Computerized decision support to optimally funnel patients through the diagnostic pathway for dementia.

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's Research & Therapy Pub Date : 2024-11-26 DOI:10.1186/s13195-024-01614-5
Aniek M van Gils, Antti Tolonen, Argonde C van Harten, Sinthujah Vigneswaran, Frederik Barkhof, Leonie N C Visser, Juha Koikkalainen, Sanna-Kaisa Herukka, Steen Gregers Hasselbalch, Patrizia Mecocci, Anne M Remes, Hilkka Soininen, Afina W Lemstra, Charlotte E Teunissen, Linus Jönsson, Jyrki Lötjönen, Wiesje M van der Flier, Hanneke F M Rhodius-Meester
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Abstract

Background: The increasing prevalence of dementia and the introduction of disease-modifying therapies (DMTs) highlight the need for efficient diagnostic pathways in memory clinics. We present a data-driven approach to efficiently guide stepwise diagnostic testing for three clinical scenarios: 1) syndrome diagnosis, 2) etiological diagnosis, and 3) eligibility for DMT.

Methods: We used data from two memory clinic cohorts (ADC, PredictND), including 504 patients with dementia (302 Alzheimer's disease, 107 frontotemporal dementia, 35 vascular dementia, 60 dementia with Lewy bodies), 191 patients with mild cognitive impairment, and 188 cognitively normal controls (CN). Tests included digital cognitive screening (cCOG), neuropsychological and functional assessment (NP), MRI with automated quantification, and CSF biomarkers. Sequential testing followed a predetermined order, guided by diagnostic certainty. Diagnostic certainty was determined using a clinical decision support system (CDSS) that generates a disease state index (DSI, 0-1), indicating the probability of the syndrome diagnosis or underlying etiology. Diagnosis was confirmed if the DSI exceeded a predefined threshold based on sensitivity/specificity cutoffs relevant to each clinical scenario. Diagnostic accuracy and the need for additional testing were assessed at each step.

Results: Using cCOG as a prescreener for 1) syndrome diagnosis has the potential to accurately reduce the need for extensive NP (42%), resulting in syndrome diagnosis in all patients, with a diagnostic accuracy of 0.71, which was comparable to using NP alone. For 2) etiological diagnosis, stepwise testing resulted in an etiological diagnosis in 80% of patients with a diagnostic accuracy of 0.77, with MRI needed in 77%, and CSF in 37%. When 3) determining DMT eligibility, stepwise testing (100% cCOG, 83% NP, 75% MRI) selected 60% of the patients for confirmatory CSF testing and eventually identified 90% of the potentially eligible patients with AD dementia.

Conclusions: Different diagnostic pathways are accurate and efficient depending on the setting. As such, a data-driven tool holds promise for assisting clinicians in selecting tests of added value across different clinical contexts. This becomes especially important with DMT availability, where the need for more efficient diagnostic pathways is crucial to maintain the accessibility and affordability of dementia diagnoses.

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计算机化决策支持,通过痴呆症诊断途径为患者提供最佳治疗方案。
背景:痴呆症发病率的不断上升和疾病改变疗法(DMT)的引入,凸显了记忆诊所对高效诊断路径的需求。我们提出了一种数据驱动方法,可有效指导三种临床情况下的逐步诊断检测:方法:我们使用了两个记忆诊所队列(ADC、PredictND)的数据,其中包括 504 名痴呆患者(302 名阿尔茨海默病患者、107 名额颞叶痴呆患者、35 名血管性痴呆患者、60 名路易体痴呆患者)、191 名轻度认知障碍患者和 188 名认知正常对照组(CN)。测试包括数字认知筛查(cCOG)、神经心理和功能评估(NP)、自动量化核磁共振成像和脑脊液生物标记物。在诊断确定性的指导下,按照预先确定的顺序依次进行检测。诊断确定性由临床决策支持系统(CDSS)确定,该系统可生成疾病状态指数(DSI,0-1),显示综合征诊断或潜在病因的可能性。根据与每种临床情况相关的敏感性/特异性临界值,如果 DSI 超过了预定义的阈值,则可确诊。每一步都对诊断准确性和是否需要进行额外检查进行评估:结果:使用 cCOG 作为 1) 综合征诊断的预检者有可能准确地减少对广泛 NP 的需求(42%),从而使所有患者都得到综合征诊断,诊断准确率为 0.71,与单独使用 NP 的诊断准确率相当。对于 2)病因诊断,逐步检测可使 80% 的患者获得病因诊断,诊断准确率为 0.77,其中 77% 的患者需要 MRI,37% 的患者需要 CSF。当3)确定DMT资格时,逐步检测(100% cCOG、83% NP、75% MRI)选择了60%的患者进行CSF确证检测,最终确定了90%可能符合条件的AD痴呆患者:结论:不同的诊断方法准确性和效率各不相同。因此,数据驱动工具有望帮助临床医生在不同的临床环境中选择具有附加值的检测项目。这一点在DMT的可用性方面变得尤为重要,因为需要更有效的诊断途径对于保持痴呆症诊断的可及性和可负担性至关重要。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
期刊最新文献
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