallel RCTs | 88 | RR: 2.74 [0.58, 12.84] | High | Could not differentiate |
Subgroup: Ranibizumab (RR less than 1 favours: Ranibizumab) | |||||
1 | Parallel RCTs | 247 | RR: 4.54 [2.41, 8.55] | High | Favours Ranibizumab |
Adverse Event: IOP increase at 24 months | |||||
Subgroup aflibercept (RR less than 1 favours: Aflibercept) | |||||
1 | Parallel RCT | 98 | RR: 11.45 [0.65, 201.60] | High | Could not differentiate |
Subgroup bevacizumab (RR less than 1 favours: Bevacizumab) | |||||
1 | Parallel RCT | 88 | RR: 2.40 [1.19, 4.82] | High | Favours bevacizumab |
Subgroup ranibizumab (RR less than 1 favours: Ranibizumab) | |||||
1 | Parallel RCT | 363 | RR: 5.03 [1.12, 22.63] | High | Favours Ranibizumab |
Table 33Intravitreal triamcinolone acetonide versus macular laser
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Visual Acuity: three or more lines improvement from baseline up to 12M | |||||
1 | Parallel RCTs | 584 | RR: 0.85[0.55,1.35] | High | Could not differentiate |
Visual Acuity: three or more lines improvement from baseline up to 24 M | |||||
1 | Parallel RCTs | 584 | RR: 0.95 [0.66, 1.35] | High | Could not differentiate |
Adverse events Cataract progression at 24 M | |||||
1 | Parallel RCT | 459 | RR: 2.68 [2.21, 3.24] | High | Favours standard threshold laser |
Adverse events IOP increase at 24 M | |||||
1 | Parallel RCT | 584 | RR: 9.20 [5.14, 16.47] | High | Favours standard threshold laser |
Table 34Number of patients meeting driving standards at month 24, n (%)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Number of patients meeting driving standards at month 24, n (%) | |||||
Lois 2023 | Pragmatic RCT | 217 | OR: 0.74 [0.16, 3.37] | High | Favours standard threshold laser |
Table 35Number of laser treatments used from baseline to month 24 in study eye, mean (SD)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Number of laser treatments used from baseline to month 24 in study eye, mean (SD) | |||||
Lois 2023 | Pragmatic RCT | 231 | −1.96 [−3.89, −0.03] | High | Favours standard threshold laser |
Table 36Comparisons vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subthreshold laser MD less than 0 favours comparison | |||||
1 Figueira 2009 | Parallel RCTs | 84 | MD −0.04 [−018,0.08] | High | Could not differentiate |
Bevacizumab MD less than 0 favours comparison | |||||
1 Soheilian 2007 | Parallel RCTs | 85 | MD −0.19 [−0.32.−0.08] | Moderate | Favours Bevacizumab |
Ranibizumab MD less than 0 favours comparison | |||||
1 Turkoglu 2015 | Parallel RCT | 70 | MD −0.10 [−0.19.−0.02] | High | Favours ranibizumab |
Triamcinolone MD less than 0 favours comparison | |||||
1 Ockrim 2008 | Parallel RCT | 83 | MD 0.04 [−0.57.0.64] | Low | Could not differentiate |
Ranibizumab + standard threshold laser MD less than 0 favours comparison | |||||
1 RELATION 2012 | Parallel RCT | 128 | MD −0.10 [−0.16.−0.04] | Low | Favours Triamcinolone |
Table 37Change in central retinal thickness from baseline (mean difference) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subthreshold laser MD less than 0 favours comparison | |||||
1 Figueira 2009 | Parallel RCTs | 84 | MD 13.20 [−31.58 , 57.98] | High | Could not differentiate |
Bevacizumab MD less than 0 favours comparison | |||||
1 Soheilian 2007 | Parallel RCTs | 85 | MD −42.00 [−95.60, −11.60] | Moderate | Could not differentiate |
Ranibizumab MD less than 0 favours comparison | |||||
1 Turkoglu 2015 | Parallel RCT | 70 | MD −66.00 [−78.59, −55.41] | High | Favours ranibizumab |
Table 38Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab MD less than 0 favours comparison | |||||
1 Soheilian 2012 | Parallel RCTs | 78 | MD −0.07 [−0.23,0.09] | High | Could not differentiate |
Bevacizumab + triamcinolone MD less than 0 favours comparison | |||||
1 Soheilian 2012 | Parallel RCTs | 75 | MD −0.06 [−0.21,0.09] | High | Could not differentiate |
Table 39Change in central retinal thickness at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab MD less than 0 favours comparison | |||||
1 Soheilian 2012 | Parallel RCTs | 75 | MD −4.00 [−66.81,58.81] | High | Could not differentiate |
Bevacizumab + triamcinolone MD less than 0 favours comparison | |||||
1 Soheilian 2012 | Parallel RCTs | 78 | MD −26.00 [−81.03, 29.03] | High | Could not differentiate |
Table 40Anti-VEGF vs sham: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab (MD less than 0 favours anti-vegf) | |||||
1 Ahmadieh 2008 | Parallel RCTs | 78 | MD −0.15 [−0.26, −0.04] | High | Favours Bevacizumab |
Table 41Subthreshold vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subthreshold laser vs standard threshold laser (MD less than 0 favours subthreshold laser) | |||||
4 | Parallel RCT | 213 | MD −0.01 [−0.12, 0.09] | Low | Could not differentiate |
Table 42bevacizumab vs bevacizumab + standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab vs bevacizumab + standard threshold laser (MD less than 0 favours vs bevacizumab + standard threshold laser) | |||||
1 (Faghihi,2010) | Parallel RCT | 80 |
MD: −0.04 [−0.17, 0.08] | High | Could not differentiate |
Table 43Anti-VEGF vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab Vs Standard threshold laser (MD less than 0 favours anti-VEGF) | |||||
2 | Parallel RCT | MD −0.17 [−0.21, −0.13] | Moderate | Favours bevacizumab | |
Aflibercept Vs Standard threshold laser (MD less than 0 favours anti-VEGF) | |||||
3 | Parallel RCT | MD −0.09 [−0.19, 0.02] | Low | Could not differentiate |
Table 44Steroids vs sham: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Fluocinolone Vs Sham (MD less than 0 favours steroid) | |||||
1 FAME 2011 (Campochiaro 2011) | Parallel RCT | 560 | MD −0.06 [−0.08, −0.03] | High | Favours Fluocinolone |
Dexamethasone Vs Sham (MD less than 0 favours steroid) | |||||
1 MEAD 2014 (Boyer 2014) | Parallel RCT | 701 | MD −0.05 [−0.09, 0.00] | High | Favour Dexamethasone |
Table 45Brolucizumab vs aflibercept: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Brolucizumab Vs Aflibercept (MD less than 0 favours Brolucizumab) | |||||
1 (Brown 2022) | Parallel RCT | 360 | MD 0.02 [−0.02, 0.07] | High | Could not differentiate |
Table 46Anti VEGF vs Anti VEGF: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Aflibercept vs. Bevacizumab (MD less than 0 favours Aflibercept) | |||||
1 DRCRnet 2015 | Parallel RCT | 386 | MD−0.06 [−0.10, −0.01] | High | Favours Aflibercept |
Aflibercept vs Ranibizumab (MD less than 0 favours Aflibercept) | |||||
1 DRCRnet 2015 | Parallel RCT | 392 | MD −0.01 [−0.06, 0.04] | High | Could not differentiate |
Ranibizumab vs Bevacizumab (MD less than 0 favours Ranibizumab) | |||||
1 DRCRnet 2015 | Parallel RCT | 376 | MD −0.05 [−0.09, −0.00] | High | Favour Ranibizumab |
Table 47Dexamethasone vs bevacizumab: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Dexamethasone Vs Bevacizumab (MD less than 0 favours Dexamethasone) | |||||
1 BEVORDEX 2014 (Gillies 2014) | Parallel RCT | 88 | MD 0.08 [−0.03, 0.19] | High | Could not differentiate |
Table 48Triamcinolone vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Triamcinolone Vs Standard threshold laser (MD less than 0 favours Triamcinolone) | |||||
1 DRCRnet 2008 | Parallel RCT | 584 | MD 0.08 [0.01, 0.15] | High | Favours Standard threshold laser |
Table 49Combination treatment vs sham + standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Ranibizumab + standard threshold laser (MD less than 0 favours ranibizumab + standard threshold laser | |||||
1 DRCRnet 2010 | Parallel RCT | 480 | MD −0.12 [−0.17, −0.07] | High | Favours ranibizumab + standard threshold laser |
Ttriamcinolone + standard threshold laser (MD less than 0 favours triamcinolone + standard threshold laser) | |||||
1 DRCRnet 2010 | Parallel RCT | 479 | MD −0.02 [−0.07, 0.03] | High | Could not differentiate |
Table 50Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab Vs Triamcinolone + Bevacizumab (MD less than 0 favours Triamcinolone + Bevacizumab) | |||||
1 Soheilian 2012 | Parallel RCT | 75 | MD 0.01 [−0.15, 0.17] | High | Could not differentiate |
Table 51Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Ranibizumab + standard threshold laser vs standard threshold laser: (MD less than 0 favours Ranibizumab + standard threshold laser) | |||||
1 DRCRnet 2010 | Parallel RCT | 253 | MD −0.08 [−0.13, −0.03] | High | Favours Ranibizumab + standard threshold laser |
Triamcinolone + standard threshold laser vs standard threshold laser: (MD less than 0 favours triamcinolone + standard threshold laser) | |||||
1 DRCRnet 2010 | Parallel RCT | 256 | MD 0.00 [−0.06, 0.06] | High | Favours triamcinolone + standard threshold laser |
Table 52Aflibercept vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Aflibercept vs standard threshold Laser (MD less than 0 favours Aflibercept) | |||||
1 VISTA & VIVID (Korobelnik 2014) | Parallel RCT | 168 | MD −0.15 [−0.15, −0.14] | High | Favours Aflibercept |
Table 53Aflibercept vs standard threshold laser: Change in visual acuity (logMAR) at 24 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Aflibercept vs standard threshold laser: (MD less than 0 favours Aflibercept) | |||||
1 VISTA & VIVID (Korobelnik 2014) | Parallel RCT | 168 | MD −0.15 [−0.16, −0.14] | High | Favours Aflibercept |
Table 54Aflibercept vs standard threshold laser: Change in central retinal thickness at 12 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Aflibercept vs standard threshold laser: (MD less than 0 favours Aflibercept) | |||||
1 VISTA & VIVID (Midena 2018) | Parallel RCT | 168 | MD −69.30 [−73.28, −65.32] | High | Favours Aflibercept |
Table 55Aflibercept vs standard threshold laser: Change in central retinal thickness at 24 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Laser vs aflibercept: change in central retinal thickness at 24 months. (MD less than 0 favours aflibercept) | |||||
1 VISTA & VIVID (Midena 2018 | Parallel RCT | 168 | MD 67.80 [63.42, 72.18] | High | Favours standard threshold laser |
Table 56Triamcinolone vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | |
---|---|---|---|---|---|
Triamcinolone vs standard threshold laser: (MD less than 0 favours Triamcinolone) | |||||
1 DRCRnet 2008 | Parallel RCT | 296 | MD 0.08 [0.01, 0.15] | High | Favours standard threshold laser |
Table 57Combination treatment vs standard threshold laser: Change in central retinal thickness from baseline (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Ranibizumab + standard threshold laser (MD less than 0 favours Ranibizumab + standard threshold laser) | |||||
1 DRCRnet 2010 | Parallel RCT | 227 | MD −44.00 [−65.63, −22.37 | High | Favours Ranibizumab + standard threshold laser |
triamcinolone + standard threshold laser (MD less than 0 favours triamcinolone + standard threshold laser | |||||
1 DRCRnet 2010 | Parallel RCT | 231 | MD −32.00 [−54.39, −9.61] | High | Favours triamcinolone + standard threshold laser |
Table 58Aflibercept vs standard threshold laser
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation 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 RCT | 168 | MD −151.70 [−154.35, −149.05] | High | Favours standard threshold laser |
Table 59Comparisons vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subthreshold laser vs standard threshold laser (MD less than 0 favours Subthreshold laser) | |||||
1 Figueira 2009 | Parallel RCT | 84 | MD −0.04 [−0.16, 0.08] | High | Could not differentiate |
Bevacizumab vs standard threshold laser (MD less than 0 favours Bevacizumab) | |||||
1 Soheilian 2007 | Parallel RCT | 85 | MD −0.19 [−0.32, −0.06] | High | Favours Bevacizumab |
Table 60Comparisons vs standard threshold laser: Change in central retinal thickness from baseline (mean difference) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Subthreshold laser vs standard threshold laser (MD less than 0 favours Subthreshold laser) | |||||
1 Figueira 2009 | Parallel RCT | 84 | MD 13.20 [−31.58, 57.98] | High | Could not differentiate |
Bevacizumab vs standard threshold laser (MD less than 0 favours Bevacizumab | |||||
1 Soheilian 2007 | Parallel RCT | 85 | MD −42.00 [−95.60, 11.60] | High | Could not differentiate |
Table 61Comparisons vs standard threshold laser: Change in visual acuity from baseline (logMAR) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Ranibizumab vs standard threshold laser | |||||
Turkoglu 2015 | Parallel RCT | 70 | MD −0.10 [−0.19, −0.02] | High | Favours Ranibizumab |
Triamcinolone vs standard threshold laser | |||||
Ockrim 2008 | Parallel RCT | 83 | MD 0.04 [−0.57, 0.64] | High | Could not differentiate |
Table 62Ranibizumab vs standard threshold laser: Change in central retinal thickness from baseline (mean difference) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Ranibizumab + standard threshold laser vs standard threshold laser | |||||
RELATION 2012 | Parallel RCT | 128 | MD −0.10 [−0.16, −0.04] | High | Favours Ranibizumab + standard threshold laser |
Table 63Bevacizumab vs sham
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab vs sham | |||||
Ahmadieh 2008 | Parallel RCT | 78 | MD −0.15 [−0.26, −0.04] | High | Favours Bevacizumab |
Table 64Ranibizumab vs standard threshold laser: Change in central retinal thickness from baseline (mean difference) at 12 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Ranibizumab vs standard threshold laser | |||||
Turkoglu 2015 | Parallel RCT | 70 | MD −66.00 [−76.59, −55.41] | High | Favours Ranibizumab |
Table 65Comparisons vs standard threshold laser: Change in visual acuity LogMAR at 24 months (mean difference)
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab | |||||
Soheilian 2012 | Parallel RCT | 77 | MD −0.07 [−0.23, 0.09] | High | Could not differentiate |
Bevacizumab + triamcinolone | |||||
Soheilian 2012 | Parallel RCT | 74 | MD −0.06 [−0.21, 0.09] | High | Could not differentiate |
Table 66Comparisons vs standard threshold laser: Change in central retinal thickness from baseline to 24 months
No. of studies | Study design | Sample size | Effect size (95% CI) | Quality | Interpretation of effect |
---|---|---|---|---|---|
Bevacizumab | |||||
Soheilian 2012 | Parallel RCT | 77 | MD −4.00 [−66.81, 58.81] | High | Could not differentiate |
Bevacizumab + triamcinolone | |||||
Soheilian 2012 | Parallel RCT | 74 | MD −26.00 [−81.03, 29.03] | High | Could not differentiate |
Table 67Economic evidence profile
Study | Applicability | Limitations | Other comments | Incremental | Uncertainty | ||
---|---|---|---|---|---|---|---|
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 perspective | Directly applicable; NHS perspective | Minor 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: £2,930 | Aflibercept 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 trial | Directly applicable; NHS perspective | Minor 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 therapies | Directly applicable; NHS perspective | Minor 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 edema | Partially applicable; Canada study setting with 5% discount rate | Minor 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 data | Partially applicable; US study; 3% discount rate from 2 years onwards | Potentially 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 edema | Partially applicable; US study (includes societal costs); 3% discount rate | Potentially 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 0.9981 | Ranibizumab compared with sham considering both eyes $4,587 (£3,193)/QALY | No 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 edema | Partially applicable; US study; 3% discount rates | Minor 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 analysis | Partially applicable; US study; 0 or 5% discount rate used | Potentially 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 RCT | Directly applicable; NHS and PSS perspective | Minor 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: −£365 | Subthreshold micro pulse laser compared with standard threshold laser: 0.008 | Subthreshold 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 edema | Partially applicable; US healthcare setting | Minor 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: 0.015 | Aflibercept 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
Strategy | Absolute costs | Absolute QALYs | Inc. costs | Inc. QALYs | ICER | NMB at £20K/QALY (95% CI) |
---|---|---|---|---|---|---|
No treatment | £3,843 | 8.485 | - | - | - | £165,850 (£152,520 to £179,419) |
Subthreshold laser | £4,431 | 8.956 | £588 | 0.471 | £1,248 | £174,682 (£160,969 to £188,956) |
Standard threshold laser | £4,823 | 8.976 | £392 | 0.020 | £19,272 | £174,697 (£161,500 to £188,126) |
Bevacizumab | £9,385 | 9.201 | £4,562 | 0.225 | £20,318 | £174,625 (£161,698 to £188,032) |
Bevacizumab plus standard laser | £11,408 | 9.216 | £2,023 | 0.015 | £133,549 | £172,905 (£159,025 to £186,478) |
Ranibizumab | £23,920 | 9.220 | £12,511 | 0.004 | Extendedly dominated | £160,471 (£147,567 to £173,477) |
Brolucizumab | £24,360 | 9.266 | £12,952 | 0.051 | £256,445 | £160,963 (£147,392 to £174,636) |
Ranibizumab plus standard laser | £24,693 | 9.199 | £333 | −0.067 | Dominated | £159,295 (£146,028 to £173,040) |
Faricimab | £33,947 | 9.266 | £9,587 | 0.000 | Dominated | £151,368 (£137,455 to £166,067) |
Aflibercept | £34,388 | 9.258 | £10,028 | −0.008 | Dominated | £150,771 (£136,228 to £165,577) |
Table 69Economic model results (list price) compared with no treatment
Strategy | Absolute costs | Absolute QALYs | Inc. costs | Inc. QALYs | ICER |
---|---|---|---|---|---|
No treatment | £3,843 | 8.485 | - | - | - |
Subthreshold laser | £4,431 | 8.956 | £588 | 0.471 | £1,248 |
Standard threshold laser | £4,823 | 8.976 | £980 | 0.491 | £1,994 |
Bevacizumab | £9,385 | 9.201 | £5,542 | 0.716 | £7,741 |
Bevacizumab plus standard laser | £11,408 | 9.216 | £7,565 | 0.731 | £10,349 |
Ranibizumab | £23,920 | 9.220 | £20,076 | 0.735 | £27,319 |
Brolucizumab | £24,360 | 9.266 | £20,517 | 0.781 | £26,253 |
Ranibizumab plus standard laser | £24,693 | 9.199 | £20,849 | 0.715 | £29,172 |
Faricimab | £33,947 | 9.266 | £30,104 | 0.781 | £38,541 |
Aflibercept | £34,388 | 9.258 | £30,545 | 0.773 | £39,500 |
Table 70Economic model results (list price) fully incremental analysis
Strategy | Absolute costs | Absolut QALYs | Inc. costs | Inc. QALYs | ICER | NMB at £20K/QALY (95% CI) |
---|---|---|---|---|---|---|
No treatment | £3,822 | 8.503 | £0 | 0.000 | £0 | £166,238 (£152,957 to £180,234) |
Subthreshold laser | £4,458 | 8.944 | £635 | 0.441 | £1,442 | £174,414 (£160,952 to £187,227) |
Standard threshold laser | £4,919 | 8.928 | £462 | −0.015 | Dominated | £173,646 (£159,605 to £187,244) |
Bevacizumab | £9,308 | 9.211 | £4,850 | 0.268 | £18,125 | £174,916 (£161,429 to £187,533) |
Bevacizumab plus standard laser | £11,325 | 9.211 | £2,017 | 0.000 | Extendedly dominated | £172,899 (£159,168 to £186,269) |
Ranibizumab | £24,039 | 9.224 | £14,731 | 0.012 | Extendedly dominated | £160,434 (£146,828 to £174,059) |
Brolucizumab | £24,348 | 9.268 | £15,040 | 0.057 | £263,607 | £161,016 (£147,669 to £173,755) |
Ranibizumab plus standard laser | £24,904 | 9.209 | £556 | −0.060 | Dominated | £159,268 (£145,571 to £172,882) |
Faricimab | £33,979 | 9.271 | £9,630 | 0.003 | £3,116,792 | £151,448 (£137,073 to £164,968) |
Aflibercept | £34,522 | 9.267 | £544 | −0.005 | Dominated | £150,813 (£136,809 to £164,845) |
Table 71Economic model results (list price) compared with no treatment
Strategy | Absolute costs | Absolute QALYs | Inc. costs | Inc. QALYs | ICER |
---|---|---|---|---|---|
No treatment | £3,822 | 8.503 | - | - | - |
Subthreshold laser | £4,458 | 8.944 | £635 | 0.441 | £1,442 |
Standard threshold laser | £4,919 | 8.928 | £1,097 | 0.425 | £2,579 |
Bevacizumab | £9,308 | 9.211 | £5,485 | 0.708 | £7,746 |
Bevacizumab plus standard laser | £11,325 | 9.211 | £7,502 | 0.708 | £10,593 |
Ranibizumab | £24,039 | 9.224 | £20,216 | 0.721 | £28,054 |
Brolucizumab | £24,348 | 9.268 | £20,526 | 0.765 | £26,824 |
Ranibizumab plus standard laser | £24,904 | 9.209 | £21,081 | 0.706 | £29,878 |
Faricimab | £33,979 | 9.271 | £30,156 | 0.768 | £39,250 |
Aflibercept | £34,522 | 9.267 | £30,700 | 0.764 | £40,196 |
Table 72List prices for treatments included in the recommendations
Resource | Unit costs | Source |
---|---|---|
Aflibercept 4.0mg/0.1ml | £816.00 | BNF (accessed 13/02/2023) |
Ranibizumab (Lucentis) 2.3mg/0.23ml | £551.00 | BNF (accessed 13/02/2023) |
Ranibizumab biosimilar (Ongavia) 2.3mg/0.23ml | £523.45 | BNF (accessed 28/04/2023) |
Bevacizumab* 1.25mg | £50.00 | Poku et al (2012) cited in NICE TA824 |
Brolucizumab 19.8mg/0.165ml | £816.00 | BNF (accessed 13/02/2023) |
Faricimab 28.8mg/0.24ml | £857.00 | BNF (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.