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

Authors :
Moayyedi P
Eikelboom JW
Bosch J
Connolly SJ
Dyal L
Shestakovska O
Leong D
Anand SS
Störk S
Branch KRH
Bhatt DL
Verhamme PB
O'Donnell M
Maggioni AP
Lonn EM
Piegas LS
Ertl G
Keltai M
Bruns NC
Muehlhofer E
Dagenais GR
Kim JH
Hori M
Steg PG
Hart RG
Diaz R
Alings M
Widimsky P
Avezum A
Probstfield J
Zhu J
Liang Y
Lopez-Jaramillo P
Kakkar AK
Parkhomenko AN
Ryden L
Pogosova N
Dans AL
Lanas F
Commerford PJ
Torp-Pedersen C
Guzik TJ
Vinereanu D
Tonkin AM
Lewis BS
Felix C
Yusoff K
Metsarinne KP
Fox KAA
Yusuf S
Source :
Gastroenterology [Gastroenterology] 2019 Sep; Vol. 157 (3), pp. 682-691.e2. Date of Electronic Publication: 2019 May 29.
Publication Year :
2019

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.<br />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.<br />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.<br />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.<br /> (Copyright © 2019 AGA Institute. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1528-0012
Volume :
157
Issue :
3
Database :
MEDLINE
Journal :
Gastroenterology
Publication Type :
Academic Journal
Accession number :
31152740
Full Text :
https://doi.org/10.1053/j.gastro.2019.05.056