Identification of mutation carriers and referral to genetic services
Outcomes
More accurate diagnosis and risk assessment of family members
Screening and surveillance for mutation carriers and family members
Identification of mutation carriers in the family
Identification and referral
to genetic services
Reinforcing factors
Referral process
Patient request
Clinical guidelines
History
Personal
Family
Enabling factors
Access to and availability of genetic services
Cost
Wait time
Predisposing factors
Clinician demographics
Awareness
Knowledge
Confidence
