Department of Physical Medicine and Rehabilitation, University of Michigan, North Campus Research Complex, 2800 Plymouth Road, Building NCRC B14, Room G216, Ann Arbor, MI, 8109-2800, USA.
Department of Psychiatry, Carver College of Medicine, The University of Iowa, Iowa City, IA, USA.
J Neurol. 2019 Oct;266(10):2406-2422. doi: 10.1007/s00415-019-09417-7. Epub 2019 Jun 12.
Huntington disease (HD) is a progressive neurodegenerative disorder. There are no HD-specific measures to assess for end-of-life (EOL) preferences that have been validated for clinical use. The purpose of this study is to demonstrate reliability and validity of three HD-specific EOL measures for use in and clinical research settings.
We examined internal reliability, test-retest reliability, floor and ceiling effects, convergent and discriminant validity, known groups' validity, measurement error, and change over time to systematically examine reliability and validity of the HDQLIFE EOL measures.
Internal consistency and test-retest reliability were > 0.70. The measures were generally free of floor and ceiling effects and measurement error was minimal. Convergent and discriminant validity were consistent with well-known constructs in the field. Hypotheses for known groups validity were partially supported (there were generally group differences for the EOL planning measures, but not for meaning and purpose or concern with death and dying). Measurement error was acceptable and there were minimal changes over time across the EOL measures.
Results support the clinical utility of the HDQLIFE EOL measures in persons with HD.
亨廷顿病(HD)是一种进行性神经退行性疾病。目前尚无针对终末期(EOL)偏好的 HD 特异性评估措施,这些措施尚未经过验证可用于临床。本研究的目的是证明三种用于临床研究的 HD 特异性 EOL 测量方法的可靠性和有效性。
我们检查了内部可靠性、重测可靠性、地板和天花板效应、收敛和判别有效性、已知群体的有效性、测量误差以及随时间的变化,以系统地检查 HDQLIFE EOL 测量方法的可靠性和有效性。
内部一致性和重测可靠性均大于 0.70。这些措施通常没有地板和天花板效应,且测量误差很小。收敛和判别有效性与该领域的知名结构一致。已知群体有效性的假设得到了部分支持(EOL 计划措施通常存在群体差异,但意义和目的或对死亡的关注则没有)。测量误差可接受,EOL 测量方法在整个过程中的变化很小。
研究结果支持 HDQLIFE EOL 测量方法在 HD 患者中的临床实用性。