Caldwell J R, Hale M E, Boyd R E, Hague J M, Iwan T, Shi M, Lacouture P G
Gainesville Clinical Research Center, Florida 32605, USA.
J Rheumatol. 1999 Apr;26(4):862-9.
To compare the efficacy and safety of controlled release oxycodone given every 12 h around the clock with immediate release oxycodone-acetaminophen (APAP) given 4 times daily for osteoarthritis (OA) pain.
Adults (n=167) with moderate to severe OA pain despite regular use of nonsteroidal antiinflammatory drugs (NSAID) entered open label titration for 30 days with immediate release oxycodone qid; 107 qualified for randomization to double blind, parallel group treatment for 30 days with placebo, controlled release oxycodone, or immediate release oxycodone-APAP.
Following titration with immediate release oxycodone, mean (SE) pain intensity (0, none to 3, severe) decreased from 2.44 (0.04) to 1.38 (0.05) (p=0.0001), and quality of sleep (1, very poor; 5, excellent) improved from 2.58 (0.08) to 3.57 (0.07) (p=0.0001). Mean dose was about 40 mg/day. Pain intensity and quality of sleep were significantly improved in both active groups compared with the placebo group (p< or =0.05) during the double blind trial. Pain intensity and sleep scores were comparable in both active groups during double blind treatment. Nausea (p=0.03) and dry mouth (p=0.09) were less common with controlled release oxycodone than immediate release oxycodone-APAP.
Controlled release oxycodone q12h and immediate release oxycodone-APAP qid, added to NSAID, were superior to placebo for reducing OA pain and improving quality of sleep. The active treatments provided comparable pain control and sleep quality. Controlled release oxycodone was associated with a lower incidence of some side effects.
比较每12小时一次的控释羟考酮与每日4次的速释羟考酮-对乙酰氨基酚(APAP)用于骨关节炎(OA)疼痛的疗效和安全性。
尽管规律使用非甾体抗炎药(NSAID)仍有中度至重度OA疼痛的成年人(n = 167)进入开放标签滴定阶段,使用速释羟考酮每日4次,持续30天;107名符合条件的患者被随机分为双盲、平行组治疗30天,分别给予安慰剂、控释羟考酮或速释羟考酮-APAP。
在用速释羟考酮滴定后,平均(SE)疼痛强度(0为无,3为重度)从2.44(0.04)降至1.38(0.05)(p = 0.0001),睡眠质量(1为非常差;5为优秀)从2.58(0.08)提高到3.57(0.07)(p = 0.0001)。平均剂量约为40毫克/天。在双盲试验期间,与安慰剂组相比,两个活性治疗组的疼痛强度和睡眠质量均有显著改善(p≤0.05)。双盲治疗期间,两个活性治疗组的疼痛强度和睡眠评分相当。控释羟考酮引起的恶心(p = 0.03)和口干(p = 0.09)比速释羟考酮-APAP少见。
每12小时一次的控释羟考酮和每日4次的速释羟考酮-APAP,加用NSAID后,在减轻OA疼痛和改善睡眠质量方面优于安慰剂。活性治疗提供了相当的疼痛控制和睡眠质量。控释羟考酮的一些副作用发生率较低。