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Randomized Controlled Trial
. 2018 Sep;20(3):182-189.

A cluster randomised, crossover, registry-embedded clinical trial of proton pump inhibitors versus histamine-2 receptor blockers for ulcer prophylaxis therapy in the intensive care unit (PEPTIC study): study protocol

Paul J Young  1 , Sean M Bagshaw  2 , Andrew Forbes  3 , Alistair Nichol  4 , Stephen E Wright  5 , Rinaldo Bellomo  4 , Michael J Bailey  4 , Richard W Beasley  6 , Glenn M Eastwood  7 , Marino Festa  8 , David Gattas  9 , Frank van Haren  10 , Edward Litton  11 , Paul R Mouncey  12 , Leanlove Navarra  6 , David Pilcher  4 , Diane M Mackle  6 , Colin J McArthur  6 , Shay P McGuinness  6 , Manoj K Saxena  13 , Steve Webb  4 , Kathryn M Rowan  12 ; Australian and New Zealand Intensive Care Society Clinical Trials Group on behalf of the PEPTIC investigators
Affiliations
  • PMID: 30153780
Randomized Controlled Trial

A cluster randomised, crossover, registry-embedded clinical trial of proton pump inhibitors versus histamine-2 receptor blockers for ulcer prophylaxis therapy in the intensive care unit (PEPTIC study): study protocol

Paul J Young et al. Crit Care Resusc. 2018 Sep.

Abstract

Background: The balance of risks and benefits with using proton pump inhibitors (PPIs) versus histamine-2 receptor blockers (H2RB) for stress ulcer prophylaxis in patients who are invasively ventilated in the intensive care unit (ICU) is uncertain.

Objective: To describe the study protocol and statistical analysis plan for the Proton Pump Inhibitors versus Histamine-2 Receptor Blockers for Ulcer Prophylaxis Therapy in the Intensive Care Unit (PEPTIC) study.

Design, setting and participants: Protocol for a prospective, multicentre, randomised, open-label, cluster crossover, registry-embedded trial to be conducted in 50 ICUs in Australia, Canada, Ireland, New Zealand and the United Kingdom. The PEPTIC study will compare two approaches to stress ulcer prophylaxis in mechanically ventilated adults implemented at the level of the ICU. One approach is to use PPIs as the default therapy and the other approach is to use H2RBs as the default therapy when stress ulcer prophylaxis is prescribed. Each ICU, by random allocation, will use one approach for 6 months and will then switch to the opposite approach for the next 6 months. The PEPTIC study began recruitment in August 2016 and will complete recruitment in January 2019.

Main outcome measures: The primary end point will be in-hospital mortality. Secondary outcomes include clinically significant upper gastrointestinal bleeding, Clostridium difficile infection, ICU length of stay and hospital length of stay.

Results and conclusions: The PEPTIC study will compare the effect on in-hospital mortality of implementing, at the level of the ICU, the use of PPI as the preferred agent for stress ulcer prophylaxis in mechanically ventilated adults in the ICU with using H2RB as the preferred agent.

Trial registration: Australian and New Zealand Clinical Trials Registry (ANZCTRN 12616000481471).

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