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

BACKGROUND: Clinical registries, which capture information about the health and healthcare use of patients with a health condition or treatment, often contain patient-reported outcomes (PROs) that provide insights about the patient’s perspectives on their health. Missing data can affect the value of...

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Detalles Bibliográficos
Autores principales: Ayilara, Olawale F., Zhang, Lisa, Sajobi, Tolulope T., Sawatzky, Richard, Bohm, Eric, Lix, Lisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585083/
https://www.ncbi.nlm.nih.gov/pubmed/31221151
http://dx.doi.org/10.1186/s12955-019-1181-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585083/
https://www.ncbi.nlm.nih.gov/pubmed/31221151
http://dx.doi.org/10.1186/s12955-019-1181-2

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