Stress ulcer prophylaxis with proton pump inhibitors or histamin-2 receptor antagonists in adult intensive care patients: a systematic review with meta-analysis and trial sequential analysis

  • Marija Barbateskovic*
  • , Søren Marker
  • , Anders Granholm
  • , Carl Thomas Anthon
  • , Mette Krag
  • , Janus Christian Jakobsen
  • , Anders Perner
  • , Jørn Wetterslev
  • , Morten Hylander Møller
  • *Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

Purpose: Most intensive care unit (ICU) patients receive stress ulcer prophylaxis. We present updated evidence on the effects of prophylactic proton pump inhibitors (PPIs) or histamine 2 receptor antagonists (H2RAs) versus placebo/no prophylaxis on patient-important outcomes in adult ICU patients. Methods: We conducted a systematic review with meta-analysis and trial sequential analysis (TSA) of randomised clinical trials assessing the effects of PPI/H2RA versus placebo/no prophylaxis on mortality, gastrointestinal (GI) bleeding, serious adverse events (SAEs), health-related quality of life (HRQoL), myocardial ischemia, pneumonia, and Clostridium (Cl.) difficile enteritis in ICU patients. Results: We identified 42 trials randomising 6899 ICU patients; 3 had overall low risk of bias. We did not find an effect of stress ulcer prophylaxis on mortality [relative risk 1.03, 95% confidence interval (CI) 0.94–1.14; TSA-adjusted CI 0.94–1.14], but the occurrence of any GI bleeding was reduced as compared with placebo/no prophylaxis (0.60, 95% CI 0.47–0.77; TSA-adjusted CI 0.36–1.00). The conventional meta-analysis indicated that clinically important GI bleeding was reduced (RR 0.63, 95% CI 0.48–0.81), but the TSA-adjusted CI 0.35–1.13 indicated lack of firm evidence. The effects of stress ulcer prophylaxis on SAEs, HRQoL, pneumonia, myocardial ischemia and Cl. difficile enteritis are uncertain. Conclusions: In this updated systematic review, we were able to refute a relative change of 20% of mortality. The occurrence of GI bleeding was reduced, but we lack firm evidence for a reduction in clinically important GI bleeding. The effects on SAEs, HRQoL, pneumonia, myocardial ischemia and Cl. difficile enteritis remain inconclusive.

OriginalsprogEngelsk
TidsskriftIntensive Care Medicine
Vol/bind45
Udgave nummer2
Sider (fra-til)143-158
ISSN0342-4642
DOI
StatusUdgivet - 27. feb. 2019

Finansiering

Marija Barbateskovic: PhD student at the Copenhagen Trial Unit and the Centre for Research in Intensive Care. Søren Marker: PhD student at the Department of Intensive Care at Rigshospitalet and the Centre for Research in Intensive Care. Coordinating investigator of the randomised clinical trial ‘Stress Ulcer Prophylaxis in the Intensive Care Unit’(SUP-ICU). Anders Granholm: Coordinating investigator of the SUP-ICU trial. Carl Thomas Anthon: Coordinating investigator of the SUP-ICU trial. Mette Krag: Coordinating investigator of the SUP-ICU trial. Janus Christian Jakobsen: Director of Research, Chief Physician, Department of Cardiology, Holbæk Sygehus, Holbæk, Denmark. Anders Perner: Head of Research at the Department of Intensive Care at Rigshospitalet. The intensive care unit receives support for research from CSL Behring, Fresenius Kabi, Ferring Pharmaceuticals and the Novo Nordisk Foundation. Dr Perner is initiator of the SUP-ICU trial. Jørn Wetterslev: Member of the Copenhagen Trial Unit task force for developing Trial Sequential Analysis theory, manual and software which is presently free-ware at www.ctu.dk/tsa. Dr Wetterslev is member of the SUP-ICU trial steering group. Morten Hylander Møller: Sponsor and initiator of the SUP-ICU trial.

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