Beinhoff Ulrike, Hilbert Verena, Bittner Daniel, Gron Georg, Riepe Matthias W
Department of Psychiatry, Charité Medical University, Berlin, Germany.
Dement Geriatr Cogn Disord. 2005;20(5):278-85. doi: 10.1159/000088249. Epub 2005 Sep 12.
The current increase in aged individuals in number and proportion of the general population warrants dependable strategies to improve early detection of cognitive impairment. It was the goal of the present study to develop a triage for bedside testing and outpatient services. In a prospective clinical cohort study at the outpatient Memory Clinic, University of Ulm, Germany, 232 subjects were diagnosed with Alzheimer's disease [AD; NINCDS-ADRDA criteria; n = 66; age 65.9 +/- 7.3 years (mean +/- SD); Mini Mental State Examination (MMSE) score 23.4 +/- 4.1], mild cognitive impairment (MCI; criteria of Petersen et al.; n = 48; age 66.4 +/- 7.1 years; MMSE score 28.3 +/- 1.5), and major depressive disorder (DSM-IV criteria; n = 61; age 63.4 +/- 8.0 years; MMSE score 28.6 +/- 1.6). Diagnosis was secured with extensive neuropsychological, clinical, radiological, and laboratory investigations. Six brief screening tests including the Memory Impairment Screen (MIS), Letter Sorting Test (LST), Verbal Fluency (VF), and Clock Drawing Test (CDT) were assessed independently from the diagnostic procedure. We compared single items and composite scores. LST yielded a diagnostic accuracy of 0.81 and 0.62 for AD and MCI patients versus controls, respectively. With the MIS, diagnostic accuracy was 0.89 and 0.71, respectively. With a combination of LST, MIS, VF, and CDT, a sensitivity for AD and MCI patients of 1.00 and 0.83 was achieved. Thus, single-item screening (e.g. LST, VF) taking little more than 1 min and suitable for bedside testing or brief screening in the general practitioner's office yields diagnostic accuracy comparable to standard laboratory tests for other diseases. A composite of screening tests suitable for application in general outpatient care in neurological and psychiatric services reliably detects patients with AD and MCI.
当前,老年个体在总人口中的数量和比例不断增加,这就需要可靠的策略来改善认知障碍的早期检测。本研究的目的是开发一种用于床边检测和门诊服务的分诊方法。在德国乌尔姆大学门诊记忆诊所进行的一项前瞻性临床队列研究中,232名受试者被诊断患有阿尔茨海默病[AD;NINCDS-ADRDA标准;n = 66;年龄65.9±7.3岁(平均值±标准差);简易精神状态检查表(MMSE)评分23.4±4.1]、轻度认知障碍(MCI;彼得森等人的标准;n = 48;年龄66.4±7.1岁;MMSE评分28.3±1.5)和重度抑郁症(DSM-IV标准;n = 61;年龄66.4±8.0岁;MMSE评分28.6±1.6)。通过广泛的神经心理学、临床、放射学和实验室检查确定诊断。六项简短筛查测试,包括记忆障碍筛查(MIS)、字母分类测试(LST)、语言流畅性(VF)和画钟测试(CDT),独立于诊断程序进行评估。我们比较了单项和综合评分。LST对AD和MCI患者与对照组的诊断准确率分别为0.81和0.62。使用MIS时,诊断准确率分别为0.89和0.71。结合LST、MIS、VF和CDT,AD和MCI患者的敏感性分别达到1.00和0.83。因此,单项筛查(如LST、VF)耗时仅1分钟多一点,适用于床边检测或在全科医生办公室进行简短筛查,其诊断准确率与其他疾病的标准实验室检测相当。一组适用于神经科和精神科门诊普通护理的筛查测试能够可靠地检测出AD和MCI患者。