Pope Janet E, Prashker Mark, Anderson Jennifer
Department of Medicine, Division of Rheumatology, University of Western Ontario, London, Ontario, Canada.
J Rheumatol. 2004 Jan;31(1):140-9.
To determine whether or not N of 1 trials with diclofenac/misoprostol (Arthrotec) are superior and cost-effective compared with standard treatment in osteoarthritis (OA).
We randomized subjects with OA who were "uncertain that nonsteroidal antiinflammatory drugs (NSAID) were helpful" to 2 different groups. One group received conventional treatment whereby they were told to stop their NSAID and to wait and see what happened. If necessary, treatment with other NSAID and all other usual OA treatment strategies were used. The other group received a series of crossover trials with diclofenac 50 mg and misoprostol 200 micro g twice a day or an identical placebo for 2 weeks each in a random double-blinded manner. Every 4 weeks they chose which treatment they preferred. By 3 months, if there was no clear preference, the N of 1 trials were discontinued. All trial participants were seen monthly for 3 months and at 6 months. All costs (direct and indirect) were collected for both groups. Costs of research-generated visits were not counted in the "conventional treatment" group.
Fifty-one subjects were randomized (stratified by most symptomatic OA area): 25 with knee, 7 with hip, and 19 with hand OA. Twenty-four were randomized into the N of 1 group. There were no differences in the baseline and followup variables including age, income, education, past and current NSAID use, global assessment, Health Assessment Questionnaire (HAQ), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and Medical Outcome Study Short Form-36 (SF-36) scores. In the N of 1 group, 11 patients preferred diclofenac in total (of whom 7 did only one round, 2 did 2 rounds, and 2 did 3 rounds). None of the N of 1 patients preferred placebo and 11 had no preference (2 dropped out at baseline). At 6 months, 15 of 19 in "conventional therapy" and 17 of 21 in N of 1 were taking NSAID. That is, NSAID appeared to be effective in 81% of N of 1 subjects and 79% of conventionally treated patients, even though subjects were initially uncertain that their NSAID were helpful. The total OA-related costs in Canadian dollars per patient (in 1996) for N of 1 treated patients at 6 months were: 551.66 dollars +/- 154.02 dollars (SD) versus 395.62 dollars +/- 226.87 dollars for controls, excluding 2 research visits for controls (p < 0.009). The HAQ pain and disability, WOMAC scales, and physician global assessments improved more in the N of 1 group (at greater cost), but no between-group differences in efficacy were seen, possibly due to small numbers.
N of 1 trials were time-consuming in these patients and are more expensive, but with slightly better outcomes. In addition, NSAID seem to be effective in a majority of subjects with OA who have been uncertain of their benefit.
确定双氯芬酸/米索前列醇(奥湿克)的单病例试验与骨关节炎(OA)的标准治疗相比是否更优且具有成本效益。
我们将那些“不确定非甾体抗炎药(NSAID)是否有帮助”的OA患者随机分为两组。一组接受常规治疗,即告知他们停用NSAID并观察情况。如有必要,可使用其他NSAID及所有其他常用的OA治疗策略。另一组接受一系列交叉试验,以随机双盲方式每天两次服用50毫克双氯芬酸和200微克米索前列醇或相同的安慰剂,各为期2周。每4周他们选择自己更喜欢的治疗方法。到3个月时,如果没有明确偏好,则停止单病例试验。所有试验参与者在3个月内每月就诊一次,6个月时再次就诊。收集两组的所有费用(直接和间接)。研究产生的就诊费用在“常规治疗”组中不计入。
51名受试者被随机分组(按症状最明显的OA部位分层):25例膝关节OA,7例髋关节OA,19例手部OA。24例被随机分入单病例试验组。在基线和随访变量方面,包括年龄、收入、教育程度、既往和当前NSAID使用情况、整体评估、健康评估问卷(HAQ)、西安大略和麦克马斯特大学骨关节炎指数(WOMAC)以及医学结局研究简表36(SF - 36)评分,均无差异。在单病例试验组中,共有11例患者更喜欢双氯芬酸(其中7例只进行了一轮,2例进行了两轮,2例进行了三轮)。单病例试验组中没有患者更喜欢安慰剂,11例无偏好(2例在基线时退出)。6个月时,常规治疗组的19例中有15例、单病例试验组的21例中有17例正在服用NSAID。也就是说,NSAID似乎对81%的单病例试验组受试者和79%的常规治疗患者有效,尽管受试者最初不确定他们的NSAID是否有帮助。以加元计算,单病例试验组患者在6个月时的每名患者与OA相关的总费用为:551.66加元±154.02加元(标准差),而对照组为395.62加元±226.87加元,不包括对照组的2次研究就诊费用(p < 0.009)。单病例试验组的HAQ疼痛和残疾评分、WOMAC量表以及医生整体评估改善更明显(成本更高),但未观察到组间疗效差异,可能是由于样本量小。
在这些患者中,单病例试验耗时且成本更高,但结果略好。此外,NSAID似乎对大多数不确定其益处的OA受试者有效。