Abstract
Background & Aims: Antiplatelets and anticoagulants are associated with increased upper gastrointestinal bleeding. We evaluated whether proton pump inhibitor therapy could reduce this risk. Methods: We performed a 3 × 2 partial factorial double-blind trial of 17,598 participants with stable cardiovascular disease and peripheral artery disease. Participants were randomly assigned to groups given pantoprazole 40 mg daily or placebo, as well as rivaroxaban 2.5 mg twice daily with aspirin 100 mg once daily, rivaroxaban 5 mg twice daily, or aspirin 100 mg alone. The primary outcome was time to first upper gastrointestinal event, defined as a composite of overt bleeding, upper gastrointestinal bleeding from a gastroduodenal lesion or of unknown origin, occult bleeding, symptomatic gastroduodenal ulcer or ≥5 erosions, upper gastrointestinal obstruction, or perforation. Results: There was no significant difference in upper gastrointestinal events between the pantoprazole group (102 of 8791 events) and the placebo group (116 of 8807 events) (hazard ratio, 0.88; 95% confidence interval [CI], 0.67–1.15). Pantoprazole significantly reduced bleeding of gastroduodenal lesions (hazard ratio, 0.52; 95% confidence interval, 0.28–0.94; P = .03); this reduction was greater when we used a post-hoc definition of bleeding gastroduodenal lesion (hazard ratio, 0.45; 95% confidence interval, 0.27–0.74), although the number needed to treat still was high (n = 982; 95% confidence interval, 609–2528). Conclusions: In a randomized placebo-controlled trial, we found that routine use of proton pump inhibitors in patients receiving low-dose anticoagulation and/or aspirin for stable cardiovascular disease does not reduce upper gastrointestinal events, but may reduce bleeding from gastroduodenal lesions. ClinicalTrials.gov ID: NCT01776424.
| Original language | English |
|---|---|
| Pages (from-to) | 403-412.e5 |
| Number of pages | 15 |
| Journal | Gastroenterology |
| Volume | 157 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Aug 2019 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Drug
- Heart Disease Prevention
- Stomach
- Thrombosis
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In: Gastroenterology, Vol. 157, No. 2, 08.2019, p. 403-412.e5.
Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - Pantoprazole to Prevent Gastroduodenal Events in Patients Receiving Rivaroxaban and/or Aspirin in a Randomized, Double-Blind, Placebo-Controlled Trial
AU - Moayyedi, Paul
AU - Eikelboom, John W.
AU - Bosch, Jackie
AU - Connolly, Stuart J.
AU - Dyal, Leanne
AU - Shestakovska, Olga
AU - Leong, Darryl
AU - Anand, Sonia S.
AU - Störk, Stefan
AU - Branch, Kelly R.H.
AU - Bhatt, Deepak L.
AU - Verhamme, Peter B.
AU - O'Donnell, Martin
AU - Maggioni, Aldo P.
AU - Lonn, E. M.
AU - Piegas, Leopoldo S.
AU - Ertl, G.
AU - Keltai, Matyas
AU - Cook Bruns, N.
AU - Muehlhofer, Eva
AU - Dagenais, Gilles R.
AU - Kim, Jae Hyung
AU - Hori, Masatsugu
AU - Steg, P. Gabriel
AU - Hart, Robert G.
AU - Diaz, Rafael
AU - Alings, M.
AU - Widimsky, Petr
AU - Avezum, Alvaro
AU - Probstfield, Jeffrey
AU - Zhu, Jun
AU - Liang, Yan
AU - Lopez-Jaramillo, Patricio
AU - Kakkar, Ajay
AU - Parkhomenko, Alexander N.
AU - Ryden, Lars
AU - Pogosova, Nana
AU - Dans, Antonio
AU - Lanas, Fernando
AU - Commerford, Patrick J.
AU - Torp-Pedersen, Christian
AU - Guzik, T.
AU - Vinereanu, Dragos
AU - Tonkin, Andrew M.
AU - Lewis, Basil S.
AU - Felix, Camilo
AU - Yusoff, Khalid
AU - Metsarinne, Kaj
AU - Fox, Keith A.A.
AU - Yusuf, S.
AU - for the COMPASS Investigators
N1 - Funding Information: Funding This study was funded by Bayer AG . Funding Information: Funding This study was funded by Bayer AG. Conflicts of interest These authors disclose the following: Dr Moayyedi has received funding for research (related to inflammatory bowel disease and irritable bowel syndrome) from Allergan and Takeda. Dr Eikelboom reports receiving grant support and honoraria from Bayer, Boehringer Ingelheim, Bristol-Myers Squibb/Pfizer, Daiichi Sankyo, Janssen, AstraZeneca, Eli Lilly, GlaxoSmithKline, and Sanofi-Aventis. Dr Connolly is receiving lecture fees and consulting fees from Bristol-Myers Squibb, Pfizer, Portola Pharmaceuticals, Boehringer Ingelheim, Servier, Daiichi Sankyo, and Medtronic. Dr Hart is receiving grant support, fees for serving as principal investigator of the Rivaroxaban Versus Aspirin in Secondary Prevention of Stroke and Prevention of Systemic Embolism in Patients With Recent Embolic Stroke of Undetermined Source (NAVIGATE ESUS) trial, and advisory board fees from Bayer. Dr Diaz is receiving grant support from the Population Health Research Institute. Dr Alings is receiving consulting fees from Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Pfizer, and Sanofi-Aventis. Dr Lonn is receiving consulting fees from Bayer, Amgen, Sanofi, Novartis, and Servier. Dr Anand is receiving consulting fees and lecture fees from Bayer and Novartis. Dr Avezum is receiving consulting fees from Boehringer Ingelheim. Dr Branch is receiving grant support from Astellas and serving on an advisory board for Janssen. Dr Bhatt is receiving grant support from Amarin, AstraZeneca, Bristol-Myers Squibb, Eisai, Ethicon, Medtronic, Sanofi-Aventis, the Medicines Company, Roche, Pfizer, Forest Laboratories/AstraZeneca, Ischemix, Amgen, Eli Lilly, Chiesi, and Ironwood Pharmaceuticals, collaborating on research (uncompensated) with FlowCo, PLx Pharma, Takeda, and Merck, receiving fees for serving on data monitoring committees, an operations committee, a publications committee (US co-national leader), and a steering committee from the Population Health Research Institute, serving as editor-in-chief of the Harvard Heart Letter for Belvoir Publications, serving as chief medical editor of Cardiology Today's Intervention for Slack Publications, receiving fees for serving on continuing medical education steering committees from WebMD, receiving advisory board fees from Elsevier, serving on uncompensated advisory boards for Medscape Cardiology and Regado Biosciences, serving as editor-in-chief of the Journal of Invasive Cardiology for HMP Communications, serving as deputy editor for Clinical Cardiology, serving as guest editor and associate editor for the Journal of the American College of Cardiology, serving as chair of the research and publications committee of the Veterans Affairs Cardiovascular Assessment, Reporting, and Tracking system for the Department of Veterans Affairs, serving as site co-investigator for Biotronik and Boston Scientific, serving on an uncompensated advisory board for Cardax, and receiving fees for serving on data monitoring committees from the Cleveland Clinic, Duke University, and Mount Sinai School of Medicine. Dr Zhu is receiving lecture fees from Bayer, Boehringer Ingelheim, and Sanofi. Dr Liang is receiving lecture fees from Bayer, Boehringer Ingelheim, and Sanofi. Dr Maggioni is receiving fees for serving as a study committee member from Novartis, Bayer, Fresenius Medical Care, and Cardiorentis. Dr Kakkar is receiving grant support and fees for serving as steering committee chairman from Bayer, and consulting fees from Boehringer Ingelheim, Daiichi Sankyo Europe, Janssen, Sanofi, and Armetheon. Dr Fox is receiving grant support and honoraria from AstraZeneca and honoraria from Sanofi/Regeneron Pharmaceuticals. Dr Parkhomenko is receiving grant support and honoraria from Pfizer, Bayer, Janssen, AstraZeneca, Sanofi, and Merck Sharp & Dohme. Dr Störk is receiving grant support from Servier and Boehringer Ingelheim, grant support and lecture fees from Novartis and Thermo Fisher Scientific, and lecture fees from Pfizer. Dr Dans is receiving lecture fees from Pfizer and Boehringer Ingelheim. Dr Torp-Pedersen is receiving grant support from Biotronik. Dr Verhamme is receiving grant support, lecture fees, and consulting fees from Bayer HealthCare, Boehringer Ingelheim, Daiichi Sankyo, Pfizer, and Brisol-Myers Squibb, grant support from Sanofi and Leo Pharma, and consulting fees from Portola Pharmaceuticals. Dr Vinereanu is receiving grant support, lecture fees, and consulting fees from Boehringer Ingelheim, Pfizer, and Novartis and grant support and lecture fees from Servier. Dr Lewis is receiving lecture fees and honoraria from Pfizer/Bristol-Myers Squibb. Dr Steg is receiving fees for serving on a steering committee from Amarin, Janssen, and CSL Behring, fees for serving on a steering committee and lecture fees from AstraZeneca, lecture fees and consulting fees from Bayer and Bristol-Myers Squibb, fees for preparation of educational material from Boehringer Ingelheim, consulting fees and fees for serving on a data and safety monitoring board from Eli Lilly and Merck Sharp & Dohme, consulting fees from Novartis and Regeneron Pharmaceuticals, fees for serving on a critical-event committee from Pfizer, fees for serving on a steering committee and consulting fees from Sanofi, and fees for serving on a steering committee, consulting fees, and fees for serving on a data and safety monitoring board from Servier. Dr Cook Bruns and Dr Muehlhofer are employed by Bayer. Dr Yusuf is receiving grant support and honoraria from Bayer, Boehringer Ingelheim, Astra-Zeneca, Bristol-Myers Squibb, and Cadila Pharmaceuticals. The remaining authors disclose no conflicts. Funding This study was funded by Bayer AG. Author contributions: All authors were involved in data acquisition, general design of the trial, interpretation of the data and critical revision of the manuscript. L. Dyal and O. Shestakovska were involved with the primary analysis of the data. P. Moayyedi, J.W. Eikelboom, J. Bosch, S.J. Connolly, and S. Yusuf were involved in the initial draft of the manuscript. P. Moayyedi, J.W. Eikelboom, J. Bosch, S.J. Connolly, N. Cook Bruns, E. Muehlhofer and S. Yusuf were involved with the design of this aspect of the trial. J.W. Eikelboom and S. Yusuf were involved in obtaining funding and N. Cook Bruns and E. Muehlhofer were involved with the decision to provide support from Bayer AG. Conflicts of interest These authors disclose the following: Dr Moayyedi has received funding for research (related to inflammatory bowel disease and irritable bowel syndrome) from Allergan and Takeda. Dr Eikelboom reports receiving grant support and honoraria from Bayer, Boehringer Ingelheim, Bristol-Myers Squibb/Pfizer, Daiichi Sankyo, Janssen, AstraZeneca, Eli Lilly, GlaxoSmithKline, and Sanofi-Aventis. Dr Connolly is receiving lecture fees and consulting fees from Bristol-Myers Squibb, Pfizer, Portola Pharmaceuticals, Boehringer Ingelheim, Servier, Daiichi Sankyo, and Medtronic. Dr Hart is receiving grant support, fees for serving as principal investigator of the Rivaroxaban Versus Aspirin in Secondary Prevention of Stroke and Prevention of Systemic Embolism in Patients With Recent Embolic Stroke of Undetermined Source (NAVIGATE ESUS) trial, and advisory board fees from Bayer. Dr Diaz is receiving grant support from the Population Health Research Institute. Dr Alings is receiving consulting fees from Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Pfizer, and Sanofi-Aventis. Dr Lonn is receiving consulting fees from Bayer, Amgen, Sanofi, Novartis, and Servier. Dr Anand is receiving consulting fees and lecture fees from Bayer and Novartis. Dr Avezum is receiving consulting fees from Boehringer Ingelheim. Dr Branch is receiving grant support from Astellas and serving on an advisory board for Janssen. Dr Bhatt is receiving grant support from Amarin, AstraZeneca, Bristol-Myers Squibb, Eisai, Ethicon, Medtronic, Sanofi-Aventis, the Medicines Company, Roche, Pfizer, Forest Laboratories/AstraZeneca, Ischemix, Amgen, Eli Lilly, Chiesi, and Ironwood Pharmaceuticals, collaborating on research (uncompensated) with FlowCo, PLx Pharma, Takeda, and Merck, receiving fees for serving on data monitoring committees, an operations committee, a publications committee (US co-national leader), and a steering committee from the Population Health Research Institute, serving as editor-in-chief of the Harvard Heart Letter for Belvoir Publications, serving as chief medical editor of Cardiology Today's Intervention for Slack Publications, receiving fees for serving on continuing medical education steering committees from WebMD, receiving advisory board fees from Elsevier, serving on uncompensated advisory boards for Medscape Cardiology and Regado Biosciences, serving as editor-in-chief of the Journal of Invasive Cardiology for HMP Communications, serving as deputy editor for Clinical Cardiology, serving as guest editor and associate editor for the Journal of the American College of Cardiology, serving as chair of the research and publications committee of the Veterans Affairs Cardiovascular Assessment, Reporting, and Tracking system for the Department of Veterans Affairs, serving as site co-investigator for Biotronik and Boston Scientific, serving on an uncompensated advisory board for Cardax, and receiving fees for serving on data monitoring committees from the Cleveland Clinic, Duke University, and Mount Sinai School of Medicine. Dr Zhu is receiving lecture fees from Bayer, Boehringer Ingelheim, and Sanofi. Dr Liang is receiving lecture fees from Bayer, Boehringer Ingelheim, and Sanofi. Dr Maggioni is receiving fees for serving as a study committee member from Novartis, Bayer, Fresenius Medical Care, and Cardiorentis. Dr Kakkar is receiving grant support and fees for serving as steering committee chairman from Bayer, and consulting fees from Boehringer Ingelheim, Daiichi Sankyo Europe, Janssen, Sanofi, and Armetheon. Dr Fox is receiving grant support and honoraria from AstraZeneca and honoraria from Sanofi/Regeneron Pharmaceuticals. Dr Parkhomenko is receiving grant support and honoraria from Pfizer, Bayer, Janssen, AstraZeneca, Sanofi, and Merck Sharp & Dohme. Dr Störk is receiving grant support from Servier and Boehringer Ingelheim, grant support and lecture fees from Novartis and Thermo Fisher Scientific, and lecture fees from Pfizer. Dr Dans is receiving lecture fees from Pfizer and Boehringer Ingelheim. Dr Torp-Pedersen is receiving grant support from Biotronik. Dr Verhamme is receiving grant support, lecture fees, and consulting fees from Bayer HealthCare, Boehringer Ingelheim, Daiichi Sankyo, Pfizer, and Brisol-Myers Squibb, grant support from Sanofi and Leo Pharma, and consulting fees from Portola Pharmaceuticals. Dr Vinereanu is receiving grant support, lecture fees, and consulting fees from Boehringer Ingelheim, Pfizer, and Novartis and grant support and lecture fees from Servier. Dr Lewis is receiving lecture fees and honoraria from Pfizer/Bristol-Myers Squibb. Dr Steg is receiving fees for serving on a steering committee from Amarin, Janssen, and CSL Behring, fees for serving on a steering committee and lecture fees from AstraZeneca, lecture fees and consulting fees from Bayer and Bristol-Myers Squibb, fees for preparation of educational material from Boehringer Ingelheim, consulting fees and fees for serving on a data and safety monitoring board from Eli Lilly and Merck Sharp & Dohme, consulting fees from Novartis and Regeneron Pharmaceuticals, fees for serving on a critical-event committee from Pfizer, fees for serving on a steering committee and consulting fees from Sanofi, and fees for serving on a steering committee, consulting fees, and fees for serving on a data and safety monitoring board from Servier. Dr Cook Bruns and Dr Muehlhofer are employed by Bayer. Dr Yusuf is receiving grant support and honoraria from Bayer, Boehringer Ingelheim, Astra-Zeneca, Bristol-Myers Squibb, and Cadila Pharmaceuticals. The remaining authors disclose no conflicts. Funding This study was funded by Bayer AG. Publisher Copyright: © 2019 AGA Institute
PY - 2019/8
Y1 - 2019/8
N2 - Background & Aims: Antiplatelets and anticoagulants are associated with increased upper gastrointestinal bleeding. We evaluated whether proton pump inhibitor therapy could reduce this risk. Methods: We performed a 3 × 2 partial factorial double-blind trial of 17,598 participants with stable cardiovascular disease and peripheral artery disease. Participants were randomly assigned to groups given pantoprazole 40 mg daily or placebo, as well as rivaroxaban 2.5 mg twice daily with aspirin 100 mg once daily, rivaroxaban 5 mg twice daily, or aspirin 100 mg alone. The primary outcome was time to first upper gastrointestinal event, defined as a composite of overt bleeding, upper gastrointestinal bleeding from a gastroduodenal lesion or of unknown origin, occult bleeding, symptomatic gastroduodenal ulcer or ≥5 erosions, upper gastrointestinal obstruction, or perforation. Results: There was no significant difference in upper gastrointestinal events between the pantoprazole group (102 of 8791 events) and the placebo group (116 of 8807 events) (hazard ratio, 0.88; 95% confidence interval [CI], 0.67–1.15). Pantoprazole significantly reduced bleeding of gastroduodenal lesions (hazard ratio, 0.52; 95% confidence interval, 0.28–0.94; P = .03); this reduction was greater when we used a post-hoc definition of bleeding gastroduodenal lesion (hazard ratio, 0.45; 95% confidence interval, 0.27–0.74), although the number needed to treat still was high (n = 982; 95% confidence interval, 609–2528). Conclusions: In a randomized placebo-controlled trial, we found that routine use of proton pump inhibitors in patients receiving low-dose anticoagulation and/or aspirin for stable cardiovascular disease does not reduce upper gastrointestinal events, but may reduce bleeding from gastroduodenal lesions. ClinicalTrials.gov ID: NCT01776424.
AB - Background & Aims: Antiplatelets and anticoagulants are associated with increased upper gastrointestinal bleeding. We evaluated whether proton pump inhibitor therapy could reduce this risk. Methods: We performed a 3 × 2 partial factorial double-blind trial of 17,598 participants with stable cardiovascular disease and peripheral artery disease. Participants were randomly assigned to groups given pantoprazole 40 mg daily or placebo, as well as rivaroxaban 2.5 mg twice daily with aspirin 100 mg once daily, rivaroxaban 5 mg twice daily, or aspirin 100 mg alone. The primary outcome was time to first upper gastrointestinal event, defined as a composite of overt bleeding, upper gastrointestinal bleeding from a gastroduodenal lesion or of unknown origin, occult bleeding, symptomatic gastroduodenal ulcer or ≥5 erosions, upper gastrointestinal obstruction, or perforation. Results: There was no significant difference in upper gastrointestinal events between the pantoprazole group (102 of 8791 events) and the placebo group (116 of 8807 events) (hazard ratio, 0.88; 95% confidence interval [CI], 0.67–1.15). Pantoprazole significantly reduced bleeding of gastroduodenal lesions (hazard ratio, 0.52; 95% confidence interval, 0.28–0.94; P = .03); this reduction was greater when we used a post-hoc definition of bleeding gastroduodenal lesion (hazard ratio, 0.45; 95% confidence interval, 0.27–0.74), although the number needed to treat still was high (n = 982; 95% confidence interval, 609–2528). Conclusions: In a randomized placebo-controlled trial, we found that routine use of proton pump inhibitors in patients receiving low-dose anticoagulation and/or aspirin for stable cardiovascular disease does not reduce upper gastrointestinal events, but may reduce bleeding from gastroduodenal lesions. ClinicalTrials.gov ID: NCT01776424.
KW - Drug
KW - Heart Disease Prevention
KW - Stomach
KW - Thrombosis
UR - https://www.scopus.com/pages/publications/85068311091
U2 - 10.1053/j.gastro.2019.04.041
DO - 10.1053/j.gastro.2019.04.041
M3 - Article
C2 - 31054846
AN - SCOPUS:85068311091
SN - 0016-5085
VL - 157
SP - 403-412.e5
JO - Gastroenterology
JF - Gastroenterology
IS - 2
ER -