Once the patient’s confusion has resolved, he should be presumed capable unless an assessment shows otherwise. MCCQE ethics objectives prioritize patient autonomy, informed decision-making, and confidentiality . Families may request “therapeutic privilege” or nondisclosure, but this is not the default and cannot override a capable patient’s right to information needed to make decisions. The appropriate first step is to explore the patient’s preferences about receiving serious news (some patients prefer limited information or to delegate decisions). Asking the patient whether he wants to know the diagnosis respects autonomy while remaining sensitive to potential distress. Simply telling him immediately (without checking preferences) may conflict with patient-centered disclosure, and automatically complying with the family’s request violates the patient’s rights and undermines informed consent for goals-of-care planning. A palliative care consult is appropriate, but only after clarifying the patient’s understanding and wishes and beginning honest, preference-guided communication. The clinician should also support the family, explain ethical duties, and reassure them that disclosure can be done gradually and compassionately.