Anemia Clinical Trial
Official title:
Randomized Trial of Liberal Versus Restrictive Guidelines for Red Blood Cell Transfusion in Preterm Infants
The purpose of this study was to determine whether restrictive guidelines for red blood cell (RBC) transfusions for preterm infants can reduce the number of transfusions without adverse consequences.
Design, Setting, and Patients. We enrolled 100 hospitalized preterm infants with birth
weights 500 to 1300 g into a randomized clinical trial comparing two levels of hematocrit
threshold for RBC transfusion.
Intervention. The infants were randomly assigned to either the liberal or the restrictive
transfusion group. For each group, transfusions were given only when the hematocrit fell
below the assigned value. In each group, the transfusion thresholds decreased with improving
clinical status.
Main Outcome Measures. We recorded the number of transfusions, the number of donor
exposures, and various clinical and physiological outcomes.
Results. Infants in the liberally transfused group received more RBC transfusions, mean 5.2
(SD 4.5) vs 3.3 (SD 2.9) in the restrictive transfusion group (P=0.025). However, the number
of donors to whom the infants were exposed was not significantly different, mean 2.8 (SD
2.5) vs 2.2 (SD 2.0). There was no difference between the groups in the percentage of
infants who avoided transfusions altogether, 12% in the liberal transfusion group vs 10% in
the restrictive group. Infants in the restrictive group were more likely to have
intraparenchymal brain hemorrhage or periventricular leukomalacia (P=0.012), and they had
more frequent episodes of apnea (P=0.004), including both mild and severe episodes.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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