Effect 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.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
18 02 2020
Historique:
pubmed: 18 1 2020
medline: 9 10 2020
entrez: 18 1 2020
Statut: ppublish

Résumé

Proton 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.

Identifiants

pubmed: 31950977
pii: 2759412
doi: 10.1001/jama.2019.22190
pmc: PMC7029750
doi:

Substances chimiques

Histamine H2 Antagonists 0
Proton Pump Inhibitors 0

Types de publication

Comparative Study Journal Article Multicenter Study Pragmatic Clinical Trial Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

616-626

Subventions

Organisme : CIHR
Pays : Canada

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

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Auteurs

Paul J Young (PJ)

Medical Research Institute of New Zealand, Wellington.
Intensive Care Unit, Wellington Hospital, Wellington, New Zealand.

Sean M Bagshaw (SM)

Department of Critical Care Medicine, University of Alberta Hospital, Edmonton, Canada.

Andrew B Forbes (AB)

Biostatistics Unit, Monash University, Melbourne, Australia.

Alistair D Nichol (AD)

Intensive Care Unit, Alfred Hospital, Melbourne, Australia.
Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia.
University College Dublin-Clinical Research Centre, St Vincent's Hospital, Dublin, Ireland.

Stephen E Wright (SE)

Intensive Care Unit, Freeman Hospital, Newcastle upon Tyne, England.

Michael Bailey (M)

Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia.
University of Melbourne, Melbourne, Australia.

Rinaldo Bellomo (R)

Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia.
University of Melbourne, Melbourne, Australia.
Intensive Care Unit, Austin Hospital, Heidelberg, Australia.

Richard Beasley (R)

Medical Research Institute of New Zealand, Wellington.

Kathy Brickell (K)

University College Dublin-Clinical Research Centre, St Vincent's Hospital, Dublin, Ireland.

Glenn M Eastwood (GM)

Intensive Care Unit, Austin Hospital, Heidelberg, Australia.

David J Gattas (DJ)

Intensive Care Unit, Royal Prince Alfred Hospital, Camperdown, Australia.
George Institute for Global Health, University of New South Wales, Sydney, Australia.

Frank van Haren (F)

Intensive Care Unit, Canberra Hospital, Canberra, Australia.

Edward Litton (E)

Intensive Care Unit, Fiona Stanley Hospital, Murdoch, Australia.

Diane M Mackle (DM)

Medical Research Institute of New Zealand, Wellington.

Colin J McArthur (CJ)

Medical Research Institute of New Zealand, Wellington.
Department of Critical Care Medicine, Auckland City Hospital, Auckland, New Zealand.

Shay P McGuinness (SP)

Medical Research Institute of New Zealand, Wellington.
Cardiothoracic and Vascular Intensive Care Unit, Auckland City Hospital, Auckland, New Zealand.

Paul R Mouncey (PR)

Intensive Care National Audit and Research Centre, London, England.

Leanlove Navarra (L)

Medical Research Institute of New Zealand, Wellington.

Dawn Opgenorth (D)

Department of Critical Care Medicine, University of Alberta Hospital, Edmonton, Canada.

David Pilcher (D)

Intensive Care Unit, Alfred Hospital, Melbourne, Australia.
Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia.
Australian and New Zealand Intensive Care Society Centre for Outcome and Resource Evaluation, Camberwell, Australia.

Manoj K Saxena (MK)

George Institute for Global Health, University of New South Wales, Sydney, Australia.
Intensive Care Unit, Bankstown Hospital, Bankstown, Australia.

Steve A Webb (SA)

Intensive Care Unit, Royal Perth Hospital, Perth, Australia.

Daisy Wiley (D)

Intensive Care National Audit and Research Centre, London, England.

Kathryn M Rowan (KM)

Intensive Care National Audit and Research Centre, London, England.

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Classifications MeSH