Heightened privacy and confidentiality stakes generate unique anonymity and nondisclosure policies and practices for HIV.

Deception’s justifiability might depend on clinicians’ commitment to solidarity and awareness of social determinants of patients’ vulnerability to HIV infection.

Patient-centered care means offering potentially beneficial interventions while avoiding retraumatizing a patient.

The AMA Code of Medical Ethics offers guidance on HIV screening that expresses respect for patient autonomy while protecting public health.

Merits and drawbacks of U = U messaging are ethically and clinically complex, and drawbacks could harm patients in whom viral suppression is hard to achieve.

Drs Oliva Kates and Monica Gandhi join Ethics Talk to discuss equity and public health messaging in ending the HIV epidemic.

Some clinicians cite absence of long-term data to justify not fully deferring surgery for children with DSD, and legal restrictions of early procedures are also at play.

Dr Nat Mulkey and Dr Carl G. Streed Jr join Ethics Talk to discuss their article coauthored with Dr Barbara M. Chubak, "A Call to Update Standard of Care for Children With Differences in Sex Development."

Financial relationships are common, and ethical questions rightly emerge about how conflicts of interest compromise investigators’ approaches to research.

Clinician-researchers deeply invested in data gathering are still obliged to respect a patient-subject’s right to stop being in research.