• S Davies and A Olujohungbe.
• NHS Executive, Department of Health, 40 Eastbourne Terrace, London, UK, W2 3QR. sdaviet@doh.gov.uk
• Cochrane Db Syst Rev. 2001 Jan 1 (2): CD002202.

BackgroundSickle cell disease is one of the most common inherited diseases world wide. It is associated with life long morbidity and a reduced life expectancy. Hydroxyurea, a chemotherapeutic drug taken by mouth, raises fetal haemoglobin and, as such, is expected to ameliorate some of the clinical problems of sickle cell disease.ObjectivesTo assess the effects of hydroxyurea therapy in sickle cell disease patients of all types, of any age, regardless of setting.Search StrategyWe searched the Cochrane Cystic Fibrosis and Genetic Disorders Group specialised register of controlled trials for haemoglobinopathies, which comprises references identified from comprehensive electronic database searches, hand-searching relevant journals, and hand-searching abstract books of conference proceedings. Date of the most recent search(es): November 2000.Selection CriteriaAll randomised or quasi-randomised controlled trials comparing the use of oral hydroxyurea for one month or longer with placebo, standard therapy or other interventions for the treatment of patients with sickle cell disease.Data Collection And AnalysisBoth reviewers independently assessed trial quality and extracted data from the two studies included.Main ResultsTwenty trials were found of which two trials, which reported results from a total of 324 adults and children were suitable for inclusion in the review. From the data provided in the published reports only one study (the MSH study to the United States of America) could be analysed. This study showed marked differences in favour of hydroxyurea treatment as compared with placebo in terms of annual crisis rate, use of transfusions, and life-threatening complications (in particular, the acute sickle chest syndrome). No serious adverse effects were reported from either study.Reviewer's ConclusionsWhile hydroxyurea appears both effective and safe in the severely affected SS adults over a two year period; further studies are required to elucidate its role in other patient groups and for other conditions.

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