Palangio M, Wideman G L, Keffer M, Landau C J, Morris E, Doyle R T, Jiang J G, Damask M, de Padova A
Medical Affairs Department, Knoll Pharmaceutical Company, Mount Olive, New Jersey 07828-1234, USA.
Clin Ther. 2000 May;22(5):600-12. doi: 10.1016/s0149-2918(00)80047-8.
The objective of this study was to compare the effectiveness of combination hydrocodone and ibuprofen with that of combination oxycodone and acetaminophen in the treatment of moderate to severe postoperative obstetric or gynecologic pain.
Hydrocodone 7.5 mg with ibuprofen 200 mg is the only approved fixed-dose combination analgesic containing an opioid and ibuprofen.
This randomized, double-blind, parallel-group, single-dose, active-comparator, placebo-controlled study compared the effects of a 2-tablet dose of hydrocodone 7.5 mg and ibuprofen 200 mg with those of a 2-tablet dose of oxycodone 5 mg and acetaminophen 325 mg and placebo. Analgesia was assessed over 8 hours.
Mean pain relief (PR) scores were similar for the hydrocodone with ibuprofen and oxycodone with acetaminophen groups (n = 61 and 59, respectively) at 0.5, 1, 1.5, 2, 2.5, 3, 4, and 7 hours and significantly greater for the hydrocodone with ibuprofen group at 5, 6, and 8 hours (P < or = 0.05). Mean pain intensity difference (PID) scores were similar for hydrocodone with ibuprofen and oxycodone with acetaminophen at 0.5, 1, 1.5, 2, 2.5, 3, and 4 hours and significantly greater for hydrocodone with ibuprofen at 5, 6, 7, and 8 hours (P < or = 0.05). Total PR scores were similar for hydrocodone with ibuprofen and oxycodone with acetaminophen for the 0- to 3- and 0- to 4-hour intervals and significantly greater for hydrocodone with ibuprofen for the 0- to 6- and 0- to 8-hour intervals (P < 0.05). The sum of the PID scores was similar for hydrocodone with ibuprofen and oxycodone with acetaminophen for the 0- to 3-, 0- to 4-, 0- to 6-, and 0- to 8-hour intervals. The median estimated time to onset of analgesia, mean peak PR score, median time to remedication, and mean global assessment score were similar for hydrocodone with ibuprofen and oxycodone with acetaminophen. Assay sensitivity was demonstrated by the presence of statistically significant differences between both active treatments and placebo (n = 60). The number of patients experiencing adverse events was similar for each of the 3 groups (11 [18.0%], hydrocodone with ibuprofen; 7 [11.9%], oxycodone with acetaminophen; and 6 [10.0%], placebo).
In this study, a 2-tablet dose of combination hydrocodone 7.5 mg and ibuprofen 200 mg was as effective as a 2-tablet dose of combination oxycodone 5 mg and acetaminophen 325 mg in the treatment of moderate to severe postoperative obstetric or gynecologic pain. Both treatments were superior to placebo. The results of this study suggest that the combination of hydrocodone 7.5 mg and ibuprofen 200 mg may offer prescribers an additional option in combination pain therapy.
本研究的目的是比较氢可酮与布洛芬联合用药和羟考酮与对乙酰氨基酚联合用药在治疗中重度产科或妇科术后疼痛方面的有效性。
7.5毫克氢可酮与200毫克布洛芬是唯一获批的含阿片类药物和布洛芬的固定剂量复方镇痛药。
本随机、双盲、平行组、单剂量、活性对照、安慰剂对照研究比较了2片剂量的7.5毫克氢可酮与200毫克布洛芬、2片剂量的5毫克羟考酮与325毫克对乙酰氨基酚以及安慰剂的效果。在8小时内评估镇痛效果。
氢可酮与布洛芬组和羟考酮与对乙酰氨基酚组(分别为n = 61和59)在0.5、1、1.5、2、2.5、3、4和7小时的平均疼痛缓解(PR)评分相似,氢可酮与布洛芬组在5、6和8小时的评分显著更高(P≤0.05)。氢可酮与布洛芬组和羟考酮与对乙酰氨基酚组在0.5、1、1.5、2、2.5、3和4小时的平均疼痛强度差异(PID)评分相似,氢可酮与布洛芬组在5、6、7和8小时的评分显著更高(P≤0.05)。氢可酮与布洛芬组和羟考酮与对乙酰氨基酚组在0至3小时和0至4小时的总PR评分相似,氢可酮与布洛芬组在0至6小时和0至8小时的评分显著更高(P < 0.05)。氢可酮与布洛芬组和羟考酮与对乙酰氨基酚组在0至3小时、0至4小时、0至6小时和0至8小时的PID评分总和相似。氢可酮与布洛芬组和羟考酮与对乙酰氨基酚组的中位镇痛起效估计时间、平均PR峰值评分、中位再次用药时间和平均总体评估评分相似。两种活性治疗与安慰剂之间存在统计学显著差异,证明了检测的敏感性(n = 60)。三组中经历不良事件的患者数量相似(氢可酮与布洛芬组11例[18.0%];羟考酮与对乙酰氨基酚组7例[11.9%];安慰剂组6例[10.0%])。
在本研究中,2片剂量的7.5毫克氢可酮与200毫克布洛芬联合用药在治疗中重度产科或妇科术后疼痛方面与2片剂量的5毫克羟考酮与325毫克对乙酰氨基酚联合用药效果相当。两种治疗均优于安慰剂。本研究结果表明,7.5毫克氢可酮与200毫克布洛芬联合用药可能为处方者在联合疼痛治疗中提供额外的选择。