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The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study

BACKGROUND: Nefopam is a non-opioid, non-steroidal, centrally acting analgesic drug. The concomitant use of opioids and nefopam is believed to have many advantages over the administration of opioids alone for postoperative pain management. We conducted a randomized, double-blind study to determine t...

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Autores principales: Moon, Jee Youn, Choi, Sang Sik, Lee, Shin Young, Lee, Mi Kyung, Kim, Jung Eun, Lee, Ji Eun, Lee, So Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pain Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837116/
https://www.ncbi.nlm.nih.gov/pubmed/27103966
http://dx.doi.org/10.3344/kjp.2016.29.2.110
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author Moon, Jee Youn
Choi, Sang Sik
Lee, Shin Young
Lee, Mi Kyung
Kim, Jung Eun
Lee, Ji Eun
Lee, So Hyun
author_facet Moon, Jee Youn
Choi, Sang Sik
Lee, Shin Young
Lee, Mi Kyung
Kim, Jung Eun
Lee, Ji Eun
Lee, So Hyun
author_sort Moon, Jee Youn
collection PubMed
description BACKGROUND: Nefopam is a non-opioid, non-steroidal, centrally acting analgesic drug. The concomitant use of opioids and nefopam is believed to have many advantages over the administration of opioids alone for postoperative pain management. We conducted a randomized, double-blind study to determine the fentanyl-sparing effect of co-administration of nefopam with fentanyl for postoperative pain management via patient controlled analgesia (PCA). METHODS: Ninety female patients who underwent laparoscopic total hysterectomy under general anesthesia were randomized into 3 groups, Group A, fentanyl 1,000 µg; Group B, fentanyl 500 µg + nefopam 200 mg; and Group C, fentanyl 500 µg + nefopam 400 mg, in a total volume of 100 ml PCA to be administered over the first 48 h postoperatively without basal infusion. The primary outcome was total fentanyl consumption during 48 h; secondary outcomes included pain scores and incidence of side effects. RESULTS: Eighty-one patients were included in the analysis. The overall fentanyl-sparing effects of PCA with concomitant administration of nefopam during the first 48 h postoperatively were 54.5% in Group B and 48.9% group C. Fentanyl use was not significantly different between Groups B and C despite the difference in the nefopam dose. There were no differences among the three groups in terms of PCA-related side effects, although the overall sedation score of Group B was significantly lower than that of Group A. CONCLUSIONS: The concomitant administration of nefopam with fentanyl for postoperative pain management may allow reduction of fentanyl dose, thereby reducing the risk of opioid-related adverse effects.
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spelling pubmed-48371162016-04-21 The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study Moon, Jee Youn Choi, Sang Sik Lee, Shin Young Lee, Mi Kyung Kim, Jung Eun Lee, Ji Eun Lee, So Hyun Korean J Pain Original Article BACKGROUND: Nefopam is a non-opioid, non-steroidal, centrally acting analgesic drug. The concomitant use of opioids and nefopam is believed to have many advantages over the administration of opioids alone for postoperative pain management. We conducted a randomized, double-blind study to determine the fentanyl-sparing effect of co-administration of nefopam with fentanyl for postoperative pain management via patient controlled analgesia (PCA). METHODS: Ninety female patients who underwent laparoscopic total hysterectomy under general anesthesia were randomized into 3 groups, Group A, fentanyl 1,000 µg; Group B, fentanyl 500 µg + nefopam 200 mg; and Group C, fentanyl 500 µg + nefopam 400 mg, in a total volume of 100 ml PCA to be administered over the first 48 h postoperatively without basal infusion. The primary outcome was total fentanyl consumption during 48 h; secondary outcomes included pain scores and incidence of side effects. RESULTS: Eighty-one patients were included in the analysis. The overall fentanyl-sparing effects of PCA with concomitant administration of nefopam during the first 48 h postoperatively were 54.5% in Group B and 48.9% group C. Fentanyl use was not significantly different between Groups B and C despite the difference in the nefopam dose. There were no differences among the three groups in terms of PCA-related side effects, although the overall sedation score of Group B was significantly lower than that of Group A. CONCLUSIONS: The concomitant administration of nefopam with fentanyl for postoperative pain management may allow reduction of fentanyl dose, thereby reducing the risk of opioid-related adverse effects. The Korean Pain Society 2016-04 2016-04-01 /pmc/articles/PMC4837116/ /pubmed/27103966 http://dx.doi.org/10.3344/kjp.2016.29.2.110 Text en Copyright © The Korean Pain Society, 2016 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 Original Article
Moon, Jee Youn
Choi, Sang Sik
Lee, Shin Young
Lee, Mi Kyung
Kim, Jung Eun
Lee, Ji Eun
Lee, So Hyun
The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study
title The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study
title_full The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study
title_fullStr The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study
title_full_unstemmed The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study
title_short The Effect of Nefopam on Postoperative Fentanyl Consumption: A Randomized, Double-blind Study
title_sort effect of nefopam on postoperative fentanyl consumption: a randomized, double-blind study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837116/
https://www.ncbi.nlm.nih.gov/pubmed/27103966
http://dx.doi.org/10.3344/kjp.2016.29.2.110
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