Children with severe anemia do not require immediate blood transfusion: TRACT clinical trial

Published On 2019-08-04 13:50 GMT   |   Update On 2019-08-04 13:50 GMT

Delhi: Children hospitalized for uncomplicated severe anemia do not require immediate transfusion, suggests findings from TRACT trial. The volume of transfusion may matter only in the context of fever.


The study, published in the New England Journal of Medicine, found that there was no significant difference in 28-day mortality and other clinical outcomes over 6 months in children who received transfusion versus children who did not.


The results suggest that there is no need to transfuse immediately or to transfuse a higher volume at least in the pediatric population in two sub-Saharan countries (Uganda and Malawi). The possible effect of higher volume transfusion in patients with fever may trigger additional and potentially useful studies.


Similarly, there was no significant difference in 28-day mortality among children who received transfusions of 20 mL/kg and those who received transfusions of 30 mL/kg. There was evidence to suggest a higher transfusion volume may benefit children without fevers, but this was an exploratory endpoint.





For the purpose, the researchers evaluated 1,565 Ugandan and Malawian children with uncomplicated, severe anemia. The patients’ median age was 26 months, and 984 (62.9%) had malaria.


The children were randomized to either immediate transfusion (n = 778) or no immediate transfusion (n = 787). Children in the control group who did not have an immediate transfusion could receive a transfusion if they showed new signs of clinical severity or had their hemoglobin decrease to below 4 g/dL.

All children in the immediate-transfusion group received a transfusion, as did 386 (49.0%) in the control group. The median time to transfusion was 1.3 hours in the immediate group and 24.9 hours in the control group. The mean total blood volume transfused per child was 314 plus or minus 228 mL and 142 plus or minus 224, respectively. The follow-up period was 180 days, and 4.5% of patients (n = 71) were lost to follow-up.


Key findings:

  • Death had occurred by 28 days in 7 children (0.9%) in the immediate-transfusion group and in 13 (1.7%) in the control group and by 180 days in 35 (4.5%) and 47 (6.0%), respectively, without evidence of interaction with other randomizations or evidence of between-group differences in readmissions, serious adverse events, or hemoglobin recovery at 180 days.

  • The mean length of hospital stay was 0.9 days longer in the control group.



The children received a transfusion of 30 mL/kg (n = 1,592) or 20 mL/kg (n = 1,596) at a median of 1.2 hours after randomization. Some children – 197 in the 30-mL/kg group and 300 in the 20-mL/kg group – received additional transfusions. The mean volume of total blood transfused per child was 475 plus or minus 385 mL, and 353 plus or minus 348 mL, respectively.


Key findings:

  • There was no significant between-group difference with regard to mortality.

  • The 28-day mortality rate was 3.4% in the 30 mL/kg group and 4.5% in the 20 mL/kg group.

  • The 28-day mortality rate did differ according to the presence of fever at the screening.

  • The mortality rate was lower in the 30 mL/kg group for children without fevers but higher in the 30 mL/kg group for febrile children.

  • For other outcomes, including readmissions and serious adverse events, the researchers found no significant between-group differences.


To read the complete study follow the link: DOI: 10.1056/NEJMoa1900105

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