Blood Transfusion Vs. Hydroxyurea for Stroke Prevention in Children With Sickle Cell Anemia: A Systematic Review and Meta-Analysis
- PMID: 36569706
- PMCID: PMC9774052
- DOI: 10.7759/cureus.31778
Blood Transfusion Vs. Hydroxyurea for Stroke Prevention in Children With Sickle Cell Anemia: A Systematic Review and Meta-Analysis
Abstract
Sickle cell anemia (SCA) is a hereditary condition that can lead to severe complications in children such as acute coronary syndrome, splenic sequestration, renal failure, and stroke. Blood transfusion and hydroxyurea (HU) therapy are used to prevent stroke in children with sickle cell disease (SCD). Preliminary data show considerable variation and inconsistency in the use of these two therapeutic interventions. Therefore, this systematic review was carried out to compare the effects of blood transfusion to HU therapy in preventing stroke for children with sickle cell disease. There was an extensive literature search in reliable and authentic databases like PubMed, Medline, Scopus, Cochrane, and Science Direct to obtain relevant articles. This study used the standards and guidelines from the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). During the systematic review, data were obtained focusing on the following parameters: the size of the sample in the study, the age of the subjects involved in the study, the type of Intervention, and the outcome. After an initial search of 163 papers, 25 studies were included. The results of the research give the first evidence that HU is effective in the treatment of cerebrovascular problems in children with SCD. However, it is unclear under what circumstances HU may prevent a second stroke. It can be concluded that children with SCA can effectively avoid primary strokes through chronic blood transfusions and HU.
Keywords: blood transfusion; children; hydroxyurea; prevention; sickle cell anemia; stroke.
Copyright © 2022, Hafiz et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
Figures







Similar articles
-
Red blood cell transfusion to treat or prevent complications in sickle cell disease: an overview of Cochrane reviews.Cochrane Database Syst Rev. 2018 Aug 1;8(8):CD012082. doi: 10.1002/14651858.CD012082.pub2. Cochrane Database Syst Rev. 2018. PMID: 30067867 Free PMC article.
-
Interventions for preventing silent cerebral infarcts in people with sickle cell disease.Cochrane Database Syst Rev. 2020 Apr 6;4(4):CD012389. doi: 10.1002/14651858.CD012389.pub3. Cochrane Database Syst Rev. 2020. PMID: 32250453 Free PMC article.
-
Interventions for preventing silent cerebral infarcts in people with sickle cell disease.Cochrane Database Syst Rev. 2017 May 13;5(5):CD012389. doi: 10.1002/14651858.CD012389.pub2. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2020 Apr 6;4:CD012389. doi: 10.1002/14651858.CD012389.pub3. PMID: 28500860 Free PMC article. Updated. Review.
-
The clinical effectiveness and cost-effectiveness of primary stroke prevention in children with sickle cell disease: a systematic review and economic evaluation.Health Technol Assess. 2012;16(43):1-129. doi: 10.3310/hta16430. Health Technol Assess. 2012. PMID: 23140544 Free PMC article. Review.
-
Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.Cochrane Database Syst Rev. 2017 Jan 17;1(1):CD003146. doi: 10.1002/14651858.CD003146.pub3. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2020 Jul 27;7:CD003146. doi: 10.1002/14651858.CD003146.pub4. PMID: 28094851 Free PMC article. Updated. Review.
Cited by
-
Overview of the Association Between the Pathophysiology, Types, and Management of Sickle Cell Disease and Stroke.Cureus. 2023 Dec 15;15(12):e50577. doi: 10.7759/cureus.50577. eCollection 2023 Dec. Cureus. 2023. PMID: 38107212 Free PMC article. Review.
-
Hydroxyurea for secondary stroke prevention in children with sickle cell anaemia: a systematic review of clinical evidence and outcomes.Ann Med Surg (Lond). 2024 Jan 3;86(2):1042-1047. doi: 10.1097/MS9.0000000000001660. eCollection 2024 Feb. Ann Med Surg (Lond). 2024. PMID: 38333270 Free PMC article. Review.
References
-
- Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease. Leikin SL, Gallagher D, Kinney TR, Sloane D, Klug P, Rida W. https://pubmed.ncbi.nlm.nih.gov/2671914/ Pediatrics. 1989;84:500–508. - PubMed
-
- The clinical features of sickle cell disease. Serjeant GR. Baillieres Clin Haematol. 1993;6:93–115. - PubMed
-
- Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease. Ware RE, Zimmerman SA, Schultz WH. https://pubmed.ncbi.nlm.nih.gov/10556185/ Blood. 1999;94:3022–3026. - PubMed
-
- Long-term stroke risk in children with sickle cell disease screened with transcranial Doppler. Adams RJ, McKie VC, Carl EM, et al. Ann Neurol. 1997;42:699–704. - PubMed
Publication types
LinkOut - more resources
Full Text Sources