Snedecor Sonya J, Botteman Marc F, Schaefer Kendyl, Sarocco Phillip, Barry Nadine, Pickard A Simon
Pharmerit North America LLC, 4350 East-West Highway, Suite 430, Bethesda, MD 20814, USA.
J Ment Health Policy Econ. 2010 Mar;13(1):27-35.
Eszopiclone is effective for the treatment of insomnia in patients with insomnia and comorbid major depressive disorder (MDD). Both conditions impose significant economic burden, with the US societal cost of depression estimated at USD 50 billion annually.
The purpose of this analysis was to examine the costs and benefits of eszopiclone co-administered with fluoxetine (ESZ+FLX) compared to placebo co-administered with fluoxetine (PBO+FLX) in adults meeting the DSM-IV criteria for insomnia and MDD.
Data from 434 patients enrolled in an 8-week clinical trial who met the economic-subanalysis criteria were examined. The costs of medical care (in 2007 USUSD ) and lost work time were estimated from the Hamilton Depression Scale (HAM-D17) scores using published algorithms. Cost of lost productivity while at work was based on responses to the Work Limitations Questionnaire. The impact of therapy on quality-adjusted life years (QALYs) was estimated by transforming HAM-D17 (base case analysis) or Short Form Health Survey (SF-12) (scenario analyses) responses into health utility scores using published algorithms. Drug costs were estimated based on average wholesale price.
The mean 8-week increases in QALYs from baseline were 0.0392 and 0.0334 for the ESZ+FLX and PBO+FLX groups, respectively. Mean per-patient costs were USD 1,279 and USD 1,198 for the respective groups. Thus, co-treatment resulted in net increases of 0.0058 QALYs and USD 81, leading to an incremental cost per QALY gained of approximately USD 14,000.
Co-administration of eszopiclone and fluoxetine improved patients' insomnia symptoms and appeared to be a cost-effective treatment strategy for patients with insomnia and comorbid MDD. One limitation of this study is that optimal utility estimation techniques were not available. Utilities were instead derived indirectly using the HAM-D17 (disease-specific, not generic) or SF-12 (generic, but potentially insensitive to important changes in some conditions) instruments.
Sleep disturbance is predictive of depression relapse, and is the most common residual symptom in patients who have been successfully treated with fluoxetine for depression. Thus, identifying cost-effective strategies for the treatment of insomnia symptoms is important for this patient population.
Treatment guidelines and drug coverage decisions should be based on clinical evidence, effectiveness, and economic criteria (i.e., whether an effective drug therapy produces sufficient benefits given its costs). This information about the overall value of eszopiclone can be measured as the cost per QALY gained with the use of ESZ+FLX compared with FLX alone. In order to make decisions based on value, payers and policy makers must have access to reliable cost-effectiveness information.
The residual efficacy observed in the clinical trial following the discontinuation of co-therapy should be explored further to determine whether intermittent treatment with ESZ+FLX is a cost-effective strategy.
艾司佐匹克隆对伴有重度抑郁症(MDD)的失眠患者的失眠治疗有效。这两种病症都会带来巨大的经济负担,据估计,美国抑郁症的社会成本每年达500亿美元。
本分析的目的是研究在符合《精神疾病诊断与统计手册》第四版(DSM-IV)失眠和MDD标准的成年人中,与氟西汀联合使用安慰剂(PBO+FLX)相比,艾司佐匹克隆联合氟西汀(ESZ+FLX)的成本和效益。
对434名参加为期8周临床试验且符合经济亚分析标准的患者的数据进行了研究。使用已发表的算法,根据汉密尔顿抑郁量表(HAM-D17)评分估算医疗费用(以2007年美元计)和误工时间。工作时生产力损失成本基于对工作限制问卷的回答。通过使用已发表的算法将HAM-D17(基础病例分析)或简短健康调查问卷(SF-12)(情景分析)的回答转换为健康效用评分,来估算治疗对质量调整生命年(QALY)的影响。药物成本根据平均批发价估算。
ESZ+FLX组和PBO+FLX组从基线开始的8周QALY平均增加量分别为0.0392和0.0334。各组患者的平均成本分别为1279美元和1198美元。因此,联合治疗使QALY净增加0.0058,成本净增加81美元,每获得一个QALY的增量成本约为14000美元。
艾司佐匹克隆与氟西汀联合使用改善了患者的失眠症状,对于伴有MDD的失眠患者似乎是一种具有成本效益的治疗策略。本研究的一个局限性是没有可用的最佳效用估计技术。相反,效用是使用HAM-D17(针对特定疾病,而非通用)或SF-12(通用,但可能对某些病症的重要变化不敏感)工具间接得出的。
睡眠障碍可预测抑郁症复发,并是已成功用氟西汀治疗抑郁症的患者中最常见的残留症状。因此,确定治疗失眠症状的具有成本效益的策略对该患者群体很重要。
治疗指南和药物覆盖范围的决定应基于临床证据、有效性和经济标准(即一种有效的药物治疗在考虑其成本的情况下是否能产生足够的效益)。关于艾司佐匹克隆总体价值的这一信息可以通过与单独使用氟西汀相比,使用ESZ+FLX获得的每个QALY的成本来衡量。为了基于价值做出决策,支付方和政策制定者必须能够获取可靠的成本效益信息。
应进一步探索联合治疗停止后在临床试验中观察到的残留疗效,以确定ESZ+FLX间歇治疗是否是一种具有成本效益的策略。