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芬太尼患者自控透皮系统用于急性术后镇痛的安全性和有效性:一项多中心、安慰剂对照试验。

The safety and efficacy of a fentanyl patient-controlled transdermal system for acute postoperative analgesia: a multicenter, placebo-controlled trial.

作者信息

Chelly Jacques E, Grass Jeffrey, Houseman Timothy W, Minkowitz Harold, Pue Alex

机构信息

*University of Pittsburgh Medical Center and †The Western Pennsylvania Hospital, Pittsburgh, Pennsylvania, ‡Thomas Hospital, Fairhope, Alabama, §Memorial City Hospital, Houston, Texas, and the ∥Mary Birch Hospital for Women, San Diego, California.

出版信息

Anesth Analg. 2004 Feb;98(2):427-433. doi: 10.1213/01.ANE.0000093314.13848.7E.

Abstract

UNLABELLED

A noninvasive method of delivery of parenteral opioids for management of acute pain may offer logistic advantages for patients and nursing staff. A patient-controlled transdermal system (PCTS) under development consists of a preprogrammed, self-contained drug-delivery system that uses electrotransport technology (E-TRANS, ALZA Corp, Mountain View, CA) to deliver 40 micro g of fentanyl HCl over 10 min per on-demand dose for patient-controlled analgesia (PCA). In this randomized, double-blinded, placebo-controlled trial we compared the efficacy and safety of on-demand fentanyl HCl PCTS 40 microg against placebo for postoperative pain up to 24 h after major abdominal, orthopedic, or thoracic surgery in 205 patients. The primary efficacy measurement was the percentage of patients withdrawn from the study because of inadequate analgesia after completing at least 3 h of treatment. Secondary efficacy measures included mean pain intensity (using visual analog scales), patient global assessments, and investigator global assessments. Of 189 patients considered evaluable for efficacy, 25% of patients in the fentanyl HCl PCTS 40 microg group withdrew because of inadequate analgesia, compared with 40.4% of the placebo group (P < 0.05). Use of fentanyl HCl PCTS 40 micro g was associated with lower VAS scores and higher mean patient and investigator global assessment scores compared with placebo. No patient experienced clinically relevant respiratory depression. This study showed that a fentanyl HCl PCTS 40 microg for PCA was superior to placebo and well tolerated for the control of moderate to severe postoperative pain for up to 24 h after major surgery.

IMPLICATIONS

This multicenter, randomized, double-blinded, placebo-controlled trial showed that an on-demand fentanyl HCl patient-controlled transdermal system (PCTS) was superior to placebo and well tolerated for the control of moderate to severe postoperative pain for up to 24 h after major surgery. This fentanyl HCl PCTS is a preprogrammed, needle free, self-contained drug-delivery system that uses electrotransport technology (iontophoresis) to deliver 40 microg of fentanyl per on-demand dose.

摘要

未标记

一种用于管理急性疼痛的非侵入性胃肠外阿片类药物给药方法,可能会为患者和护理人员带来后勤方面的便利。正在研发的患者自控透皮系统(PCTS)由一个预编程的、独立的药物输送系统组成,该系统使用电转运技术(E-TRANS,阿尔扎公司,加利福尼亚州山景城),每次按需剂量在10分钟内输送40微克盐酸芬太尼用于患者自控镇痛(PCA)。在这项随机、双盲、安慰剂对照试验中,我们比较了205例接受腹部、骨科或胸科大手术后长达24小时的术后疼痛患者,按需使用40微克盐酸芬太尼PCTS与安慰剂的疗效和安全性。主要疗效指标是在完成至少3小时治疗后,因镇痛不足而退出研究的患者百分比。次要疗效指标包括平均疼痛强度(使用视觉模拟量表)、患者总体评估和研究者总体评估。在189例被认为可进行疗效评估的患者中,40微克盐酸芬太尼PCTS组有25%的患者因镇痛不足而退出,而安慰剂组为40.4%(P<0.05)。与安慰剂相比,使用40微克盐酸芬太尼PCTS的患者视觉模拟量表评分更低,患者和研究者总体评估平均得分更高。没有患者出现临床相关的呼吸抑制。这项研究表明,用于PCA的40微克盐酸芬太尼PCTS优于安慰剂,在大手术后长达24小时控制中度至重度术后疼痛时耐受性良好。

启示

这项多中心、随机、双盲、安慰剂对照试验表明,按需使用盐酸芬太尼患者自控透皮系统(PCTS)优于安慰剂,在大手术后长达24小时控制中度至重度术后疼痛时耐受性良好。这种盐酸芬太尼PCTS是一个预编程的、无针的、独立的药物输送系统,使用电转运技术(离子电渗疗法)每次按需剂量输送40微克芬太尼。

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