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Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography

BACKGROUND: We evaluated whether the addition of a small dose of ketamine or fentanyl would lead to a reduction in the total dose of propofol consumed without compromising the safety and recovery of patients having endoscopic ultrasonography (EUS). METHODS: A total of 210 adult patients undergoing e...

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Autores principales: Singh, Shweta A, Prakash, Kelika, Sharma, Sandeep, Dhakate, Gaurav, Bhatia, Vikram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809707/
https://www.ncbi.nlm.nih.gov/pubmed/29441174
http://dx.doi.org/10.4097/kjae.2018.71.1.43
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author Singh, Shweta A
Prakash, Kelika
Sharma, Sandeep
Dhakate, Gaurav
Bhatia, Vikram
author_facet Singh, Shweta A
Prakash, Kelika
Sharma, Sandeep
Dhakate, Gaurav
Bhatia, Vikram
author_sort Singh, Shweta A
collection PubMed
description BACKGROUND: We evaluated whether the addition of a small dose of ketamine or fentanyl would lead to a reduction in the total dose of propofol consumed without compromising the safety and recovery of patients having endoscopic ultrasonography (EUS). METHODS: A total of 210 adult patients undergoing elective EUS under sedation were included in the study. Patients were randomized into three groups. Patients were premedicated intravenously with normal saline in group 1, 50 µg fentanyl in group 2, and 0.5 mg/kg ketamine in group 3. All patients received intravenous propofol for sedation. Propofol consumption in mg/kg/h was noted. The incidence of hypotension, bradycardia, desaturation, and coughing was noted. The time to achieve a Post Anesthesia Discharge Score (PADS) of 10 was also noted. RESULTS: There were 68 patients in group 1, 70 in group 2, and 72 in group 3. The amount of propofol consumed was significantly higher in group 1 (9.25 [7.3–13.2]) than in group 2 (8.8 [6.8–12.2]) and group 3 (7.6 [5.7–9.8]). Patient hemodynamics and oxygenation were well maintained and comparable in all groups. The time to achieve a PADS of 10 was significantly higher in group 3 compared to the other two groups. CONCLUSIONS: The use of 50 µg fentanyl or 0.5 mg/kg ketamine in a single dose during EUS reduces the dose of propofol required for sedation. However, unlike the addition of fentanyl, the addition of ketamine increased the time to recovery. Thus, 50 µg fentanyl is a good additive to propofol infusion for sedation during EUS to reduce the requirement for propofol without affecting the time to recovery.
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spelling pubmed-58097072018-02-13 Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography Singh, Shweta A Prakash, Kelika Sharma, Sandeep Dhakate, Gaurav Bhatia, Vikram Korean J Anesthesiol Clinical Research Article BACKGROUND: We evaluated whether the addition of a small dose of ketamine or fentanyl would lead to a reduction in the total dose of propofol consumed without compromising the safety and recovery of patients having endoscopic ultrasonography (EUS). METHODS: A total of 210 adult patients undergoing elective EUS under sedation were included in the study. Patients were randomized into three groups. Patients were premedicated intravenously with normal saline in group 1, 50 µg fentanyl in group 2, and 0.5 mg/kg ketamine in group 3. All patients received intravenous propofol for sedation. Propofol consumption in mg/kg/h was noted. The incidence of hypotension, bradycardia, desaturation, and coughing was noted. The time to achieve a Post Anesthesia Discharge Score (PADS) of 10 was also noted. RESULTS: There were 68 patients in group 1, 70 in group 2, and 72 in group 3. The amount of propofol consumed was significantly higher in group 1 (9.25 [7.3–13.2]) than in group 2 (8.8 [6.8–12.2]) and group 3 (7.6 [5.7–9.8]). Patient hemodynamics and oxygenation were well maintained and comparable in all groups. The time to achieve a PADS of 10 was significantly higher in group 3 compared to the other two groups. CONCLUSIONS: The use of 50 µg fentanyl or 0.5 mg/kg ketamine in a single dose during EUS reduces the dose of propofol required for sedation. However, unlike the addition of fentanyl, the addition of ketamine increased the time to recovery. Thus, 50 µg fentanyl is a good additive to propofol infusion for sedation during EUS to reduce the requirement for propofol without affecting the time to recovery. The Korean Society of Anesthesiologists 2018-02 2017-06-14 /pmc/articles/PMC5809707/ /pubmed/29441174 http://dx.doi.org/10.4097/kjae.2018.71.1.43 Text en Copyright © The Korean Society of Anesthesiologists, 2018 http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Article
Singh, Shweta A
Prakash, Kelika
Sharma, Sandeep
Dhakate, Gaurav
Bhatia, Vikram
Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
title Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
title_full Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
title_fullStr Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
title_full_unstemmed Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
title_short Comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
title_sort comparison of propofol alone and in combination with ketamine or fentanyl for sedation in endoscopic ultrasonography
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809707/
https://www.ncbi.nlm.nih.gov/pubmed/29441174
http://dx.doi.org/10.4097/kjae.2018.71.1.43
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