TY - JOUR
T1 - Safety of Proton Pump Inhibitors Based on a Large, Multi-Year, Randomized Trial of Patients Receiving Rivaroxaban or Aspirin
AU - COMPASS Investigators
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, Kelley R.H.
AU - Bhatt, Deepak L.
AU - Verhamme, Peter B.
AU - O'Donnell, Martin
AU - Maggioni, Aldo P.
AU - Lonn, Eva M.
AU - Piegas, Leopoldo S.
AU - Ertl, Georg
AU - Keltai, Matyas
AU - Bruns, Nancy Cook
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, Marco
AU - Widimsky, Petr
AU - Avezum, Alvaro
AU - Probstfield, Jeffrey
AU - Zhu, Jun
AU - Liang, Yan
AU - Lopez-Jaramillo, Patricio
AU - Kakkar, Ajay K.
AU - Parkhomenko, Alexander N.
AU - Ryden, Lars
AU - Pogosova, Nana
AU - Dans, Antonio L.
AU - Lanas, Fernando
AU - Commerford, Patrick J.
AU - Torp-Pedersen, Christian
AU - Guzik, Tomek J.
AU - Vinereanu, Dragos
AU - Tonkin, Andrew M.
AU - Lewis, Basil S.
AU - Felix, Camilo
AU - Yusoff, Khalid
AU - Metsarinne, Kaj P.
AU - Fox, Keith A.A.
AU - Yusuf, Salim
N1 - Publisher Copyright:
© 2019 AGA Institute
PY - 2019/9
Y1 - 2019/9
N2 - 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.
AB - 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.
KW - Bacteria
KW - CVD
KW - Reflux
KW - Thrombosis
UR - http://www.scopus.com/inward/record.url?scp=85070685740&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2019.05.056
DO - 10.1053/j.gastro.2019.05.056
M3 - Artículo Científico
C2 - 31152740
AN - SCOPUS:85070685740
SN - 0016-5085
VL - 157
SP - 682-691.e2
JO - Gastroenterology
JF - Gastroenterology
IS - 3
ER -