COMPETENCY STANDARDS

Below you will see the competency standards for genetics and a set of learning outcomes at three academic levels devised by the GeneSense team.

 

1. Identify clients who might benefit from genetic information and services.

Level 1 Outcomes:
1.1.1 Outline the relevance of a three generation family history in relation to assessing genetic health risk.
1.1.2 Describe basic patterns of biological inheritance and their variation in families and populations.
1.1.3 List resources available for clients and professionals seeking genetic information.
1.1.4 Identify the roles of the specialist genetics services and the referral pathway for access to genetics services.
Level 2 Outcomes:
1.2.1 Acquire and record accurate information for the construction of a three generation family history to assess genetic health risk.
1.2.2 Explore significant family history to assess genetic risk of altered health states.
1.2.3 Distinguish patterns of biological inheritance and their variation in families and populations.
1.2.4 Utilise relevant genetic information resources to inform practice.
1.2.5 Discuss the roles of the specialist genetics services and the referral pathway for appropriate patients/clients.
Level 3 Outcomes:
1.3.1 Construct a three generation family history for the process of assessing genetic health risk.
1.3.2 Appraise significant family history to assess genetic risk of altered health states.
1.3.3 Differentiate patterns of biological inheritance & communicate how these may vary in families and populations.
1.3.4 Use and evaluate relevant genetic information resources to inform practice.
1.3.5 Explain and communicate the roles of the specialist genetics services and the referral pathway for appropriate patients/clients.

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2. Appreciate the importance of sensitivity in tailoring genetic information and services to clients' culture, knowledge and language.

Level 1 Outcomes:
2.1.1 Recognise how communication of genetics issues should take into account the client’s level of understanding.
2.1.2 Outline how a client’s cultural, ethnic and religious background may influence their use of genetic information and services.
Level 2 Outcomes:
2.2.1 Demonstrate the use of appropriate communication skills in relation to the client’s level of understanding of genetics issues.
2.2.2 Discuss the impact of culture, ethnicity and religion on a client’s potential use of genetic information and services.
Level 3 Outcomes:
2.3.1 Effectively communicate genetic issues at a clients level of understanding.

2.3.2 Critically evaluate the significance of culture, ethnicity and religion on a client’s potential use of genetic information and services.

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3. Uphold the rights of all clients to informed decision making and voluntary action.

Level 1 Outcomes:
3.1.1 Identify past and potential future misuse of genetic information.
3.1.2 Explain how own beliefs and values can influence client care.
3.1.3 Recognise the rights of all individuals to informed decision making and voluntary action.
Level 2 Outcomes:
3.2.1 Discuss how the misuse of genetic information could potentially influence a client’s ability to make an informed decision and act voluntarily.
3.2.2 Explore how personal values and beliefs in relation to ethical, cultural, religious and ethnic issues could impact on client care.
3.2.3 Facilitate clients’ rights to self determination through ensuring informed decision making and voluntary action.
3.2.4 Ensure that the particular needs of those unable to give informed consent in relation to accessing genetic information are addressed.
Level 3 Outcomes:
3.3.1 Appraise the impact of genetic information misuse on a clients ability to make an informed decision and take voluntary action.
3.3.2 Critically evaluate the significance of personal values and beliefs in relation to ethical, cultural, religious and ethnic issues in the context of client care.
3.3.3 Uphold clients’ rights to self determination through ensuring informed decision making and voluntary action.
3.3.4 Advocate the particular needs of those unable to give informed consent in relation to accessing genetic information.
3.3.5 Analyse how the principle of a non directive approach underpins the process of genetic counselling, in facilitating client autonomy and empowerment.

 

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4. Demonstrate knowledge and understanding of the role of genetic and other factors in maintaining health and in the manifestation, modification and prevention of disease expression to underpin effective practice.

Level 1 Outcomes:

4.1.1 Discuss how genetic factors affect health and disease.

4.1.2 Outline how disease expression throughout the life cycle is affected by both genetic & environmental factors.
Level 2 Outcomes:
4.2.1 Explore the role of genetic factors in altered health states using examples of common inherited conditions.
4.2.2 Explain with examples, how disease expression throughout the lifecycle may be influenced by genetic and environmental factors.
4.2.3 Discuss the influence of family genetic history on health education for both individuals and populations.
Level 3 Outcomes:
4.3.1 Evaluate the role of genetic factors in the human health-disease continuum.
4.3.2 Critically appraise the impact of genotype and environment throughout the human life cycle.
4.3.3 Promote the importance of family genetic history in health education.
4.3.4 Distinguish between genetic susceptibility and clinical manifestation of disease using basic concepts of risk.

 

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5. Demonstrate a knowledge and understanding of the utility and limitations of genetic testing and information.

Level 1 Outcomes:
5.1.1 Explain the need for and maintain privacy and confidentiality when discussing and recording genetic information.
5.1.2 Discuss the process of genetic testing and its limitations.
Level 2 Outcomes:
5.2.1 Demonstrate confidentiality and maintains privacy when discussing and recording genetic information.
5.2.2 Explore potential risks, benefits and limitations of genetic testing and access to genetic information.
5.2.3 Debate the ethical, legal and social implications of genetic information for individuals and families.
5.2.4 Respond appropriately to enquiries about genetic concerns.
Level 3 Outcomes:
5.3.1 Ensure confidentiality and privacy when discussing and recording genetic information.
5.3.2 Evaluate potential risks, benefits and limitations of genetic testing and access to genetic information.
5.3.3 Critically appraise the ethical, legal and social implications of genetic information for individuals and families.
5.2.4 Respond appropriately and effectively to enquiries about genetic concerns.

 

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6. Recognise the limitation of one's own genetic expertise.

Level 1 Outcomes:
6.1.1 Recognise the limitations of their own genetic knowledge and practice.
6.1.2 Identify the role of the specialist genetics services and other agencies in providing appropriate patient/client care.
Level 2 Outcomes:
6.2.1 Explore own strengths and weaknesses in genetic knowledge and practice.
6.2.2 Explain how specialist genetic services and other agencies provide appropriate patient/client care.
6.2.3 Develop a collaborative approach to patient/client care in relation to genetics, with other statutory and voluntary organisations.
Level 3 Outcomes:
6.3.1 Critically assess personal genetic knowledge and practice
6.3.2 Appraise the role of specialist genetic services and other agencies in the provison of appropriate patient/client care.
6.3.3 Promote a collaborative approach to enhance patient/client care in relation to genetics with other statutory and voluntary organisations.

 

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7.Obtain and communicate credible current information about genetics for self, clients and colleagues.

Level 1 Outcomes:
7.1.1 List resources available for accessing genetic information.
7.1.2 Recognise the importance of regularly updating genetics knowledge from reputable sources.
Level 2 Outcomes:
7.2.1 Employ a range of appropriate genetic information resources to inform practice.
7.2.2 Incorporate current genetic knowledge from reputable sources into practice.
7.2.3 Utilise reliable genetic evidence when communicating with patient/clients.
Level 3 Outcomes:
7.3.1 Critically appraise information and evidence from a range of reliable sources
7.3.2 Evaluate and incorporate current reputable genetic information into own practice.
7.3.3 Develop effective communication strategies to inform clients and colleagues of relevant genetic information.


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