What are the first steps in the ethical decision-making process?
Collect the data and consider the alternatives.
Collect, analyze, and interpret the data.
Collect data and consider the consequences of the actions.
Collect the data and make a decision.
The Correct Answer is B
Collect the data and consider the alternatives: This step involves gathering all relevant information about the situation and identifying possible courses of action. It's essential to have a clear understanding of the problem and the available options before making a decision. However, this is not typically the very first step in the ethical decision-making process, as collecting data often precedes considering alternatives.
Collect, analyze, and interpret the data: This is the correct first step in the ethical decision-making process. It emphasizes the importance of systematically gathering information, analyzing it to identify ethical concerns, and interpreting the data to understand the ethical implications.
Collect data and consider the consequences of the actions: While considering the consequences is a crucial part of ethical decision-making, it usually comes after collecting and analyzing the data. It's important to evaluate the potential outcomes of each alternative once you have a clear grasp of the ethical issues involved.
Collect the data and make a decision: Making a decision is the final step in the ethical decision-making process. While data collection is an essential part of the process, making a decision should follow a careful analysis and consideration of the ethical implications. Jumping straight to a decision without thorough analysis can lead to unethical choices.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
A) Refuse to give the information over the phone:
This option respects the patient's confidentiality and is the best course of action. Sharing sensitive medical information over the phone without proper verification and consent is not appropriate.
B) Give a noncommittal response that "everything is normal" even though it is untrue:
Providing false information compromises the integrity of the healthcare professional and can lead to serious consequences if discovered. It's essential to be honest and accurate when sharing medical information.
C) Give the results as they are reported on the laboratory sheet because the insurance company is paying for the test anyway:
Sharing medical information without proper consent, especially over the phone, is a violation of patient privacy and confidentiality. Insurance payment does not negate the need for patient consent and confidentiality.
D) Tell the representative that the test results are not back yet:
If the results are not yet available, it is appropriate to inform the insurance representative truthfully. However, if the results are available, the nurse should not provide them without proper authorization.
Correct Answer is A
Explanation
Living will: A living will is a legal document in which a person specifies what actions should be taken for their health if they are no longer able to make decisions for themselves due to illness or incapacity. It outlines the medical treatments an individual would like to receive or not receive, particularly in end-of-life situations.
Client's Bill of Rights: This document outlines the rights and responsibilities of clients receiving medical care. It does not specifically contain a client's written wishes about healthcare decisions in case of incapacity.
Welfare rights: Welfare rights refer to the legal rights of individuals to receive assistance from the government, typically in the form of financial aid or social services, to meet basic needs like food, shelter, and healthcare. This is not related to healthcare decision-making for incapacitated individuals.
Informed consent: Informed consent is the process where a patient is informed about the potential risks, benefits, and alternatives of a medical procedure or treatment. While important for medical decision-making, it is not the specific document where a client's written wishes about healthcare decisions are recorded for situations where they are unable to make decisions themselves.
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