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利用二级数据源验证帕金森病与临床诊断标准的符合度。

Validation of secondary data sources to identify Parkinson disease against clinical diagnostic criteria.

出版信息

Am J Epidemiol. 2015 Feb 1;181(3):185-90. doi: 10.1093/aje/kwu326. Epub 2014 Dec 29.

Abstract

Parkinson disease (PD) is the second most common neurodegenerative disorder. Its diagnosis relies solely on a clinical examination and is not straightforward because no diagnostic test exists. Large, population-based, prospective cohort studies designed to examine other outcomes that are more common than PD might provide cost-efficient alternatives for studying the disease. However, most cohort studies have not implemented rigorous systematic screening for PD. A majority of epidemiologic studies that utilize population-based prospective designs rely on secondary data sources to identify PD cases. Direct validation of these secondary sources against clinical diagnostic criteria is lacking. The Framingham Heart Study has prospectively screened and evaluated participants for PD based on clinical diagnostic criteria. We assessed the predictive value of secondary sources for PD identification relative to clinical diagnostic criteria in the Framingham Heart Study (2001-2012). We found positive predictive values of 1.0 (95% confidence interval: 0.868, 1.0), 1.0 (95% confidence interval: 0.839, 1.0), and 0.50 (95% confidence interval: 0.307, 0.694) for PD identified from self-report, use of antiparkinsonian medications, and Medicare claims, respectively. The negative predictive values were all higher than 0.99. Our results highlight the limitations of using only Medicare claims data and suggest that population-based cohorts may be utilized for the study of PD determined via self-report or medication inventories while preserving a high degree of confidence in the validity of PD case identification.

摘要

帕金森病(PD)是第二常见的神经退行性疾病。它的诊断仅依赖于临床检查,而且并不简单,因为目前还没有诊断测试。设计用于检查比 PD 更常见的其他结果的大型、基于人群的前瞻性队列研究可能为研究该疾病提供具有成本效益的替代方案。然而,大多数队列研究并未对 PD 进行严格的系统筛查。大多数利用基于人群的前瞻性设计的流行病学研究依赖于二级数据源来确定 PD 病例。缺乏对这些二级来源与临床诊断标准进行直接验证。弗雷明汉心脏研究(Framingham Heart Study)根据临床诊断标准前瞻性筛选和评估 PD 参与者。我们评估了二级来源相对于 Framingham Heart Study(2001-2012 年)中临床诊断标准对 PD 识别的预测价值。我们发现,通过自我报告、使用抗帕金森病药物和医疗保险索赔识别的 PD 的阳性预测值分别为 1.0(95%置信区间:0.868,1.0)、1.0(95%置信区间:0.839,1.0)和 0.50(95%置信区间:0.307,0.694)。阴性预测值均高于 0.99。我们的结果突出了仅使用医疗保险索赔数据的局限性,并表明基于人群的队列可能用于通过自我报告或药物清单研究 PD,同时保持对 PD 病例识别的高度信心。

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