Patients have the right to do what regarding their treatment information?

Patients possess the right to refuse additional information and delegate decision-making regarding their treatment. This aspect of patient autonomy respects the belief that individuals should have control over their own health care choices, including the information they wish to receive or not receive. Patients may opt to not be given certain details if they believe it would negatively affect their well-being or if they wish to delegate decisions to a trusted family member or healthcare proxy. This empowers patients to manage their healthcare journey in a way that aligns with their preferences and values.

The other options do not correctly convey the nuances of patient rights. While patients should be informed about their treatment, the choice to receive all possible information can be overwhelming and may not be preferred by everyone. Sharing medical records widely can pose confidentiality and privacy issues, as patients have the right to keep their information private. Lastly, while discussing treatment with family members can be important, it is crucial that patients are able to set their own boundaries on who is included in these discussions, rather than being restricted to only family members.