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REVISE: re-evaluating the inhibition of stress erosions in the ICU-statistical analysis plan for a randomized trial.
Heels-Ansdell, Diane; Billot, Laurent; Thabane, Lehana; Alhazzani, Waleed; Deane, Adam; Guyatt, Gordon; Finfer, Simon; Lauzier, François; Myburgh, John; Young, Paul; Arabi, Yaseen; Marshall, John; English, Shane; Muscedere, John; Ostermann, Marlies; Venkatesh, Bala; Zytaruk, Nicole; Hardie, Miranda; Hammond, Naomi; Knowles, Serena; Saunders, Lois; Poole, Alexis; Al-Fares, Abdulrahman; Xie, Feng; Hall, Richard; Cook, Deborah.
Afiliación
  • Heels-Ansdell D; Department of Health Research Methods Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Billot L; The George Institute for Global Health, University of New South Wales, University of New South Wales Medicine & Health, Sydney, New South Wales, Australia.
  • Thabane L; Department of Health Research Methods Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Alhazzani W; Department of Health Research Methods Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Deane A; Department of Critical Care, Melbourne Medical School, University of Melbourne, Melbourne, Australia.
  • Guyatt G; Department of Health Research Methods Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Finfer S; Critical Care Division, The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Lauzier F; Division of Critical Care, Department of MedicineDepartment of Anesthesiology and Critical CareFaculty of Medicine, at l`Université LavalLaval UniversityUniversite Laval Faculte de medicine, Quebec, Canada.
  • Myburgh J; Critical Care Division, The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Young P; Medical Research Institute of New Zealand, Wellington, New Zealand.
  • Arabi Y; King Saud bin Abdulaziz University for Health Sciences, Riyad, Saudi Arabia.
  • Marshall J; Department of Surgery and Critical Care Medicine, Unity Health Toronto, University of Toronto, Toronto, Canada.
  • English S; Department of Medicine (Critical Care), Faculty of Medicine, University of Ottawa, Ottawa, Canada.
  • Muscedere J; Department of Critical Care Medicine, Queens University| Kingston Health Sciences Centre, Kingston, Ontario, Canada.
  • Ostermann M; Department of Critical Care, King's College London, London, UK.
  • Venkatesh B; The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Zytaruk N; Department of Health Research Methods Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Hardie M; Academic Critical Care Office Room D176, Critical Care Medicine, St. Joseph's Healthcare Hamilton, 50 Charlton Avenue East, Hamilton, Ontario, Canada.
  • Hammond N; The George Institute for Global Health, Newton, Australia.
  • Knowles S; University of New South Wales, Sydney, New South Wales, Australia.
  • Saunders L; The George Institute for Global Health, Newton, Australia.
  • Poole A; Academic Critical Care Office Room D176, Critical Care Medicine, St. Joseph's Healthcare Hamilton, 50 Charlton Avenue East, Hamilton, Ontario, Canada.
  • Al-Fares A; The University of Adelaide, Adelaide, Australia.
  • Xie F; Interdepartment Division of Critical Care Medicine, University of Toronto, Toronto, Canada.
  • Hall R; Department of Health Research Methods Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Cook D; Dalhousie University Faculty of Medicine, Halifax, Canada.
Trials ; 24(1): 796, 2023 Dec 06.
Article en En | MEDLINE | ID: mdl-38057875
ABSTRACT

BACKGROUND:

The REVISE (Re-Evaluating the Inhibition of Stress Erosions in the ICU) trial will evaluate the impact of the proton pump inhibitor pantoprazole compared to placebo in invasively ventilated critically ill patients.

OBJECTIVE:

To outline the statistical analysis plan for the REVISE trial.

METHODS:

REVISE is a randomized clinical trial ongoing in intensive care units (ICUs) internationally. Patients ≥ 18 years old, receiving invasive mechanical ventilation, and expected to remain ventilated beyond the calendar day after randomization are allocated to either 40 mg pantoprazole intravenously or placebo while mechanically ventilated.

RESULTS:

The primary efficacy outcome is clinically important upper GI bleeding; the primary safety outcome is 90-day mortality. Secondary outcomes are ventilator-associated pneumonia, Clostridioides difficile infection, new renal replacement therapy, ICU and hospital mortality, and patient-important GI bleeding. Tertiary outcomes are total red blood cells transfused, peak serum creatinine concentration, and duration of mechanical ventilation, ICU, and hospital length of stay. Following an interim analysis of results from 2400 patients (50% of 4800 target sample size), the data monitoring committee recommended continuing enrolment.

CONCLUSIONS:

This statistical analysis plan outlines the statistical analyses of all outcomes, sensitivity analyses, and subgroup analyses. REVISE will inform clinical practice and guidelines worldwide. TRIAL REGISTRATION www. CLINICALTRIALS gov NCT03374800. November 21, 2017.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neumonía Asociada al Ventilador / Unidades de Cuidados Intensivos Límite: Adolescent / Adult / Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neumonía Asociada al Ventilador / Unidades de Cuidados Intensivos Límite: Adolescent / Adult / Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Canadá