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First-time adverse drug reactions, survival analysis, and the share of adverse drug reactions in treatment discontinuation in real-world rheumatoid arthritis patients

Authors :
Kimberly Velthuis
Naomi T. Jessurun
Thi D.M. Nguyen
Joep Scholl
Jurriaan R.G. Jansen
Jette A. van Lint
Leanne J. Kosse
Peter M. ten Klooster
Harald E. Vonkeman
Psychology, Health & Technology
TechMed Centre
Source :
Expert opinion on drug safety. Taylor & Francis
Publication Year :
2023

Abstract

Background: This study aims to compare nature and frequency of adverse drug reactions (ADRs), time to first ADR, drug survival, and the share of ADRs in treatment discontinuation of first-time treatment with adalimumab (ADA) and etanercept (ETN) in real-world RA patients. Research design and methods: Retrospective, single-center cohort study including naïve patients treated between January 2003-April 2020. Time to first ADR and drug survival of first-time treatment were studied using Kaplan–Meier and Cox-regression models up to 10 years, with 2- and 5-year post-hoc sensitivity analysis. Nature and frequencies of first-time ADRs and causes of treatment discontinuation were assessed. Results: In total, 416 patients (ADA: 255, ETN: 161, 4865 patient years) were included, of which 92 (22.1%) experienced ADR(s) (ADA: 59, 23.1%; ETN: 33, 20.4%). Adjusted for age, gender and concomitant conventional DMARD use, ADA was more likely to be discontinued than ETN up to 2-, 5- and 10-year follow-up (adjusted HRs 1.63; 1.62; 1.59 (all p

Details

Language :
English
ISSN :
14740338
Database :
OpenAIRE
Journal :
Expert opinion on drug safety
Accession number :
edsair.doi.dedup.....485b1a6ff4e7681393aee9871670ab8a
Full Text :
https://doi.org/10.1080/14740338.2023.2172157