The risks of misinformation being spread through online patient forums can be mitigated by communication strategies aimed at physicians and organizations.

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

The Holocaust and the racial hygiene doctrine that helped rationalize it still overshadow contemporary debates about using gene editing for disease prevention.

Raciolinguistic hierarchies can undermine the quality of Latinx patients’ health experiences.

Improving health outcomes through patient-centered care is one way to build value for stakeholders in health care.

Justification for using WTP values and QALYs lies in incorporating preferences of those whose treatment could be affected.

Allocating resources for interventions requires consensus among stakeholders with a plurality of perspectives about how to weigh antimicrobial stewardship interventions’ risks and benefits.

CEA has been increasingly used to inform public and private organizations’ reimbursement decisions, benefit designs, and price negotiations worldwide.

Co-creative health systems planning requires engaging patients and learning from peers.

Information different patients need or want about cybersecurity risk varies, so communicating clearly is always key.