Psychosocial approaches to participation in BRCA1 / 2 genetic risk assessment among African American women: a systematic
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REVIEW
Psychosocial approaches to participation in BRCA1/2 genetic risk assessment among African American women: a systematic review Kerry A. Sherman & Suzanne M. Miller & Laura-Kate Shaw & Karen Cavanagh & Sherri Sheinfeld Gorin Received: 29 May 2013 / Accepted: 18 July 2013 # Springer-Verlag Berlin Heidelberg 2013
Abstract Breast cancer is a significant health concern for African American women. Nonetheless, uptake of genetic risk assessment (including both genetic counseling and testing) for breast cancer gene mutations among these populations remains low. This paper systematically reviews cognitive (i.e., beliefs) and affective (i.e., emotions) factors influencing BRCA1/2 genetic risk assessment among African American women as well as psychosocial interventions to facilitate informed decision making in this population. A systematic search of CINAHL, PubMed, and PsycINFO was undertaken, yielding 112 published studies. Of these, 18 met the eligibility criteria. African American woman are likely to participate in genetic risk assessment if they are knowledgeable about cancer genetics, perceive a high risk of developing breast cancer, have low expectancies of stigmatization from medical professionals, view themselves as independent from family, and have fatalistic beliefs and a future temporal orientation. Anticipated negative affective responses, such as an inability to “handle” the results of testing, are barriers to uptake. Specific perceptions, beliefs, and emotional factors are associated with genetic risk assessment among African American women. Understanding these factors is key in the K. A. Sherman (*) : L.
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