Clinicians must advocate for decriminalization of SUDs during pregnancy and for improving access to comprehensive, evidence-based care.

“Race” is a product of European-American views of phenotypic and cultural differences and continues to influence Native health decision making.

Social media platforms and organizational websites that facilitate organ procurement should respect potential donors’ autonomy and confidentiality.

The AMA Code of Medical Ethics’ opinions related to organ donors’ informed, voluntary decisions and equitable distribution of organs and tissues.

Large precision health initiatives like the National Institutes of Health’s All of Us campaign raise important ethical questions about consent, privacy, and inclusivity. This month on Ethics Talk, we explore with Dr Katie Johansen Taber and Ysabel Duron strategies for protecting participants and ensuring that diverse communities are represented.

Although the World Health Organization defines infertility as a disease, insurance coverage gaps generate disparities in access to care and treatment, especially for tubal factor infertility and oncofertility.

Practices changed when hospitals became places of recovery rather than death.

With a focus on health justice, literature review suggests possible relationships between HPV type and geography and demonstrates that insurance status matters.

Researchers and clinicians face ethical and policy-based challenges in disclosing, preventing and treating psychosis. Which diagnostic labels should be considered to motivate more effective public and professional dialogue about psychosis risk?

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