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The psychometric properties of the K10 and K6 scales in screening for mood and anxiety disorders in the South African Stress and Health study

机译:南非压力与健康研究中K10和K6量表的心理测量特性用于筛查情绪和焦虑症

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摘要

Emerging research has provided support for the use of the Kessler Psychological Distress Scales in developing countries; however, this research has yet to be extended to southern Africa. This study sought to evaluate the performance of the Kessler scales in screening for depression and anxiety disorders in the South African population. The scales along with the Composite International Diagnostic Interview (CIDI) were included in the South African Stress and Health study, a nationally representative household survey. The K10/K6 demonstrated moderate discriminating ability in detecting depression and anxiety disorders in the general population; evidenced by area under the receiver operating curves of 0.73 and 0.72 respectively. However, both scales failed to meet our acceptability criteria of high sensitivity and high positive predictive value. Examinations of differences in responding by race/ethnicity revealed that the K10/K6 [Kessler Psychological Distress Scale 10‐item (K10) and the abbreviated six‐item (K6)] had significantly lower discriminating ability with respect to depression and anxiety disorders among the Black group (0.71) than among the combined minority race/ethnic groups of White, Colored, and Indian/Asian (0.78;  = 0.016). The difference in time period assessed on the K10/K6 (past 30 days) versus the CIDI (past 12 months) was a notable limitation of this study. Additional validation studies using clinician diagnostic instruments are recommended.
机译:新兴研究为在发展中国家使用凯斯勒心理困扰量表提供了支持;但是,这项研究尚未扩展到南部非洲。这项研究旨在评估Kessler量表在筛查南非人群抑郁和焦虑症中的表现。该量表与综合国际诊断访谈(CIDI)一起纳入了南非压力与健康研究,该研究是全国性的家庭调查。 K10 / K6在普通人群中表现出中等的辨别能力,可用于检测抑郁症和焦虑症。由接收器工作曲线下方的面积分别证明为0.73和0.72。但是,这两个量表均未达到我们的高灵敏度和高阳性预测值的可接受标准。通过种族/民族回应的差异调查显示,K10 / K6 [凯斯勒心理困扰量表10-项(K10)和缩写的六项(K6)]在抑郁症和焦虑症中的辨别能力明显较低。黑人(0.71)比白人,有色人种和印度/亚洲人的少数民族/种族组合(0.78; = minority0.016)高。在K10 / K6(过去30天)与CIDI(过去12天)之间评估的时间差异是该研究的显着局限。建议使用临床医生的诊断仪器进行其他验证研究。

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