优化阿尔茨海默病诊断和治疗:评估在临床实践中整合血液生物标记物进行疾病调整治疗的成本效益

IF 4.3 Q2 BUSINESS
Sandar Aye, R. Handels, B. Winblad, L. Jönsson
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引用次数: 0

摘要

背景近期血液生物标记物(BBM)的发展在诊断阿尔茨海默病(AD)的淀粉样病理方面取得了令人鼓舞的成果。目标我们旨在评估在疾病调整治疗(DMT)背景下血液生物标志物在阿尔茨海默病诊断中的潜在价值。设计我们开发了一个决策分析模型,以评估在阿尔茨海默病诊断中使用血液生物标志物的长期健康结果。我们比较了标准护理(SOC)诊断工作流程与 BBM 作为(1)初级保健中心(PHC)转诊决策工具和(2)专科记忆诊所(MC)侵入性 CSF 检查分流工具的整合情况。我们将决策树和马尔可夫模型相结合,模拟患者的诊断过程、诊断后的治疗决策和长期健康结果。模型的输入参数来自已发表的文献和登记数据分析。我们从社会角度进行了成本效用分析,周期为一年,期限为 30 年(终生)。我们报告了与每种诊断策略相关的正确诊断百分比、成本(2022 欧元)、质量调整生命年 (QALY) 和增量成本效益比 (ICER) 等模拟结果。在 SOC 和 PHC 路径中,被诊断为 AD 患者的终生成本分别为 249,685 欧元和 250,287 欧元,QALY 分别为 9.5 和 9.52。成本增量为 603 欧元,QALYs 收益为 0.01,ICER 为 48,296 欧元。结论在PHC使用BBM做出转诊决定可能会增加初始诊断成本,但可以避免与疾病进展相关的高成本,前提是可以获得具有成本效益的DMT,而在MC使用BBM可以降低初始评估成本,但会产生与疾病进展相关的高成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimising Alzheimer’s Disease Diagnosis and Treatment: Assessing Cost-Utility of Integrating Blood Biomarkers in Clinical Practice for Disease-Modifying Treatment

Optimising Alzheimer’s Disease Diagnosis and Treatment: Assessing Cost-Utility of Integrating Blood Biomarkers in Clinical Practice for Disease-Modifying Treatment

Background

Recent developments in blood biomarkers (BBM) have shown promising results in diagnosing amyloid pathology in Alzheimer’s Disease (AD). However, information on how these BBMs can best be used in clinical settings to optimise clinical decision-making and long-term health outcomes for individuals with AD is still lacking.

Objectives

We aim to assess the potential value of BBM in AD diagnosis within the context of disease-modifying treatment (DMT).

Design

We developed a decision analytic model to evaluate the long-term health outcomes using BBM in AD diagnosis. We compared standard of care (SOC) diagnosis workflow to the integration of BBM as a (1) referral decision tool in primary health center (PHC) and (2) triaging tool for invasive CSF examination in specialist memory clinic (MC). We combined a decision tree and a Markov model to simulate the patient’s diagnostic journey, treatment decisions following diagnosis and long-term health outcomes. Input parameters for the model were identified from published literature and registry data analysis. We conducted a cost-utility analysis from the societal perspective using a one-year cycle length and a 30-year (lifetime) horizon.

Measurements

We reported the simulated outcomes in the percentage of correct diagnosis, costs (in 2022 Euros), quality-adjusted life year (QALY), and incremental cost-effectiveness ratios (ICER) associated with each diagnosis strategy.

Results

Compared to SOC, integrating BBM in PHC increased patient referrals by 8% and true positive AD diagnoses by 10.4%. The lifetime costs for individuals diagnosed with AD were € 249,685 and €250,287, and QALYs were 9.5 and 9.52 in SOC and PHC pathways, respectively. The cost increments were €603, and QALYs gained were 0.01, resulting in an ICER of €48,296. Using BBM in MC reduced the exposure to invasive CSF procedures and costs but also reduced true positive AD diagnoses and QALYs.

Conclusions

Using BBM at PHC to make referral decisions might increase initial diagnostic costs but can prevent high costs associated with disease progression, providing a cost-effective DMT is available, whereas using BBM in MC could reduce the initial evaluation cost but incur high costs associated with disease progression.

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来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
自引率
0.00%
发文量
0
期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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