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Lack of association between fluoroquinolone and aortic aneurysm or dissection

Authors
Huh, KyungminKang, MinsunJung, Jaehun
Issue Date
Nov-2023
Publisher
OXFORD UNIV PRESS
Keywords
Fluoroquinolones; Antibiotics; Aortic aneurysm; Aortic dissection
Citation
EUROPEAN HEART JOURNAL, v.44, no.42, pp 4476 - 4484
Pages
9
Journal Title
EUROPEAN HEART JOURNAL
Volume
44
Number
42
Start Page
4476
End Page
4484
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/90329
DOI
10.1093/eurheartj/ehad627
ISSN
0195-668X
1522-9645
Abstract
Background and Aims An increased risk of aortic aneurysm and aortic dissection (AA/AD) has been reported with fluoroquinolone (FQ) use. However, recent studies suggested confounding factors by indication. This study aimed to investigate the risk of AA/AD associated with FQ use.Methods This nationwide population-based study included adults aged >= 20 years who received a prescription of oral FQ or third-generation cephalosporins (3GC) during outpatient visits from 2005 to 2016. Data source was the National Health Insurance Service reimbursement database. The primary outcome was hospitalization or in-hospital death with a primary diagnosis of AA/AD. A self-controlled case series (SCCS) and Cox proportional hazards model were used. Self-controlled case series compared the incidence of the primary outcome in the risk period vs. the control periods.Results A total of 954 308 patients (777 109 with FQ and 177 199 with 3GC use) were included. The incidence rate ratios for AA/AD between the risk period and the pre-risk period were higher in the 3GC group [11.000; 95% confidence interval (CI) 1.420-85.200] compared to the FQ group (2.000; 95% CI 0.970-4.124). The overall incidence of AA/AD among the patients who received FQ and 3GC was 5.40 and 8.47 per 100 000 person-years. There was no significant difference in the risk between the two groups (adjusted hazard ratio 0.752; 95% CI 0.515-1.100) in the inverse probability of treatment-weighted Cox proportional hazards model. Subgroup and sensitivity analysis showed consistent results.Conclusions There was no significant difference in the risk of AA/AD in patients who were administered oral FQ compared to those administered 3GC. The study findings suggest that the use of FQ should not be deterred when clinically indicated. Structured Graphical Abstract FQ, fluoroquinolone; 3GC, 3rd generation cephalosporin; HR, hazard ratio; CI, confidence interval; IPTW, inverse probability of treatment weighting.
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