Table 2 Themes and subthemes

From: A step forward in genetic counselling: defining practice and ethics through the Genetic Counselling Practice Consortium in Hong Kong

 

Theme

Subtheme

Scope of practice

Pre-assessment

Building rapport

Obtaining informed consent

 

Assessing risk

Collecting medical history

Discussing genetic/medical conditions/diseases

 

Ordering laboratory/genomic tests

Facilitating tests

Interpreting test results

 

Discussing clinical implications

Explaining clinical significance

Evaluating risk of recurrence

Promoting psychological adaptations

 

Making referrals to support services

Referring patients to physical health services

Referring patients to psychological support

 

Other duties

Involving in research

Developing public health policies

Advocating public education

Code of ethics

To self

Duty of candour

Professional indemnity arrangements

 

To clients/patients

Duty of care

Communication, consent and confidentiality

Record keeping

Minimising risk

 

To colleagues

Maintaining boundaries

Minimising risk

 

To society