| Literature DB >> 26637472 |
Navya Nair1, Cecelia Bellcross2, Lisa Haddad3, Monique Martin4, Roland Matthews5, Sheryl Gabram-Mendola6, Barbara Crane4, Dana Meaney-Delman3.
Abstract
Hereditary breast and ovarian cancer syndrome (HBOC) is an inherited condition associated with mutations in the BRCA1 or BRCA2 (BRCA) genes. Identification of individuals with HBOC requires that primary care providers understand the genetic principles required to appropriately collect family history and refer individuals for genetic evaluation. A survey was developed and administered to primary care providers in Georgia to assess their existing knowledge of HBOC and direct targeted educational efforts.We found that Georgia providers demonstrate some knowledge of basic genetic principles but were unable to consistently identify individuals at risk for HBOC. Knowledge deficits included lack of understanding of inheritance patterns and failure to recognize the significance of ovarian cancer history. Strategies for improving identification of patients with HBOC include increasing provider knowledge and integrating HBOC risk assessment tools into practice. Identification of individuals at risk is the critical first step in the process of reducing incidence of breast and ovarian cancer associated with BRCA mutations.Entities:
Keywords: BRCA; Breast cancer; Hereditary; Ovarian cancer
Mesh:
Year: 2017 PMID: 26637472 DOI: 10.1007/s13187-015-0950-9
Source DB: PubMed Journal: J Cancer Educ ISSN: 0885-8195 Impact factor: 2.037