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  • Higher or Lower Hemoglobin ...
    Kirpalani, Haresh; Bell, Edward F; Hintz, Susan R; Tan, Sylvia; Schmidt, Barbara; Chaudhary, Aasma S; Johnson, Karen J; Crawford, Margaret M; Newman, Jamie E; Vohr, Betty R; Carlo, Waldemar A; D'Angio, Carl T; Kennedy, Kathleen A; Ohls, Robin K; Poindexter, Brenda B; Schibler, Kurt; Whyte, Robin K; Widness, John A; Zupancic, John A F; Wyckoff, Myra H; Truog, William E; Walsh, Michele C; Chock, Valerie Y; Laptook, Abbot R; Sokol, Gregory M; Yoder, Bradley A; Patel, Ravi M; Cotten, C Michael; Carmen, Melissa F; Devaskar, Uday; Chawla, Sanjay; Seabrook, Ruth; Higgins, Rosemary D; Das, Abhik

    New England journal of medicine/˜The œNew England journal of medicine, 12/2020, Letnik: 383, Številka: 27
    Journal Article

    Limited data suggest that higher hemoglobin thresholds for red-cell transfusions may reduce the risk of cognitive delay among extremely-low-birth-weight infants with anemia. We performed an open, multicenter trial in which infants with a birth weight of 1000 g or less and a gestational age between 22 weeks 0 days and 28 weeks 6 days were randomly assigned within 48 hours after delivery to receive red-cell transfusions at higher or lower hemoglobin thresholds until 36 weeks of postmenstrual age or discharge, whichever occurred first. The primary outcome was a composite of death or neurodevelopmental impairment (cognitive delay, cerebral palsy, or hearing or vision loss) at 22 to 26 months of age, corrected for prematurity. A total of 1824 infants (mean birth weight, 756 g; mean gestational age, 25.9 weeks) underwent randomization. There was a between-group difference of 1.9 g per deciliter (19 g per liter) in the pretransfusion mean hemoglobin levels throughout the treatment period. Primary outcome data were available for 1692 infants (92.8%). Of 845 infants in the higher-threshold group, 423 (50.1%) died or survived with neurodevelopmental impairment, as compared with 422 of 847 infants (49.8%) in the lower-threshold group (relative risk adjusted for birth-weight stratum and center, 1.00; 95% confidence interval CI, 0.92 to 1.10; P = 0.93). At 2 years, the higher- and lower-threshold groups had similar incidences of death (16.2% and 15.0%, respectively) and neurodevelopmental impairment (39.6% and 40.3%, respectively). At discharge from the hospital, the incidences of survival without severe complications were 28.5% and 30.9%, respectively. Serious adverse events occurred in 22.7% and 21.7%, respectively. In extremely-low-birth-weight infants, a higher hemoglobin threshold for red-cell transfusion did not improve survival without neurodevelopmental impairment at 22 to 26 months of age, corrected for prematurity. (Funded by the National Heart, Lung, and Blood Institute and others; TOP ClinicalTrials.gov number, NCT01702805.).