Genetics E2- Ethical & Legal issues

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11 Terms

1
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What pretest genetic counseling should patients and family members receive?

Risk assessment, discussion of testing alternatives, & predictive value and interpretive limitations of the tests

2
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What are potential benefits of genetic testing?

Anxiety relief, opportunities for behavior modification, & inc surveillance or interventions that may reduce risk

3
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What are negative consequences to genetic testing?

inc anxiety, depression, & anger, potential for discrimination by insurers and employers, “survivors guilt”

4
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Why is post-test counseling necessary?

To ensure results are interpreted correctly

*+ result only represents probability of dz; - result does not guarantee dz won’t develop

5
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What law classifies genetic information as PHI to protect a patient’s privacy?

HIPAA

6
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What federal law prohibits discrimination in health coverage and employment based on genetic information?

GINA

7
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What does GINA not cover?

Life insurance, long-term care insurance, & disability insurance

8
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What law prohibits health insurers from using genetic information to determine eligibility, charge higher premiums, and require genetic testing?

GINA

9
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What law prohibits employers from using genetic information to make employment decisions or requiring genetic tests as a condition of employment?

GINA

10
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In most countries, including the US, is there a legal obligation to inform family members of an increased risk to a disease after genetic testing?

No

11
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T/F: In the UK, healthcare practitioners may be liable for failing to disclose a patient’s Huntington gene status, if affected, to offspring.

True