Objective: To determine the effect of remifentanil infusion on the minimum alveolar concentration of sevoflurane preventing movement (SEVOMAC) and bispectral index (BIS) in dogs.
Study Design: Prospective, unmasked study.
Animals: A total of 10 adult Beagle dogs weighing 9.0 ± 1.1 kg.
Methods: Dogs were anesthetized with sevoflurane and baseline SEVOMAC was determined. Remifentanil was infused at 5, 10 and 20 μg kg hour, in sequence, with 20 minutes washout between infusions. Variables monitored throughout anesthesia included heart rate (HR), oscillometric blood pressure, end-tidal partial pressure of carbon dioxide, end-tidal sevoflurane concentration (Fe'Sevo) and BIS. SEVOMAC after remifentanil infusion (SEVOMAC) determination started 20 minutes after the start of each infusion. Venous blood samples were collected for plasma remifentanil concentration determination at baseline, SEVOMAC determination time points, and 20 minutes after each infusion was stopped. A mixed model analysis was used to determine the effect of remifentanil infusion on response variables. The relationships between BIS and Fe'Sevo, plasma remifentanil concentrations and the percentage decrease in baseline SEVOMAC were evaluated (p < 0.05).
Results: The overall SEVOMAC at baseline was 2.47 ± 0.11%. Addition of remifentanil at all infusion rates significantly decreased SEVOMAC, but the medium and high doses resulted in significantly greater decreases in SEVOMAC than the lower dose. There was no difference in SEVOMAC percentage change between infusions 10 and 20 μg kg hour. Plasma remifentanil concentrations were significantly different in all infusion rates. Baseline BIS value was 70 ± 1 and was lower than the BIS values recorded during all remifentanil infusions. BIS values were not significantly different among infusion rates. HR was lower and mean arterial pressure was higher during remifentanil infusions than at baseline.
Conclusions And Clinical Relevance: All remifentanil infusions decreased SEVOMAC in dogs. Remifentanil infusion at any rate studied did not reduce BIS values.
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http://dx.doi.org/10.1016/j.vaa.2022.12.004 | DOI Listing |
Br J Anaesth
January 2025
Department of Anesthesiology, Duke University School of Medicine, Durham, NC, USA; Bermaride LLC, Durham, NC, USA. Electronic address:
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Anesthesiology and Pain and Palliative Medicine, Radboud University Medical Center, Nijmegen, NLD.
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January 2025
Takeda Development Center Americas, Inc., Lexington, MA, USA.
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Department of Anaesthesia and Intensive care, Odense university hospital, 5000 Odense, Denmark.
Breast cancer surgeries offer challenges in perioperative pain management, especially in the presence of inherent risk of postoperative nausea and vomiting (PONV) and postmastectomy pain syndrome (PMPS). Inappropriate opioid consumption was speculated as one of the reasons. Through this study, the influence of objective pain monitoring through a nociception level monitor (NOL) on perioperative course in breast surgeries was investigated.
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December 2024
Department of Anesthesiology and Reanimation, Ankara Bilkent City Hospital, Ankara 06800, Turkey.
Postoperative delirium is a frequent complication in children undergoing general anesthesia. It has been suggested that inflammation and oxidative stress contribute to the pathophysiology of delirium. The aim of our study was to investigate the relationship between inflammatory markers and delirium.
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