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A comparison of oxycodone prolonged-release vs. oxycodone + naloxone prolonged-release after laparoscopic hysterectomy

机译:腹腔镜子宫切除术后羟考酮缓释与羟考酮+纳洛酮缓释的比较

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Background: Targiniq? , an oxycodone prolonged-release (PR) formulation combined with the opioid antagonist naloxone PR, aims to prevent opioid-induced constipation without impairing the analgesic efficacy. This has been confirmed during prolonged use in chronic pain or cancer patients. The purpose of our study was to compare clinical effects of oxycodone PR with oxycodone PR + naloxone PR for short-term post-operative pain management. Methods: This randomised, double-blind, prospective study included 85 women undergoing laparoscopic hysterectomy. The two groups received either oxycodone PR 10 mg or oxycodone PR 10 mg + naloxone PR 5 mg as pre-medication and twice daily for 3 days. As rescue analgesic, the patients received oxycodone intravenous during the first 24 h post-operatively and oxycodone tablets in the 2472-h period. Constipation, other side effects, pain and satisfaction were registered during the first 7 post-operative days. Results: Demographic, pre-and perioperative variables and the use of rescue analgesics were similar in the groups. There were no significant differences in variables related to constipation. In the oxycodone PR + naloxone PR group, 25% had no defecation during the first 72 h post-operatively, compared with 20% in the oxycodone PR group (mean 1.2 ± 1.1 vs. 2.1 ± 2.4 defecations). Other opioid-induced effects and side effects showed no significant differences. Only 7% were dissatisfied with their oral pain treatment. Conclusion: Addition of naloxone to oxycodone PR tablets in a pain regimen administered twice daily the first three postoperative days had no significant clinical effects on constipation or other variables during the first week after hysterectomy.
机译:背景:Targiniq?羟考酮缓释(PR)制剂与阿片类药物拮抗剂纳洛酮PR结合使用,旨在预防阿片类药物引起的便秘而不损害其止痛效果。在慢性疼痛或癌症患者中长期使用期间已确认这一点。我们研究的目的是比较羟考酮PR与羟考酮PR +纳洛酮PR在短期术后疼痛管理中的临床效果。方法:这项随机,双盲,前瞻性研究纳入了85名接受腹腔镜子宫切除术的妇女。两组患者均接受羟考酮PR 10 mg或羟考酮PR 10 mg +纳洛酮PR 5 mg的预用药,每天两次,共3天。作为抢救性镇痛剂,患者在术后头24小时内静脉注射羟考酮,并在2472-h期间接受羟考酮片剂。在术后的前7天记录便秘,其他副作用,疼痛和满意度。结果:两组的人口统计学,术前和围手术期变量以及抢救性镇痛药的使用情况相似。与便秘相关的变量没有显着差异。羟考酮PR +纳洛酮PR组在术后头72小时无排便,而羟考酮PR组为20%(平均排便1.2±1.1 vs. 2.1±2.4)。其他阿片样物质诱导的作用和副作用均无明显差异。只有7%对他们的口腔疼痛治疗不满意。结论:在术后三天每天两次给予止痛药,将纳洛酮添加到羟考酮PR片中,在子宫切除后的第一周内对便秘或其他变量无明显临床效果。

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