Schlander Michael
Institute for Innovation & Valuation in Health Care (InnoVal HC), Eschborn, Germany.
Curr Med Res Opin. 2008 Feb;24(2):515-35. doi: 10.1185/030079908x260808.
Conclusions of the recent NICE technology appraisal of treatments for attention-deficit/hyperactivity disorder (ADHD) differ from recommendations by other Health Technology Assessment (HTA) agencies, such as the Scottish Medicines Consortium (CMS) and the Australian Pharmaceutical Benefits Advisory Committee (PBAC). NICE did not identify differences on grounds of clinical effectiveness between treatment options studied and issued technology guidance based on clinical profiles of compounds and on drug acquisition costs. The aim of the present study was to explore the robustness of NICE assessment methods when addressing a complex clinical problem such as the evaluation of ADHD treatment strategies. This robustness will be of interest to international policy-makers, given the widespread perception of NICE as a role model for the implementation of HTAs including economic evaluation.
A qualitative case study was performed to critically appraise the technology assessment report (AR) underlying NICE conclusions, including a systematic search for and analysis of relevant literature.
The AR produced on behalf of NICE was found to exhibit a range of anomalies. Search criteria were not applied consistently, and the available clinical evidence was not used optimally; selection of clinical endpoints and clinical trials for analysis were idiosyncratic. The primary cost-effectiveness model relied on six short-term studies only, and secondary extensions combined heterogeneous study designs and different clinical endpoints. Neither the distinction between efficacy and effectiveness nor the role of treatment compliance in ADHD was addressed adequately. Long-term extensions of the model were impaired by use of inappropriate discount rates and absence of consideration of long-term sequelae associated with ADHD.
A review of the literature strongly suggests that the NICE assessment of ADHD treatment strategies was incomplete and likely prone to bias. It is concluded that NICE did not adequately accommodate a complex clinical decision problem. Although the present qualitative case study of one assessment cannot, and was not designed to, invalidate the NICE approach to economic evaluation of healthcare programs, this observation may have potentially far-reaching implications for the generalizability of NICE-like approaches.
英国国家卫生与临床优化研究所(NICE)近期对注意力缺陷多动障碍(ADHD)治疗方法的技术评估结论,与其他卫生技术评估(HTA)机构的建议不同,如苏格兰药品委员会(CMS)和澳大利亚药物福利咨询委员会(PBAC)。NICE并未基于所研究治疗方案的临床疗效来确定差异,而是根据化合物的临床特征和药物采购成本发布技术指南。本研究的目的是探讨NICE评估方法在解决诸如ADHD治疗策略评估这类复杂临床问题时的稳健性。鉴于人们普遍认为NICE是包括经济评估在内的卫生技术评估实施的典范,这种稳健性将受到国际政策制定者的关注。
进行了一项定性案例研究,以批判性地评估NICE结论所依据的技术评估报告(AR),包括对相关文献的系统检索和分析。
发现代表NICE编写的AR存在一系列异常情况。检索标准未得到一致应用,可用的临床证据未得到最佳利用;临床终点的选择和用于分析的临床试验具有特殊性。主要的成本效益模型仅依赖六项短期研究,二次扩展则结合了不同类型的研究设计和不同的临床终点。疗效与有效性之间的区别以及治疗依从性在ADHD中的作用均未得到充分探讨。该模型的长期扩展受到不当贴现率的影响,且未考虑与ADHD相关的长期后遗症。
文献综述强烈表明,NICE对ADHD治疗策略的评估并不完整,可能存在偏差。得出的结论是,NICE没有充分考虑复杂的临床决策问题。尽管本研究对一项评估的定性案例研究无法且并非旨在使NICE对医疗保健项目的经济评估方法无效,但这一观察结果可能对类似NICE方法的推广产生潜在的深远影响。