Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Hydromorphone Compared to Fentanyl in Patients Receiving Extracorporeal Membrane Oxygenation

View through CrossRef
Fentanyl is commonly used in critically ill patients receiving extracorporeal membrane oxygenation (ECMO). Fentanyl’s lipophilicity and protein binding may contribute to a sequestration of the drug in the ECMO circuit. Hydromorphone lacks these characteristics potentially leading to a more predictable drug delivery and improved pain and sedation management among ECMO patients. This study compared hydromorphone to fentanyl in patients receiving ECMO. This retrospective study included adult patients receiving ECMO for ≥48 hours. Patients were excluded if they required neuromuscular blockade, received both fentanyl and hydromorphone during therapy, or had opioid use before hospitalization. Baseline characteristics included patient demographics, ECMO indication and settings, and details regarding mechanical ventilation. The primary outcome was opioid requirements at 48 hours post cannulation described in morphine milligram equivalent (MME). Secondary endpoints included 24-hour opioid requirements, concurrent sedative use, and differences in pain and sedation scores. No differences were noted between the patients receiving fentanyl (n = 32) or hydromorphone (n = 20). Patients receiving hydromorphone required lower MME compared to fentanyl at 24 hours (88 [37–121] vs. 131 [137–227], p < 0.01) and 48 hours (168 [80–281] vs. 325 [270–449], p < 0.01). The proportion of within-goal pain and sedation scores between groups was similar at 24 and 48 hours. Sedative requirements did not differ between the groups. Patients receiving hydromorphone required less MME compared to fentanyl without any differences in sedative requirements, or agitation-sedation scores at 48 hours. Prospective studies should be completed to validate these findings.
Title: Hydromorphone Compared to Fentanyl in Patients Receiving Extracorporeal Membrane Oxygenation
Description:
Fentanyl is commonly used in critically ill patients receiving extracorporeal membrane oxygenation (ECMO).
Fentanyl’s lipophilicity and protein binding may contribute to a sequestration of the drug in the ECMO circuit.
Hydromorphone lacks these characteristics potentially leading to a more predictable drug delivery and improved pain and sedation management among ECMO patients.
This study compared hydromorphone to fentanyl in patients receiving ECMO.
This retrospective study included adult patients receiving ECMO for ≥48 hours.
Patients were excluded if they required neuromuscular blockade, received both fentanyl and hydromorphone during therapy, or had opioid use before hospitalization.
Baseline characteristics included patient demographics, ECMO indication and settings, and details regarding mechanical ventilation.
The primary outcome was opioid requirements at 48 hours post cannulation described in morphine milligram equivalent (MME).
Secondary endpoints included 24-hour opioid requirements, concurrent sedative use, and differences in pain and sedation scores.
No differences were noted between the patients receiving fentanyl (n = 32) or hydromorphone (n = 20).
Patients receiving hydromorphone required lower MME compared to fentanyl at 24 hours (88 [37–121] vs.
131 [137–227], p < 0.
01) and 48 hours (168 [80–281] vs.
325 [270–449], p < 0.
01).
The proportion of within-goal pain and sedation scores between groups was similar at 24 and 48 hours.
Sedative requirements did not differ between the groups.
Patients receiving hydromorphone required less MME compared to fentanyl without any differences in sedative requirements, or agitation-sedation scores at 48 hours.
Prospective studies should be completed to validate these findings.

Related Results

Venoarterial extracorporeal membrane oxygenation in adult patients: predictors of mortality
Venoarterial extracorporeal membrane oxygenation in adult patients: predictors of mortality
Background: Extracorporeal membrane oxygenation is a cardiopulmonary supportive therapy. In this study, we reviewed our experience with extracorporeal membrane oxygenation support ...
Neuroinflammation and Neurometabolomic Profiling in Fentanyl Overdose Mouse Model Treated with Novel β-Lactam, MC-100093, and Ceftriaxone
Neuroinflammation and Neurometabolomic Profiling in Fentanyl Overdose Mouse Model Treated with Novel β-Lactam, MC-100093, and Ceftriaxone
Opioid-related deaths are attributed to overdoses, and fentanyl overdose has been on the rise in many parts of the world, including the USA. Glutamate transporter 1 (GLT-1) has bee...
Procedure for Western blot v1
Procedure for Western blot v1
Goal: This document has the objective of standardizing the protocol for Western blot. This technique allows the detection of specific proteins separated on polyacrylamide gel and t...
Opioid antagonism in fentanyl antinociception experimental
Opioid antagonism in fentanyl antinociception experimental
Among the most commonly used drugs to reduce pain and inflammation are nonsteroidal anti-inflammatory drugs (NSAIDs) and opioids. Opioids are a wide group of drugs including fentan...
Liver Metabolomics and Inflammatory Profiles in Mouse Model of Fentanyl Overdose Treated with Beta-Lactams
Liver Metabolomics and Inflammatory Profiles in Mouse Model of Fentanyl Overdose Treated with Beta-Lactams
Fentanyl is a highly potent opioid analgesic that is approved medically to treat acute and chronic pain. There is a high potential for overdose-induced organ toxicities, including ...

Back to Top