Association of fluoroquinolones with the risk of spontaneous pneumothorax: nationwide case-time-control study.

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM Thorax Pub Date : 2024-10-11 DOI:10.1136/thorax-2024-221779
Anne Bénard-Laribière, Elodie Pambrun, Serge Kouzan, Jean-Luc Faillie, Julien Bezin, Antoine Pariente
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Abstract

Introduction: Fluoroquinolones can cause severe collagen-associated adverse effects, potentially impacting the pulmonary connective tissue. We investigated the association between fluoroquinolones and spontaneous pneumothorax.

Methods: A case-time-control study was performed using the nationwide French reimbursement healthcare system database (SNDS). Cases were adults ≥18 years admitted for spontaneous pneumothorax between 2017 and 2022. For each case, fluoroquinolone use was compared between the risk period immediately preceding the admission date (days -30 to -1), and three earlier reference periods (days -180 to -151, -150 to -121, -120 to -91), adjusting for time-varying confounders. OR estimates were corrected for potential exposure-trend bias using a reference group without the event (matched on age, sex, chronic obstructive pulmonary disease history, calendar time). Amoxicillin use was studied similarly to control for indication bias.

Results: Of the 246 pneumothorax cases exposed to fluoroquinolones (63.8% men; mean age, 43.0±18.4 years), 63 were exposed in the 30-day risk period preceding pneumothorax and 128 in the reference periods. Of the 3316 amoxicillin cases (72.9% men; mean age, 39.4±17.6 years), 1210 were exposed in the 30-day risk period and 1603 in the reference ones. OR adjusted for exposure-trend and covariates was 1.59 (95% CI 1.14 to 2.22) for fluoroquinolones and 2.25 (2.07 to 2.45) for amoxicillin.

Conclusion: An increased risk of spontaneous pneumothorax was associated with both fluoroquinolone and amoxicillin use, with an even higher association for amoxicillin. This strongly suggests the role of the underlying infections rather than a causal effect of the individual antibiotics and can be considered reassuring regarding a potential lung connective toxicity of fluoroquinolones.

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氟喹诺酮类药物与自发性气胸风险的关系:全国病例-时间对照研究。
简介氟喹诺酮类药物可导致严重的胶原相关不良反应,对肺结缔组织造成潜在影响。我们研究了氟喹诺酮类药物与自发性气胸之间的关系:方法:我们利用法国全国报销医疗系统数据库(SNDS)进行了一项病例-时间对照研究。病例为2017年至2022年期间因自发性气胸入院的≥18岁成年人。对每个病例的氟喹诺酮类药物使用情况,在入院日期前的风险期(-30 天至-1 天)和三个较早的参照期(-180 天至-151 天、-150 天至-121 天、-120 天至-91 天)之间进行了比较,并对随时间变化的混杂因素进行了调整。使用未发生事件的参照组(年龄、性别、慢性阻塞性肺病病史、日历时间匹配)对 OR 估计值进行了校正,以消除潜在的暴露趋势偏差。对阿莫西林的使用情况也进行了类似研究,以控制适应症偏倚:结果:在暴露于氟喹诺酮类药物的 246 例气胸病例中(63.8% 为男性,平均年龄(43.0±18.4)岁),63 例在气胸前 30 天的风险期内暴露于氟喹诺酮类药物,128 例在参照期内暴露于氟喹诺酮类药物。在3316例阿莫西林病例(72.9%为男性;平均年龄为39.4±17.6岁)中,1210例在气胸前30天的风险期内接触过阿莫西林,1603例在参考期内接触过阿莫西林。根据暴露趋势和协变量调整后,氟喹诺酮类药物的OR为1.59(95% CI为1.14至2.22),阿莫西林为2.25(2.07至2.45):结论:使用氟喹诺酮类药物和阿莫西林都会增加自发性气胸的风险,而使用阿莫西林的风险更高。这有力地说明了潜在感染的作用,而不是单种抗生素的因果效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Thorax
Thorax 医学-呼吸系统
CiteScore
16.10
自引率
2.00%
发文量
197
审稿时长
1 months
期刊介绍: Thorax stands as one of the premier respiratory medicine journals globally, featuring clinical and experimental research articles spanning respiratory medicine, pediatrics, immunology, pharmacology, pathology, and surgery. The journal's mission is to publish noteworthy advancements in scientific understanding that are poised to influence clinical practice significantly. This encompasses articles delving into basic and translational mechanisms applicable to clinical material, covering areas such as cell and molecular biology, genetics, epidemiology, and immunology.
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