4.6 Article

Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten years

Journal

BRITISH JOURNAL OF HAEMATOLOGY
Volume 152, Issue 6, Pages 766-770

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1365-2141.2010.08451.x

Keywords

blood transfusion; sickle cell disease; iron overload

Categories

Funding

  1. Medical Research Council [G0000111] Funding Source: researchfish
  2. Medical Research Council [G0000111] Funding Source: Medline
  3. MRC [G0000111] Funding Source: UKRI

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P>Transfusion of red blood cells is a major therapeutic option in sickle cell disease (SCD). There is strong evidence for its efficacy, particularly in primary and secondary stroke prevention in children, however, its use in other areas remains controversial. This study assessed the patterns of transfusion in the adult cohort attending King's College Hospital over a 10-year period, from 2000 to 2009. Total blood usage has increased significantly (P = 0 center dot 006) during this time, with 78% of the blood received by only 6% of the patients. The increase is explained by increased automated red cell exchange and increased usage for planned and acute transfusions for sickle-related complications.

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