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Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis

BACKGROUND: Proton pump inhibitors (PPIs) are widely prescribed, often without clear indications. There are conflicting data on its association with mortality risk and hepatic decompensation in cirrhotic patients. Furthermore, PPI users and PPI exposure in some studies have been poorly defined with...

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Autores principales: De Roza, Marianne Anastasia, Kai, Lim, Kam, Jia Wen, Chan, Yiong Huak, Kwek, Andrew, Ang, Tiing Leong, Hsiang, John Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737311/
https://www.ncbi.nlm.nih.gov/pubmed/31543684
http://dx.doi.org/10.3748/wjg.v25.i33.4933
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author De Roza, Marianne Anastasia
Kai, Lim
Kam, Jia Wen
Chan, Yiong Huak
Kwek, Andrew
Ang, Tiing Leong
Hsiang, John Chen
author_facet De Roza, Marianne Anastasia
Kai, Lim
Kam, Jia Wen
Chan, Yiong Huak
Kwek, Andrew
Ang, Tiing Leong
Hsiang, John Chen
author_sort De Roza, Marianne Anastasia
collection PubMed
description BACKGROUND: Proton pump inhibitors (PPIs) are widely prescribed, often without clear indications. There are conflicting data on its association with mortality risk and hepatic decompensation in cirrhotic patients. Furthermore, PPI users and PPI exposure in some studies have been poorly defined with many confounding factors. AIM: To examine if PPI use increases mortality and hepatic decompensation and the impact of cumulative PPI dose exposure. METHODS: Data from patients with decompensated liver cirrhosis were extracted from a hospital database between 2013 to 2017. PPI users were defined as cumulative defined daily dose (cDDD) ≥ 28 within a landmark period, after hospitalisation for hepatic decompensation. Cox regression analysis for comparison was done after propensity score adjustment. Further risk of hepatic decompensation was analysed by Poisson regression. RESULTS: Among 295 decompensated cirrhosis patients, 238 were PPI users and 57 were non-users. PPI users had higher mortality compared to non-users [adjusted HR = 2.10, (1.20-3.67); P = 0.009]. Longer PPI use with cDDD > 90 was associated with higher mortality, compared to non-users [aHR = 2.27, (1.10-5.14); P = 0.038]. PPI users had a higher incidence of hospitalization for hepatic decompensation [aRR = 1.61, (1.30-2.11); P < 0.001]. CONCLUSION: PPI use in decompensated cirrhosis is associated with increased risk of mortality and hepatic decompensation. Longer PPI exposure with cDDD > 90 increases the risk of mortality.
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spelling pubmed-67373112019-09-22 Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis De Roza, Marianne Anastasia Kai, Lim Kam, Jia Wen Chan, Yiong Huak Kwek, Andrew Ang, Tiing Leong Hsiang, John Chen World J Gastroenterol Retrospective Cohort Study BACKGROUND: Proton pump inhibitors (PPIs) are widely prescribed, often without clear indications. There are conflicting data on its association with mortality risk and hepatic decompensation in cirrhotic patients. Furthermore, PPI users and PPI exposure in some studies have been poorly defined with many confounding factors. AIM: To examine if PPI use increases mortality and hepatic decompensation and the impact of cumulative PPI dose exposure. METHODS: Data from patients with decompensated liver cirrhosis were extracted from a hospital database between 2013 to 2017. PPI users were defined as cumulative defined daily dose (cDDD) ≥ 28 within a landmark period, after hospitalisation for hepatic decompensation. Cox regression analysis for comparison was done after propensity score adjustment. Further risk of hepatic decompensation was analysed by Poisson regression. RESULTS: Among 295 decompensated cirrhosis patients, 238 were PPI users and 57 were non-users. PPI users had higher mortality compared to non-users [adjusted HR = 2.10, (1.20-3.67); P = 0.009]. Longer PPI use with cDDD > 90 was associated with higher mortality, compared to non-users [aHR = 2.27, (1.10-5.14); P = 0.038]. PPI users had a higher incidence of hospitalization for hepatic decompensation [aRR = 1.61, (1.30-2.11); P < 0.001]. CONCLUSION: PPI use in decompensated cirrhosis is associated with increased risk of mortality and hepatic decompensation. Longer PPI exposure with cDDD > 90 increases the risk of mortality. Baishideng Publishing Group Inc 2019-09-07 2019-09-07 /pmc/articles/PMC6737311/ /pubmed/31543684 http://dx.doi.org/10.3748/wjg.v25.i33.4933 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Retrospective Cohort Study
De Roza, Marianne Anastasia
Kai, Lim
Kam, Jia Wen
Chan, Yiong Huak
Kwek, Andrew
Ang, Tiing Leong
Hsiang, John Chen
Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
title Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
title_full Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
title_fullStr Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
title_full_unstemmed Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
title_short Proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
title_sort proton pump inhibitor use increases mortality and hepatic decompensation in liver cirrhosis
topic Retrospective Cohort Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737311/
https://www.ncbi.nlm.nih.gov/pubmed/31543684
http://dx.doi.org/10.3748/wjg.v25.i33.4933
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