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Effect of red blood cell transfusion on the development of retinopathy of prematurity: A systematic review and meta-analysis
Author(s) -
Zhe Zhu,
Xin Hua,
Yang Yu,
Pan Zhu,
Kairui Hong,
Yefang Ke
Publication year - 2020
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0234266
Subject(s) - medicine , retinopathy of prematurity , publication bias , meta analysis , funnel plot , gestational age , cochrane library , subgroup analysis , blood transfusion , web of science , red blood cell transfusion , pediatrics , observational study , pregnancy , biology , genetics
Background The effect of red blood cell (RBC) transfusion on retinopathy of prematurity (ROP) is difficult to establish, because ROP may also be influenced by other factors. Therefore, we carried out a systematic review and meta-analysis to explore the relationship between RBC transfusion and the development of ROP. Methods The PubMed, Embase, Cochrane Library and Web of Science databases were searched from their inception to September 1, 2019. Observational studies that reported the relationship between RBC transfusion and ROP after adjusting for other potential risk factors were included. The combined result was analyzed by a random effect model. Heterogeneity and publication bias were tested, and sensitivity analysis was performed. Results Of the 2628 identified records, 18 studies including 15072 preterm infants and 5620 cases of ROP were included. A random effect model was used and revealed that RBC transfusion was significantly associated with ROP (pooled OR = 1.50, 95% CI: 1.27–1.76), with moderate heterogeneity among the included studies (I 2 = 44.2%). Subgroup analysis indicated that RBC transfusion was more closely related to ROP in the group with a gestational age (GA) ≤32 weeks (OR = 1.77, 95% CI: 1.29–2.43) but not in the groups with a GA ≤34 weeks (OR = 1.36, 95% CI: 0.85–2.18) or a GA <37 weeks (OR = 1.25, 95% CI: 0.86–1.82). No obvious publication bias was found based on the funnel plot and Egger’s test. Removing any single study did not significantly alter the combined result in the sensitivity analysis. Conclusions Our study revealed that RBC transfusion is an independent risk factor for the development of ROP, especially in younger preterm infants. However, there seemed to be no evidence to support an effect of RBC transfusion on ROP in older groups. Further studies addressing this issue in older preterm neonates are warranted.

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