Clinician-related |
Lack familiarity with Lynch syndrome |
Knowledge of family history and age at diagnosis |
Lack of adherence to guidelines |
Knowledge of tumour test results |
Negative attitude toward genetic testing |
Improvement for patient diagnosis, treatment and clinical management |
Lack of professional experience |
|
Uncertain of who or when to refer |
|
Lack of awareness to importance of family history |
|
Patient-related |
Patients disinterest |
Patients requests |
Lack of family history knowledge to guide referral |
Organizational-related |
Uncertain or perceived long wait time for a genetics appointment or test results |
Practical information about genetic services (e.g., the availability and cost of testing, turnaround time) |
Unknown cost or assumed high costs of testing |
Specific criteria or guidelines for referral |
Unfamiliar with genetic services |
Increased collaboration with genetics specialist |
|
Prompts or triggers for referral |
|
Ease of access for services |
|
Continuing education for clinicians |
|
Better follow-up care or referral pathway |