Cottrell Suzi, Tilden Dominic, Robinson Paul, Bae Jay, Arellano Jorge, Edgell Eric, Aristides Mike, Boye Kristina S
IMS Health, London, UK.
Value Health. 2008 May-Jun;11(3):376-88. doi: 10.1111/j.1524-4733.2007.00256.x.
To estimate the cost-effectiveness of atomoxetine for children with attention-deficity/hyperactivity disorder (ADHD) in the United Kingdom compared with current alternatives.
An economic model with Markov processes was developed to estimate the costs and benefits of atomoxetine versus other current ADHD treatment options. The model evaluated atomoxetine in five patient subgroups according to treatment history and the existence of comorbidities precluding stimulant medication. The incremental cost per quality-adjusted life-year (QALY) was calculated for atomoxetine treatment algorithms compared with comparator algorithms. The Markov process incorporated 18 health states, representing a range of outcomes across all treatment options included in the algorithms. Utility values were derived from a survey of 83 parents of children with ADHD. The effectiveness and safety aspects of the treatment options were based on a thorough review of controlled clinical trials and other clinical literature, and validated by international experts. Costs and outcomes were estimated using Monte Carlo simulation over a 1-year duration, with costs estimated from the perspective of the National Health Service in England and Wales.
For stimulant-naive patients, the incremental cost per QALY gained for the atomoxetine algorithm compared with immediate-release methylphenidate hydrochloride (MPH) was pound 15,224 ( pound 13,241 compared with extended-release MPH). In the stimulant-exposed populations, the incremental cost per QALY for the atomoxetine algorithm was between pound 14,169 and pound 15,878. For patients contraindicated for stimulant therapies, the incremental cost per QALY was pound 11,523 and pound 12,370 for stimulant-naive and stimulant-exposed populations, respectively.
The economic evaluation showed atomoxetine is an effective alternative across a range of ADHD populations and offers value-for-money in the treatment of ADHD.
评估在英国,与当前其他治疗方法相比,托莫西汀治疗注意力缺陷/多动障碍(ADHD)儿童的成本效益。
构建一个包含马尔可夫过程的经济模型,以估计托莫西汀与其他当前ADHD治疗方案的成本和效益。该模型根据治疗史和存在排除使用兴奋剂药物的合并症情况,将患者分为五个亚组来评估托莫西汀。计算托莫西汀治疗方案相对于对照方案每获得一个质量调整生命年(QALY)的增量成本。马尔可夫过程纳入了18种健康状态,代表了各治疗方案中一系列的结局。效用值来自对83名ADHD儿童家长的调查。治疗方案的有效性和安全性基于对对照临床试验及其他临床文献的全面回顾,并经国际专家验证。成本和结局通过为期1年的蒙特卡洛模拟进行估计,成本从英格兰和威尔士国民医疗服务体系的角度进行估算。
对于未使用过兴奋剂的患者,与速释盐酸哌甲酯(MPH)相比,托莫西汀方案每获得一个QALY的增量成本为15,224英镑(与缓释MPH相比为13,241英镑)。在使用过兴奋剂的人群中,托莫西汀方案每QALY的增量成本在14,169英镑至15,878英镑之间。对于禁用兴奋剂治疗的患者,未使用过兴奋剂和使用过兴奋剂的人群每QALY的增量成本分别为11,523英镑和12,370英镑。
经济评估表明,托莫西汀在一系列ADHD人群中是一种有效的替代药物,在ADHD治疗中具有性价比。