Your browser doesn't support javascript.
loading
Benzodiazepine-Free Cardiac Anesthesia for Reduction of Postoperative Delirium (B-Free): A Protocol for a Multi-centre Randomized Cluster Crossover Trial.
Spence, Jessica; Belley-Côté, Emilie; Jacobsohn, Eric; Lee, Shun Fu; D'Aragon, Frederick; Avidan, Michael; Mazer, C David; Rousseau-Saine, Nicolas; Rajamohan, Raja; Pryor, Kane; Klein, Rael; Tan, Edmund Chong-How; Cameron, Matthew; Di Sante, Emily; DeBorba, Erin; Mustard, Mary; Couture, Etienne; Zamper, Raffael; Law, Michael; Djaiani, George; Saha, Tarit; Choi, Stephen; Hedlin, Peter; Pikaluk, Ryan; Lam, Wing Ying; Deschamps, Alain; Whitlock, Richard; Dulong, Braden; Devereaux, P J; Beaver, Chris; Kloppenburg, Shelley; Oczkowski, Simon; McIntyre, William Finlay; McFarling, Matthew; Lamy, Andre; Vincent, Jessica; Connolly, Stuart.
Afiliación
  • Spence J; Departments of Anesthesia and Critical Care and Health Research Methods, Evaluation, and Impact, McMaster University; and Perioperative Research Division, Population Health Research Institute, Hamilton, Ontario, Canada.
  • Belley-Côté E; Departments of Medicine (Cardiology and Critical Care), and Health Research Methods, Evaluation, and Impact, McMaster University, and Perioperative Research Division, Population Health Research Institute, Hamilton, Ontario, Canada.
  • Jacobsohn E; Departments of Anesthesia and Perioperative Medicine and Medicine (Critical Care), University of Manitoba, Winnipeg, Manitoba, Canada.
  • Lee SF; Department of Health Research Methods, Evaluation, and Impact, McMaster University, and Population Health Research Institute, Hamilton, Ontario, Canada.
  • D'Aragon F; Département d'anesthésiologie, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
  • Avidan M; Department of Anesthesia, Washington University at St. Louis, St. Louis, Missouri, USA.
  • Mazer CD; Department of Anesthesia and Li Ka Shing Knowledge Institute, St. Michael's Hospital, and Department of Anesthesiology and Pain Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Rousseau-Saine N; Département d'anesthésiologie, Université de Montréal, Montréal, Quebec, Canada.
  • Rajamohan R; Department of Anesthesia, University of British Columbia, Vancouver, British Columbia, Canada.
  • Pryor K; Department of Anesthesiology, Weill Cornell Medical College, New York, New York, USA.
  • Klein R; Department of Anesthesia, University of British Columbia, Vancouver, British Columbia, Canada.
  • Tan EC; Department of Anesthesia, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Cameron M; Department of Anesthesia, McGill University, Montreal, Quebec, Canada.
  • Di Sante E; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • DeBorba E; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Mustard M; St. Michael's Hospital, Toronto, Ontario, Canada.
  • Couture E; Département d'anesthésiologie, Université Laval, Quebec City, Quebec, Canada.
  • Zamper R; Department of Anesthesia, University of Western Ontario, London, Ontario, Canada.
  • Law M; Department of Anesthesia, University of British Columbia, Vancouver, British Columbia, Canada.
  • Djaiani G; Department of Anesthesiology and Pain Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Saha T; Department of Anesthesia, Queen's University, Kingston, Ontario, Canada.
  • Choi S; Department of Anesthesiology and Pain Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Hedlin P; Department of Anesthesia, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
  • Pikaluk R; Department of Anesthesia, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
  • Lam WY; Department of Anesthesia, University of Alberta, Edmonton, Alberta, Canada.
  • Deschamps A; Département d'anesthésiologie, Université de Montréal, Montréal, Quebec, Canada.
  • Whitlock R; Departments of Surgery (Cardiac Surgery) and Health Research Methods, Evaluation, and Impact, McMaster University, and Perioperative Research Division, Population Health Research Institute, Hamilton, Ontario, Canada.
  • Dulong B; Department of Anesthesia, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Devereaux PJ; Departments of Medicine (Cardiology and Critical Care), and Health Research Methods, Evaluation, and Impact, McMaster University, and Perioperative Research Division, Population Health Research Institute, Hamilton, Ontario, Canada.
  • Beaver C; Sheridan College, Brampton, Ontario, Canada.
  • Kloppenburg S; Population Health Research Institute, Hamilton, Ontario, Canada.
  • Oczkowski S; Department of Medicine (Critical Care), McMaster University, Hamilton, Ontario, Canada.
  • McIntyre WF; Department of Medicine (Cardiology), McMaster University, and Perioperative Research Division, Population Health Research Institute, Hamilton, Ontario, Canada.
  • McFarling M; Department of Anesthesia, McMaster University, Hamilton, Ontario, Canada.
  • Lamy A; Departments of Surgery (Cardiac Surgery) and Health Research Methods, Evaluation, and Impact, McMaster University, Perioperative Research Division, Population Health Research Institute, Hamilton, Ontario, Canada.
  • Vincent J; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Connolly S; Department of Medicine (Cardiology), McMaster University, and Population Health Research Institute, Hamilton, Ontario, Canada.
CJC Open ; 5(9): 691-699, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37744662
ABSTRACT
Delirium is common after cardiac surgery and is associated with adverse outcomes. Administration of benzodiazepines before and after cardiac surgery is associated with delirium; guidelines recommend minimizing their use. Benzodiazepine administration during cardiac surgery remains common because of its recognized benefits. The Benzodiazepine-Free Cardiac Anesthesia for Reduction of Postoperative Delirium (B-Free) trial is a randomized cluster crossover trial evaluating whether an institutional policy of restricting intraoperative benzodiazepine administration (ie, ≥ 90% of patients do not receive benzodiazepines during cardiac surgery), as compared with a policy of liberal intraoperative benzodiazepine administration (ie, ≥ 90% of patients receive ≥ 0.03 mg/kg midazolam equivalent), reduces delirium. Hospitals performing ≥ 250 cardiac surgeries a year are included if their cardiac anesthesia group agrees to apply both benzodiazepine policies per their randomization, and patients are assessed for postoperative delirium every 12 hours in routine clinical care. Hospitals apply the restricted or liberal benzodiazepine policy during 12 to 18 crossover periods of 4 weeks each. Randomization for all periods takes place in advance of site startup; sites are notified of their allocated policy during the last week of each crossover period. Policies are applied to all patients undergoing cardiac surgery during the trial period. The primary outcome is the incidence of delirium at up to 72 hours after surgery. The B-Free trial will enroll ≥ 18,000 patients undergoing cardiac surgery at 20 hospitals across North America. Delirium is common after cardiac surgery, and benzodiazepines are associated with the occurrence of delirium. The B-Free trial will determine whether an institutional policy restricting the administration of benzodiazepines during cardiac surgery reduces the incidence of delirium after cardiac surgery. Clinicaltrials.gov registration number NCT03928236 (First registered April 26, 2019).
L'état confusionnel est fréquent après une chirurgie cardiaque et il est associé à des complications. L'administration de benzodiazépines avant et après une chirurgie cardiaque est associée à l'état confusionnel; dans les lignes directrices, on recommande de réduire leur utilisation au minimum. L'administration de benzodiazépines pendant une chirurgie cardiaque demeure fréquente, en raison des leurs bienfaits reconnus. L'essai B-Free (Benzodiazepine-Free Cardiac Anesthesia for Reduction of Postoperative Delirium ou l'anesthésie sans benzodiazépine en contexte de chirurgie cardiaque pour la réduction de l'état confusionnel postopératoire) est un essai à répartition aléatoire par grappes et avec permutation, visant à évaluer si une politique institutionnelle de restriction de l'administration peropératoire de benzodiazépines (c.-à-d. que ≥ 90 % des patients ne reçoivent pas de benzodiazépines durant une chirurgie cardiaque) réduit l'état confusionnel, comparativement à une politique d'administration peropératoire libérale de benzodiazépines (c.-à-d. que ≥ 90 % des patients reçoivent ≥ 0,03 mg/kg d'équivalent du midazolam). Des hôpitaux effectuant au moins 250 chirurgies cardiaques par année sont inclus dans l'essai si leurs équipes d'anesthésie cardiaque acceptent d'appliquer les deux politiques relatives aux benzodiazépines en vertu de la répartition aléatoire et si les patients sont évalués toutes les 12 heures, en ce qui a trait à l'état confusionnel postopératoire, dans le cadre des soins cliniques habituels. Les hôpitaux mettent en œuvre la politique d'administration restreinte ou libérale de benzodiazépines durant 12 à 18 périodes de permutation de 4 semaines chacune. La répartition aléatoire de l'ensemble des périodes a lieu avant le début de l'essai à l'hôpital; les établissements sont avisés de la politique qui leur est attribuée au cours de la dernière semaine de chaque période de permutation. Les politiques sont appliquées à tous les patients qui subissent une chirurgie cardiaque durant la période de l'essai. Le critère d'évaluation principal est l'incidence de l'état confusionnel dans les 72 heures suivant l'intervention chirurgicale. L'étude B-Free inclura au moins 18 000 patients qui subiront une chirurgie cardiaque dans 20 hôpitaux en l'Amérique du Nord. L'état confusionnel est fréquent après une chirurgie cardiaque, et les benzodiazépines sont associées à la survenue de l'état confusionnel. L'essai B-Free permettra de déterminer si une politique institutionnelle de restriction de l'administration de benzodiazépines durant une chirurgie cardiaque réduit l'incidence de l'état confusionnel après une telle chirurgie.Clinicaltrials.gov registration number NCT03928236 (First registered April 26, 2019).

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Guideline Idioma: En Revista: CJC Open Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Guideline Idioma: En Revista: CJC Open Año: 2023 Tipo del documento: Article País de afiliación: Canadá