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Risk of aortic aneurysm and dissection following exposure to fluoroquinolones, common antibiotics, and febrile illness using a self-controlled case series study design: Retrospective analyses of three large healthcare databases in the US.
Londhe, Ajit A; Holy, Chantal E; Weaver, James; Fonseca, Sergio; Villasis, Angelina; Fife, Daniel.
Affiliation
  • Londhe AA; Janssen Pharmaceutical Research and Development, LLC, Titusville, NJ, United States of America.
  • Holy CE; Johnson & Johnson, New Brunswick, NJ, United States of America.
  • Weaver J; Janssen Pharmaceutical Research and Development, LLC, Titusville, NJ, United States of America.
  • Fonseca S; Janssen Pharmaceutical Research and Development, LLC, Titusville, NJ, United States of America.
  • Villasis A; Janssen Pharmaceutical Research and Development, LLC, Titusville, NJ, United States of America.
  • Fife D; Janssen Pharmaceutical Research and Development, LLC, Titusville, NJ, United States of America.
PLoS One ; 16(8): e0255887, 2021.
Article in En | MEDLINE | ID: mdl-34398907
OBJECTIVE: Recent observational studies suggest increased aortic aneurysm or dissection (AAD) risk following fluoroquinolone (FQ) exposure but acknowledge potential for residual bias from unreported patient characteristics. The objective of our study is to evaluate the potential association between FQ, other common antibiotics and febrile illness with risk of AAD using a self-controlled case series (SCCS) study design. DESIGN: Retrospective database analysis-SCCS. SETTING: Primary and Secondary Care. STUDY POPULATION: 51,898 patients across 3 US claims databases (IBM® MarketScan® commercial and Medicare databases, Optum Clinformatics). EXPOSURE: FQ or other common antibiotics or febrile illness. OUTCOME: AAD. METHODS: We studied patients with exposures and AAD between 2012 and 2017 in 3 databases. Risk windows were defined as exposure period plus 30 days. Diagnostic analyses included p-value calibration to account for residual error using negative control exposures (NCE), and pre-exposure outcome analyses to evaluate exposure-outcome timing. The measure of association was the incidence rate ratio (IRR) comparing exposed and unexposed time. RESULTS: Most NCEs produced effect estimates greater than the hypothetical null, indicating positive residual error; calibrated p (Cp) values were therefore used. The IRR following FQ exposure ranged from 1.13 (95% CI: 1.04-1.22 -Cp: 0.503) to 1.63 (95% CI: 1.45-1.84 -Cp: 0.329). An AAD event peak was identified 60 days before first FQ exposure, with IRR increasing between the 60- to 30- and 29- to 1-day pre-exposure periods. It is uncertain how much this pre-exposure AAD event peak reflects confounding versus increased antibiotic use after a surgical correction of AADs. CONCLUSION: This study does not confirm prior studies. Using Cp values to account for residual error, the observed FQ-AAD association cannot be interpreted as significant. Additionally, an AAD event surge in the 60 days before FQ exposure is consistent with confounding by indication, or increased use of antibiotics post-surgery. REGISTRATION: NCT03479736.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Medicare / Fluoroquinolones Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans / Middle aged Country/Region as subject: America do norte Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Medicare / Fluoroquinolones Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans / Middle aged Country/Region as subject: America do norte Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States