Patient experience of the informed consent process during acute myocardial infarction: a sub-study of the VALIDATE-SWEDEHEART trial

OBJECTIVE: We aimed to assess the patient experience of informed consent (IC) during acute myocardial infarction (AMI) in a sub-study of the VALIDATE-SWEDEHEART trial. The original trial compared two anticoagulant agents in patients undergoing coronary intervention. A witnessed oral IC was required...

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Detalles Bibliográficos
Autores principales: Olsson, Anneli, Ring, Camilla, Josefsson, Johan, Eriksson, Annika, Rylance, Rebecca, Fröbert, Ole, James, Stefan, Sparv, David, Erlinge, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059267/
https://www.ncbi.nlm.nih.gov/pubmed/32143733
http://dx.doi.org/10.1186/s13063-020-4147-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059267/
https://www.ncbi.nlm.nih.gov/pubmed/32143733
http://dx.doi.org/10.1186/s13063-020-4147-0

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