Potential harms associated with routine collection of patient sociodemographic information: A rapid review

BACKGROUND: Health systems are recommended to capture routine patient sociodemographic data as a key step in providing equitable person‐centred care. However, collection of this information has the potential to cause harm, especially for vulnerable or potentially disadvantaged patients. OBJECTIVE: T...

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Detalles Bibliográficos
Autores principales: Petkovic, Jennifer, Duench, Stephanie L., Welch, Vivian, Rader, Tamara, Jennings, Alison, Forster, Alan J., Tugwell, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Research Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351414/
https://www.ncbi.nlm.nih.gov/pubmed/30341795
http://dx.doi.org/10.1111/hex.12837

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351414/
https://www.ncbi.nlm.nih.gov/pubmed/30341795
http://dx.doi.org/10.1111/hex.12837

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