Fluoroquinolones and Risk of Aortic Aneurysm or Dissection in Patients With Congenital Aortic Disease and Marfan Syndrome.


Journal

Circulation journal : official journal of the Japanese Circulation Society
ISSN: 1347-4820
Titre abrégé: Circ J
Pays: Japan
ID NLM: 101137683

Informations de publication

Date de publication:
25 08 2023
Historique:
medline: 29 8 2023
pubmed: 24 2 2023
entrez: 23 2 2023
Statut: ppublish

Résumé

Fluoroquinolone use can be associated with an increased risk of aortic aneurysm (AA) or aortic dissection (AD). The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between fluoroquinolone use and AA/AD risk was unknown in these high-risk patients and therefore it was studied in this work.Methods and Results: Data were collected from a national database between 2000 and 2017 for 550 patients with AA/AD and any congenital aortic disease (mean age 41.5 years; 415 with Marfan syndrome). A case cross-over study was conducted to compare the risk of aortic events (AA/AD) associated with fluoroquinolone and amoxicillin use between the hazard period (from -60 days to -1 day) and a randomly selected reference period (-180 to -121 days; -240 to -181 days; and -300 to -241 days). Compared to the reference period without fluoroquinolone use, fluoroquinolone use during the hazard period was not associated with a greater risk of AA/AD (1.09% vs. 1.09%; odds ratio [OR] 1.000; 95% confidence interval [CI] 0.32-3.10), AA (OR 0.67; 95% CI 0.11-3.99), or AD (OR 1.33; 95% CI 0.30-5.96) in patients with congenital aortic disease or Marfan syndrome. This lack of association was maintained in subgroup analysis, including Marfan syndrome or not, age (≤50 vs. >50 years) and sex. Fluoroquinolone use was not associated with an increased risk of AA/AD in patients with congenital aortic disease, including Marfan syndrome. More evidence is required for a fluoroquinolone pharmacovigilance plan in these patients.

Sections du résumé

BACKGROUND
Fluoroquinolone use can be associated with an increased risk of aortic aneurysm (AA) or aortic dissection (AD). The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between fluoroquinolone use and AA/AD risk was unknown in these high-risk patients and therefore it was studied in this work.Methods and Results: Data were collected from a national database between 2000 and 2017 for 550 patients with AA/AD and any congenital aortic disease (mean age 41.5 years; 415 with Marfan syndrome). A case cross-over study was conducted to compare the risk of aortic events (AA/AD) associated with fluoroquinolone and amoxicillin use between the hazard period (from -60 days to -1 day) and a randomly selected reference period (-180 to -121 days; -240 to -181 days; and -300 to -241 days). Compared to the reference period without fluoroquinolone use, fluoroquinolone use during the hazard period was not associated with a greater risk of AA/AD (1.09% vs. 1.09%; odds ratio [OR] 1.000; 95% confidence interval [CI] 0.32-3.10), AA (OR 0.67; 95% CI 0.11-3.99), or AD (OR 1.33; 95% CI 0.30-5.96) in patients with congenital aortic disease or Marfan syndrome. This lack of association was maintained in subgroup analysis, including Marfan syndrome or not, age (≤50 vs. >50 years) and sex.
CONCLUSIONS
Fluoroquinolone use was not associated with an increased risk of AA/AD in patients with congenital aortic disease, including Marfan syndrome. More evidence is required for a fluoroquinolone pharmacovigilance plan in these patients.

Identifiants

pubmed: 36823078
doi: 10.1253/circj.CJ-22-0682
doi:

Substances chimiques

Fluoroquinolones 0

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1164-1172

Auteurs

Shao-Wei Chen (SW)

Division of Thoracic and Cardiovascular Surgery, Department of Surgery, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.
Center for Big Data Analytics and Statistics, Chang Gung Memorial Hospital, Linkou Medical Center.

Chia-Pin Lin (CP)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Yi-Hsin Chan (YH)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Victor Chien-Chia Wu (VC)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Yu-Ting Cheng (YT)

Division of Thoracic and Cardiovascular Surgery, Department of Surgery, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Ying-Chang Tung (YC)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Fu-Chih Hsiao (FC)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Dong-Yi Chen (DY)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Kuo-Chun Hung (KC)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

An-Hsun Chou (AH)

Department of Anesthesiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

Pao-Hsien Chu (PH)

Department of Cardiology, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University.

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