首页> 外文期刊>The Professional Medical Journal >PROPHYLAXIS OF POSTOPERATIVE NAUSEA AND VOMITING LAPAROSCOPIC PROCEDURES WITH 5-HT3 RECEPTOR ANTAGONISTS, A RANDOMIZED CONTROLLED TRIAL.
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PROPHYLAXIS OF POSTOPERATIVE NAUSEA AND VOMITING LAPAROSCOPIC PROCEDURES WITH 5-HT3 RECEPTOR ANTAGONISTS, A RANDOMIZED CONTROLLED TRIAL.

机译:术后恶心的预后和呕吐的腹腔镜手术与5-HT 3受体拮抗剂,随机对照试验。

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In this study we aim to study the efficacy of Ramosetron and Palonosetronin preventing post-operative nausea and vomiting in high risk patients. Study Design: Arandomized controlled trial. Setting: A Large Tertiary Care Centre in Karachi. Period: 9 monthsfrom January 2017 to September 2017. Materials and Methods: N=81 participants tookpart in the study. The patient population was divided into three groups.. Patients belongingto group A received Palonosetron 0.075mg mixed with normal saline in a mixture of 3ml, priorto induction, and received 3ml of normal saline half an hour prior to the end of the procedure.Patients in group B received 3ml of normal saline prior to induction and a mixture of 0.3mg ofRamosetron mixed with normal saline as 3ml half an hour before end of procedure. In groupC patients received normal saline 3ml both before induction and half an hour prior to end ofsurgery. Results: The patient demographics were similar in all the groups and no significantdifference was found. The incidence of post-operative nausea and vomiting during 2 hours postoperatively was 41.97%, the incidence of nausea at 2 hours was in group A= 33.33%, in groupB= 29.62%, in group C= 62.96% respectively, having a p value of 0.014 refer to table 2. After48 hours of surgery the overall incidence of vomiting in the groups was not significant havinga p value of 0.428 and an incidence of 6.172%. Conclusion: Palonosetron and Ramosetronare equally effective in prevention of post-operative nausea and vomiting in high risk patientsundergoing laparoscopic gynecological procedures.
机译:在这项研究中,我们旨在研究雷莫司琼和帕洛诺司琼林预防高危患者术后恶心和呕吐的功效。研究设计:随机对照试验。地点:卡拉奇的大型三级护理中心。从2017年1月至2017年9月,为期9个月。材料与方法:N = 81名参与者参加了研究。将患者分为三组。A组患者在诱导前先接受0.075mg帕洛诺司琼与3ml生理盐水混合,然后在手术结束前半小时接受3ml生理盐水。 B组在手术前半小时接受诱导前3ml生理盐水和0.3mg拉莫司琼与生理盐水混合的混合物3ml。 C组患者在诱导前和手术结束前半小时均接受3ml生理盐水。结果:各组患者的人口统计学特征相似,未发现显着差异。术后2小时内恶心和呕吐的发生率为41.97%,A组2小时时恶心的发生率分别为A组的33.33%,B组的29.62%,C组的62.96%。 0.014见表2。手术48小时后,各组的呕吐总发生率不显着,p值为0.428,发生率为6.172%。结论:帕洛诺司琼和雷莫司琼在腹腔镜妇科手术中对高危患者术后恶心和呕吐的预防效果相同。

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