Question

What term describesWhen a client receives accurate and relevant information about a medical procedure?

a. Informed consent
b. Procedural disclosure
c. Patient briefing
d. Medical briefing

Answer 1

The term describing when a client is fully informed about a medical procedure is 'informed consent.' It is essential for ethical and legal compliance in healthcare and research, ensuring clients can make educated decisions on whether to proceed with the procedure or participation in a study.

Step-by-step explanation:

The term that describes when a client receives accurate and relevant information about a medical procedure is informed consent. This process ensures that the client is fully aware of the potential risks, benefits, and alternatives associated with the procedure, which allows them to make an educated decision about whether to proceed. Informed consent is a fundamental ethical and legal requirement in the medical field and research involving human subjects. It is important that all risks and benefits must be clearly outlined to study participants to give appropriate consent. Violations of this requirement, such as offering incentives to inmates for participation or not fully disclosing information about a research study, can lead to ethical and legal issues.

Inductive reasoning is used in research to draw conclusions from observations, and it is essential that participants are informed of what to expect during an experiment, any risks involved, and the implications of the research before obtaining their consent to participate.

Answer 2

The term that describes when a client receives accurate and relevant information about a medical procedure is 'informed consent'. It is crucial for patients and research participants to be fully aware of and agree to the procedure or study after being informed of the potential risks and benefits. Informed consent is also essential to uphold the ethics of medical practice and research.

Step-by-step explanation:

The term that describes when a client receives accurate and relevant information about a medical procedure is informed consent. Informed consent is a process that ensures patients or research subjects are fully aware of the potential risks, benefits, and alternatives associated with the procedure or study they are considering, and that they agree to proceed with full knowledge of this information.

Informed consent is not only applicable to medical procedures but also extends to research involving human subjects. Participants must be informed of all relevant aspects of the study, the potential risks involved, and the implications of the research before they can give their consent to participate. Moreover, all risks and benefits must be clearly explained for the consent to be considered valid.

Potential violations of informed consent

Examples of potential violations include offering incentives to inmates in a correctional facility for participation, misinforming participants about the nature of the treatment they will receive in a study, or not disclosing that a placebo may be administered as part of the study.