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Faculty Suggestions / Strategies

Clinical Outcomes

Expected Nursing Students' Clinical Outcomes in Genetics

Group 1

  1. Recognize when a diagnosis is genetic or has a genetic component.
  2. Recognize common phenotypes.
  3. Obtain genetic family history.
  4. Generate pedigree .
  5. Recognize at-risk family members based on pedigree.
  6. Recognize ethnic and racial predisposition to gene specific diseases.
  7. Recognize presence of dysmorphology.
  8. Identify and refer to genetic resources ( medical, support groups, quality web sites).
  9. Assist individual and family with interpretation of genetic information.
  10. Use health promotion/disease prevention techniques shown to alter phenotypical expression of genes.
  11. Identify and anticipate risk factors specific to gender, race and/or ethnicity.
  12. Identify genetic disorders common to a population.
  13. Identify, anticipate and deliberate the ethical, legal and social implications of genetic advances .
  14. Function as self-directed learners who update their knowledge about and competence in the clinical application of genetic advances.
  15. Anticipate the phenotypic effects of potential ethnic / racial genetic differences (e.g., pharmacogenetics).
  16. Anticipate ethnic, cultural differences as they relate to personal/group responses to genetic information, technology and services.

Group 2

  1. Management of genetic information.
  2. Recognize genetic components of common disorders.
  3. Awareness that genetic condition affects whole family.
  4. Phenotypical assessment.
  5. Case management.
  6. Facilitate referral process and obtain resources.
  7. Construct three generation pedigree.
  8. Recognize and anticipate interaction between genetics and environment.
  9. Facilitate discussion of ethical dilemma with individual and family.
  10. Awareness of pharmacogenetics.
  11. Critical understanding of genetics language.
  12. Provide basic genetic information.
  13. Assess families' understanding of and response to genetic information / technology / services.
  14. Active listening.
  15. Support decisions.
  16. Refer.
    • Avoid contributing to horror stories or inaccurate genetic information.
    • Advocate through health care policy.

    Group 3

    1. Assessment.
    2. Collect genetic history.
    3. generation pedigree.
    4. interviewing skills.
    5. recognize common deviations from normal through the lifespan.
      • Understanding legal, social and ethical implications of genetics in clinical practice.
      • Sensitivity to cultural diversity.
      • Intervention.
      • Recognize need for referral.
      • Make appropriate referral.
      • Identify resources.
      • Provide basic information.
      • Recognize own strength and weaknesses.
      • Provide safe, supportive care to clients and families.

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      Email: gepn@cchmc.org