Hong Jihyung, Dilla Tatiana, Arellano Jorge
LSE Health, London School of Economics, London, UK.
BMC Psychiatry. 2009 Apr 14;9:15. doi: 10.1186/1471-244X-9-15.
Attention Deficit/Hyperactivity Disorder (ADHD) is a neurobehavioural disorder, affecting 3-6% of school age children and adolescents in Spain. Methylphenidate (MPH), a mild stimulant, had long been the only approved medication available for ADHD children in Spain. Atomoxetine is a non-stimulant alternative in the treatment of ADHD with once-a-day oral dosing. This study aims to estimate the cost-effectiveness of atomoxetine compared to MPH. In addition, atomoxetine is compared to 'no medication' for patient populations who are ineligible for MPH (i.e. having stimulant-failure experience or co-morbidities precluding stimulant medication).
An economic model with Markov processes was developed to estimate the costs and benefits of atomoxetine versus either MPH or 'no medication'. The incremental cost per quality-adjusted life-year (QALY) was calculated for atomoxetine relative to the comparators. The Markov process incorporated 14 health states, representing a range of outcomes associated with treatment options. Utility values were obtained from the utility valuation survey of 83 parents of children with ADHD. The clinical data 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 Spain.
For stimulant-naive patients without contra-indications to stimulants, the incremental costs per QALY gained for atomoxetine were euro 34,308 (compared to an immediate-release MPH) and euro 24,310 (compared to an extended-release MPH). For those patients who have stimulant-failure experience or contra-indications to stimulants, the incremental costs per QALY gained of atomoxetine compared to 'no medication' were euro 23,820 and euro 23,323, respectively.
The economic evaluation showed that atomoxetine is an effective alternative across a range of ADHD populations and offers value-for money in the treatment of ADHD.
注意力缺陷多动障碍(ADHD)是一种神经行为障碍,在西班牙影响3%至6%的学龄儿童和青少年。哌甲酯(MPH)是一种温和的兴奋剂,长期以来一直是西班牙唯一被批准用于治疗ADHD儿童的药物。托莫西汀是一种治疗ADHD的非兴奋剂替代品,每日口服一次。本研究旨在评估托莫西汀与MPH相比的成本效益。此外,将托莫西汀与不符合使用MPH条件(即有兴奋剂治疗失败经历或存在排除使用兴奋剂药物的合并症)的患者群体的“不使用药物”情况进行比较。
开发了一个具有马尔可夫过程的经济模型,以估计托莫西汀与MPH或“不使用药物”相比的成本和效益。计算了托莫西汀相对于对照药物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14种健康状态,代表了与治疗选择相关的一系列结果。效用值来自对83名ADHD儿童家长的效用评估调查。临床数据基于对对照临床试验和其他临床文献的全面审查,并经国际专家验证。成本和结果通过为期1年的蒙特卡洛模拟进行估计,成本从西班牙国家卫生服务的角度进行估计。
对于无兴奋剂使用禁忌的初治患者,托莫西汀每获得一个QALY的增量成本分别为34308欧元(与速释MPH相比)和24310欧元(与缓释MPH相比)。对于有兴奋剂治疗失败经历或有兴奋剂使用禁忌的患者,托莫西汀与“不使用药物”相比每获得一个QALY的增量成本分别为23820欧元和23323欧元。
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。