关于评估多病症随时间变化的方法的修订建议:使方法与目的相一致。

Corey L Nagel, Nicholas J Bishop, Anda Botoseneanu, Heather G Allore, Jason T Newsom, David A Dorr, Ana R Quiñones
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引用次数: 0

摘要

背景:快速发展的多病症研究领域表明,中年和晚年多病症的变化会对以人为本的重要结果(如与健康相关的生活质量)产生深远影响。然而,在多病症纵向研究中,很少有组织框架和相对较少的工作来权衡各种定量方法的优点和局限性:我们确定并讨论了与特定研究目标相一致的方法,目的是:1)建立评估多病症纵向变化的通用语言;2)揭示我们在多病症进展和变化关键期方面的知识差距;3)为研究提供信息,以确定哪些群体经历了不同的疾病进展速度和不同的病因途径,并与重要健康相关结果的恶化联系在一起:我们回顾了多病症测量、健康相关数据纵向分析、随时间变化的可操作性等方面的实际问题,并讨论了与多病症纵向研究目标的四种一般类型相一致的方法:1)研究多病症的个体变化;2)识别遵循类似多病症发展轨迹的亚群体;3)了解个体或群体何时、如何以及为何转变到多病症的更晚期阶段;以及 4)研究多病症与关键健康领域的共同发展:这项工作鼓励采用系统的方法对多病症的变化进行定量研究,并为研究人员提供了宝贵的资源,以衡量和尽量减少多病症对老龄人口的有害影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recommendations on Methods for Assessing Multimorbidity Changes Over Time: Aligning the Method to the Purpose.

Background: The rapidly growing field of multimorbidity research demonstrates that changes in multimorbidity in mid- and late-life have far reaching effects on important person-centered outcomes, such as health-related quality of life. However, there are few organizing frameworks and comparatively little work weighing the merits and limitations of various quantitative methods applied to the longitudinal study of multimorbidity.

Methods: We identify and discuss methods aligned to specific research objectives with the goals of (i) establishing a common language for assessing longitudinal changes in multimorbidity, (ii) illuminating gaps in our knowledge regarding multimorbidity progression and critical periods of change, and (iii) informing research to identify groups that experience different rates and divergent etiological pathways of disease progression linked to deterioration in important health-related outcomes.

Results: We review practical issues in the measurement of multimorbidity, longitudinal analysis of health-related data, operationalizing change over time, and discuss methods that align with 4 general typologies for research objectives in the longitudinal study of multimorbidity: (i) examine individual change in multimorbidity, (ii) identify subgroups that follow similar trajectories of multimorbidity progression, (iii) understand when, how, and why individuals or groups shift to more advanced stages of multimorbidity, and (iv) examine the coprogression of multimorbidity with key health domains.

Conclusions: This work encourages a systematic approach to the quantitative study of change in multimorbidity and provides a valuable resource for researchers working to measure and minimize the deleterious effects of multimorbidity on aging populations.

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