Martinez-Martin Pablo, Kulisevsky Jaime, Mir Pablo, Tolosa Eduardo, García-Delgado Pilar, Luquin María-Rosario
1Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.
2National Center of Epidemiology, Carlos III Institute of Health, Madrid, Spain.
NPJ Parkinsons Dis. 2018 Jul 2;4:20. doi: 10.1038/s41531-018-0056-2. eCollection 2018.
Early clinical diagnosis of advanced Parkinson's disease (APD) may be difficult. This study aimed to validate a simple screening tool, the CDEPA questionnaire ("Cuestionario De Enfermedad de Parkinson Avanzada" [Questionnaire for Advanced Parkinson's Disease]), for the identification of APD in daily practice. The study included 173 consecutively selected patients with PD (40% were women, mean age was 68.4 ± 10.5 years), stratified according to the Hoehn and Yahr (HY) scale. The CDEPA questionnaire defined APD as the presence of severe disability requiring help for activities of daily living (ADL), motor fluctuations with limitation or inability to perform ADL, severe dysphagia, recurrent falls, or dementia. The diagnostic performance of the questionnaire was assessed against the gold standard criterion based on clinical judgment. PD was categorized as advanced in 65 (38%) patients when using the gold standard and in 109 (63%) patients when the CDEPA questionnaire was used. The CDEPA questionnaire and the gold standard agreed moderately (kappa statistic of 0.48, < 0.001). The CDEPA classified APD with a sensitivity of 97%; specificity of 57%; total accuracy of 72.3%; and area under the curve (for a binary classifier) of 77.2%. Significant differences were found between the groups created by the CDEPA in several usual PD evaluations (HY Scale, SCOPA Motor Scale, Non-motor Symptoms Scale for PD, Clinical Impression of Severity Index for PD, Clinical Global Impression-Severity Scale, and Patient Global Impression-Severity Scale). CDEPA showed satisfactory inter-rater agreement (kappa = 0.88) and test-retest concordance (kappa 0.83). In conclusion, the CDEPA questionnaire is a valid, reliable, and useful instrument for easily screening APD.
晚期帕金森病(APD)的早期临床诊断可能具有挑战性。本研究旨在验证一种简单的筛查工具,即CDEPA问卷(“帕金森病晚期问卷”),以便在日常实践中识别APD。该研究纳入了173例连续入选的帕金森病患者(40%为女性,平均年龄为68.4±10.5岁),并根据霍恩和亚尔(HY)分级进行分层。CDEPA问卷将APD定义为存在严重残疾,日常生活活动(ADL)需要帮助,出现运动波动且限制或无法进行ADL,严重吞咽困难,反复跌倒或痴呆。根据临床判断,以金标准为对照评估该问卷的诊断性能。使用金标准时,65例(38%)患者的帕金森病被归类为晚期;使用CDEPA问卷时,109例(63%)患者被归类为晚期。CDEPA问卷与金标准的一致性中等(kappa统计量为0.48,P<0.001)。CDEPA对APD的分类敏感性为97%;特异性为57%;总准确率为72.3%;二元分类器的曲线下面积为77.2%。在一些常见的帕金森病评估中(HY分级、SCOPA运动量表、帕金森病非运动症状量表、帕金森病严重程度临床印象指数、临床总体印象-严重程度量表和患者总体印象-严重程度量表),CDEPA所划分的组间存在显著差异。CDEPA显示出令人满意的评分者间一致性(kappa=0.88)和重测一致性(kappa 0.83)。总之,CDEPA问卷是一种有效、可靠且实用的工具,可用于轻松筛查APD。