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2
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本文引用的文献

1
Consensus guidelines for the management of postoperative nausea and vomiting.术后恶心呕吐管理的共识指南。
Anesth Analg. 2014 Jan;118(1):85-113. doi: 10.1213/ANE.0000000000000002.
2
Update on the management of postoperative nausea and vomiting.术后恶心呕吐管理的最新进展。
Drugs. 2013 Sep;73(14):1525-47. doi: 10.1007/s40265-013-0110-7.
3
Reevaluation of the effectiveness of ramosetron for preventing postoperative nausea and vomiting: a systematic review and meta-analysis.雷莫司琼预防术后恶心呕吐有效性的再评价:系统评价和荟萃分析。
Anesth Analg. 2013 Aug;117(2):329-39. doi: 10.1213/ANE.0b013e31829847a1. Epub 2013 Jun 11.
4
A meta-analysis of prevention of postoperative nausea and vomiting: randomised controlled trials by Fujii et al. compared with other authors.一项荟萃分析:预防术后恶心呕吐:Fujii 等人的随机对照试验与其他作者的比较。
Anaesthesia. 2012 Oct;67(10):1076-90. doi: 10.1111/j.1365-2044.2012.07232.x. Epub 2012 Jun 27.
5
Intravenous, oral, and the combination of intravenous and oral ramosetron for the prevention of nausea and vomiting after laparoscopic cholecystectomy: a randomized, double-blind, controlled trial.静脉注射、口服和静脉注射联合口服雷莫司琼预防腹腔镜胆囊切除术后恶心呕吐的随机、双盲、对照试验。
Clin Ther. 2011 Sep;33(9):1162-72. doi: 10.1016/j.clinthera.2011.07.018.
6
Ramosetron versus ondansetron for the prevention of postoperative nausea and vomiting after laparoscopic cholecystectomy.雷莫司琼与昂丹司琼预防腹腔镜胆囊切除术后恶心呕吐的比较。
Surg Endosc. 2010 Apr;24(4):812-7. doi: 10.1007/s00464-009-0670-5. Epub 2009 Aug 26.
7
Comparison of ramosetron with ondansetron for prevention of postoperative nausea and vomiting in patients undergoing gynaecological surgery.雷莫司琼与昂丹司琼预防妇科手术患者术后恶心呕吐的比较。
Br J Anaesth. 2009 Oct;103(4):549-53. doi: 10.1093/bja/aep209. Epub 2009 Aug 21.
8
Society for Ambulatory Anesthesia guidelines for the management of postoperative nausea and vomiting.门诊麻醉学会术后恶心呕吐管理指南。
Anesth Analg. 2007 Dec;105(6):1615-28, table of contents. doi: 10.1213/01.ane.0000295230.55439.f4.
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Ramosetron versus ondansetron in the prevention of chemotherapy-induced gastrointestinal side effects: A prospective randomized controlled study.雷莫司琼与昂丹司琼预防化疗引起的胃肠道副作用的前瞻性随机对照研究。
Chemotherapy. 2007;53(1):44-50. doi: 10.1159/000098418. Epub 2007 Jan 3.
10
Prevention and treatment of postoperative nausea and vomiting.术后恶心呕吐的预防与治疗。
Am J Health Syst Pharm. 2005 Jun 15;62(12):1247-60; quiz 1261-2. doi: 10.1093/ajhp/62.12.1247.

雷莫司琼预防高危患者术后恶心呕吐的有效剂量

Effective Dose of Ramosetron for Prophylaxis of Postoperative Nausea and Vomiting in High-Risk Patients.

作者信息

Lee Seongheon, Jeong Sinho, Kim Joungmin, Jeong Seongwook

机构信息

Department of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju 519-763, Republic of Korea.

出版信息

Biomed Res Int. 2015;2015:951474. doi: 10.1155/2015/951474. Epub 2015 Jul 14.

DOI:10.1155/2015/951474
PMID:26258145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4516817/
Abstract

BACKGROUND

Postoperative nausea and vomiting (PONV) are common adverse events with an incidence of up to 80% in high-risk patients. Ramosetron, a selective 5-HT3 receptor antagonist, is widely used to prevent PONV. The purpose of this study was to evaluate the effective dose of ramosetron for the prevention of PONV in high-risk patients.

METHODS

Fifty-one patients were randomly allocated to 3 groups and were administered ramosetron 0.3 mg (group A), 0.45 mg (group B), or 0.6 mg (group C), at the end of their surgery. The episodes of PONV were assessed 1, 6, 24, and 48 hours after the injection and all the adverse events were observed.

RESULTS

The complete response rate in the postoperative period 6-24 hours after the anesthesia was higher in group C than in group A: 93% versus 44%. Group C's experience score of Rhodes index was lower than group A's: 0.81 ± 2.56 versus 3.94 ± 5.25. No adverse drug reaction could be observed in all groups.

CONCLUSIONS

The effective dose of ramosetron to be injected for the near-complete prophylaxis of PONV 6 to 24 hours after surgery in high-risk patients is a 0.6 mg bolus injection at the end of the surgery.

摘要

背景

术后恶心呕吐(PONV)是常见的不良事件,高危患者的发生率高达80%。雷莫司琼是一种选择性5-HT3受体拮抗剂,广泛用于预防PONV。本研究的目的是评估雷莫司琼预防高危患者PONV的有效剂量。

方法

51例患者随机分为3组,在手术结束时分别给予0.3mg雷莫司琼(A组)、0.45mg雷莫司琼(B组)或0.6mg雷莫司琼(C组)。在注射后1、6、24和48小时评估PONV发作情况,并观察所有不良事件。

结果

麻醉后6-24小时术后完全缓解率C组高于A组:93%对44%。C组的Rhodes指数经验评分低于A组:0.81±2.56对3.94±5.25。所有组均未观察到药物不良反应。

结论

高危患者术后6至24小时近乎完全预防PONV所需注射的雷莫司琼有效剂量为手术结束时静脉推注0.6mg。