Do proton pump inhibitors increase mortality? A systematic review and in‐depth analysis of the evidence
Proton pump inhibitors (PPIs) were primarily approved for short‐term use (2 to 8 weeks). However, PPI use continues to expand. Widely believed to be safe, we reviewed emerging evidence on increased mortality with PPI long‐term use. Our 2016 systematic PPI drug class review found that mortality was n...
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description | Proton pump inhibitors (PPIs) were primarily approved for short‐term use (2 to 8 weeks). However, PPI use continues to expand. Widely believed to be safe, we reviewed emerging evidence on increased mortality with PPI long‐term use. Our 2016 systematic PPI drug class review found that mortality was not reported as an outcome in randomized controlled trials (RCTs) that directly compared different PPIs. We sought more recent and comprehensive data on PPI harm outcomes from research syntheses as a follow‐on. A search was conducted from January 2014 to January 2020. We searched MEDLINE, EMBASE, and Cochrane Central for evidence from systematic reviews (SRs) and primary studies reporting all‐cause mortality in adults treated with a PPI for any indication (duration >12 weeks) compared to patients without PPI treatment (no use, placebo, or H2RA use). Two independent investigators assessed study eligibility, synthesized evidence, and assessed the quality of the included studies. Data on all‐cause mortality were sought, analyzed, critically examined, and interpreted herein. From 1304 articles, one SR was identified that reported on all‐cause mortality. The SRs pooled three observational studies with data to 1 year: odds ratio, 95% confidence interval (CI) 1.53‐1.84. A RCT, the COMPASS (Cardiovascular Outcomes for People Using Anticoagulant Strategies) RCT with data to 3 years: hazard ratio (HR) 1.03, 95% CI 0.92‐1.15. The US Veterans Affairs cohort study using a large national dataset with data to 10 years found a HR of 1.17, 95% CI (1.10‐1.24) and (NNH) of 22. The most common causes of death were from cardiovascular and chronic kidney diseases, with an excess death of 15 and 4 per 1000 patients, respectively, over the 10‐year period. Harms arising from real‐world medication use are best evaluated using a pharmacovigilance “convergence of proof” approach using data from a variety of sources and various study designs. Given that most PPI indications for use recommended a treatment duration of less than 12 weeks, it seems clear that PPIs were significantly overused in older patients. The median exposure time to PPI ranged from 1 to 4.6 years. Signals of serious harms including increased mortality with long‐term PPI use are reported in observational studies. The COMPASS trial findings are not inconsistent with contemporaneous findings from observational studies. The COMPASS RCT was unlikely to detect an increase in mortality given the trial was not powered to detect th |
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A systematic review and in‐depth analysis of the evidence</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Access via Wiley Online Library</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library (Open Access Collection)</source><source>PubMed Central</source><creator>Ben‐Eltriki, Mohamed ; Green, Carolyn J. ; Maclure, Malcolm ; Musini, Vijaya ; Bassett, Ken L. ; Wright, James M.</creator><creatorcontrib>Ben‐Eltriki, Mohamed ; Green, Carolyn J. ; Maclure, Malcolm ; Musini, Vijaya ; Bassett, Ken L. ; Wright, James M.</creatorcontrib><description>Proton pump inhibitors (PPIs) were primarily approved for short‐term use (2 to 8 weeks). However, PPI use continues to expand. Widely believed to be safe, we reviewed emerging evidence on increased mortality with PPI long‐term use. Our 2016 systematic PPI drug class review found that mortality was not reported as an outcome in randomized controlled trials (RCTs) that directly compared different PPIs. We sought more recent and comprehensive data on PPI harm outcomes from research syntheses as a follow‐on. A search was conducted from January 2014 to January 2020. We searched MEDLINE, EMBASE, and Cochrane Central for evidence from systematic reviews (SRs) and primary studies reporting all‐cause mortality in adults treated with a PPI for any indication (duration >12 weeks) compared to patients without PPI treatment (no use, placebo, or H2RA use). Two independent investigators assessed study eligibility, synthesized evidence, and assessed the quality of the included studies. Data on all‐cause mortality were sought, analyzed, critically examined, and interpreted herein. From 1304 articles, one SR was identified that reported on all‐cause mortality. The SRs pooled three observational studies with data to 1 year: odds ratio, 95% confidence interval (CI) 1.53‐1.84. A RCT, the COMPASS (Cardiovascular Outcomes for People Using Anticoagulant Strategies) RCT with data to 3 years: hazard ratio (HR) 1.03, 95% CI 0.92‐1.15. The US Veterans Affairs cohort study using a large national dataset with data to 10 years found a HR of 1.17, 95% CI (1.10‐1.24) and (NNH) of 22. The most common causes of death were from cardiovascular and chronic kidney diseases, with an excess death of 15 and 4 per 1000 patients, respectively, over the 10‐year period. Harms arising from real‐world medication use are best evaluated using a pharmacovigilance “convergence of proof” approach using data from a variety of sources and various study designs. Given that most PPI indications for use recommended a treatment duration of less than 12 weeks, it seems clear that PPIs were significantly overused in older patients. The median exposure time to PPI ranged from 1 to 4.6 years. Signals of serious harms including increased mortality with long‐term PPI use are reported in observational studies. The COMPASS trial findings are not inconsistent with contemporaneous findings from observational studies. The COMPASS RCT was unlikely to detect an increase in mortality given the trial was not powered to detect this outcome. The potential increase in mortality in older patients associated with prolonged PPI exposure needs to be conveyed to health professionals. Clinicians and patients may be able to reverse the relentless expansion of long‐term PPI exposure by reviewing indications and considering potential harms as well as benefits.</description><identifier>ISSN: 2052-1707</identifier><identifier>EISSN: 2052-1707</identifier><identifier>DOI: 10.1002/prp2.651</identifier><identifier>PMID: 32996701</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Adult ; Aged ; Anticoagulants ; Cardiovascular Diseases - mortality ; Cause of Death - trends ; Clinical trials ; Cohort Studies ; Confidence intervals ; Drug interactions ; FDA approval ; Female ; Fractures ; Humans ; long‐term use ; Male ; medication harms ; Middle Aged ; Mortality ; Mortality - trends ; mortality studies ; Observational Studies as Topic ; Pharmacology ; Pharmacovigilance ; Prescription Drug Overuse - mortality ; proton pump inhibitors ; Proton Pump Inhibitors - adverse effects ; Proton Pump Inhibitors - therapeutic use ; Randomized Controlled Trials as Topic ; Renal Insufficiency, Chronic - mortality ; Review ; Reviews ; Systematic review ; systematic reviews ; Veterans</subject><ispartof>Pharmacology research & perspectives, 2020-10, Vol.8 (5), p.e00651-n/a</ispartof><rights>2020 The Authors. published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd</rights><rights>2020 The Authors. Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4661-195c46a2d8a1d40a25634658498a330aa7ba46b0ec3a0e9d7c1d9a37d1bf08d3</citedby><cites>FETCH-LOGICAL-c4661-195c46a2d8a1d40a25634658498a330aa7ba46b0ec3a0e9d7c1d9a37d1bf08d3</cites><orcidid>0000-0002-2129-981X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525804/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525804/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32996701$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ben‐Eltriki, Mohamed</creatorcontrib><creatorcontrib>Green, Carolyn J.</creatorcontrib><creatorcontrib>Maclure, Malcolm</creatorcontrib><creatorcontrib>Musini, Vijaya</creatorcontrib><creatorcontrib>Bassett, Ken L.</creatorcontrib><creatorcontrib>Wright, James M.</creatorcontrib><title>Do proton pump inhibitors increase mortality? A systematic review and in‐depth analysis of the evidence</title><title>Pharmacology research & perspectives</title><addtitle>Pharmacol Res Perspect</addtitle><description>Proton pump inhibitors (PPIs) were primarily approved for short‐term use (2 to 8 weeks). However, PPI use continues to expand. Widely believed to be safe, we reviewed emerging evidence on increased mortality with PPI long‐term use. Our 2016 systematic PPI drug class review found that mortality was not reported as an outcome in randomized controlled trials (RCTs) that directly compared different PPIs. We sought more recent and comprehensive data on PPI harm outcomes from research syntheses as a follow‐on. A search was conducted from January 2014 to January 2020. 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The US Veterans Affairs cohort study using a large national dataset with data to 10 years found a HR of 1.17, 95% CI (1.10‐1.24) and (NNH) of 22. The most common causes of death were from cardiovascular and chronic kidney diseases, with an excess death of 15 and 4 per 1000 patients, respectively, over the 10‐year period. Harms arising from real‐world medication use are best evaluated using a pharmacovigilance “convergence of proof” approach using data from a variety of sources and various study designs. Given that most PPI indications for use recommended a treatment duration of less than 12 weeks, it seems clear that PPIs were significantly overused in older patients. The median exposure time to PPI ranged from 1 to 4.6 years. Signals of serious harms including increased mortality with long‐term PPI use are reported in observational studies. The COMPASS trial findings are not inconsistent with contemporaneous findings from observational studies. The COMPASS RCT was unlikely to detect an increase in mortality given the trial was not powered to detect this outcome. The potential increase in mortality in older patients associated with prolonged PPI exposure needs to be conveyed to health professionals. 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A systematic review and in‐depth analysis of the evidence</atitle><jtitle>Pharmacology research & perspectives</jtitle><addtitle>Pharmacol Res Perspect</addtitle><date>2020-10</date><risdate>2020</risdate><volume>8</volume><issue>5</issue><spage>e00651</spage><epage>n/a</epage><pages>e00651-n/a</pages><issn>2052-1707</issn><eissn>2052-1707</eissn><abstract>Proton pump inhibitors (PPIs) were primarily approved for short‐term use (2 to 8 weeks). However, PPI use continues to expand. Widely believed to be safe, we reviewed emerging evidence on increased mortality with PPI long‐term use. Our 2016 systematic PPI drug class review found that mortality was not reported as an outcome in randomized controlled trials (RCTs) that directly compared different PPIs. We sought more recent and comprehensive data on PPI harm outcomes from research syntheses as a follow‐on. A search was conducted from January 2014 to January 2020. We searched MEDLINE, EMBASE, and Cochrane Central for evidence from systematic reviews (SRs) and primary studies reporting all‐cause mortality in adults treated with a PPI for any indication (duration >12 weeks) compared to patients without PPI treatment (no use, placebo, or H2RA use). Two independent investigators assessed study eligibility, synthesized evidence, and assessed the quality of the included studies. Data on all‐cause mortality were sought, analyzed, critically examined, and interpreted herein. From 1304 articles, one SR was identified that reported on all‐cause mortality. The SRs pooled three observational studies with data to 1 year: odds ratio, 95% confidence interval (CI) 1.53‐1.84. A RCT, the COMPASS (Cardiovascular Outcomes for People Using Anticoagulant Strategies) RCT with data to 3 years: hazard ratio (HR) 1.03, 95% CI 0.92‐1.15. The US Veterans Affairs cohort study using a large national dataset with data to 10 years found a HR of 1.17, 95% CI (1.10‐1.24) and (NNH) of 22. The most common causes of death were from cardiovascular and chronic kidney diseases, with an excess death of 15 and 4 per 1000 patients, respectively, over the 10‐year period. Harms arising from real‐world medication use are best evaluated using a pharmacovigilance “convergence of proof” approach using data from a variety of sources and various study designs. Given that most PPI indications for use recommended a treatment duration of less than 12 weeks, it seems clear that PPIs were significantly overused in older patients. The median exposure time to PPI ranged from 1 to 4.6 years. Signals of serious harms including increased mortality with long‐term PPI use are reported in observational studies. The COMPASS trial findings are not inconsistent with contemporaneous findings from observational studies. The COMPASS RCT was unlikely to detect an increase in mortality given the trial was not powered to detect this outcome. The potential increase in mortality in older patients associated with prolonged PPI exposure needs to be conveyed to health professionals. Clinicians and patients may be able to reverse the relentless expansion of long‐term PPI exposure by reviewing indications and considering potential harms as well as benefits.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>32996701</pmid><doi>10.1002/prp2.651</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-2129-981X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Anticoagulants Cardiovascular Diseases - mortality Cause of Death - trends Clinical trials Cohort Studies Confidence intervals Drug interactions FDA approval Female Fractures Humans long‐term use Male medication harms Middle Aged Mortality Mortality - trends mortality studies Observational Studies as Topic Pharmacology Pharmacovigilance Prescription Drug Overuse - mortality proton pump inhibitors Proton Pump Inhibitors - adverse effects Proton Pump Inhibitors - therapeutic use Randomized Controlled Trials as Topic Renal Insufficiency, Chronic - mortality Review Reviews Systematic review systematic reviews Veterans |
title | Do proton pump inhibitors increase mortality? A systematic review and in‐depth analysis of the evidence |
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