Certified Clinical Medical Assistant CCMA Practice Test

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What is one purpose of informed consent?

To allow patients to refuse treatment

To ensure patient awareness of potential risks

Informed consent serves several essential purposes in clinical practice, with one of the primary aims being to ensure that patients are made fully aware of the potential risks associated with a medical procedure or treatment. This is crucial because it empowers patients to make educated decisions regarding their health care. They are informed of not only the benefits of a treatment but also any adverse effects or complications that may arise, allowing them to weigh their options carefully.

By understanding the risks involved, patients can engage in a meaningful dialogue with their healthcare providers about their concerns and preferences, which leads to a more collaborative approach to medical care. This process is foundational in promoting ethical medical practices and protecting patient autonomy. The emphasis on informed consent also helps to establish trust between patients and their healthcare providers.

The other options, while they may pertain to the medical context, do not capture the essence of informed consent as well as ensuring patient awareness of potential risks does.

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To obtain insurance approval

To expedite the treatment process

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