Correlates of Depressive Symptoms Among Women Seeking Cancer Genetic Counseling and Risk Assessment at a High-Risk Cancer Clinic

2006 ◽  
Vol 15 (4) ◽  
pp. 267-276 ◽  
Author(s):  
Molly Middlecamp Kodl ◽  
Judith W. Lee ◽  
Alicia K. Matthews ◽  
Shelly A. Cummings ◽  
Olufunmilayo I. Olopade
2001 ◽  
Vol 10 (2) ◽  
pp. 133-150 ◽  
Author(s):  
June A. Peters ◽  
Carol L. McAllister ◽  
Wendy S. Rubinstein

2020 ◽  
Vol 19 (4) ◽  
Author(s):  
Reyna J. Martínez-Arriaga ◽  
Leivy P. González-Ramírez ◽  
Azucena Del Toro-Valero ◽  
Rebeca Robles-García ◽  
Antonio Oceguera-Villanueva ◽  
...  

2016 ◽  
Vol 14 (4) ◽  
pp. 162-168 ◽  
Author(s):  
Lindsey Mette ◽  
Anna Saldivar ◽  
Natalie Poullard ◽  
Ivette Torres ◽  
Sarah Seth ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Beth Anderson ◽  
Jennifer McLosky ◽  
Elizabeth Wasilevich ◽  
Sarah Lyon-Callo ◽  
Debra Duquette ◽  
...  

Introduction. Women diagnosed with breast cancer at a young age are more likely to carry a cancer predisposing genetic mutation. Per the current NCCN recommendations, women diagnosed under age 50 should be referred to cancer genetic counseling for further risk evaluation. This study seeks to assess patient-reported barriers and facilitators to receiving genetic counseling and risk assessment among a community-based population of young breast cancer survivors (YBCS).Methods. Through the Michigan Cancer Surveillance Program, a state-based cancer registry, 488 women diagnosed with breast cancer before age 50 in 2006-2007 were identified. They received a mail survey regarding family history and facilitators and barriers to receiving genetic counseling and risk assessment.Results. Responses were received from 289 women (59.2%). One hundred twenty-two (42.2%) reported having received cancer genetic counseling. The most frequent reason identified for receiving services was to benefit their family's future. The top reasons for not attending were “no one recommended it” and “medical insurance coverage issues.”Discussion. This study is the first published report using a state cancer registry to determine facilitators and barriers to receiving genetic counseling and risk assessment among YBCS. These findings demonstrate the need for additional awareness and education about appropriate indications for genetic services.


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