The use of medical records in research: what do patients want?
about
"Let's get the best quality research we can": public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study.Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative StudyDynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical researchA Protocol for the secure linking of registries for HPV surveillanceGenomic research and wide data sharing: views of prospective participantsPhysician privacy concerns when disclosing patient data for public health purposes during a pandemic influenza outbreakAlternatives to project-specific consent for access to personal information for health research: insights from a public dialogueConsent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?Big data and ambulatory care: breaking down legal barriers to support effective useComparative effectiveness research and big data: balancing potential with legal and ethical considerations.The acceptability of conducting data linkage research without obtaining consent: lay people's views and justifications.Legal and ethical values in the resolution of research-related disputes: how can IRBS respond to participant complaints?Saudi views on consenting for research on medical records and leftover tissue samples.The re-identification risk of Canadians from longitudinal demographics.Estimating the re-identification risk of clinical data setsPublic trust in health information sharing: implications for biobanking and electronic health record systemsA survey of patient perspectives on the research use of health information and biospecimensAlternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?Privacy and confidentiality in pragmatic clinical trials.Self-report versus medical record - perinatal factors in a study of infant leukaemia: a study from the Children's Oncology GroupPatient and public views on electronic health records and their uses in the United kingdom: cross-sectional surveyPublic opinion about the importance of privacy in biobank research.Stakeholders' views on data sharing in multicenter studies.Perspectives of Patients With Cancer on the Ethics of Rapid-Learning Health Systems.Parental opinions regarding an opt-out consent process for inpatient pediatric prospective observational research in the US.Patient preferences toward an interactive e-consent application for research using electronic health records.Research on medical records without informed consent.Developing a UK registry to investigate the role of cardiovascular magnetic resonance (CMR) in patients who activate the primary percutaneous coronary intervention (PPCI) pathway: a multicentre, feasibility study linking routinely collected electronAccess to health insurance: experiences and attitudes of those with genetic versus non-genetic medical conditions.
P2860
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P2860
The use of medical records in research: what do patients want?
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
The use of medical records in research: what do patients want?
@en
type
label
The use of medical records in research: what do patients want?
@en
prefLabel
The use of medical records in research: what do patients want?
@en
P2093
P2860
P50
P1476
The use of medical records in research: what do patients want?
@en
P2093
Julia Slutsman
Laura Plantinga
Marvin R Natowicz
Sara Chandros Hull
P2860
P304
P356
10.1111/J.1748-720X.2003.TB00105.X
P577
2003-01-01T00:00:00Z