1.
Intern Med J
; 51(6): 988-992, 2021 06.
Artículo
en Inglés
| MEDLINE
| ID: mdl-34155757
RESUMEN
Clinical quality registries are increasingly utilised to monitor and improve healthcare quality. Opt-out consent is recommended to maximise participation and ensure validity of data, however, presents specific considerations when including persons with impaired decision-making abilities. This paper describes the innovative Australian Dementia Network Registry recruitment framework designed to optimise inclusion of people with dementia and mild cognitive impairment.