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The use of personal health information outside the circle of care: consent preferences of patients from an academic health care institution.
Tosoni, Sarah; Voruganti, Indu; Lajkosz, Katherine; Habal, Flavio; Murphy, Patricia; Wong, Rebecca K S; Willison, Donald; Virtanen, Carl; Heesters, Ann; Liu, Fei-Fei.
Afiliação
  • Tosoni S; Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Voruganti I; Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Lajkosz K; Department of Radiation Oncology, University of Toronto, Toronto, ON, Canada.
  • Habal F; Department of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Murphy P; Department of Medicine, University Health Network, Toronto, ON, Canada.
  • Wong RKS; Department of Anaesthesia, University Health Network, Toronto, ON, Canada.
  • Willison D; Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Virtanen C; Department of Radiation Oncology, University of Toronto, Toronto, ON, Canada.
  • Heesters A; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada.
  • Liu FF; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada.
BMC Med Ethics ; 22(1): 29, 2021 03 24.
Article em En | MEDLINE | ID: mdl-33761938
ABSTRACT

BACKGROUND:

Immense volumes of personal health information (PHI) are required to realize the anticipated benefits of artificial intelligence in clinical medicine. To maintain public trust in medical research, consent policies must evolve to reflect contemporary patient preferences.

METHODS:

Patients were invited to complete a 27-item survey focusing on (a) broad versus specific consent; (b) opt-in versus opt-out approaches; (c) comfort level sharing with different recipients; (d) attitudes towards commercialization; and (e) options to track PHI use and study results.

RESULTS:

222 participants were included in the analysis; 83% were comfortable sharing PHI with researchers at their own hospital, although younger patients (≤ 49 years) were more uncomfortable than older patients (50 + years; 13% versus 2% uncomfortable, p < 0.05). While 56% of patients preferred broad consent, 38% preferred specific consent; 6% preferred not sharing at all. The majority of patients (63%) preferred to be asked for permission before entry into a contact pool. Again, this trend was more pronounced for younger patients (≤ 49 years 76%). Approximately half of patients were uncomfortable sharing PHI with commercial enterprises (51% uncomfortable, 27% comfortable, 22% neutral). Most patients preferred to track PHI usage (61%), with the highest proportion once again reported by the youngest patients (≤ 49 years 71%). A majority of patients also wished to be notified regarding study results (70%).

CONCLUSIONS:

While most patients were willing to share their PHI with researchers within their own institution, many preferred a transparent and reciprocal consent process. These data also suggest a generational shift, wherein younger patients preferred more specific consent options. Modernizing consent policies to reflect increased autonomy is crucial in fostering sustained public engagement with medical research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Registros de Saúde Pessoal Limite: Humans Idioma: En Revista: BMC Med Ethics Assunto da revista: ETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Registros de Saúde Pessoal Limite: Humans Idioma: En Revista: BMC Med Ethics Assunto da revista: ETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Canadá