Cargando…
Trials using deferred consent in the emergency setting: a systematic review and narrative synthesis of stakeholders’ attitudes
BACKGROUND: Patients with acute conditions often lack the capacity to provide informed consent, and narrow therapeutic windows mean there is no time to seek consent from surrogates prior to treatment being commenced. One method to enable the inclusion of this study population in emergency research i...
Autores principales: | Fitzpatrick, Aran, Wood, Fiona, Shepherd, Victoria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109432/ https://www.ncbi.nlm.nih.gov/pubmed/35578362 http://dx.doi.org/10.1186/s13063-022-06304-x |
Ejemplares similares
-
Use of deferred proxy consent in two emergency critical care trials
por: Kompanje, E, et al.
Publicado: (2009) -
Exploring the inclusion of under-served groups in trials methodology research: an example from ethnic minority populations’ views on deferred consent
por: Raven-Gregg, Timia, et al.
Publicado: (2021) -
Practitioner views and experiences of deferred consent in paediatric and neonatal emergency care trials: the connect study
por: Woolfall, Kerry, et al.
Publicado: (2013) -
Patient and proxies’ attitudes towards deferred consent in randomised trials of acute treatment for stroke: A qualitative survey
por: van den Bos, Noa, et al.
Publicado: (2021) -
Deferred consent in emergency intensive care research: what if the patient dies early? Use the data or not?
por: Jansen, T. C., et al.
Publicado: (2007)