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Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study

OBJECTIVE: To evaluate the preemptive analgesic effect of combination pregabalin with celecoxib for lumbar spine surgery. METHODS: A prospective, randomized study was conducted among 60 lumbar spine surgery patients and divided into two groups. Postoperative pain relief was achieved with intravenous...

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Autores principales: Kien, Nguyen Trung, Geiger, Phillip, Van Chuong, Hoang, Cuong, Nguyen Manh, Van Dinh, Ngo, Pho, Dinh Cong, Anh, Vu The, Giang, Nguyen Truong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613459/
https://www.ncbi.nlm.nih.gov/pubmed/31308627
http://dx.doi.org/10.2147/DDDT.S202410
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author Kien, Nguyen Trung
Geiger, Phillip
Van Chuong, Hoang
Cuong, Nguyen Manh
Van Dinh, Ngo
Pho, Dinh Cong
Anh, Vu The
Giang, Nguyen Truong
author_facet Kien, Nguyen Trung
Geiger, Phillip
Van Chuong, Hoang
Cuong, Nguyen Manh
Van Dinh, Ngo
Pho, Dinh Cong
Anh, Vu The
Giang, Nguyen Truong
author_sort Kien, Nguyen Trung
collection PubMed
description OBJECTIVE: To evaluate the preemptive analgesic effect of combination pregabalin with celecoxib for lumbar spine surgery. METHODS: A prospective, randomized study was conducted among 60 lumbar spine surgery patients and divided into two groups. Postoperative pain relief was achieved with intravenous patient-controlled analgesia with morphine. The preemptive analgesia group received oral pregabalin (150 mg) and celecoxib (200 mg) 2 hrs before surgery, and the control group received a placebo. Pain was assessed by visual analogue scale (VAS). Side effects and morphine consumption were monitored until 48 hrs after surgery. RESULTS: VAS score at rest and during movement was statistically significantly lower in the preemptive analgesia group at most time points (p<0.05). Morphine consumption was significantly lower in the preemptive analgesia group compared with control group in the 24 first hours (29.03±4.38 mg vs 24.43±4.94) and 48 hrs (52.23±9.57 mg vs 44.20±10.21 mg), p<0.05. Hemodynamics, respiratory rate, and SpO(2) were similar for both groups. The sedation score was only statistically significant at H8 time point. The incidence of nausea/vomiting in the preemptive group did not statistically differ from the control group. CONCLUSION: Preoperative administration of pregabalin combined with celecoxib had a good preemptive analgesia effect and reduced intravenous morphine consumption after lumbar spine surgery. Side effects were mild and transient.
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spelling pubmed-66134592019-07-15 Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study Kien, Nguyen Trung Geiger, Phillip Van Chuong, Hoang Cuong, Nguyen Manh Van Dinh, Ngo Pho, Dinh Cong Anh, Vu The Giang, Nguyen Truong Drug Des Devel Ther Original Research OBJECTIVE: To evaluate the preemptive analgesic effect of combination pregabalin with celecoxib for lumbar spine surgery. METHODS: A prospective, randomized study was conducted among 60 lumbar spine surgery patients and divided into two groups. Postoperative pain relief was achieved with intravenous patient-controlled analgesia with morphine. The preemptive analgesia group received oral pregabalin (150 mg) and celecoxib (200 mg) 2 hrs before surgery, and the control group received a placebo. Pain was assessed by visual analogue scale (VAS). Side effects and morphine consumption were monitored until 48 hrs after surgery. RESULTS: VAS score at rest and during movement was statistically significantly lower in the preemptive analgesia group at most time points (p<0.05). Morphine consumption was significantly lower in the preemptive analgesia group compared with control group in the 24 first hours (29.03±4.38 mg vs 24.43±4.94) and 48 hrs (52.23±9.57 mg vs 44.20±10.21 mg), p<0.05. Hemodynamics, respiratory rate, and SpO(2) were similar for both groups. The sedation score was only statistically significant at H8 time point. The incidence of nausea/vomiting in the preemptive group did not statistically differ from the control group. CONCLUSION: Preoperative administration of pregabalin combined with celecoxib had a good preemptive analgesia effect and reduced intravenous morphine consumption after lumbar spine surgery. Side effects were mild and transient. Dove 2019-07-03 /pmc/articles/PMC6613459/ /pubmed/31308627 http://dx.doi.org/10.2147/DDDT.S202410 Text en © 2019 Kien et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Kien, Nguyen Trung
Geiger, Phillip
Van Chuong, Hoang
Cuong, Nguyen Manh
Van Dinh, Ngo
Pho, Dinh Cong
Anh, Vu The
Giang, Nguyen Truong
Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
title Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
title_full Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
title_fullStr Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
title_full_unstemmed Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
title_short Preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
title_sort preemptive analgesia after lumbar spine surgery by pregabalin and celecoxib: a prospective study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613459/
https://www.ncbi.nlm.nih.gov/pubmed/31308627
http://dx.doi.org/10.2147/DDDT.S202410
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