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Br J Haematol ; 145(4): 524-8, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19344396

RESUMEN

Chronic transfusions to maintain haemoglobin S (HbS) < or =30% are the mainstay of treatment for children with sickle cell anaemia (SCA) and previous stroke. This HbS target is often hard to maintain, however, and values achieved in current practice are unknown. In preparation for the Phase III Stroke With Transfusions Changing to Hydroxyurea (SWiTCH) trial, we collected data on 295 children with SCA and stroke who received transfusions at 23 institutions. The overall average pre-transfusion %HbS was 35 +/- 11% (institutional range 22-51%). Receiving scheduled transfusions on time was the most predictive variable for maintaining HbS at the < or =30% goal.


Asunto(s)
Anemia de Células Falciformes/terapia , Transfusión Sanguínea/métodos , Adolescente , Anemia de Células Falciformes/sangre , Niño , Hemoglobina Falciforme/análisis , Humanos , Guías de Práctica Clínica como Asunto , Estudios Retrospectivos , Accidente Cerebrovascular/sangre , Accidente Cerebrovascular/prevención & control , Resultado del Tratamiento , Estados Unidos
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