合并症和全身性类固醇驱动炎症性肠病的肺炎风险:倾向评分匹配队列研究

Yong Eun, Joan Culpepper-Morgan, Abiodun M Akanmode, Myint B Thu, Aprilee A Sta Lucia, Marie S Thearle, Rhonda K Trousdale
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引用次数: 0

摘要

背景:炎症性肠病(IBD)患者发生细菌性肺炎的风险增加,导致显著的发病率和死亡率。虽然以前的研究已经确定了各种风险因素,包括药物和合并症,但IBD对肺炎风险的独立贡献仍不清楚。我们假设增加的肺炎风险主要是由IBD本身以外的因素驱动的。目的:探讨IBD、合并症和药物对IBD患者肺炎风险的相对贡献。方法:我们使用All of Us Research Program数据库(2010-2022)进行了一项回顾性队列研究。我们使用四种倾向评分模型将2810名IBD患者与对照组1:1匹配:(1)仅人口统计学/生活方式;(2)合并合并症;(3)加药;(4)各因素综合。然后,我们使用Cox比例风险模型评估肺炎风险,并使用logistic回归评估危险因素。结果:在5620名匹配的参与者的初步分析中,当所有因素匹配时,IBD与肺炎风险增加没有独立相关[危险比(HR) = 1.07, 95%CI: 0.84-1.35]。然而,当仅匹配人口统计学和生活方式因素时,IBD患者的风险明显更高(HR = 2.08, 95%CI: 1.56-2.78)。在IBD队列中,高合并症负担(Charlson共病指数≥10)[比值比(OR) = 12.20, 95%CI: 6.69-23.00]和全身性类固醇使用(OR = 2.26, 95%CI: 1.21-4.64)与肺炎风险增加独立相关。结论:合并症和全身性类固醇,而不是IBD本身,驱动肺炎的风险。管理人员应关注这些因素,并优先考虑高危患者的疫苗接种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comorbidities and systemic steroids drive pneumonia risk in inflammatory bowel disease: Propensity score-matched cohort study.

Background: Patients with inflammatory bowel disease (IBD) are at an increased risk of bacterial pneumonia, contributing to significant morbidity and mortality. While previous studies have identified various risk factors, including medications and comorbidities, the independent contribution of IBD to pneumonia risk remains unclear. We hypothesized that the increased pneumonia risk is primarily driven by factors other than IBD itself.

Aim: To investigate the relative contributions of IBD, comorbidities, and medications to pneumonia risk in patients with IBD.

Methods: We conducted a retrospective cohort study using the All of Us Research Program database (2010-2022). We matched 2810 participants with IBD 1:1 with controls using four propensity score models: (1) Demographics/Lifestyle only; (2) Plus comorbidities; (3) Plus medications; and (4) All factors combined. Then we used Cox proportional hazards models to assess pneumonia risk and logistic regression to evaluate risk factors.

Results: In the primary analysis of 5620 matched participants, IBD was not independently associated with increased pneumonia risk [hazard ratio (HR) = 1.07, 95%CI: 0.84-1.35] when matched for all factors. However, participants with IBD had significantly higher risk (HR = 2.08, 95%CI: 1.56-2.78) when matched only for demographics and lifestyle factors. Within the IBD cohort, a high comorbidity burden (Charlson Comorbidity Index ≥ 10) [odds ratio (OR) = 12.20, 95%CI: 6.69-23.00] and systemic steroid use (OR = 2.26, 95%CI: 1.21-4.64) were independently associated with increased pneumonia risk.

Conclusion: Comorbidities and systemic steroids, rather than IBD itself, drive pneumonia risk. Management should focus on these factors and prioritize vaccination in high-risk patients.

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