4.5 Article

A New Procedure to Assess When Estimates from the Cumulative Link Model Can Be Interpreted as Differences for Ordinal Scales in Quality of Life Studies

期刊

CLINICAL EPIDEMIOLOGY
卷 13, 期 -, 页码 53-65

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/CLEPS.S288801

关键词

cumulative link model; ordered probit model; ordinal outcome; ordinal regression; probit link; quality of life

资金

  1. National Medical Research Council [R-608-000-093-511]
  2. Saw Swee Hock School of Public Health Programme of Research Seed Funding [SSHSPH-ResProg]
  3. Asian Breast Cancer Fund [N-176000-023-091]
  4. Swedish Cancer Society (Cancerfonden) [CAN 2015/493]

向作者/读者索取更多资源

Assessing the proxy assumption and estimating the exposure effect using the cumulative link model (CLM) offers a valid test for the presence of an association. The CLM had good performance in estimating the difference in means with simulated ordinal data and provided a method for assessing the proxy assumption, highlighting the importance of evaluating the proxy assumption to avoid reporting invalid estimates in terms of the difference in scores.
Purpose: Assessing the clinical importance of an exposure effect on a quality of life (QoL) score often requires quantifying the effect in terms of a difference in scores. Using the linear regression model (LRM) for this purpose assumes the ordinal score is a proxy for an underlying continuous variable, but the analysis offers no assessment for the validity of the assumption. We propose an approach that assesses the proxy assumption and estimates the exposure effect by using the cumulative link model (CLM). Patients and methods: CLM is a well-established regression model that assumes an ordinal score is an ordered category generated from applying thresholds to a latent continuous variable. Our approach assesses the proxy assumption by testing whether these thresholds are equidistant. We compared the performance of CLM and LRM using simulated ordinal data and illustrated their application to the effect of time since diagnosis on five subscales of fatigue among breast cancer survivors measured using the Multidimensional Fatigue Inventory. Results: CLM had good performance in estimating the difference in means with simulated ordinal data satisfying the proxy assumption, even when the outcome had only a few categories. When the proxy assumption was inadequate, both the CLM and LRM had biased estimates with poor coverage. The proxy assumption was appropriate for four of the five subscales in our real data application to fatigue scores, which highlighted the importance of assessing the proxy assumption to avoid reporting invalid estimates in terms of the difference in scores. Conclusion: The proxy assumption is critical to the interpretation of the exposure effect on the difference in mean QoL scores. CLM offers a valid test for the presence of an association, a method for assessing the proxy assumption, and when the assumption is adequate, an assessment for clinical significance using the difference in means.

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