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Combination of gabapentin and ramosetron for the prevention of postoperative nausea and vomiting after gynecologic laparoscopic surgery: a prospective randomized comparative study

机译:加巴喷丁联合雷莫司琼预防妇科腹腔镜手术后恶心和呕吐的前瞻性随机对照研究

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Background As a drug originally introduced for its anticonvulsant effects, gabapentin has been recently shown to be effective in the treatment of nausea and vomiting in various clinical settings. This study compared the antiemetic efficacy of oral gabapentin, intravenous ramosetron and gabapentin plus ramosetron in patients receiving fentanyl-based patient-controlled analgesia after laparoscopic gynecologic surgery. Methods One hundred and thirty two patients undergoing laparoscopic gynecologic surgery under general anesthesia were allocated randomly into three groups: group G received 300?mg oral gabapentin 1?h before anesthesia, group R received 0.3?mg intravenous ramosetron at the end of surgery, and group GR received a combination of 300?mg oral gabapentin 1?h before anesthesia and 0.3?mg intravenous ramosetron at the end of surgery. Postoperative nausea, retching, vomiting, rescue antiemetic drug use, pain, rescue analgesic requirements and adverse effects were assessed at 0–2, 2–24 and 24–48?h after surgery. Postoperative nausea and vomiting (PONV) was defined as the presence of nausea, retching or vomiting. Results The incidence of complete response (no PONV and no rescue antiemetics up to 48?h postoperatively) was significantly higher in group GR (26/40, 65%) than group G (16/40, 40%; P =?0.025) and group R (18/44, 41%; P =?0.027), whereas there was no significant difference between group G and group R ( P =?0.932). There were no significant between-group differences in the incidence of emetic episodes, use of rescue antiemetics, severe emesis, use of rescue analgesics or any adverse effects. Postoperative pain scores were also similar among groups. Conclusions The combination with gabapentin and ramosetron is superior to either drug alone for prevention of PONV after laparoscopic gynecologic surgery. Trial registration ClinicalTrials.gov NCT02617121 , registered November 25, 2015.
机译:背景技术作为最初因抗惊厥作用而引入的药物,加巴喷丁最近已被证明在各种临床环境中可有效治疗恶心和呕吐。这项研究比较了口服加巴喷丁,静脉内雷莫司琼和加巴喷丁加雷莫司琼在以妇科腹腔镜手术后接受以芬太尼为基础的患者自控镇痛的患者中的止吐效果。方法132例行全身麻醉的腹腔镜妇科手术患者随机分为三组:G组在麻醉前1 h口服300 mg的加巴喷丁,R组在手术结束时接受0.3 mg的雷莫司琼静脉注射; GR组在麻醉前1小时服用300?mg口服加巴喷丁并在手术结束时接受0.3?mg静脉内雷莫司琼的联合治疗。术后0–2、2–24和24–48?h评估术后恶心,呕吐,呕吐,止吐药物的使用,疼痛,止痛要求和不良反应。术后恶心呕吐(PONV)定义为存在恶心,呕吐或呕吐。结果GR组(26/40,65%)的完全缓解率(术后长达48?h无PONV且无抢救止吐药)明显高于G组(16/40,40%; P =?0.025)和R组(18 / 44,41%; P =?0.027),而G组和R组之间没有显着差异(P =?0.932)。呕吐发作,使用止吐药,严重的呕吐,使用止痛药或任何不良反应的发生率之间没有显着的组间差异。各组的术后疼痛评分也相似。结论加巴喷丁和雷莫司琼联合使用在预防腹腔镜妇科手术后PONV方面优于单独使用两种药物。试用注册ClinicalTrials.gov NCT02617121,2015年11月25日注册。

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