2020
DOI: 10.1097/hcm.0000000000000302
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Ethical Issues and the Electronic Health Record

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Cited by 18 publications
(17 citation statements)
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References 53 publications
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“…13 25 Besides, providing users control over their health information is crucial since it promotes autonomy—an ethical principle that is often violated when patients' information in electronic medical records is accessed or shared without permission. 32 33…”
Section: Discussionmentioning
confidence: 99%
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“…13 25 Besides, providing users control over their health information is crucial since it promotes autonomy—an ethical principle that is often violated when patients' information in electronic medical records is accessed or shared without permission. 32 33…”
Section: Discussionmentioning
confidence: 99%
“…13,25 Besides, providing users control over their health information is crucial since it promotes autonomy-an ethical principle that is often violated when patients' information in electronic medical records is accessed or shared without permission. 32,33 MediLinker was also viewed positively by the participants because of its utility during a pandemic. For instance, as the COVID-19 pandemic forced health care institutions to limit face-to-face interactions, enabling patients to access, add, or revoke personal health information remotely in a secure, efficient, and convenient manner is something that enticed participants to hold positive attitudes toward it.…”
Section: Positive Aspects Representative Quotesmentioning
confidence: 99%
“…This is an important step, as the quality of record keeping can affect the quality of care and the well-being of patients. The process must lead to high quality EPR data as mistakes or omissions can lead to medical errors [69][70][71][72][73][74][75][76] negatively affecting the well-being of patients. Therefore, clinician personal behaviours, such as honesty, accuracy, and conscientiousness in completing patient records and entering data to the EPR is fundamental to the quality and safety of care.…”
Section: Data Collectionmentioning
confidence: 99%
“…What are the potential harms resulting from the distribution of this information and how can these be mitigated? When determining rules regarding access to EPR data for clinical purposes, a tension between the data needs of the HCP to fulfil their healthcare responsibilities and the patient's ability to decide that sharing their record (or parts of their record) is in their best interests [31,74,[85][86][87][88][89][90][91][92][93][94][95][96][97]] must be addressed. However, as previously noted, the process of capturing patient consent can be challenging.…”
Section: Data Accessmentioning
confidence: 99%
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