Research on experiences of practicing physicians who have disabilities could help medical schools counsel applicants and increase enrollment among students with disabilities. This can ultimately improve care for patients with disabilities.

After years of funding disease-specific treatment, donation trends have shifted to support broader health systems infrastructure development. A remaining challenge is how to sustain antiretroviral therapy (ART) for patients in resource-poor regions.

Emergency medical consultations share with other emergencies the need for prompt action, potentially without information or tools ordinarily available.

Lack of ethical, legal, and clinical consensus about best practice sometimes combines with a poor clinical evidence base.

This article considers relevant history that informs the AMA Code of Medical Ethics' opinions about neurological criteria for death.

After the Indiana HIV outbreak in 2015, Congress partially repealed the ban on needle exchange programs, providing funding for operations but not syringes.

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.