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Genetic Counseling and Testing in a Community Setting: Quality, Access, and Efficiency
Stephanie A Cohen1, Angela Bradbury2, Vida Henderson3
11 Cancer Genetics Risk Assessment Program, Ascension St. Vincent, Indianapolis, IN.
Genetic counseling and testing are crucial for cancer patients and those at risk. Improving access through various models enhances early detection, prevention, and personalized treatment strategies for hereditary cancers.
Area of Science:
- Oncology
- Genetics
- Public Health
Background:
- Approximately 10% of all cancers have hereditary origins.
- Genetic testing results can significantly impact cancer treatment decisions.
- Early identification of hereditary cancer risk enables proactive surveillance and prevention.
Purpose of the Study:
- To address the growing need for improved access to genetic counseling and testing for cancer.
- To explore innovative models for identifying at-risk individuals, including those in underserved communities.
- To enhance the efficiency and accessibility of genetic services in clinical practice.
Main Methods:
- Reviewing models for identifying patients at high risk for hereditary cancer.
- Examining the integration of genetic counseling and testing into community practices.
- Evaluating the role of telehealth and collaboration with non-genetics healthcare providers.
- Considering technological solutions to optimize service delivery.
Main Results:
- Multiple models exist for identifying at-risk populations, including underserved groups.
- Community-based practices, telehealth, and interdisciplinary collaboration can expand access.
- Technological advancements offer potential for increased efficiency in genetic service delivery.
Conclusions:
- Expanding access to genetic counseling and testing is essential for optimal cancer care.
- Innovative service delivery models are needed to meet the demand for hereditary cancer risk assessment.
- Multifaceted approaches involving various healthcare settings and technologies are key to improving patient outcomes.
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