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The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy

BACKGROUND: Postoperative nausea and vomiting (PONV) frequently develops in patients undergoing thyroidectomy, and propofol-based total intravenous anesthesia (TIVA) has been reported to reduce the incidence of PONV. The present study was undertaken to compare the effects of ramosetron on PONV in wo...

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Autores principales: Lee, Dong Chul, Kwak, Hyun Jeong, Kim, Hong Soon, Choi, Sung Ho, Lee, Ji Yeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167136/
https://www.ncbi.nlm.nih.gov/pubmed/21927687
http://dx.doi.org/10.4097/kjae.2011.61.2.154
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author Lee, Dong Chul
Kwak, Hyun Jeong
Kim, Hong Soon
Choi, Sung Ho
Lee, Ji Yeon
author_facet Lee, Dong Chul
Kwak, Hyun Jeong
Kim, Hong Soon
Choi, Sung Ho
Lee, Ji Yeon
author_sort Lee, Dong Chul
collection PubMed
description BACKGROUND: Postoperative nausea and vomiting (PONV) frequently develops in patients undergoing thyroidectomy, and propofol-based total intravenous anesthesia (TIVA) has been reported to reduce the incidence of PONV. The present study was undertaken to compare the effects of ramosetron on PONV in women following total thyroidectomy under TIVA. METHODS: One hundred and thirty women scheduled for thyroidectomy were allocated to either a control group (n = 65) or a ramosetron group (n = 65). Propofol in combination with remifentanil was used for TIVA in all patients. 2 ml of either intravenous saline (control group) or 0.3 mg of ramosetron (ramosetron group) were administered at the end of the surgery. Fentanyl-based patient-controlled analgesia was implemented for 48 h after surgery in all patients. The incidences and severities of PONV, pain scores, administrations of rescue antiemetics, and the side effects of the antiemetics were documented during the first 48 h after surgery. RESULTS: The incidences of complete response (no PONV, no rescue) in the control and ramosetron groups were 71% and 88%, respectively, during the first 6 h (P = 0.029), 85% and 94% during the next 6 to 24 h period (P = 0.155), and 97% and 95% during the last 24 to 48 h period (P = 1.00). During the first 6 h, the severity of nausea and the use of rescue antiemetic medication were significantly lower in the ramosetron group. CONCLUSIONS: Ramosetron was found to be effective at reducing the incidence and severity of postoperative nausea in women that underwent total thyroidectomy with propofol-based TIVA, especially during the first 6 hours postoperatively.
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spelling pubmed-31671362011-09-16 The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy Lee, Dong Chul Kwak, Hyun Jeong Kim, Hong Soon Choi, Sung Ho Lee, Ji Yeon Korean J Anesthesiol Clinical Research Article BACKGROUND: Postoperative nausea and vomiting (PONV) frequently develops in patients undergoing thyroidectomy, and propofol-based total intravenous anesthesia (TIVA) has been reported to reduce the incidence of PONV. The present study was undertaken to compare the effects of ramosetron on PONV in women following total thyroidectomy under TIVA. METHODS: One hundred and thirty women scheduled for thyroidectomy were allocated to either a control group (n = 65) or a ramosetron group (n = 65). Propofol in combination with remifentanil was used for TIVA in all patients. 2 ml of either intravenous saline (control group) or 0.3 mg of ramosetron (ramosetron group) were administered at the end of the surgery. Fentanyl-based patient-controlled analgesia was implemented for 48 h after surgery in all patients. The incidences and severities of PONV, pain scores, administrations of rescue antiemetics, and the side effects of the antiemetics were documented during the first 48 h after surgery. RESULTS: The incidences of complete response (no PONV, no rescue) in the control and ramosetron groups were 71% and 88%, respectively, during the first 6 h (P = 0.029), 85% and 94% during the next 6 to 24 h period (P = 0.155), and 97% and 95% during the last 24 to 48 h period (P = 1.00). During the first 6 h, the severity of nausea and the use of rescue antiemetic medication were significantly lower in the ramosetron group. CONCLUSIONS: Ramosetron was found to be effective at reducing the incidence and severity of postoperative nausea in women that underwent total thyroidectomy with propofol-based TIVA, especially during the first 6 hours postoperatively. The Korean Society of Anesthesiologists 2011-08 2011-08-23 /pmc/articles/PMC3167136/ /pubmed/21927687 http://dx.doi.org/10.4097/kjae.2011.61.2.154 Text en Copyright © the Korean Society of Anesthesiologists, 2011 http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Article
Lee, Dong Chul
Kwak, Hyun Jeong
Kim, Hong Soon
Choi, Sung Ho
Lee, Ji Yeon
The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
title The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
title_full The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
title_fullStr The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
title_full_unstemmed The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
title_short The preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
title_sort preventative effect of ramosetron on postoperative nausea and vomiting after total thyroidectomy
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167136/
https://www.ncbi.nlm.nih.gov/pubmed/21927687
http://dx.doi.org/10.4097/kjae.2011.61.2.154
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