Which elements are key components of a genetic nursing assessment?

Prepare for the AMNH Genetic and Genomic in Nursing Exam. Study with multiple-choice questions, hints, and explanations. Enhance your knowledge in genetics and genomics to excel in the field of nursing. Get exam-ready today!

Multiple Choice

Which elements are key components of a genetic nursing assessment?

Explanation:
A genetic nursing assessment is a comprehensive evaluation that incorporates various elements to gain a thorough understanding of a patient's genetic background and health. One of the key components is the collection of family history and personal medical history. This information is crucial because it helps identify patterns of inheritance and assess the risk of genetic conditions within families. Family history provides insights into hereditary diseases and conditions that may be present among relatives, which can significantly influence a patient's health risks. Personal medical history allows the healthcare provider to consider any past medical issues that could be related to genetic factors. Together, these components build a framework for understanding the patient's health in the context of genetic predispositions. The other options focus on more isolated aspects that do not encompass the broad and integrative nature of a genetic nursing assessment. For example, physical activity levels and social media usage might be relevant in some healthcare contexts but are not core to evaluating genetic risks. Similarly, while genetic testing results are valuable, the full context of a patient’s history and family background is essential for a thorough assessment, making the combination of family history and personal medical history the most critical components.

A genetic nursing assessment is a comprehensive evaluation that incorporates various elements to gain a thorough understanding of a patient's genetic background and health. One of the key components is the collection of family history and personal medical history. This information is crucial because it helps identify patterns of inheritance and assess the risk of genetic conditions within families.

Family history provides insights into hereditary diseases and conditions that may be present among relatives, which can significantly influence a patient's health risks. Personal medical history allows the healthcare provider to consider any past medical issues that could be related to genetic factors. Together, these components build a framework for understanding the patient's health in the context of genetic predispositions.

The other options focus on more isolated aspects that do not encompass the broad and integrative nature of a genetic nursing assessment. For example, physical activity levels and social media usage might be relevant in some healthcare contexts but are not core to evaluating genetic risks. Similarly, while genetic testing results are valuable, the full context of a patient’s history and family background is essential for a thorough assessment, making the combination of family history and personal medical history the most critical components.

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