Who provides information about treatment risks and benefits to the patient before signing an informed consent?

Who provides information about treatment risks and benefits to the patient before signing an informed consent?

• A. The social worker
• B. The patient navigator
• C. The genetic counselor
• D. The healthcare provider

Answer: (D)

The healthcare provider is responsible for discussing the treatment risks and benefits with the patient prior to obtaining informed consent. This is essential because the healthcare provider holds the clinical expertise and understanding of the specific treatment options, including their potential outcomes, side effects, and the rationale behind the recommended course of action. During this discussion, the provider ensures that the patient has a clear understanding of the treatment, which empowers the patient to make an informed decision regarding their care. Informed consent is not just a formality; it is a process that reflects respect for patient autonomy and decision-making. While other roles, such as social workers, patient navigators, or genetic counselors, may provide valuable support and additional information, they typically do not have the primary responsibility for conveying comprehensive details about treatment risks and benefits in the context of medical procedures. Each of these other professionals may play a part in the overall care team, but the healthcare provider's role is central to the informed consent process due to their clinical training and direct relationship with the treatment plan.

The healthcare provider is responsible for discussing the treatment risks and benefits with the patient prior to obtaining informed consent. This is essential because the healthcare provider holds the clinical expertise and understanding of the specific treatment options, including their potential outcomes, side effects, and the rationale behind the recommended course of action.

During this discussion, the provider ensures that the patient has a clear understanding of the treatment, which empowers the patient to make an informed decision regarding their care. Informed consent is not just a formality; it is a process that reflects respect for patient autonomy and decision-making.

While other roles, such as social workers, patient navigators, or genetic counselors, may provide valuable support and additional information, they typically do not have the primary responsibility for conveying comprehensive details about treatment risks and benefits in the context of medical procedures. Each of these other professionals may play a part in the overall care team, but the healthcare provider's role is central to the informed consent process due to their clinical training and direct relationship with the treatment plan.