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Effects of dexmedetomidine and propofol on patient-ventilator interaction in difficult-to-wean, mechanically ventilated patients: A prospective, open-label, randomised, multicentre study

Title: Effects of dexmedetomidine and propofol on patient-ventilator interaction in difficult-to-wean, mechanically ventilated patients: A prospective, open-label, randomised, multicentre study
Authors: Conti, Giorgio; Costa, Roberta; Spinazzola, Giorgia; Ferrone, Giuliano; Antonelli, Massimo
Contributors: Conti, Giorgio; Ranieri, Vito Marco; Costa, Roberta; Garratt, Chri; Wighton, Andrew; Spinazzola, Giorgia; Urbino, Rosario; Mascia, Luciana; Ferrone, Giuliano; Pohjanjousi, Pasi; Ferreyra, Gabriela; Antonelli, Massimo
Publisher Information: BioMed Central Ltd.
Publication Year: 2016
Collection: Università Cattolica del Sacro Cuore: PubliCatt
Subject Terms: Dexmedetomidine; Mechanical ventilation; Patient-ventilator synchrony; Propofol; Sedation; Critical Care and Intensive Care Medicine; Settore MED/41 - ANESTESIOLOGIA
Description: Background: Dexmedetomidine can be used for sedation of mechanically ventilated patients and has minor respiratory effects. The aim of this study was to compare the incidence of patient-ventilator dyssynchronies during sedation with dexmedetomidine or propofol. Methods: We conducted a multicentre, prospective, open-label, randomised clinical trial, comparing dexmedetomidine with standard propofol sedation at three intensive care units of university hospitals in Italy. Twenty difficult-to-wean patients for whom the first weaning trial had failed and who were on pressure support ventilation were randomised to receive sedation with either dexmedetomidine or propofol at a similar level of sedation (Richmond Agitation-Sedation Scale [RASS] score +1 to -2). The asynchrony index (AI) was calculated using tracings of airflow, airway pressure and electrical activity of the diaphragm sampled at 0, 0.5, 1, 2, 6, 12, 18 and 24 h. Results: The mean AI was lower with dexmedetomidine than with propofol from 2 h onwards, although the two groups significantly differed only at 12 h (2.68 % vs 9.10 %, p < 0.05). No further difference was observed at 18 and 24 h. Conclusions: When sedation with propofol and dexmedetomidine was compared at similar RASS scores of patients in whom first weaning trial had failed, the AI was lower with dexmedetomidine than with propofol, and this difference was statistically significant at 12 h. These results suggest that sedation with dexmedetomidine may offer some advantages in terms of patient-ventilator synchrony.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/27368279; info:eu-repo/semantics/altIdentifier/wos/WOS:000379589200001; volume:20; issue:1; firstpage:1386; lastpage:1392; numberofpages:7; issueyear:2016; journal:CRITICAL CARE; https://hdl.handle.net/10807/119396; http://ccforum.com/content/17
DOI: 10.1186/s13054-016-1386-2
Availability: https://hdl.handle.net/10807/119396; https://doi.org/10.1186/s13054-016-1386-2; http://ccforum.com/content/17
Rights: info:eu-repo/semantics/openAccess ; license:Creative commons ; license uri:http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.C781DFDB
Database: BASE