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Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study

BACKGROUND: Analgesia after Cesarean delivery (CD) requires early ambulation to prevent thromboembolic disease and to facilitate baby care. We retrospectively reviewed anesthesia charts and medical records of patients who underwent CD to compare the efficacy of spinal anesthesia supplemented with in...

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Autores principales: Suzuki, Hiroko, Kamiya, Yoshinori, Fujiwara, Takashi, Yoshida, Takayuki, Takamatsu, Misako, Sato, Kazunori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818688/
https://www.ncbi.nlm.nih.gov/pubmed/29497635
http://dx.doi.org/10.1186/s40981-015-0005-6
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author Suzuki, Hiroko
Kamiya, Yoshinori
Fujiwara, Takashi
Yoshida, Takayuki
Takamatsu, Misako
Sato, Kazunori
author_facet Suzuki, Hiroko
Kamiya, Yoshinori
Fujiwara, Takashi
Yoshida, Takayuki
Takamatsu, Misako
Sato, Kazunori
author_sort Suzuki, Hiroko
collection PubMed
description BACKGROUND: Analgesia after Cesarean delivery (CD) requires early ambulation to prevent thromboembolic disease and to facilitate baby care. We retrospectively reviewed anesthesia charts and medical records of patients who underwent CD to compare the efficacy of spinal anesthesia supplemented with intrathecal morphine hydrochloride (ITM) and combined spinal–epidural anesthesia followed by opioid-free epidural analgesia (CSEA-EDA). FINDINGS: All subjects underwent CD at Nagaoka Chuo General Hospital between February 2012 and January 2013. Patient characteristics, time to first analgesic rescue after CD, and analgesic use after CD were examined. Incidences of postural hypotension, lower extremity numbness/weakness, postoperative nausea/vomiting (PONV), and pruritus were also examined for 48 h after CD. Average time to first analgesic use after CD (ITM 25.13 ± 16.07 h, CSEA-EDA 22.42 ± 16.27 h, p = 0.521) and cumulative probability of rescue analgesic use (p = 0.139 by log-rank test) were comparable between groups. However, average analgesic use within 24 h was lower in the ITM group (0.75 ± 1.05 times) than in the CSEA-EDA group (1.52 ± 1.72 times, p = 0.0497). Numbness or motor weakness in lower extremities only occurred in the CSEA-EDA group, and pruritus only occurred in the ITM group. CONCLUSIONS: The results of this study suggest that ITM is better than CSEA-EDA for anesthesia following CD with regard to pain control. Also, ITM would be advantageous for early ambulation following CD because of lower incidence of numbness and motor weakness in lower extremities compared to CSEA-EDA.
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spelling pubmed-58186882018-02-27 Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study Suzuki, Hiroko Kamiya, Yoshinori Fujiwara, Takashi Yoshida, Takayuki Takamatsu, Misako Sato, Kazunori JA Clin Rep Clinical Research Letter BACKGROUND: Analgesia after Cesarean delivery (CD) requires early ambulation to prevent thromboembolic disease and to facilitate baby care. We retrospectively reviewed anesthesia charts and medical records of patients who underwent CD to compare the efficacy of spinal anesthesia supplemented with intrathecal morphine hydrochloride (ITM) and combined spinal–epidural anesthesia followed by opioid-free epidural analgesia (CSEA-EDA). FINDINGS: All subjects underwent CD at Nagaoka Chuo General Hospital between February 2012 and January 2013. Patient characteristics, time to first analgesic rescue after CD, and analgesic use after CD were examined. Incidences of postural hypotension, lower extremity numbness/weakness, postoperative nausea/vomiting (PONV), and pruritus were also examined for 48 h after CD. Average time to first analgesic use after CD (ITM 25.13 ± 16.07 h, CSEA-EDA 22.42 ± 16.27 h, p = 0.521) and cumulative probability of rescue analgesic use (p = 0.139 by log-rank test) were comparable between groups. However, average analgesic use within 24 h was lower in the ITM group (0.75 ± 1.05 times) than in the CSEA-EDA group (1.52 ± 1.72 times, p = 0.0497). Numbness or motor weakness in lower extremities only occurred in the CSEA-EDA group, and pruritus only occurred in the ITM group. CONCLUSIONS: The results of this study suggest that ITM is better than CSEA-EDA for anesthesia following CD with regard to pain control. Also, ITM would be advantageous for early ambulation following CD because of lower incidence of numbness and motor weakness in lower extremities compared to CSEA-EDA. Springer Berlin Heidelberg 2015-08-27 2015 /pmc/articles/PMC5818688/ /pubmed/29497635 http://dx.doi.org/10.1186/s40981-015-0005-6 Text en © The Author(s) 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Clinical Research Letter
Suzuki, Hiroko
Kamiya, Yoshinori
Fujiwara, Takashi
Yoshida, Takayuki
Takamatsu, Misako
Sato, Kazunori
Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study
title Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study
title_full Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study
title_fullStr Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study
title_full_unstemmed Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study
title_short Intrathecal morphine versus epidural ropivacaine infusion for analgesia after Cesarean section: a retrospective study
title_sort intrathecal morphine versus epidural ropivacaine infusion for analgesia after cesarean section: a retrospective study
topic Clinical Research Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818688/
https://www.ncbi.nlm.nih.gov/pubmed/29497635
http://dx.doi.org/10.1186/s40981-015-0005-6
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