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首页> 外文期刊>Acta anaesthesiologica Belgica >Comparison ropivacaine and bupivacaine in sphenopalatine ganglion block for postoperative analgesia after functional endoscopic sinus surgery : a randomized controlled trial
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Comparison ropivacaine and bupivacaine in sphenopalatine ganglion block for postoperative analgesia after functional endoscopic sinus surgery : a randomized controlled trial

机译:在功能内镜鼻窦外科术后术后镇痛术后术治疗术治疗的比较罗哌卡因和Bupivacaine:随机对照试验

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摘要

Objective: In this study the efficacy of sphenopalatine ganglion (SPG) block will be evaluated using bupivacaine or ropivacaine in adult patients undergoing functional endoscopic sinus surgery (FESS) under general anesthesia.Methods : Sixty adult patients undergoing FESS under general anesthesia has been randomized in three groups to receive bupivacaine, ropivacaine or normal saline in SPG block before surgery.Results : Time to recovery from anesthesia was significantly higher in patients who received normal saline than bupivacaine or ropivacaine. VAS scores were significantly lower in both bupivacaine and ropivacaine groups at all recorded time points when compared to saline group. Five patients in the bupivacaine group (25%) and six patients in the ropivacaine group (30%) required rescue analgesia whereas fifteen patients (75%) in the saline group required rescue analgesia.Conclusion : Preoperative SPG with either bupivacaine or ropivacaine is an effective method of postoperative analgesia after FESS in adult patients up to 8 hours postsurgery.
机译:目的:在这项研究中,将使用Bupivacaine或Ropivacaine在一般性麻醉下使用Bupivacaine或Ropivacain评估SpHenopalatine GaNLION(SPG)块的功效。在手术前,在SPG块中接受Bupivacaine,Ropivacaine或刚性盐水的三组。结果:从Bupivaine或Ropivacaine或Ropivacaine获得正常盐水的患者中,麻醉的时间显着高。与盐碱组相比,Bupivacaine和Ropivacaine基团的VAS分数明显较低。五个患者在罗比卡因组(25%)和六位患者中罗哌卡因组(30%)所需的救援镇痛,而15名患者(75%)在盐水组中需要救援镇痛。结论:与Bupivacaine或Ropivacaine的术前SPG是一种成人患者患者后8小时后术后镇痛的有效方法。

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