Department of Neonatology, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City (Longgang Maternity and Child Institute of Shantou University Medical College), Shenzhen, 518172, Guangdong, China.
Department of Neonatology, Nanshan Maternity & Child Healthcare Hospital, Shenzhen, 518067, Guangdong, China.
Eur J Pediatr. 2024 Jul;183(7):2965-2981. doi: 10.1007/s00431-024-05565-9. Epub 2024 Apr 18.
Bronchopulmonary dysplasia (BPD) is the most common serious complication of very preterm infants (VPI) or very low birth weight (VLBW) infants. Studies implicate viral infections in etiopathogenesis. The aim of this study was to summarize the relationship between viral infections and BPD through a systematic review and meta-analysis. We searched PubMed, Embase, the Web of Science Core Collection, and the Cochrane Database on December 19, 2023. We included observational studies that examined the association between viral infections and BPD in preterm infants. We extracted data on study methods, participant characteristics, exposure assessment, and outcome measures. We assessed study risk of bias using the Newcastle-Ottawa Scale (NOS). We included 17 and 15 studies in the qualitative review and meta-analysis, respectively. The meta-analysis showed a significant association between viral infection and BPD diagnosed at 36 weeks postmenstrual age (odds ratio (OR): 2.42, 95% confidence interval: 1.89-3.09, 13 studies, very low certainty of evidence). In a subgroup analysis of specific viruses, cytomegalovirus (CMV) proved to be significantly associated with BPD diagnosed at 36 weeks postmenstrual age (OR: 2.34, 95% confidence interval: 1.80-3.05, 11 studies). We did not find an association between viral infection and BPD diagnosed on the 28th day of life, probably due to the small sample size of the included prospective studies. Conclusion: Viral infections, especially CMV, are associated with an increased risk of BPD in preterm infants. Methodologically reliable prospective studies with large samples are needed to validate our conclusions, and high-quality randomized controlled studies are needed to explore the effect of prevention or treatment of viral infections on the incidence of BPD. What is Known: • Studies have attempted to identify viral infections and bronchopulmonary dysplasia in preterm infants; however, results have been inconsistent. What is New: • Systematic demonstration that viral infections, particularly cytomegalovirus, are positively associated with bronchopulmonary dysplasia diagnosed in preterm infants at the 36th week of postmenstrual age. • The importance of screening for viral infections in preterm infants, especially cytomegalovirus. More high-quality studies should be produced in the future to investigate the causal relationship between viral infections and bronchopulmonary dysplasia.
支气管肺发育不良(BPD)是极早产儿(VLBW)或极低出生体重儿(VLBW)最常见的严重并发症。研究表明病毒感染与发病机制有关。本研究旨在通过系统评价和荟萃分析总结病毒感染与 BPD 的关系。我们于 2023 年 12 月 19 日检索了 PubMed、Embase、Web of Science 核心合集和 Cochrane 数据库。我们纳入了研究早产婴儿病毒感染与 BPD 之间关系的观察性研究。我们提取了研究方法、参与者特征、暴露评估和结局测量的数据。我们使用纽卡斯尔-渥太华量表(NOS)评估研究偏倚风险。我们分别纳入了 17 项和 15 项研究进行定性综述和荟萃分析。荟萃分析显示,病毒感染与 36 孕周校正后胎龄时诊断的 BPD 显著相关(比值比(OR):2.42,95%置信区间:1.89-3.09,13 项研究,证据确定性为极低)。在特定病毒的亚组分析中,巨细胞病毒(CMV)与 36 孕周校正后胎龄时诊断的 BPD 显著相关(OR:2.34,95%置信区间:1.80-3.05,11 项研究)。我们未发现病毒感染与 28 天龄时诊断的 BPD 之间存在关联,这可能是由于纳入的前瞻性研究样本量较小。结论:病毒感染,尤其是 CMV,与早产儿患 BPD 的风险增加有关。需要进行方法学可靠的大型样本前瞻性研究来验证我们的结论,需要进行高质量的随机对照研究来探讨预防或治疗病毒感染对 BPD 发生率的影响。已知:• 已有研究试图确定病毒感染与早产儿的支气管肺发育不良之间的关系,但结果不一致。新发现:• 系统地证明病毒感染,尤其是巨细胞病毒,与校正后胎龄 36 周时诊断的早产儿支气管肺发育不良呈正相关。• 筛查早产儿,尤其是巨细胞病毒感染的重要性。未来应开展更多高质量的研究来探讨病毒感染与支气管肺发育不良之间的因果关系。