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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| 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 |