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Study protocol for a randomized controlled trial of Proportional Assist Ventilation for Minimizing the Duration of Mechanical Ventilation: the PROMIZING study.
Bosma, Karen J; Martin, Claudio M; Burns, Karen E A; Mancebo Cortes, Jordi; Suárez Montero, Juan Carlos; Skrobik, Yoanna; Thorpe, Kevin E; Amaral, Andre Carlos Kajdacsy-Balla; Arabi, Yaseen; Basmaji, John; Beduneau, Gaëtan; Beloncle, Francois; Carteaux, Guillaume; Charbonney, Emmanuel; Demoule, Alexandre; Dres, Martin; Fanelli, Vito; Geagea, Anna; Goligher, Ewan; Lellouche, François; Maraffi, Tommaso; Mercat, Alain; Rodriguez, Pablo O; Shahin, Jason; Sibley, Stephanie; Spadaro, Savino; Vaporidi, Katerina; Wilcox, M Elizabeth; Brochard, Laurent.
  • Bosma KJ; Division of Critical Care, Department of Medicine, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada. KarenJ.Bosma@lhsc.on.ca.
  • Martin CM; Lawson Health Research Institute, London Health Sciences Centre, London, ON, Canada. KarenJ.Bosma@lhsc.on.ca.
  • Burns KEA; Division of Critical Care, Department of Medicine, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.
  • Mancebo Cortes J; Lawson Health Research Institute, London Health Sciences Centre, London, ON, Canada.
  • Suárez Montero JC; Interdepartmental Division of Critical Care, University of Toronto, Toronto, ON, Canada.
  • Skrobik Y; Division of Critical Care, Unity Health Toronto - St. Michael's Hospital, Toronto, ON, Canada.
  • Thorpe KE; Intensive Care Department, Hospital Universitari Sant Pau, Barcelona, Spain.
  • Amaral ACK; Intensive Care Department, Hospital Universitari Sant Pau, Barcelona, Spain.
  • Arabi Y; Department of Medicine, McGill University, Québec, Canada.
  • Basmaji J; Dalla Lana School of Public Health, Biostatistics Division, University of Toronto, Toronto, ON, Canada.
  • Beduneau G; Applied Health Research Centre (AHRC), Li Ka Shing Knowledge Institute of St. Michael's Hospital, Toronto, Canada.
  • Beloncle F; Interdepartmental Division of Critical Care, University of Toronto, Toronto, ON, Canada.
  • Carteaux G; Department of Critical Care Medicine, Sunnybrook Health Sciences Centre, 2075 Bayview Ave, Toronto, ON, Canada.
  • Charbonney E; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Kingdom of Saudi Arabia.
  • Demoule A; Division of Critical Care, Department of Medicine, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.
  • Dres M; Lawson Health Research Institute, London Health Sciences Centre, London, ON, Canada.
  • Fanelli V; Medical Intensive Care Unit, Normandie Univ, UNIROUEN, EA 3830, Rouen University Hospital, 76000, Rouen, France.
  • Geagea A; Medical Intensive Care Department, Angers University Hospital, Angers, France.
  • Goligher E; Service de Médecine Intensive Réanimation, Assistance Publique-Hôpitaux de Paris, CHU Henri Mondor-Albert Chenevier, Creteil, France.
  • Lellouche F; Centre Hospitalier de l'Université de Montréal (CHUM) and Hôpital du Sacré-Coeur de Montréal, Montreal, QC, Canada.
  • Maraffi T; Service de Médecine intensive - Réanimation Département, Hôpital Universitaire Pitié-Salpêtrière and Sorbonne Université Médecine, Paris, France.
  • Mercat A; Service de Médecine intensive - Réanimation Département, Hôpital Universitaire Pitié-Salpêtrière and Sorbonne Université Médecine, Paris, France.
  • Rodriguez PO; Department of Surgical Sciences, University of Turin, Turin, Italy.
  • Shahin J; Department of Anaesthesia, Critical Care and Emergency - Città della Salute e della Scienza Hospital - University of Turin, Turin, Italy.
  • Sibley S; Division of Critical Care Medicine, Department of Medicine, North York General Hospital, Toronto, ON, Canada.
  • Spadaro S; Interdepartmental Division of Critical Care, University of Toronto, Toronto, ON, Canada.
  • Vaporidi K; Department of Medicine, Toronto General Hospital, Toronto, ON, Canada.
  • Wilcox ME; Centre de recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ) - Université Laval, Québec City, QC, Canada.
  • Brochard L; Intensive Care Unit, Hôpital Intercommunal de Créteil, Créteil, France.
Trials ; 24(1): 232, 2023 Mar 27.
Article en En | MEDLINE | ID: mdl-36973743
BACKGROUND: Proportional assist ventilation with load-adjustable gain factors (PAV+) is a mechanical ventilation mode that delivers assistance to breathe in proportion to the patient's effort. The proportional assistance, called the gain, can be adjusted by the clinician to maintain the patient's respiratory effort or workload within a normal range. Short-term and physiological benefits of this mode compared to pressure support ventilation (PSV) include better patient-ventilator synchrony and a more physiological response to changes in ventilatory demand. METHODS: The objective of this multi-centre randomized controlled trial (RCT) is to determine if, for patients with acute respiratory failure, ventilation with PAV+ will result in a shorter time to successful extubation than with PSV. This multi-centre open-label clinical trial plans to involve approximately 20 sites in several continents. Once eligibility is determined, patients must tolerate a short-term PSV trial and either (1) not meet general weaning criteria or (2) fail a 2-min Zero Continuous Positive Airway Pressure (CPAP) Trial using the rapid shallow breathing index, or (3) fail a spontaneous breathing trial (SBT), in this sequence. Then, participants in this study will be randomized to either PSV or PAV+ in a 1:1 ratio. PAV+ will be set according to a target of muscular pressure. The weaning process will be identical in the two arms. Time to liberation will be the primary outcome; ventilator-free days and other outcomes will be measured. DISCUSSION: Meta-analyses comparing PAV+ to PSV suggest PAV+ may benefit patients and decrease healthcare costs but no powered study to date has targeted the difficult to wean patient population most likely to benefit from the intervention, or used consistent timing for the implementation of PAV+. Our enrolment strategy, primary outcome measure, and liberation approaches may be useful for studying mechanical ventilation and weaning and can offer important results for patients. TRIAL REGISTRATION: ClinicalTrials.gov NCT02447692 . Prospectively registered on May 19, 2015.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Respiración Artificial / Soporte Ventilatorio Interactivo Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Respiración Artificial / Soporte Ventilatorio Interactivo Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article