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使用氟喹诺酮类药物后发生主动脉瘤或夹层的风险:一项回顾性跨国网络队列研究。

Risk of aortic aneurysm or dissection following use of fluoroquinolones: a retrospective multinational network cohort study.

作者信息

Janetzki Jack L, Kim Jung Ho, Minty Evan, Lee Jung Ah, Morales Daniel R, Khera Rohan, Kim Chungsoo, Alshammari Thamir M, DuVall Scott L, Matheny Michael E, Falconer Thomas, Kim Seonji, Phan Thanh-Phuc, Nguyen Phung-Anh, Hsu Min-Huei, Hsu Jason C, Park Rae Woong, Man Kenneth K C, Seager Sarah, Van Zandt Mui, Gilbert James P, Ryan Patrick B, Schuemie Martijn J, Suchard Marc A, Hripcsak George, Pratt Nicole, Chan You Seng

机构信息

Clinical and Health Sciences, Quality Use of Medicines and Pharmacy Research Centre, University of South Australia, Adelaide, Australia.

Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea.

出版信息

EClinicalMedicine. 2025 Feb 1;81:103096. doi: 10.1016/j.eclinm.2025.103096. eCollection 2025 Mar.

DOI:10.1016/j.eclinm.2025.103096
PMID:39975698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11836508/
Abstract

BACKGROUND

Fluoroquinolones (FQs) are commonly used to treat urinary tract infections (UTIs), but some studies have suggested they may increase the risk of aortic aneurysm or dissection (AA/AD). However, no large-scale international study has thoroughly assessed this risk.

METHODS

A retrospective cohort study was conducted using a large, distributed network analysis across 14 databases from 5 countries (United States, South Korea, Japan, Taiwan, and Australia). The study included 13,588,837 patients aged 35 or older who initiated systemic fluoroquinolones (FQs) or comparable antibiotics (trimethoprim with or without sulfamethoxazole [TMP] or cephalosporins [CPHs]) for UTI treatment in the outpatient setting between JAN 01, 2010 and DEC 31, 2019. Patients were included if at the index date they had at least 365 days of prior observation and were not hospitalised for any reason on or within 7 days prior to the index date. The primary outcome was AA/AD occurrence within 60 days of exposure, with secondary outcomes examining AA and AD separately. Cox proportional hazards models with 1:1 propensity score (PS) matching were used to estimate the risk, with results calibrated using negative control outcomes. Analyses were subjected to pre-defined study diagnostics, and only those passing all diagnostics were reported. Hazard ratios (HRs) were pooled using Bayesian random-effects meta-analysis.

FINDINGS

Among analyses that passed diagnostics there were 1,954,798 and 1,195,962 propensity-matched pairs for the FQ versus TMP and FQ versus CPH comparisons respectively. For the 60-day follow-up there was no difference in risk of AA/AD between FQ and TMP (absolute rate difference [ARD], 0.21 per 1000 person-year; calibrated HR, 0.91 [95% CI 0.73-1.10]). There was no significant difference in risk for FQ versus CPH (ARD, 0.11 per 1000 person-year; calibrated HR, 1.01 [95% CI 0.82-1.25]).

INTERPRETATION

This large-scale study used a rigorous design with objective diagnostics to address bias and confounding. There was no increased risk of AA/AD associated with FQ compared to TMP or CPH in patients treated for UTI in the outpatient setting. As we only examined FQ used to treat UTIs in the outpatient setting, the results may not be generalisable to other indications with different severity.

FUNDING

Yonsei University College of Medicine, Government-wide R&D Fund project for infectious disease research (GFID), Republic of Korea, National Health and Medical Research Council (NHMRC) Australian Government. Department of Veterans Affairs (VA) Informatics and Computing Infrastructure (VINCI), Department of Veterans Affairs, the United States Government.

摘要

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/36202d40b72c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/d52b903def26/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/b466723ef9a4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/36202d40b72c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/d52b903def26/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/b466723ef9a4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/11836508/36202d40b72c/gr3.jpg

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Stud Health Technol Inform. 2024 Jan 25;310:966-970. doi: 10.3233/SHTI231108.
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Fluoroquinolone antibiotics: Prescribe only as last resort, says UK regulator.英国监管机构称:氟喹诺酮类抗生素仅作为最后手段使用。
BMJ. 2024 Jan 24;384:q183. doi: 10.1136/bmj.q183.
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Lack of association between fluoroquinolone and aortic aneurysm or dissection.氟喹诺酮与主动脉瘤或主动脉夹层之间无关联。
Eur Heart J. 2023 Nov 7;44(42):4476-4484. doi: 10.1093/eurheartj/ehad627.
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Association Between Fluoroquinolone Use and Hospitalization With Aortic Aneurysm or Aortic Dissection.氟喹诺酮类药物的使用与主动脉瘤或主动脉夹层住院之间的关联。
JAMA Cardiol. 2023 Sep 1;8(9):865-870. doi: 10.1001/jamacardio.2023.2418.
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Risk Factors for Mortality From Aortic Aneurysm and Dissection: Results From a 26-Year Follow-Up of a Community-Based Population.主动脉瘤和夹层致死的风险因素:一项基于社区人群的 26 年随访研究结果。
J Am Heart Assoc. 2023 Apr 18;12(8):e027045. doi: 10.1161/JAHA.122.027045. Epub 2023 Apr 12.
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Combining cox regressions across a heterogeneous distributed research network facing small and zero counts.在面对小计数和零计数的异构分布式研究网络中合并Cox回归。
Stat Methods Med Res. 2022 Mar;31(3):438-450. doi: 10.1177/09622802211060518. Epub 2021 Nov 29.
7
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