低剂量肝素钠是腺病毒感染后形成阻塞性支气管炎的保护因素。

Annals of medicine Pub Date : 2025-12-01 Epub Date: 2024-12-16 DOI:10.1080/07853890.2024.2440130
Li Peng, Lili Zhong, Rong Hu, Lei Cui, Silan Liu, Han Huang, Xiaofang Ding, Min Chen, Lin Lin
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引用次数: 0

摘要

背景:儿童腺病毒(ADV)肺炎是导致感染后阻塞性支气管炎(BO)发生的重要原因。肝素钠具有已知的抗炎、免疫调节和组织修复特性。然而,肝素钠在治疗 ADV 感染后阻塞性支气管炎中的作用仍不明确:方法:对2019年1月至2019年12月期间南部地区确诊为ADV肺炎并住院治疗的793名儿童进行回顾性分析。其中,307 例被归类为单一 ADV 肺炎。我们利用有向无环图分析了各种变量之间的因果关系,这进一步帮助我们确定了构建回归模型的独立变量和混杂变量。我们还采用了倾向得分匹配法(PSM)来控制本研究中无法干预的混杂变量,确保基线水平的平衡和校正。我们利用单变量逻辑回归分析探讨了影响ADV肺炎后BO发展的因素:在确诊为 ADV 肺炎的 793 名儿童中,有 86 例(10.84%)发展为 BO。PSM后,非BO组使用肝素的比例高于BO组。单变量回归分析显示,急性呼吸衰竭、神经系统受累和纤维蛋白原(FIB)是ADV肺炎病例发展为BO的风险因素(OR > 1,P 1,P 结论:ADV肺炎病例中,急性呼吸衰竭、神经系统受累和纤维蛋白原(FIB)是发展为BO的风险因素:低剂量肝素钠治疗可能是 ADV 肺炎感染后发生 BO 的保护因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-dose heparin sodium as a protective factor against bronchiolitis obliterans formation after adenovirus infection.

Background: Adenovirus (ADV) pneumonia in children is a significant contributor to the occurrence of post-infectious bronchiolitis obliterans (BO). Heparin sodium has known anti-inflammatory, immunomodulatory, and tissue repair properties. However, its role in treating BO after ADV infection remains unclear.

Methods: A retrospective analysis was conducted on 793 children diagnosed with ADV pneumonia and hospitalized in the southern region from January 2019 to December 2019. Among them, 307 cases were classified as single ADV pneumonia. We utilized directed acyclic graphs to analyze the causal relationships between various variables, which further helped us identify the independent and confounding variables for constructing our regression model. Propensity score matching (PSM) was also employed to control for confounding variables that could not be intervened in this study, ensuring baseline level equilibrium and correction. We utilized univariate logistic regression analysis to explore the factors influencing BO development after ADV pneumonia.

Results: Among the 793 children diagnosed with ADV pneumonia, 86 cases (10.84%) progressed to BO. The proportion of heparin use was higher in the non-BO group than in the BO group after PSM. The univariate regression analysis revealed that acute respiratory failure, neurological involvement and fibrinogen (FIB) were risk factors for the development of BO in ADV pneumonia cases (OR > 1, p < 0.05), but low-dose heparin sodium treatment and hemoglobin (OR < 1, p < 0.05) exhibited protective effects against BO formation. Among the 307 children with single ADV pneumonia (excluding confounding factors), 33 cases (10.75%) developed BO. The univariate regression analysis further indicated that fever duration, acute respiratory failure and FIB were risk factors for the development of BO in single ADV pneumonia (OR > 1, p < 0.05), while low-dose heparin sodium treatment (OR < 1, p < 0.05) was protective against BO formation after a single ADV pneumonia.

Conclusion: Low-dose heparin sodium treatment may be a protective factor against the development of BO after ADV pneumonia infection.

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