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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Clinical follow-up of hydroxyurea-treated adults with sickle cell disease
Ruben Nzouakou1, Dora Bachir, Anne Lavaud
1Sickle Cell Disease Center, Groupe Hospitalier Albert-Chenevier - Henri-Mondor, AP-HP, Créteil, France. ruben.nzouakou@hmn.aphp.fr
Abstract:
Hydroxyurea-derived clinical and biological benefits and safety were retrospectively studied for 123 adult patients from 2 sickle cell disease referral centers during a total follow-up of 654 patient-years and total hydroxyurea exposure of 549 patient-years. Fifty-six adverse events occurred (incidence: 12%/patient-year), with leg ulcers being the most frequent. Adverse events could arise at any time and were usually reversible. No malignancy was observed. Clinical and biological benefits of our cohort were similar to those previously reported. Based on this relatively long retrospective study, the risk/benefit ratio for moderate hydroxyurea doses was satisfactory.
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