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Safety of Proton Pump Inhibitors Based on a Large, Multi-Year, Randomized Trial of Patients Receiving Rivaroxaban or Aspirin

  • COMPASS Investigators
  • McMaster University and Hamilton Health Sciences
  • University of Wuerzburg
  • University of Washington Medical Center
  • Brigham and Women's Hospital
  • KU Leuven
  • Associazione Nazionale Medici Cardiologi Ospedalieri
  • Hospital do Coracao
  • Semmelweis University
  • Bayer AG
  • Institut Universitaire de Cardiologie et de Pneumologie de Québec
  • Catholic University of Korea
  • Osaka International Cancer Institute
  • Université Paris Descartes-Sorbonne Paris Cité
  • Instituto Cardiovascular de Rosario
  • Werkgroep Cardiologische centra Nederland (WCN)
  • Charles University in Prague
  • Dante Pazzanese Institute of Cardiology
  • University of Washington
  • Chinese Academy of Medical Sciences
  • National Association of Hospital Research Institute
  • University College London
  • Institute of Cardiology
  • Karolinska Institutet
  • Directorate
  • University of the Philippines Manila
  • Universidad de la Frontera
  • University of Cape Town
  • Aalborg University
  • University of Glasgow
  • Jagiellonian University Medical College
  • Carol Davila University of Medicine and Pharmacy
  • Monash University
  • Lady Davis Carmel Medical Center
  • Universidad UTE
  • Universiti Teknologi MARA
  • Turku University Hospital
  • University of Edinburgh

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

445 Citations (Scopus)

Abstract

Background & Aims: Proton pump inhibitors (PPIs) are effective at treating acid-related disorders. These drugs are well tolerated in the short term, but long-term treatment was associated with adverse events in observational studies. We aimed to confirm these findings in an adequately powered randomized trial. Methods: We performed a 3 × 2 partial factorial double-blind trial of 17,598 participants with stable cardiovascular disease and peripheral artery disease randomly assigned to groups given pantoprazole (40 mg daily, n = 8791) or placebo (n = 8807). Participants were also randomly assigned to groups that received rivaroxaban (2.5 mg twice daily) with aspirin (100 mg once daily), rivaroxaban (5 mg twice daily), or aspirin (100 mg) alone. We collected data on development of pneumonia, Clostridium difficile infection, other enteric infections, fractures, gastric atrophy, chronic kidney disease, diabetes, chronic obstructive lung disease, dementia, cardiovascular disease, cancer, hospitalizations, and all-cause mortality every 6 months. Patients were followed up for a median of 3.01 years, with 53,152 patient-years of follow-up. Results: There was no statistically significant difference between the pantoprazole and placebo groups in safety events except for enteric infections (1.4% vs 1.0% in the placebo group; odds ratio, 1.33; 95% confidence interval, 1.01–1.75). For all other safety outcomes, proportions were similar between groups except for C difficile infection, which was approximately twice as common in the pantoprazole vs the placebo group, although there were only 13 events, so this difference was not statistically significant. Conclusions: In a large placebo-controlled randomized trial, we found that pantoprazole is not associated with any adverse event when used for 3 years, with the possible exception of an increased risk of enteric infections. ClinicalTrials.gov Number: NCT01776424.

Original languageEnglish
Pages (from-to)682-691.e2
JournalGastroenterology
Volume157
Issue number3
DOIs
Publication statusPublished - Sep 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Bacteria
  • CVD
  • Reflux
  • Thrombosis

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