早产儿视网膜病变发生率的红细胞输注:前瞻性多中心队列研究。

IF 2.1 Q2 PEDIATRICS JMIR Pediatrics and Parenting Pub Date : 2024-09-18 DOI:10.2196/60330
Xiaoling Wang, Rui Rao, Hua Li, Xiaoping Lei, Wenbin Dong
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引用次数: 0

摘要

背景:早产儿视网膜病变(ROP早产儿视网膜病变(ROP)是早产儿视力受损和失明的主要原因:本研究旨在调查早产儿输注红细胞(RBC)与早产儿视网膜病变之间的关系,为预防和治疗早产儿视网膜病变的临床策略提供依据:我们设计了一项前瞻性多中心队列研究,纳入了3个新生儿临床医学中心2017年1月至2022年12月的VPI和随访数据。他们被分为输血组(4周内接受过RBC输血的婴儿)和非输血组。采用二元逻辑回归评估输注红细胞与 ROP 发生率之间的关系,并根据胎龄、出生体重、性别和败血症状态进行亚组分析。为了考虑所有可能影响 ROP 发生的潜在混杂因素,采用了逆概率治疗加权法和倾向得分匹配法,然后进行了敏感性分析:研究共纳入 832 例 VPI,其中未输血组 327 例,输血组 505 例。输血组的平均出生体重和胎龄较低,ROP、≥2 期 ROP 和严重 ROP 的发生率较高。逻辑回归分析显示,输血组发生 ROP(调整后的几率比 [aOR] 1.70,95% CI 1.14-2.53,P=.009)和≥2 期 ROP(aOR 1.68,95% CI 1.02-2.78,P=.04)的风险明显更高,但发生严重 ROP(aOR 1.75,95% CI 0.61-5.02,P=.30)的风险并不高。趋势分析还显示,随着输血次数和输血量的增加,发生 ROP 的风险也随之增加(P 为趋势结论):对于 VPIs,输注红细胞会显著增加 ROP 的风险,而且随着输血次数和输血量的增加,风险也会增加。
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Red Blood Cell Transfusion for Incidence of Retinopathy of Prematurity: Prospective Multicenter Cohort Study.

Background: Retinopathy of prematurity (ROP) is a leading cause of visual impairment and blindness in preterm infants.

Objective: This study sought to investigate the association between red blood cell (RBC) transfusion and ROP in very preterm infants (VPIs) to inform clinical strategies for ROP prevention and treatment.

Methods: We designed a prospective multicenter cohort study that included VPIs and follow-up data from January 2017 to December 2022 at 3 neonatal clinical medicine centers. They were categorized into a transfusion group (infants who received an RBC transfusion within 4 wk) and a nontransfusion group. The relationship between RBC transfusion and ROP incidence was assessed using binary logistic regression, with subgroup analyses based on gestational age, birth weight, sex, and sepsis status. Inverse probability of treatment weighting and propensity score matching were applied to account for all potential confounding factors that could affect ROP development, followed by sensitivity analysis.

Results: The study included 832 VPIs, including 327 in the nontransfusion group and 505 in the transfusion group. The transfusion group had a lower average birth weight and gestational age and a greater incidence of ROP, ≥stage 2 ROP, and severe ROP. Logistic regression analysis revealed that the transfusion group had a significantly greater risk of ROP (adjusted odds ratio [aOR] 1.70, 95% CI 1.14-2.53, P=.009) and ≥stage 2 ROP (aOR 1.68, 95% CI 1.02-2.78, P=.04) but not severe ROP (aOR 1.75, 95% CI 0.61-5.02, P=.30). The trend analysis also revealed an increased risk of ROP with an increasing number of transfusions and a larger volume of blood transfused (P for trend<.001). Subgroup analyses confirmed a consistent trend, with the transfusion group at a higher risk for ROP across all subgroups. Inverse probability of treatment weighting and propensity score matching analyses supported the initial findings.

Conclusions: For VPIs, RBC transfusion significantly increases the risk of ROP, and the risk increases with an increasing number of transfusions and volume of blood transfused.

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来源期刊
JMIR Pediatrics and Parenting
JMIR Pediatrics and Parenting Medicine-Pediatrics, Perinatology and Child Health
CiteScore
5.00
自引率
5.40%
发文量
62
审稿时长
12 weeks
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