Early post-operative cognitive dysfunction after closed-loop versus manual target controlled-infusion of propofol and remifentanil in patients undergoing elective major non-cardiac surgery Protocol of the randomized controlled single-blind POCD-ELA trial

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TitreEarly post-operative cognitive dysfunction after closed-loop versus manual target controlled-infusion of propofol and remifentanil in patients undergoing elective major non-cardiac surgery Protocol of the randomized controlled single-blind POCD-ELA trial
Type de publicationJournal Article
Year of Publication2018
AuteursBesch G, Vettoretti L, Claveau M, Boichut N, Mahr N, Bouhake Y, Liu N, Chazot T, Samain E, Pili-Floury S
JournalMEDICINE
Volume97
Paginatione12558
Date PublishedOCT
Type of ArticleArticle
ISSN0025-7974
Mots-clés(MeSH terms) cognitive dysfunction, anesthesia, bispectral index, consciousness monitor, general, intravenous, monitor
Résumé

Introduction: Post-operative cognitive dysfunction (POCD) is frequent in patients older than 60 years undergoing major non-cardiac surgery, and increases both morbidity and mortality. Anesthetic drugs may exert neurotoxic effects and contribute to the genesis of POCD. The hypothesis of the POCD-ELA trial was that closed-loop target-controlled infusion of propofol and remifentanil could reduce the occurrence of POCD by decreasing the risk of excessive depth of anesthesia and the dose of anesthetic drugs. Methods and analysis: We designed a single-center, single-blind, randomized, controlled, parallel trial and aim to include 204 patients aged >60 years undergoing elective major non-cardiac surgery. Patients will be randomized to receive closed-loop versus manual target-controlled infusion of propofol and remifentanil guided by bispectral index monitoring. Cognitive assessment will be performed the day before surgery (baseline) and within 72hours after surgery, using a battery of validated neuropsychological tests. The primary outcome is the incidence of POCD within 72hours after surgery. POCD is defined as a Z-score value >1.96 for at least 2 different tests or a Z-score composite value > 1.96. The calculation of the Z-score is based on data from an age-matched control population who did not undergo surgery or general anesthesia. Ethics and dissemination: This study was approved by the Ethics Committee (Comite de Protection des Personnes Est-II) and authorized by the French Health Products Agency (Agence Nationale de Securite des Medicaments, Saint-Denis, France). The University Hospital of Besancon is the trial sponsor and the holder of all data and publication rights. Results of the study will be submitted for publication in a peer-review international medical journal and for presentation in abstract (oral or poster) in international peer-reviewed congresses.

DOI10.1097/MD.0000000000012558