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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Randomized, double-blind, placebo-controlled comparison of the analgesic efficacy of oxycodone 10 mg/acetaminophen 325 mg versus controlled-release oxycodone 20 mg in postsurgical pain.
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Randomized, double-blind, placebo-controlled comparison of the analgesic efficacy of oxycodone 10 mg/acetaminophen 325 mg versus controlled-release oxycodone 20 mg in postsurgical pain.

机译:羟考酮10 mg /对乙酰氨基酚325 mg与控释羟考酮20 mg在术后疼痛中的镇痛效果的随机,双盲,安慰剂对照比较。

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摘要

This randomized, controlled trial compared the analgesic efficacy and safety of the new oxycodone 10-mg/acetaminophen 325-mg formulation (Percocet) for the treatment of acute pain following oral surgery with double the dose of oxycodone alone (controlled-release [CR] oxycodone 20 mg [OxyContin]). A total of 150 male and female patients with > or = 2 full or partial bone-impacted mandibular molars, at least moderate persistent pain, and moderate trauma received a single dose of combination agent, CR oxycodone, or placebo following oral surgery and rated pain intensity and pain relief over the next 6 hours. The intent-to-treat population comprised 141 patients (55 on combination agent, 56 on oxycodone, and 30 on placebo). Combination agent and CR oxycodone were significantly superior to placebo for all efficacy measures. Combination agent was statistically superior to CR oxycodone in four of five outcome measures of pain intensity and pain relief (PPID, PPAR, SPID, and SPRID). It also provided a faster onset and 24% reduction in the number of patients reporting treatment-related adverse events compared with twice the dose of opioid alone. This new formulation offers the combination of two analgesic drugs with complementary mechanisms of action, which results in enhanced analgesia, an "opioid-sparing" effect, and an improved side effect and safety profile.
机译:这项随机对照试验比较了新的羟考酮10毫克/对乙酰氨基酚325毫克制剂(Percocet)在口服外科手术后急性疼痛中的镇痛效果和安全性,单用羟考酮的剂量加倍(控制释放[CR]羟考酮20毫克[OxyContin]。总共150名患有或超过2个完全或部分受骨骼影响的下颌磨牙,至少中度持续性疼痛和中度创伤的男性和女性患者在接受口服手术并达到额定疼痛后接受了单剂量的联合剂,CR羟考酮或安慰剂在接下来的6小时内强度和疼痛缓解。意向性治疗人群包括141例患者(联合用药55例,羟考酮56例,安慰剂30例)。在所有功效指标上,联合用药和CR羟考酮均明显优于安慰剂。在五项疼痛强度和缓解疼痛的指标(PPID,PPAR,SID和SPRID)中,有四项在统计学上优于CR羟考酮。与单次使用阿片类药物的剂量相比,它还提供了更快的发作率,并且报告了与治疗相关的不良事件的患者数量减少了24%。这种新配方将两种止痛药结合起来,具有互补的作用机理,从而增强了止痛效果,具有“阿片类药物的保护作用”,并改善了副作用和安全性。

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