Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22440
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dc.contributor.authorYoung, Paul J-
dc.contributor.authorBagshaw, Sean M-
dc.contributor.authorForbes, Andrew B-
dc.contributor.authorNichol, Alistair D-
dc.contributor.authorWright, Stephen E-
dc.contributor.authorBailey, Michael-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorBeasley, Richard-
dc.contributor.authorBrickell, Kathy-
dc.contributor.authorEastwood, Glenn M-
dc.contributor.authorGattas, David J-
dc.contributor.authorvan Haren, Frank-
dc.contributor.authorLitton, Edward-
dc.contributor.authorMackle, Diane M-
dc.contributor.authorMcArthur, Colin J-
dc.contributor.authorMcGuinness, Shay P-
dc.contributor.authorMouncey, Paul R-
dc.contributor.authorNavarra, Leanlove-
dc.contributor.authorOpgenorth, Dawn-
dc.contributor.authorPilcher, David-
dc.contributor.authorSaxena, Manoj K-
dc.contributor.authorWebb, Steve A-
dc.contributor.authorWiley, Daisy-
dc.contributor.authorRowan, Kathryn M-
dc.date2020-01-17-
dc.date.accessioned2020-01-20T05:24:55Z-
dc.date.available2020-01-20T05:24:55Z-
dc.date.issued2020-02-
dc.identifier.citationJAMA 2020; 323(7): 616-626-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22440-
dc.description.abstractProton pump inhibitors (PPIs) or histamine-2 receptor blockers (H2RBs) are often prescribed for patients as stress ulcer prophylaxis drugs in the intensive care unit (ICU). The comparative effect of these drugs on mortality is unknown. To compare in-hospital mortality rates using PPIs vs H2RBs for stress ulcer prophylaxis. Cluster crossover randomized clinical trial conducted at 50 ICUs in 5 countries between August 2016 and January 2019. Patients requiring invasive mechanical ventilation within 24 hours of ICU admission were followed up for 90 days at the hospital. Two stress ulcer prophylaxis strategies were compared (preferential use with PPIs vs preferential use with H2RBs). Each ICU used each strategy sequentially for 6 months in random order; 25 ICUs were randomized to the sequence with use of PPIs and then use of H2RBs and 25 ICUs were randomized to the sequence with use of H2RBs and then use of PPIs (13 436 patients randomized by site to PPIs and 13 392 randomized by site to H2RBs). The primary outcome was all-cause mortality within 90 days during index hospitalization. Secondary outcomes were clinically important upper gastrointestinal bleeding, Clostridioides difficile infection, and ICU and hospital lengths of stay. Among 26 982 patients who were randomized, 154 opted out, and 26 828 were analyzed (mean [SD] age, 58 [17.0] years; 9691 [36.1%] were women). There were 26 771 patients (99.2%) included in the mortality analysis; 2459 of 13 415 patients (18.3%) in the PPI group died at the hospital by day 90 and 2333 of 13 356 patients (17.5%) in the H2RB group died at the hospital by day 90 (risk ratio, 1.05 [95% CI, 1.00 to 1.10]; absolute risk difference, 0.93 percentage points [95% CI, -0.01 to 1.88] percentage points; P = .054). An estimated 4.1% of patients randomized by ICU site to PPIs actually received H2RBs and an estimated 20.1% of patients randomized by ICU site to H2RBs actually received PPIs. Clinically important upper gastrointestinal bleeding occurred in 1.3% of the PPI group and 1.8% of the H2RB group (risk ratio, 0.73 [95% CI, 0.57 to 0.92]; absolute risk difference, -0.51 percentage points [95% CI, -0.90 to -0.12 percentage points]; P = .009). Rates of Clostridioides difficile infection and ICU and hospital lengths of stay were not significantly different by treatment group. One adverse event (an allergic reaction) was reported in 1 patient in the PPI group. Among ICU patients requiring mechanical ventilation, a strategy of stress ulcer prophylaxis with use of proton pump inhibitors vs histamine-2 receptor blockers resulted in hospital mortality rates of 18.3% vs 17.5%, respectively, a difference that did not reach the significance threshold. However, study interpretation may be limited by crossover in the use of the assigned medication. anzctr.org.au Identifier: ACTRN12616000481471.-
dc.language.isoeng-
dc.titleEffect of Stress Ulcer Prophylaxis With Proton Pump Inhibitors vs Histamine-2 Receptor Blockers on In-Hospital Mortality Among ICU Patients Receiving Invasive Mechanical Ventilation: The PEPTIC Randomized Clinical Trial.-
dc.typeJournal Article-
dc.identifier.journaltitleJAMA-
dc.identifier.affiliationIntensive Care Unit, Royal Perth Hospital, Perth, Australiaen
dc.identifier.affiliationUniversity of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationIntensive Care Unit, Fiona Stanley Hospital, Murdoch, Australiaen
dc.identifier.affiliationIntensive Care Unit, Canberra Hospital, Canberra, Australiaen
dc.identifier.affiliationCardiothoracic and Vascular Intensive Care Unit, Auckland City Hospital, Auckland, New Zealanden
dc.identifier.affiliationDepartment of Critical Care Medicine, Auckland City Hospital, Auckland, New Zealanden
dc.identifier.affiliationIntensive Care Unit, Royal Prince Alfred Hospital, Camperdown, Australiaen
dc.identifier.affiliationGeorge Institute for Global Health, University of New South Wales, Sydney, Australiaen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Society Centre for Outcome and Resource Evaluation, Camberwell, Australiaen
dc.identifier.affiliationIntensive Care Unit, Bankstown Hospital, Bankstown, Australiaen
dc.identifier.affiliationDepartment of Critical Care Medicine, University of Alberta Hospital, Edmonton, Canada-
dc.identifier.affiliationBiostatistics Unit, Monash University, Melbourne, Australiaen
dc.identifier.affiliationIntensive Care Unit, Alfred Hospital, Melbourne, Australiaen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australiaen
dc.identifier.affiliationUniversity College Dublin-Clinical Research Centre, St Vincent's Hospital, Dublin, Irelanden
dc.identifier.affiliationMedical Research Institute of New Zealand, Wellingtonen
dc.identifier.affiliationIntensive Care Unit, Wellington Hospital, Wellington, New Zealanden
dc.identifier.affiliationIntensive Care Unit, Freeman Hospital, Newcastle upon Tyne, England-
dc.identifier.affiliationMedical Research Institute of New Zealand, Wellington-
dc.identifier.affiliationUniversity College Dublin-Clinical Research Centre, St Vincent's Hospital, Dublin, Ireland-
dc.identifier.affiliationMedical Research Institute of New Zealand, Wellington-
dc.identifier.affiliationIntensive Care National Audit and Research Centre, London, England-
dc.identifier.affiliationMedical Research Institute of New Zealand, Wellington-
dc.identifier.affiliationDepartment of Critical Care Medicine, University of Alberta Hospital, Edmonton, Canada-
dc.identifier.affiliationIntensive Care National Audit and Research Centre, London, England-
dc.identifier.doi10.1001/jama.2019.22190-
dc.identifier.orcid0000-0002-1650-8939-
dc.identifier.pubmedid31950977-
dc.type.austinJournal Article-
local.name.researcherBellomo, Rinaldo
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
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