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Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty

BACKGROUND: The purpose of this study was to assess the efficacy of duloxetine as an alternative to opioid treatment for postoperative pain management following total knee arthroplasty (TKA). METHODS: Among 944 patients, 290 (30.7%) of patients received opioid or duloxetine for pain control for 6 we...

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Autores principales: Kim, Man Soo, Koh, In Jun, Choi, Keun Young, Yang, Sung Cheol, In, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253394/
https://www.ncbi.nlm.nih.gov/pubmed/34214098
http://dx.doi.org/10.1371/journal.pone.0253641
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author Kim, Man Soo
Koh, In Jun
Choi, Keun Young
Yang, Sung Cheol
In, Yong
author_facet Kim, Man Soo
Koh, In Jun
Choi, Keun Young
Yang, Sung Cheol
In, Yong
author_sort Kim, Man Soo
collection PubMed
description BACKGROUND: The purpose of this study was to assess the efficacy of duloxetine as an alternative to opioid treatment for postoperative pain management following total knee arthroplasty (TKA). METHODS: Among 944 patients, 290 (30.7%) of patients received opioid or duloxetine for pain control for 6 weeks when the pain Visual Analogue Scale (VAS) score was greater than 4 out of 10 at the time of discharge. 121 patients in the Opioid group and 118 in the Duloxetine group were followed up for more than one year. Preoperative and postoperative patient reported outcome measures (pain VAS score, Western Ontario and McMaster Universities OA Index (WOMAC) score were compared. The rate of further drug prescription (opioid or duloxetine) after 6 weeks of first prescription, 30-day readmission rate, and side effects were also investigated. RESULTS: There was no significant difference in pain VAS score, WOMAC Pain and Function score, at each time point between before and after surgery (all p>0.05). Fifteen (9.8%) patients in the opioid group and six (4.4%) patients in the duloxetine group were prescribed additional medication after first 6 weeks, showing no significant (p>0.05) difference in proportion. The 30-day readmission rate and the incidence of side effects were also similar (all p>0.05). There was no difference in the incidence of side effects between the two groups (p>0.05). CONCLUSION: Duloxetine and opioid did not show any difference in pain control, function, and side effects for up to one year after TKA. Although large-scale randomized controlled trials are still required to further confirm the side effects of duloxetine, it can be considered as an alternative to opioid for postoperative pain control following TKA.
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spelling pubmed-82533942021-07-13 Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty Kim, Man Soo Koh, In Jun Choi, Keun Young Yang, Sung Cheol In, Yong PLoS One Research Article BACKGROUND: The purpose of this study was to assess the efficacy of duloxetine as an alternative to opioid treatment for postoperative pain management following total knee arthroplasty (TKA). METHODS: Among 944 patients, 290 (30.7%) of patients received opioid or duloxetine for pain control for 6 weeks when the pain Visual Analogue Scale (VAS) score was greater than 4 out of 10 at the time of discharge. 121 patients in the Opioid group and 118 in the Duloxetine group were followed up for more than one year. Preoperative and postoperative patient reported outcome measures (pain VAS score, Western Ontario and McMaster Universities OA Index (WOMAC) score were compared. The rate of further drug prescription (opioid or duloxetine) after 6 weeks of first prescription, 30-day readmission rate, and side effects were also investigated. RESULTS: There was no significant difference in pain VAS score, WOMAC Pain and Function score, at each time point between before and after surgery (all p>0.05). Fifteen (9.8%) patients in the opioid group and six (4.4%) patients in the duloxetine group were prescribed additional medication after first 6 weeks, showing no significant (p>0.05) difference in proportion. The 30-day readmission rate and the incidence of side effects were also similar (all p>0.05). There was no difference in the incidence of side effects between the two groups (p>0.05). CONCLUSION: Duloxetine and opioid did not show any difference in pain control, function, and side effects for up to one year after TKA. Although large-scale randomized controlled trials are still required to further confirm the side effects of duloxetine, it can be considered as an alternative to opioid for postoperative pain control following TKA. Public Library of Science 2021-07-02 /pmc/articles/PMC8253394/ /pubmed/34214098 http://dx.doi.org/10.1371/journal.pone.0253641 Text en © 2021 Kim et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kim, Man Soo
Koh, In Jun
Choi, Keun Young
Yang, Sung Cheol
In, Yong
Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
title Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
title_full Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
title_fullStr Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
title_full_unstemmed Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
title_short Efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
title_sort efficacy of duloxetine compared with opioid for postoperative pain control following total knee arthroplasty
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253394/
https://www.ncbi.nlm.nih.gov/pubmed/34214098
http://dx.doi.org/10.1371/journal.pone.0253641
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