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首页> 外文期刊>Kaohsiung Journal of Medical Sciences >Comparison of the postoperative analgesic effects of paracetamol–codeine phosphate and naproxen sodium–codeine phosphate for lumbar disk surgery
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Comparison of the postoperative analgesic effects of paracetamol–codeine phosphate and naproxen sodium–codeine phosphate for lumbar disk surgery

机译:扑热息痛-磷酸可待因和萘普生钠-磷酸可待因在腰椎间盘手术中的镇痛效果比较

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The aim of this study was to compared the efficacy of paracetamol–codeine phosphate and naproxen sodium–codeine phosphate on postoperative pain and tramadol consumption during the first 24 hours after a lumbar disk surgery. After Ethics Committee approval and informed consent had been obtained, 64 patients were allocated into three groups. Patients received oral paracetamol–codeine (300?mg?+?30?mg; Group P), naproxen sodium–codeine (550?mg?+?30?mg; Group N), or placebo tablets (Group C) 30 minutes prior to induction of anesthesia. Patient-controlled analgesia was supplied postoperatively using tramadol. Pain intensity, tramadol consumption, and side effects were recorded every 1 hour, 2 hours, 6 hours, 12 hours, and 24 hours after surgery. Whole study period pain intensity (visual analogue scale scores) was lower in Group P ( p ?=?0.007) and Group N ( p ?=?0.001), compared with Group C, however, there was no statistically significant difference between Group P and Group N regarding pain intensity ( p ??0.05). Tramadol consumption was lower in Group P and Group N, compared with Group C ( p ??0.001), and in turn the lowest incidence of tramadol consumption was detected in Group P compared with Group N ( p ??0.001) and Group C ( p ??0.001). Side effects were similar between the groups. Preemptive administration of paracetamol–codeine and naproxen sodium–codeine combination significantly reduced tramadol consumption and provided more effective analgesia compared with placebo. The paracetamol–codeine combination was superior to naproxen sodium–codeine with regard to tramadol consumption.
机译:这项研究的目的是比较对乙酰氨基酚磷酸可待因和萘普生钠磷酸可待因在腰椎间盘手术后的最初24小时内对术后疼痛和曲马多的消耗的疗效。在获得伦理委员会的批准和知情同意后,将64例患者分为三组。患者在30分钟前接受口服对乙酰氨基酚-可待因(300?mg?+?30?mg; P组),萘普生钠-可待因(550?mg?+?30?mg; N组)或安慰剂片(C组);诱导麻醉。术后使用曲马多进行患者自控镇痛。术后每1小时,2小时,6小时,12小时和24小时记录疼痛强度,曲马多的消耗量和副作用。与C组相比,P组(p = 0.007)和N组(p = 0.001)的整个研究期疼痛强度(视觉模拟量表评分)较低,但是P组之间没有统计学上的显着差异N组为疼痛强度(p≥0.05)。与C组相比,P组和N组曲马多的消费量较低(p 0.001),而与N组相比,P组中曲马多的消费发生率最低(p 0.001)和组。 C(p≤0.001)。两组之间的副作用相似。与安慰剂相比,扑热息痛-可待因和萘普生钠-可待因钠的抢先给药显着减少了曲马多的消耗,并提供了更有效的镇痛作用。就曲马多的消费而言,对乙酰氨基酚-可待因的组合优于萘普生钠-可待因。

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