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丙帕他莫在骨科术后疼痛中的镇痛增效作用。

The morphine-sparing effect of propacetamol in orthopedic postoperative pain.

作者信息

Delbos A, Boccard E

机构信息

Clinique St-Michel, Toulouse, France.

出版信息

J Pain Symptom Manage. 1995 May;10(4):279-86. doi: 10.1016/0885-3924(95)00004-I.

DOI:10.1016/0885-3924(95)00004-I
PMID:7541435
Abstract

The analgesic efficacy and safety of propacetamol (Pro-Dafalgan), an injectable prodrug of acetaminophen, in combination with morphine administered by patient-controlled analgesia (PCA) were studied in 60 patients (56 men, 4 women; age 18-40 years; mean age, 26 years) after knee ligamentoplasty. Using a double-blind, randomized, parallel-group design, the effects of four (every 6 hr) intravenous injections of 2 g propacetamol (= 1 g acetaminophen) were compared with four injections of placebo (PL) in the recovery room immediately after surgery. Efficacy was assessed over 24 hr by automatic recording on the PCA device of the cumulative dose of morphine and the number of boluses requested. It was also assessed on pain scores rated on a five-point verbal scale and a visual analogue scale before administration, at 1, 2, 3, and 4 hr, and then every 2 hr until the 24th hr after administration. A five-point global efficacy scale was also administered. Any side effects were recorded throughout the duration of the study, and the ability to tolerate the drug was assessed by recording arterial pressure, cardiac and respiratory frequency, and sedation at the same assessment times as the pain scores. The 24-hr morphine consumption was significantly decreased in the propacetamol group (number of 1 mg boluses: 14.7 +/- 11.3 versus 23.2 +/- 13.8, P = 0.01; PCA usage: 26.4 +/- 12.3 mg versus 34.6 +/- 15.4 mg, P = 0.03; PCA usage + titration: 34.5 +/- 12.7 mg versus 43.1 +/- 15.9 mg, P = 0.02).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在60例(56例男性,4例女性;年龄18 - 40岁;平均年龄26岁)膝关节韧带成形术后患者中,研究了对乙酰氨基酚的注射用前体药物丙帕他莫(痛力克)与吗啡联合患者自控镇痛(PCA)的镇痛效果及安全性。采用双盲、随机、平行组设计,在术后恢复室将4次(每6小时一次)静脉注射2g丙帕他莫(相当于1g对乙酰氨基酚)的效果与4次注射安慰剂(PL)的效果进行比较。通过PCA装置自动记录吗啡累积剂量和追加剂量次数,评估24小时内的疗效。还在给药前、给药后1、2、3和4小时以及之后每2小时直至24小时,根据五点语言量表和视觉模拟量表对疼痛评分进行评估。同时采用五点整体疗效量表。在研究期间记录所有副作用,并在与疼痛评分相同的评估时间记录动脉压、心率、呼吸频率和镇静情况,以评估对药物的耐受性。丙帕他莫组24小时吗啡消耗量显著降低(1mg追加剂量次数:14.7±11.3对23.2±13.8,P = 0.01;PCA用量:26.4±12.3mg对34.6±15.4mg,P = 0.03;PCA用量 + 滴定:34.5±12.7mg对43.1±15.9mg,P = 0.02)。(摘要截短于250字)

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