Early cost-utility analysis of general and cerebrospinal fluid-specific Alzheimer's disease biomarkers for hypothetical disease-modifying treatment decision in mild cognitive impairment

被引:17
|
作者
Handels, Ron L. H. [1 ,2 ]
Joore, Manuela A. [2 ,3 ]
Tran-Duy, An [3 ,4 ,5 ]
Wimo, Anders [6 ]
Wolfs, Claire A. G. [1 ]
Verhey, Frans R. J. [1 ]
Severens, Johan L. [7 ]
机构
[1] Maastricht Univ, Sch Mental Hlth & Neurosci, Dept Psychiat & Neuropsychol, Alzheimer Ctr Limburg, Maastricht, Netherlands
[2] Sch Publ Hlth & Primary Care, Dept Hlth Org Policy & Econ, Maastricht, Netherlands
[3] Maastricht Univ, Med Ctr, Dept Clin Epidemiol & Med Technol Assessment, Maastricht, Netherlands
[4] Maastricht Univ, Med Ctr, Dept Internal Med, Maastricht, Netherlands
[5] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[6] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Stockholm, Sweden
[7] Erasmus Univ, Inst Hlth Policy & Management, Rotterdam, Netherlands
关键词
Alzheimer's disease; Mild cognitive impairment; Cerebrospinal fluid; Biomarker; Decision analytic modeling; Economic evaluation; Cost-utility; Hypothetical disease-modifying treatment; ECONOMIC-EVALUATION; DEMENTIA; DIAGNOSIS; IMPACT; TESTS;
D O I
10.1016/j.jalz.2015.02.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The study aimed to determine the room for improvement of a perfect cerebrospinal fluid (CSF) biomarker and the societal incremental net monetary benefit of CSF in subjects with mild cognitive impairment (MCI) assuming a hypothetical disease-modifying Alzheimer's disease (AD) treatment. Methods: A decision model compared current practice to a perfect biomarker and to two strategies positioning CSF as add- on test when current practice concluded the presence or absence of AD. Results: The simulated MCI population was aged on average 68.3 and 49% had AD. The room for improvement by the perfect CSF test was 0.39 quality adjusted life years, V33,622 ($ 43,372) savings, 2.0 potential beneficial treatment years, and 1.3-year delay in dementia conversion. Discussion: The results indicated more potential benefit from a biomarker positioned to verify subjects who are not expected to have AD (i.e., to prevent undertreatment) rather than to verify subjects expected to have AD (prevent overtreatment). Sensitivity analyses explored different CSF positions. (C) 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:896 / 905
页数:10
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