Impact of missing data on bias and precision when estimating change in patient-reported outcomes from a clinical registry

Author:

Ayilara Olawale F.,Zhang Lisa,Sajobi Tolulope T.,Sawatzky Richard,Bohm Eric,Lix Lisa M.ORCID

Funder

Canadian Institutes of Health Research

Canada Research Chairs

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health,General Medicine

Reference36 articles.

1. Franklin PD, Ayers DC, Berliner E. The essential role of patient-centered registries in an era of electronic health records. NEJM Catal. 2018 [cited 2018 Nov 20]; Available from: https://catalyst.nejm.org/force-tjr-patient-centered-registries/

2. Johnston BC, Patrick DL, Thorlund K, Busse J, da Costa B, Schunemann H, et al. Patient-reported outcomes in meta-analyses, part 2: methods for improving interpretability for decision-makers. Health Qual Life Outcomes. 2013;11(211):1–9.

3. Bell MB, Fairclough DL. Practical and statistical issues in missing data for longitudinal patient-reported outcomes. Stat Methods Med Res. 2014;23(5):440–9.

4. Schafer JL. Analysis of incomplete multivariate data. London: Chapman and Hall; 1997.

5. Molenberghs G, Kenward MG. Missing data in clinical studies. West Sussex: John Wiley & Sons; 2007.

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