Study Design and Cohort Comparability in a Study of Major Cardiovascular Events in New Users of Prucalopride Versus Polyethylene Glycol 3350
Autor: | Thomas M. MacDonald, Joan Fortuny, Miguel Cainzos-Achirica, Elizabeth Andrews, Love Linnér, Ryan Ziemiecki, Alicia Gilsenan, Ana Ruigómez, Bianca Kollhorst, Oscar F. Cantero, Estel Plana, Tania Schink, Luis A. García-Rodríguez, Pär Karlsson, Robert W. V. Flynn |
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Rok vydání: | 2019 |
Předmět: |
Male
Research design medicine.medical_specialty Databases Factual Population Toxicology 030226 pharmacology & pharmacy Polyethylene Glycols Cohort Studies 03 medical and health sciences 0302 clinical medicine Germany Internal medicine Humans Medicine Pharmacology (medical) 030212 general & internal medicine Propensity Score education Benzofurans Sweden Pharmacology education.field_of_study Study Design Prucalopride business.industry United Kingdom Laxatives Research Design Propensity score matching Cohort Female Observational study Diagnosis code business Constipation Cohort study medicine.drug |
Zdroj: | Drug safety, 42(10):1167-1177 Drug Safety |
ISSN: | 1179-1942 0114-5916 |
DOI: | 10.1007/s40264-019-00836-z |
Popis: | Introduction Given prior safety experience with other 5-HT4 agonists for chronic constipation, an observational, population-based cohort study in five data sources from Germany, Sweden, and the UK was conducted to evaluate the cardiovascular safety of prucalopride. Objectives Our objective is to describe the methods and resulting comparability of cohorts in a multi-database, multinational study of prucalopride initiators and polyethylene glycol 3350 (PEG) initiators following a harmonized protocol. Methods Prucalopride initiators were matched on age, sex, and index date to PEG initiators (1:5 ratio). Study exposures, cardiovascular risk factors, and other covariates were identified from healthcare utilization codes harmonized across databases. Cardiovascular outcomes were identified using database-specific algorithms based on diagnosis codes. The propensity score (PS) in each database was estimated using logistic regression, with prucalopride versus PEG as the outcome and including clinically relevant variables associated with major adverse cardiovascular events. Results In total, 12,030 prucalopride initiators and 59,985 PEG initiators were identified. After matching and trimming, cohorts from the UK and Sweden were well-balanced for cardiovascular risk factors and cancer. However, in Germany, PEG initiators remained older and sicker than prucalopride initiators. The prevalence of these characteristics also differed from those in the UK and Sweden. The pooled analyses included only data from the UK and Sweden. Conclusions Matching, trimming, and PS stratification yielded comparable cohorts in four of five data sources. Use of these methods could not achieve balance for key covariates within the German cohort, likely due to reimbursement differences in Germany. Electronic supplementary material The online version of this article (10.1007/s40264-019-00836-z) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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