Proton pump inhibitor use and risk of hepatic encephalopathy : a multicentre study

dc.contributor.authorGairing, Simon Johannes
dc.contributor.authorMangini, Chiara
dc.contributor.authorZarantonello, Lisa
dc.contributor.authorJonasson, Elise
dc.contributor.authorDobbermann, Henrike
dc.contributor.authorSultanik, Philippe
dc.contributor.authorGalle, Peter Robert
dc.contributor.authorLabenz, Joachim
dc.contributor.authorThabut, Dominique
dc.contributor.authorMarquardt, Jens Uwe
dc.contributor.authorBloom, Patricia P.
dc.contributor.authorLauridsen, Mette Munk
dc.contributor.authorMontagnese, Sara
dc.contributor.authorLabenz, Christian
dc.date.accessioned2024-09-19T13:32:49Z
dc.date.available2024-09-19T13:32:49Z
dc.date.issued2024
dc.description.abstractBackground & Aims: Data on the association between proton pump inhibitor (PPI) use and hepatic encephalopathy (HE) are conflicting, and data from multicentre studies are scarce. The aim of this study was to dissect the potential association between PPI use and minimal (MHE) and overt HE (OHE). Methods: Data from patients with cirrhosis recruited at seven centres across Europe and the US were analysed. MHE was defined by the psychometric hepatic encephalopathy score (PHES). PPI use was recorded on the day of testing with PHES. Patients were followed for OHE development and death/liver transplantation. Results: A total of 1,160 patients with a median MELD of 11 were included (Child-Pugh stages: A 49%/B 39%/C 11%). PPI use was noted in 58% of patients. Median follow-up time was 18.1 months, during which 230 (20%) developed an OHE episode, and 224 (19%) reached the composite endpoint of death/liver transplantation. In multivariable analyses, PPI use was neither associated with the presence of MHE at baseline nor OHE development during follow-up. These findings were consistent in subgroup analyses of patients with Child-Pugh A or B cirrhosis and after excluding patients with a history of OHE. PPI use was also not associated with a higher risk of OHE, neither in patients with an indication for treatment nor in patients without an indication. Conclusions: PPI use is not associated with a higher risk of HE in patients with cirrhosis. Based on these findings, at present, a prescription should not be prohibited in case of a generally accepted indication. Impact and implications: Data on the association between proton pump inhibitor (PPI) use and hepatic encephalopathy (HE) are conflicting. In this study, PPI use was not associated with a higher risk of minimal HE at baseline or overt HE during follow-up in patients with cirrhosis. Based on these findings, prescription of a PPI for a generally accepted indication should not be prohibited in patients with cirrhosis.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-10716
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/10735
dc.language.isoengde
dc.rightsCC-BY-4.0*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleProton pump inhibitor use and risk of hepatic encephalopathy : a multicentre studyen_GB
dc.typeZeitschriftenaufsatzde
jgu.journal.issue8de
jgu.journal.titleJHEP reportsde
jgu.journal.volume6de
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative101104de
jgu.publisher.doi10.1016/j.jhepr.2024.101104de
jgu.publisher.issn2589-5559de
jgu.publisher.nameElsevierde
jgu.publisher.placeAmsterdamde
jgu.publisher.year2024
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610de
jgu.subject.dfgLebenswissenschaftende
jgu.type.contenttypeScientific articlede
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde

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