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- W2585053973 abstract "All patients with HbSS (SCA) share the same genetic mutation but the clinical phenotype is variable and difficult to predict early in life. A reliable severity predictor would be invaluable toward directing therapeutic decisions in those patients at highest risk of SCA complications. A search of PubMed, Cochrane Clinical Trials Register, and Scopus was performed to determine which SCA severity predictors have been validated in pediatric patients. The full text of 94 of the 590 references identified was reviewed based on the title/abstract. Fifty-four articles were included in the analysis. Alpha globin gene number was the most commonly studied severity predictor, followed by fetal hemoglobin (HbF) and reticulocyte count. Alpha thalassemia trait was protective against overt stroke and abnormal transcranial Doppler (TCD) in all but one study, but not frequency of painful crisis or silent cerebral infarct. Two thirds of the HbF studies reported beneficial effects with increasing HbF levels; however, increased HbF levels were not associated with lower hospitalization or stroke rates in others. The ability to predict SCA complications was mixed for all variables, except TCD and absolute reticulocyte count. More reliable predictors are urgently needed to guide therapeutic decisions in children with SCA." @default.
- W2585053973 created "2017-02-10" @default.
- W2585053973 creator A5000449507 @default.
- W2585053973 creator A5025514706 @default.
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- W2585053973 date "2017-06-01" @default.
- W2585053973 modified "2023-10-16" @default.
- W2585053973 title "A systematic review of the literature for severity predictors in children with sickle cell anemia" @default.
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- W2585053973 doi "https://doi.org/10.1016/j.bcmd.2017.01.014" @default.
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