Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28502
Title: A Phase II Cluster-Crossover Randomized Trial of Fentanyl versus Morphine for Analgosedation in Mechanically Ventilated Patients.
Austin Authors: Casamento, Andrew J;Serpa Neto, Ary ;Young, Marcus ;Lawrence, Mervin;Taplin, Christina;Eastwood, Glenn M ;Ghosh, Angajendra;Bellomo, Rinaldo 
Affiliation: Intensive Care..
Data Analytics Research and Evaluation (DARE) Centre..
Department of Intensive Care, Northern Hospital, Melbourne, Australia..
University of Melbourne, Melbourne, Australia..
Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia..
Department of Medical Education, University of Melbourne, Melbourne, Australia..
Department of Critical Care, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia..
Department of Critical Care Medicine, Hospital Israelita Albert Einstein, Sao Paulo, Brazil..
Issue Date: 1-Dec-2021
Publication information: American journal of respiratory and critical care medicine 2021; 204(11): 1286-1294
Abstract: Rationale: The continuous infusion of fentanyl or morphine is often prescribed to assist with analgesia and sedation (analgosedation) during mechanical ventilation. Objectives: To compare the effect of fentanyl versus morphine on patient-centered outcomes in ventilated patients. Methods: We conducted a cluster-randomized, cluster-crossover trial between July 2019 and August 2020 in two adult ICUs. We compared two continuous infusion regimens (fentanyl versus morphine). One ICU was randomized to the fentanyl-morphine sequence and the other to the morphine-fentanyl sequence. The primary outcome was the number of ventilator-free days at Day 28. Secondary outcomes included, among others, duration of mechanical ventilation in survivors and ICU-free days at Day 28. Measurements and Main Results: Via cluster allocation, we randomized 737 patients. Of these, 56 were excluded because of the opt-out consent process, leaving 681 (344 to fentanyl and 337 to morphine) for primary analysis (median [interquartile range] age, 59 [44-69] years). Median ventilator-free days at Day 28 were 26.1 (20.7-27.3) in the fentanyl versus 25.3 (19.1-27.2) in the morphine group (median difference, 0.79 [95% confidence interval, 0.31 to 1.28], P = 0.001). ICU-free days were greater (P < 0.001) and length of stay in the ICU for survivors shorter (P < 0.001) in the fentanyl group. All other secondary outcomes were not statistically different by treatment group. Conclusions: Among adult patients requiring mechanical ventilation, compared with morphine, fentanyl infusion significantly increased the median number of ventilator-free days at Day 28. The choice of opioid infusion agent may affect clinical outcomes and requires further investigation.
URI: https://ahro.austin.org.au/austinjspui/handle/1/28502
DOI: 10.1164/rccm.202106-1515OC
ORCID: 0000-0001-6289-524X
0000-0002-6195-660X
0000-0002-2067-7276
0000-0002-1650-8939
0000-0003-1520-9387
Journal: American journal of respiratory and critical care medicine
PubMed URL: 34543581
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/34543581/
Type: Journal Article
Subjects: analgesia
fentanyl
mechanical ventilation
morphine
sedation
Appears in Collections:Journal articles

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