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右美托咪定联合舒芬太尼用于电视胸腔镜手术术后静脉镇痛的量效关系

[Dose-response Relationship of Dexmedetomidine Combined with Sufentail for Postoperative Intravenous Analgesia in Video-assisted Thoracoscopic Surgery].

作者信息

Tan Xiao Lu, Chen Ya Yu, Hu Bo, Zhou Qiao Mei, Shao Wei Dong, Xu Bo, Xiao Hai Ping, Zhang Xing An

机构信息

Department of Anesthesiology, General Hospital of Southern Theater Command of Chinese PLA,Guangzhou University of Chinese Medicine,Guangzhou 510010,China.

Department of Thoracic Surgery, General Hospital of Southern Theater Command of Chinese PLA,Guangzhou University of Chinese Medicine,Guangzhou 510010,China.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2019 Jun 30;41(3):373-378. doi: 10.3881/j.issn.1000-503X.10881.

Abstract

Objective To investigate the 50% effective dose(ED)and 95% effective dose(ED)of dexmedetomidine(DEX)combined with 0.032 μg/(kg·h)sufentanil as well as its analgesic effect for patient-controlled intravenous analgesia(PCIA)after video-assisted thoracoscopic surgery(VATS).Methods Totally 25 patients undergoing elective VATS were enrolled. DEX and 0.032 μg/(kg·h)sufentanil were used for postoperative PCIA. The loading dose of DEX was 0.048 μg/(kg·h),and the dose difference between two adjacent patients was 0.008 μg/(kg·h). The DEX dose of a current patient was determined by whether the previous patient was satisfied with postoperative analgesic effect. If the previous patient was satisfied with postoperative analgesic effect,the DEX dose of the current patient was decreased by 0.008 μg/(kg·h);and if the previous analgestic effect was not satisfactory,DEX dose of the current patient was increased by 0.008 μg/(kg·h). The study endpoint was dexmedetomidine dose was<0.008 μg/(kg· h) within 7 upper and lower cycles in 7 consecutive cases. Finally,the probability unit regression was used to estimate the ED and ED of DEX and their 95% .Results When DEX combined with 0.032 μg/(kg·h) sufentanil was used for postoperative PCIA in young patients undergoing VATS,the ED and EDof DEX were 0.0346 μg/(kg· h)[95%:0.0283-0.0408 μg/(kg·h)] and 0.0459 μg/(kg·h)[95%:0.0400-0.0880 μg/(kg·h)],respectively. No adverse reaction such as vomiting,respiratory depression,or bradycardia occurred. The average Visual Analogue Scale(VAS)scores at rest(=-5.128,=0.000)and cough(Z=-6.642,=0.000)and the Ramsay sedation score(Z=-2.335,=0.020)within 6 hours after surgery were higher than those after 6 hour.Conclusion DEX combined with 0.032 μg/(kg·h) sufentanil are effective for postoperative PCIA in patients undergoing VATS when the ED and ED are 0.0346 μg/(kg·h)and 0.0459 μg/(kg·h),respectively.

摘要

目的 探讨右美托咪定(DEX)联合0.032 μg/(kg·h)舒芬太尼用于电视胸腔镜手术(VATS)后患者自控静脉镇痛(PCIA)的半数有效剂量(ED)和95%有效剂量(ED)及其镇痛效果。方法 选取择期行VATS的患者25例。DEX与0.032 μg/(kg·h)舒芬太尼用于术后PCIA。DEX负荷剂量为0.048 μg/(kg·h),相邻2例患者的剂量差为0.008 μg/(kg·h)。根据前1例患者术后镇痛效果是否满意确定当前患者的DEX剂量。若前1例患者术后镇痛效果满意,则当前患者的DEX剂量减少0.008 μg/(kg·h);若前1例患者镇痛效果不满意,则当前患者的DEX剂量增加0.008 μg/(kg·h)。研究终点为连续7例患者在7个上下周期内右美托咪定剂量<0.008 μg/(kg·h)。最后,采用概率单位回归法估算DEX的ED和ED及其95%可信区间。结果 DEX联合0.032 μg/(kg·h)舒芬太尼用于VATS术后年轻患者PCIA时,DEX的ED和ED分别为0.0346 μg/(kg·h)[95%可信区间:0.02830.0408 μg/(kg·h)]和0.0459 μg/(kg·h)[95%可信区间:0.04000.0880 μg/(kg·h)]。未发生呕吐、呼吸抑制或心动过缓等不良反应。术后6小时内静息时视觉模拟评分(VAS)均值(Z=-5.128,P=0.000)、咳嗽时VAS均值(Z=-6.642,P=0.000)及Ramsay镇静评分(Z=-2.335,P=0.020)均高于术后6小时。结论 DEX联合0.032 μg/(kg·h)舒芬太尼用于VATS术后患者PCIA有效时,DEX的ED和ED分别为0.0346 μg/(kg·h)和0.0459 μg/(kg·h)。

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