Document Type
Article
Publication Date
8-30-2021
Abstract
BACKGROUND: To assess the efficacy and safety of restrictive versus liberal red blood cell transfusion thresholds in very low birth weight infants.
METHODS: We searched MEDLINE, EMBASE, and Cochrane database without any language restrictions. The last search was conducted in August 15, 2020. All randomized controlled trials comparing the use of restrictive versus liberal red blood cell transfusion thresholds in very low birth weight (VLBW) infants were selected. Pooled risk ratio (RR) for dichotomous variable with 95% confidence intervals were assessed by a random-effects model. The primary outcome was all-cause mortality.
RESULTS: Overall, this meta-analysis included 6 randomized controlled trials comprising 3,483 participants. Restrictive transfusion does not increase the risk of all-cause mortality (RR, 0.99; 95% CI, 0.84 to 1.17; I2 = 0%; high-quality evidence), and does not increase the composite outcome of death or neurodevelopmental impairment (RR, 1.01, 95% CI, 0.93-1.09; I2 = 7%; high-quality evidence) or other serious adverse events. Results were similar in subgroup analyses of all-cause mortality by weight of infants, gestational age, male infants, and transfusion volume.
CONCLUSIONS: In very low birth weight infants, a restrictive threshold for red blood cell transfusion was not associated with increased risk of all-cause mortality, in either short term or long term.
Recommended Citation
Wang, Peng; Wang, Xing; Deng, Haidong; Li, Linjie; Chong, Weelic; Hai, Yang; and Zhang, Yu, "Restrictive versus liberal transfusion thresholds in very low birth weight infants: A systematic review with meta-analysis" (2021). Department of Medicine Faculty Papers. Paper 310.
https://jdc.jefferson.edu/medfp/310
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
34460843
Language
English
Comments
This article is the author’s final published version in PLoS ONE, Volume 16, Issue 8, August 2021, Article number e0256810.
The published version is available at https://doi.org/10.1371/journal.pone.0256810. Copyright © Wang et al.