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Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial
Objective: This prospective study evaluated the 50% effective dose (ED(50)) and 95% effective dose (ED(95)) of nalbuphine combined with propofol during painless gastroscopy. Methods: Seventy-five patients who underwent painless gastroscopy were randomly divided into five groups (group N(0), N(0.05),...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672217/ https://www.ncbi.nlm.nih.gov/pubmed/34924999 http://dx.doi.org/10.3389/fphar.2021.673550 |
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author | Li, Shuangfeng Wang, Ying Chen, Xiaojian Huang, Tingwan Li, Na |
author_facet | Li, Shuangfeng Wang, Ying Chen, Xiaojian Huang, Tingwan Li, Na |
author_sort | Li, Shuangfeng |
collection | PubMed |
description | Objective: This prospective study evaluated the 50% effective dose (ED(50)) and 95% effective dose (ED(95)) of nalbuphine combined with propofol during painless gastroscopy. Methods: Seventy-five patients who underwent painless gastroscopy were randomly divided into five groups (group N(0), N(0.05), N(0.1), N(0.15,) and N(0.2)), with doses of 0, 0.05, 0.1, 0.15, or 0.2 mg/kg nalbuphine in each group. Propofol was given to all groups as the sedative. The bispectral index (BIS) value, propofol dose, examination time, and awakening time were recorded. The number of patients with intolerance indexes (coughing, retching, swallowing, or limb movement) was recorded in each group. The ED(50)/ED(95) of nalbuphine combined with propofol for gastroscopy were calculated. Results: Compared with those of groups N(0), N(0.05), or N(0.1), the propofol dose and awakening time were significantly reduced in group N(0.15) or N(0.2) (p < 0.05). The successful rate of painless gastroscopy in group N(0.15) or N(0.2) significantly increased compared to that of group N(0) or N(0.05) (p < 0.05). When combined with propofol, nalbuphine had an ED(50) and ED(95) for painless gastroscopy of 0.078 mg/kg (95% CI, 0.056–0.098 mg/kg) and 0.162 mg/kg (95% CI, 0.134–0.217 mg/kg), respectively. Conclusion: The ED(50)/ED(95) of nalbuphine combined with propofol are 0.078 and 0.162 mg/kg, respectively, for painless gastroscopy. Nalbuphine at 0.162 mg/kg combined with propofol is effective and safe for painless gastroscopy in adults. |
format | Online Article Text |
id | pubmed-8672217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86722172021-12-16 Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial Li, Shuangfeng Wang, Ying Chen, Xiaojian Huang, Tingwan Li, Na Front Pharmacol Pharmacology Objective: This prospective study evaluated the 50% effective dose (ED(50)) and 95% effective dose (ED(95)) of nalbuphine combined with propofol during painless gastroscopy. Methods: Seventy-five patients who underwent painless gastroscopy were randomly divided into five groups (group N(0), N(0.05), N(0.1), N(0.15,) and N(0.2)), with doses of 0, 0.05, 0.1, 0.15, or 0.2 mg/kg nalbuphine in each group. Propofol was given to all groups as the sedative. The bispectral index (BIS) value, propofol dose, examination time, and awakening time were recorded. The number of patients with intolerance indexes (coughing, retching, swallowing, or limb movement) was recorded in each group. The ED(50)/ED(95) of nalbuphine combined with propofol for gastroscopy were calculated. Results: Compared with those of groups N(0), N(0.05), or N(0.1), the propofol dose and awakening time were significantly reduced in group N(0.15) or N(0.2) (p < 0.05). The successful rate of painless gastroscopy in group N(0.15) or N(0.2) significantly increased compared to that of group N(0) or N(0.05) (p < 0.05). When combined with propofol, nalbuphine had an ED(50) and ED(95) for painless gastroscopy of 0.078 mg/kg (95% CI, 0.056–0.098 mg/kg) and 0.162 mg/kg (95% CI, 0.134–0.217 mg/kg), respectively. Conclusion: The ED(50)/ED(95) of nalbuphine combined with propofol are 0.078 and 0.162 mg/kg, respectively, for painless gastroscopy. Nalbuphine at 0.162 mg/kg combined with propofol is effective and safe for painless gastroscopy in adults. Frontiers Media S.A. 2021-12-01 /pmc/articles/PMC8672217/ /pubmed/34924999 http://dx.doi.org/10.3389/fphar.2021.673550 Text en Copyright © 2021 Li, Wang, Chen, Huang and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Shuangfeng Wang, Ying Chen, Xiaojian Huang, Tingwan Li, Na Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial |
title | Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial |
title_full | Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial |
title_fullStr | Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial |
title_full_unstemmed | Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial |
title_short | Effective Doses of Nalbuphine Combined With Propofol for Painless Gastroscopy in Adults: A Randomized Controlled Trial |
title_sort | effective doses of nalbuphine combined with propofol for painless gastroscopy in adults: a randomized controlled trial |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672217/ https://www.ncbi.nlm.nih.gov/pubmed/34924999 http://dx.doi.org/10.3389/fphar.2021.673550 |
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