Date of Award
Spring 2-11-2025
Degree Type
Dissertation
Degree Name
PhD Nursing
Department
Nursing
Advisor
Bonnie Sturm, EdD, RN
Committee Member
Nancy Innella, PhD
Committee Member
Joyce Maglione, PhD
Keywords
Genetic testing, Genetic counseling, Latinas, BRCA1/2, qualitative
Abstract
Healthy women with BRCA1 (BReast CAncer gene 1) or BRCA2 (BReast CAncer gene 2), (henceforth, BRCA1/2 mutation) without a diagnosis of breast or ovarian cancer (unaffected), have up to 80% increased lifetime risk of developing breast cancer, and up to 40% increased lifetime risk of ovarian cancer. Genetic counseling and testing based upon family history is essential to diagnose genetic mutations increasing one’s risk for certain cancers. Latinas have the second highest prevalence of BRCA1/2 mutations after Ashkenazi Jewish women, and cancer is now the leading cause of death among Latinos, surpassing cardiovascular disease. However, no qualitative study has been published in which interviews have been conducted with Latinas once a genetic mutation has been identified. The purpose of this study is to describe the experience of genetic testing among Latinas diagnosed with BRCA1/2 mutation. Thorne’s (2016) method of Interpretive Description will provide a framework to this qualitative inquiry. New knowledge describing Latinas’ experiences will have clinical implications to help address cancer disparities in genetic testing and counseling. This research will fill a gap in the women’s health literature and will inform nursing research, education, and clinical practice.
Recommended Citation
Milli, Lisania, "The Experience of Genetic Testing among Latinas with BRCA1/2 mutation" (2025). Seton Hall University Dissertations and Theses (ETDs). 3229.
https://scholarship.shu.edu/dissertations/3229