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Randomized Controlled Trial
. 2014 Aug 21;371(8):699-710.
doi: 10.1056/NEJMoa1401731.

Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia

Affiliations
Randomized Controlled Trial

Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia

Michael R DeBaun et al. N Engl J Med. .

Abstract

Background: Silent cerebral infarcts are the most common neurologic injury in children with sickle cell anemia and are associated with the recurrence of an infarct (stroke or silent cerebral infarct). We tested the hypothesis that the incidence of the recurrence of an infarct would be lower among children who underwent regular blood-transfusion therapy than among those who received standard care.

Methods: In this randomized, single-blind clinical trial, we randomly assigned children with sickle cell anemia to receive regular blood transfusions (transfusion group) or standard care (observation group). Participants were between 5 and 15 years of age, with no history of stroke and with one or more silent cerebral infarcts on magnetic resonance imaging and a neurologic examination showing no abnormalities corresponding to these lesions. The primary end point was the recurrence of an infarct, defined as a stroke or a new or enlarged silent cerebral infarct.

Results: A total of 196 children (mean age, 10 years) were randomly assigned to the observation or transfusion group and were followed for a median of 3 years. In the transfusion group, 6 of 99 children (6%) had an end-point event (1 had a stroke, and 5 had new or enlarged silent cerebral infarcts). In the observation group, 14 of 97 children (14%) had an end-point event (7 had strokes, and 7 had new or enlarged silent cerebral infarcts). The incidence of the primary end point in the transfusion and observation groups was 2.0 and 4.8 events, respectively, per 100 years at risk, corresponding to an incidence rate ratio of 0.41 (95% confidence interval, 0.12 to 0.99; P=0.04).

Conclusions: Regular blood-transfusion therapy significantly reduced the incidence of the recurrence of cerebral infarct in children with sickle cell anemia. (Funded by the National Institute of Neurological Disorders and Stroke and others; Silent Cerebral Infarct Multi-Center Clinical Trial ClinicalTrials.gov number, NCT00072761, and Current Controlled Trials number, ISRCTN52713285.).

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Figures

Figure 1
Figure 1. Screening, Randomization, and Follow-up
The screening and randomization process extended from December 2004 through May 2010. Participants may have had more than one reason for exclusion or withdrawal from the study. For participants who were lost to follow-up, data that had accrued before withdrawal were used in the analysis.
Figure 2
Figure 2. Hemoglobin S and Ferritin Levels in the Transfusion Group
The box plots show the hemoglobin S levels (Panel A) and the ferritin levels (Panel B) in the transfusion group, in 6-month intervals. The horizontal line in the boxes represents the median, the lower and upper boundaries of the boxes represent the 25th and 75th percentiles, respectively, the I bars represent the 10th and 90th percentiles, and the circles represent values outside the 10th and 90th percentiles. The number of participants listed does not include nine participants who declined transfusion therapy immediately after they underwent randomization.

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