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Cardiovascular Safety of Prucalopride in Patients with Chronic Constipation: A Multinational Population-Based Cohort Study

Author

Listed:
  • Alicia Gilsenan

    (RTI Health Solutions)

  • Joan Fortuny

    (RTI Health Solutions)

  • Miguel Cainzos-Achirica

    (RTI Health Solutions
    Hospital Universitari de Bellvitge)

  • Oscar F. Cantero

    (Centro Español de Investigación Farmacoepidemiológica)

  • Robert W. V. Flynn

    (University of Dundee)

  • Luis Garcia-Rodriguez

    (Centro Español de Investigación Farmacoepidemiológica)

  • Abenah Harding

    (RTI Health Solutions)

  • Bianca Kollhorst

    (Leibniz Institute for Prevention Research and Epidemiology-BIPS)

  • Pär Karlsson

    (Karolinska Institutet)

  • Love Linnér

    (Karolinska Institutet)

  • Thomas M. MacDonald

    (University of Dundee)

  • Ingvild Odsbu

    (Karolinska Institutet)

  • Estel Plana

    (RTI Health Solutions)

  • Ana Ruigómez

    (Centro Español de Investigación Farmacoepidemiológica)

  • Tania Schink

    (Leibniz Institute for Prevention Research and Epidemiology-BIPS)

  • Ryan Ziemiecki

    (RTI Health Solutions)

  • Elizabeth B. Andrews

    (RTI Health Solutions)

Abstract

Introduction The serotonin 5-HT4 receptor agonist prucalopride is approved in the European Union for the treatment of chronic constipation. This offered the unique opportunity to include real-world observational data on cardiovascular safety in the new drug application for approval of prucalopride in the USA. Methods This observational population-based cohort study (EUPAS9200) conducted in five data sources (three in the UK, one in Sweden, and one in Germany [which was subsequently excluded from the pooled analyses]) aimed to estimate the pooled adjusted incidence rate ratio for major adverse cardiovascular events (defined as hospitalization for non-fatal acute myocardial infarction or stroke, and in-hospital cardiovascular death) in adult initiators of prucalopride compared with initiators of polyethylene glycol 3350 (PEG) following a common protocol. Standardized incidence rates and incidence rate ratios of major adverse cardiovascular events were derived using propensity score stratification. Sensitivity analyses explored the impact of exposure definition, outcome categories, interim cancer, and unmeasured confounding. Results The pooled analyses included 5715 initiators of prucalopride and 29,372 initiators of PEG. Average duration of use was 175 days for prucalopride and 82 days for PEG. The pooled standardized incidence rate per 1000 person-years (95% confidence interval) of major adverse cardiovascular events was 6.57 (3.90–10.39) for patients initiating prucalopride and 10.24 (6.97–14.13) for PEG. The pooled adjusted incidence rate ratio for major adverse cardiovascular events was 0.64 (95% confidence interval 0.36–1.14). Results remained consistent in various sensitivity analyses. Conclusions The pooled incidence rate ratio estimate was consistent with no indication of an increased risk above the pre-specified safety threshold of 3.00 for major adverse cardiovascular events in patients with chronic constipation using prucalopride as compared with PEG.

Suggested Citation

  • Alicia Gilsenan & Joan Fortuny & Miguel Cainzos-Achirica & Oscar F. Cantero & Robert W. V. Flynn & Luis Garcia-Rodriguez & Abenah Harding & Bianca Kollhorst & Pär Karlsson & Love Linnér & Thomas M. Ma, 2019. "Cardiovascular Safety of Prucalopride in Patients with Chronic Constipation: A Multinational Population-Based Cohort Study," Drug Safety, Springer, vol. 42(10), pages 1179-1190, October.
  • Handle: RePEc:spr:drugsa:v:42:y:2019:i:10:d:10.1007_s40264-019-00835-0
    DOI: 10.1007/s40264-019-00835-0
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    1. Joan Fortuny & Alicia Gilsenan & Miguel Cainzos-Achirica & Oscar F. Cantero & Robert W. V. Flynn & Luis Garcia-Rodriguez & Bianca Kollhorst & Pär Karlsson & Love Linnér & Thomas M. MacDonald & Estel P, 2019. "Study Design and Cohort Comparability in a Study of Major Cardiovascular Events in New Users of Prucalopride Versus Polyethylene Glycol 3350," Drug Safety, Springer, vol. 42(10), pages 1167-1177, October.
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    1. Joan Fortuny & Alicia Gilsenan & Miguel Cainzos-Achirica & Oscar F. Cantero & Robert W. V. Flynn & Luis Garcia-Rodriguez & Bianca Kollhorst & Pär Karlsson & Love Linnér & Thomas M. MacDonald & Estel P, 2019. "Study Design and Cohort Comparability in a Study of Major Cardiovascular Events in New Users of Prucalopride Versus Polyethylene Glycol 3350," Drug Safety, Springer, vol. 42(10), pages 1167-1177, October.

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