Chapter 8: Overview of Genetics and Genomics in Nursing - Nurselytic

Questions 40

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Brunner & Suddarth's Textbook of Medical-Surgical Nursing 14e (Hinkle 2017)

Chapter 8 : Overview of Genetics and Genomics in Nursing Questions

Question 1 of 5

What legislation has as its purpose to protect Americans against improper use of genetic and genomic information?

Correct Answer: A

Rationale: The Genetic Information Nondiscrimination Act (GIN
A), signed into law in 2008, protects Americans against improper use of genetic and genomic information in insurance and employment decisions. The other options do not exist.

Question 2 of 5

What should the nurse do?

Correct Answer: B

Rationale: Nurses assess the patient's capacity and ability to give voluntary consent. Language differences prevent the husband from giving informed consent without a translator. Having the wife translate or explaining in simple English does not ensure accurate understanding, and signing without comprehension is unethical.

Question 3 of 5

What is the nurses best response?

Correct Answer: C

Rationale: Nurses obtain patient consent to obtain medical records to ensure appropriate information and counseling, including risk interpretation, are provided. Vague responses like â??just in case' or â??due diligence' do not adequately explain the need for medical records.

Question 4 of 5

According to this legislation, insurers may use genetics testing as a justification for what action?

Correct Answer: B

Rationale: HIPAA prohibits the use of genetics information to establish insurance eligibility. However, it does not prohibit group plans from increasing premiums, excluding coverage for a specific condition, or imposing a lifetime cap on benefits. Mandating Medicaid enrollment or health promotion plans is not allowed.

Question 5 of 5

When planning this couples follow-up counseling, the nurse should recognize what implication of this assessment finding?

Correct Answer: A

Rationale: Sickle cell anemia follows an autosomal recessive pattern of inheritance. When carriers have children together, there is a 25% chance that each child may inherit the gene mutation from both parents and have the condition. Carriers do not develop the disease, and lifestyle factors do not directly influence this mendelian inheritance pattern.

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