Articles Tagged With: Privacy
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Patients Share Preferences About Data Privacy
Most want security and accountability, are concerned about who can access their information and for what purposes.
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Biden Signs Executive Order Protecting Reproductive Rights
Action aims to protect access to healthcare services, patient privacy.
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Admissibility of ED Recordings Depends on Multiple Factors
Even if the patient recorded the entire discharge instructions, relevant discussions might have happened throughout the visit. The defense can challenge the admissibility based on that argument, but the ruling could go either way.
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Emergency Providers Uneasy About Recording Visits
Clinicians might need more information, such as specifics on who would record the discharge instructions, whether it would be recorded on the patient’s personal smartphone, and what safeguards could be required to ensure patient privacy. Combined with possible involvement of the hospital’s legal department, this might make providers more comfortable with the idea.
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NFTs Could Give Patients Control Over Who Accesses Medical Data
Personal health information carries indisputable value to individuals — both clinically and financially. Yet, as it stands, patients have little or no say on how their own health data are shared. Some ethicists argue nonfungible tokens (NFTs) can be used to create a more ethical and transparent system.
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Take Stock of Your Cybersecurity on Data Privacy Day
Part of building patient trust is ensuring personal information remains private and protected.
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IRBs Scrutinizing Recruitment of Adolescents via Social Media
When recruiting adolescents online, investigators should think about how they would proceed if recruitment was conducted in person. Researchers would not be able to barge into an in-person group meeting without an invitation, just as they cannot post in a private Facebook group without the moderator’s permission.
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Many Ethical Considerations for MDs if Patient Is Unvaccinated
Beyond the ethical questions, there are logistics, privacy, and even equity concerns to consider. -
OCR Seeking Ways to Improve HIPAA, Respond to Value Concerns
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‘It’s a No-Man’s Land’: The Pitfalls of Genetic Data-Sharing and Informed Consent
It is unclear how well participants really understand all the potential risks of sharing their DNA. Researchers are ethically obligated to be sure that what they are asking people to consent to is just, fair, appropriate, and respectful of human rights.