Bénard-Laribière Anne, Pambrun Elodie, Kouzan Serge, Faillie Jean-Luc, Bezin Julien, Pariente Antoine
Université de Bordeaux, INSERM, BPH, team AHeaD, U1219, Bordeaux, France
Université de Bordeaux, INSERM, BPH, team AHeaD, U1219, Bordeaux, France.
Thorax. 2025 Feb 17;80(3):159-166. doi: 10.1136/thorax-2024-221779.
Fluoroquinolones can cause severe collagen-associated adverse effects, potentially impacting the pulmonary connective tissue. We investigated the association between fluoroquinolones and spontaneous pneumothorax.
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.
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.
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.
氟喹诺酮类药物可引起严重的胶原相关不良反应,可能影响肺结缔组织。我们研究了氟喹诺酮类药物与自发性气胸之间的关联。
使用法国全国性医保报销医疗系统数据库(SNDS)进行病例-时间-对照研究。病例为2017年至2022年间因自发性气胸入院的18岁及以上成年人。对于每个病例,比较入院日期前紧接的风险期(第-30天至-1天)与三个更早的参考期(第-180天至-151天、-150天至-121天、-120天至-91天)的氟喹诺酮类药物使用情况,并对随时间变化的混杂因素进行调整。使用无该事件的参考组(根据年龄、性别、慢性阻塞性肺疾病病史、日历时间进行匹配)对OR估计值进行潜在暴露趋势偏倚校正。对阿莫西林的使用进行类似研究以控制指征偏倚。
在246例暴露于氟喹诺酮类药物的气胸病例中(63.8%为男性;平均年龄43.0±18.4岁),63例在气胸前30天风险期暴露,128例在参考期暴露。在3316例阿莫西林病例中(72.9%为男性;平均年龄39.4±17.6岁),1210例在30天风险期暴露,1603例在参考期暴露。校正暴露趋势和协变量后的OR值,氟喹诺酮类药物为1.59(95%CI 1.14至2.22),阿莫西林为2.25(2.07至2.45)。
自发性气胸风险增加与氟喹诺酮类药物和阿莫西林的使用均相关,阿莫西林的相关性更高。这强烈提示潜在感染的作用而非个别抗生素的因果效应,并且对于氟喹诺酮类药物潜在的肺结缔组织毒性而言可认为是令人安心的。