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Analgosedation: The Use of Fentanyl Compared to Hydromorphone

BACKGROUND: The 2018 Society of Critical Care Medicine guidelines on the “Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICU” advocate for protocol-based analgosedation practices. There are limited data available to guide wh...

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Autores principales: Choi, Hahnl, Radparvar, Sara, Aitken, Samuel L., Altshuler, Jerry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519389/
https://www.ncbi.nlm.nih.gov/pubmed/34722922
http://dx.doi.org/10.2478/jccm-2021-0026
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author Choi, Hahnl
Radparvar, Sara
Aitken, Samuel L.
Altshuler, Jerry
author_facet Choi, Hahnl
Radparvar, Sara
Aitken, Samuel L.
Altshuler, Jerry
author_sort Choi, Hahnl
collection PubMed
description BACKGROUND: The 2018 Society of Critical Care Medicine guidelines on the “Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICU” advocate for protocol-based analgosedation practices. There are limited data available to guide which analgesic to use. This study compares outcomes in patients who received continuous infusions of fentanyl or hydromorphone as sedative agents in the intensive care setting. METHODS: This retrospective cohort study evaluated patients admitted into the medical intensive care unit, the surgical intensive care unit, and the cardiac intensive care unit from April 1, 2017, to August 1, 2018, who were placed on continuous analgesics. Patients were divided according to receipt of fentanyl or hydromorphone as a continuous infusion as a sedative agent. The primary endpoints were ICU length of stay and time on mechanical ventilation. RESULTS: A total of 177 patients were included in the study; 103 received fentanyl as a continuous infusion, and 74 received hydromorphone as a continuous infusion. Baseline characteristics were similar between groups. Patients in the hydromorphone group had deeper sedation targets. Median ICU length of stay was eight days in the fentanyl group compared to seven days in the hydromorphone group (p = 0.11) and median time on mechanical ventilation was 146.47 hours in the fentanyl group and 122.33 hours in the hydromorphone group (p = 0.31). There were no statistically significant differences in the primary endpoints of ICU length of stay and time on mechanical ventilation between fentanyl and hydromorphone for analgosedation purposes. CONCLUSION: No statistically significant differences were found in the primary endpoints studied. Patients in the hydromorphone group required more tracheostomies, restraints, and were more likely to have a higher proportion of Critical Care Pain Observation Tool (CPOT) scores > 2.
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spelling pubmed-85193892021-10-28 Analgosedation: The Use of Fentanyl Compared to Hydromorphone Choi, Hahnl Radparvar, Sara Aitken, Samuel L. Altshuler, Jerry J Crit Care Med (Targu Mures) Research Article BACKGROUND: The 2018 Society of Critical Care Medicine guidelines on the “Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICU” advocate for protocol-based analgosedation practices. There are limited data available to guide which analgesic to use. This study compares outcomes in patients who received continuous infusions of fentanyl or hydromorphone as sedative agents in the intensive care setting. METHODS: This retrospective cohort study evaluated patients admitted into the medical intensive care unit, the surgical intensive care unit, and the cardiac intensive care unit from April 1, 2017, to August 1, 2018, who were placed on continuous analgesics. Patients were divided according to receipt of fentanyl or hydromorphone as a continuous infusion as a sedative agent. The primary endpoints were ICU length of stay and time on mechanical ventilation. RESULTS: A total of 177 patients were included in the study; 103 received fentanyl as a continuous infusion, and 74 received hydromorphone as a continuous infusion. Baseline characteristics were similar between groups. Patients in the hydromorphone group had deeper sedation targets. Median ICU length of stay was eight days in the fentanyl group compared to seven days in the hydromorphone group (p = 0.11) and median time on mechanical ventilation was 146.47 hours in the fentanyl group and 122.33 hours in the hydromorphone group (p = 0.31). There were no statistically significant differences in the primary endpoints of ICU length of stay and time on mechanical ventilation between fentanyl and hydromorphone for analgosedation purposes. CONCLUSION: No statistically significant differences were found in the primary endpoints studied. Patients in the hydromorphone group required more tracheostomies, restraints, and were more likely to have a higher proportion of Critical Care Pain Observation Tool (CPOT) scores > 2. Sciendo 2021-08-05 /pmc/articles/PMC8519389/ /pubmed/34722922 http://dx.doi.org/10.2478/jccm-2021-0026 Text en © 2021 Hahnl Choi, Sara Radparvar, Samuel L. Aitken, Jerry Altshuler, published by Sciendo https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Research Article
Choi, Hahnl
Radparvar, Sara
Aitken, Samuel L.
Altshuler, Jerry
Analgosedation: The Use of Fentanyl Compared to Hydromorphone
title Analgosedation: The Use of Fentanyl Compared to Hydromorphone
title_full Analgosedation: The Use of Fentanyl Compared to Hydromorphone
title_fullStr Analgosedation: The Use of Fentanyl Compared to Hydromorphone
title_full_unstemmed Analgosedation: The Use of Fentanyl Compared to Hydromorphone
title_short Analgosedation: The Use of Fentanyl Compared to Hydromorphone
title_sort analgosedation: the use of fentanyl compared to hydromorphone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519389/
https://www.ncbi.nlm.nih.gov/pubmed/34722922
http://dx.doi.org/10.2478/jccm-2021-0026
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