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作 者:董稳[1] 刘瑞昌[1] 刘克英[1] 关明[1] 杨旭东[1]
机构地区:[1]北京大学口腔医学院.口腔医院麻醉科,北京100081
出 处:《北京大学学报(医学版)》2009年第1期109-111,共3页Journal of Peking University:Health Sciences
摘 要:目的:比较氯诺昔康(lornoxicam)和舒芬太尼(sufentanil)用于颌面外科术后自控静脉镇痛(patient—controlled intravenous analgesia,PCIA)的作用和不良反应。方法:200例美国麻醉医师协会(American Society of Anesthesiologists,ASA)Ⅰ~Ⅱ级择期口腔颌面外科手术全麻患者,分为氯诺昔康组(L组)和舒芬太尼组(S组),每组100例,分别接受氯诺昔康和舒芬太尼作为术后镇痛药物。记录开始镇痛后4,8,12,24,48h两组的疼痛视觉模拟评分(visual analogue scale,VAS)、Prince—Henry疼痛评分(Prince—Henry score,PHS)、Ramsay镇静评分(Ramsay sedation score,RSS)和治疗期间可能出现的不良反应,镇痛结束后统计患者对镇痛治疗的总体满意度。结果:两组术后镇痛治疗期间各时间点疼痛VAS、PHS及RSS组间比较差异无统计学意义。两组镇痛结束后对镇痛治疗的总体满意度差异无统计学意义。镇痛治疗期间L组恶心、呕吐和头晕的发生率低于S组(1% vs 9%,0 vs 4%,0 vs 3%,P〈0.05);两组其他不良反应的比较差异无统计学意义。结论:氯诺昔康和舒芬太尼用于颌面外科术后镇痛,均能取得满意的镇痛效果,氯诺昔康不良反应发生率较低。Objective:To compare the analgesic efficiency and adverse effects of postoperative patientcontrolled intravenous an algesia (PCIA) with lornoxicam and sufentanil in patients undergoing oral maxillofacial surgery. Methods: 200 ASA(American Society of Anesthesiologists)Ⅰ - Ⅱ patients who undertook oral maxillofacial operation were divided into two groups: lornoxicam group (group L) and sufentanil group (group S) ,with 100 patients in each group. The effectiveness was assessed with visual analogu scale (VAS), Prince-Henry score(PHS) and Ramsay sedation Score(RSS) at different time points: 4, 8, 12, 24 and 48 h after the beginning of analgesia. The analgesic efficacy of analgesia and the adverse effects during analgesia period were observed. Results: Statistical analysis revealed no significant difference in VAS, PHS and RSS at 4, 8, 12, 24, 48 h and the overall satisfaction on analgesia therapy. The percentage of nausea, vomiting and dizziness was significantly lower in group L than that in group S ( 1% vs 9% ,0 vs 4% ,0 vs 3%, P 〈0. 05). Conclusion: Lornoxicam could provide an identical efficacy as sufentanil in the postoperative PCIA in patients undergoing oral maxillofacial surgery. In addition, lornoxieam caused less adversed effects.
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