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帕瑞昔布钠抑制瑞芬太尼术后痛觉过敏的量效关系
引用本文:苏志源,陈郡兴,谭正玲,詹鸿. 帕瑞昔布钠抑制瑞芬太尼术后痛觉过敏的量效关系[J]. 医疗保健器具, 2011, 18(4): 528-530. DOI: 10.3936/j.issn.1674-4659.2011.04.0528
作者姓名:苏志源  陈郡兴  谭正玲  詹鸿
作者单位:广州医学院第三附属医院麻醉科,广东广州,510150
摘    要:
目的探讨帕瑞昔布钠抑制瑞芬太尼致患者术后痛觉过敏的量效关系。方法选择我院2010年1~6月期间,择期全麻下妇科腹腔镜手术患者40例,年龄19~45岁,体重45~70 kg,ASA I~II级。静脉注射芬太尼、丙泊酚和阿曲库铵麻醉诱导后,气管插管行全凭静脉全麻。术中静脉输注0.12μg.kg-1.min-1瑞芬太尼和75~200 mg.kg-1.min-1丙泊酚,间断静脉注射阿曲库铵维持麻醉。麻醉诱导后,采用序贯法静脉注射帕瑞昔布钠,初始剂量为0.6 mg/kg,相邻梯度为0.2 mg/kg,采用概率单位法计算患者术后痛觉过敏抑制时(气管拔管后10 min时VAS评分〈4分)帕瑞昔布钠的半数有效剂量(ED50)、95%有效剂量(ED95)及其95%可信区间。结果帕瑞昔布钠抑制瑞芬太尼致患者术后痛觉过敏的ED50(95%可信区间)为0.63 mg/kg(0.52mg/kg~0.75 mg/kg),ED95(95%可信区间)为1.10 mg/kg(0.86 mg/kg~2.81 mg/kg)。结论帕瑞昔布钠抑制瑞芬太尼致患者术后痛觉过敏的ED50和ED95分别为0.63 mg/kg和1.10 mg/kg。

关 键 词:帕瑞昔布钠  瑞芬太尼  痛觉过敏  量效关系

Dose-response Relationship of Parecoxib for Inhibiting Postoperative Hyperalgesia after Remifentanil-based Anesthesia
SU Zhiyuan,CHEN Junxing,TAN Zhengling,ZHAN Hong. Dose-response Relationship of Parecoxib for Inhibiting Postoperative Hyperalgesia after Remifentanil-based Anesthesia[J]. Medicine Healthcare Apparatus, 2011, 18(4): 528-530. DOI: 10.3936/j.issn.1674-4659.2011.04.0528
Authors:SU Zhiyuan  CHEN Junxing  TAN Zhengling  ZHAN Hong
Affiliation:SU Zhiyuan,CHEN Junxing,TAN Zhengling,ZHAN Hong(Department of Anesthesia,the Third Affiliated Hopital of Guangzhou Medical College,Guangzhou 510150,China)
Abstract:
Objective To investigate dose-response relationship of parecoxib for inhibiting postoperative hyperalgesia after remifentanil-based anesthesia in patients undergoing gynecological laparoscopy.Methods Forty patients aged 19 ~ 45 years with ASA I or II,weighing 45 ~ 70 kg and undergoing gynecological laparoscopy under remifentanil-based general anesthesia were studied.Anesthesia used propofol 2 mg/kg,fentanyl 4 μg/kg and atracurium 0.6 mg/kg.Patients were given infusion of remifentail(0.12 μg·kg-1·min-1) and propofol(75 ~ 200 mg·kg-1·min-1) during the operation.Atracurium was given intermittently.The patients were mechanically ventilated after tracheal intubation.Parecoxib was given before skin incision for inhibiting remifentanil-induced postoperative hyperalgesia.Pain was assessed using VAS at 10 min after tracheal extubation.VAS score 4 was defined as effective.The optimal dose was determined by Dixon's up-and-down method.If the VAS score was 4,the next patient received a lower dose of parecoxib.If ineffective,a high dose was given in the next patient.The up-and-down sequences were analyzed by using probit method to determine the ED50,ED95 and 95% confidence interval(CI).Results The ED50 and ED95 of parecoxib for inhibiting postoperative hyperalgesia after remifentanil-based anesthesia in patients following gynecological laparoscopy were 0.63 mg/kg(95% CI: 0.52 mg/kg ~ 0.75 mg/kg) and 1.10 mg/kg(95% CI: 0.86 mg/kg ~ 2.81mg/kg).Conclusion The ED50 and ED95 of parecoxib for inhibiting postoperative hyperalgesia after remifentanil-based anesthesia in patients following gynecological laparoscopy are 0.63 mg/kg and 1.10 mg/kg respectively.
Keywords:Parecoxib  Remifentanil  Hyperalgesia  Dose-response relationship  
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