Evaluation of Patterns in Access to Breast Cancer Care and Breast Cancer Presentation in a Safety Net Patient Population

2021 ◽  
pp. 000313482096628
Author(s):  
Erica Choe ◽  
Hayoung Park ◽  
Ma’at Hembrick ◽  
Christine Dauphine ◽  
Junko Ozao-Choy

Background While prior studies have shown the apparent health disparities in breast cancer diagnosis and treatment, there is a gap in knowledge with respect to access to breast cancer care among minority women. Methods We performed a retrospective analysis of patients with newly diagnosed breast cancer from 2014 to 2016 to evaluate how patients presented and accessed cancer care services in our urban safety net hospital. Patient demographics, cancer stage, history of breast cancer screening, and process of referral to cancer care were collected and analyzed. Results Of the 202 patients identified, 61 (30%) patients were younger than the age of 50 and 75 (63%) were of racial minority background. Only 39% of patients with a new breast cancer were diagnosed on screening mammogram. Women younger than the age of 50 ( P < .001) and minority women ( P < .001) were significantly less likely to have had any prior screening mammograms. Furthermore, in patients who met the screening guideline age, more than half did not have prior screening mammograms. Discussion Future research should explore how to improve breast cancer screening rates within our county patient population and the potential need for revision of screening guidelines for minority patients.

2014 ◽  
Vol 10 (2) ◽  
pp. e107-e112 ◽  
Author(s):  
Meaghan M. Crowley ◽  
Molly E. McCoy ◽  
Sharon M. Bak ◽  
Sarah E. Caron ◽  
Naomi Y. Ko ◽  
...  

Urgently needed interventions to reduce disparities in breast cancer treatment should take into account obstacles inherent among immigrant and indigent populations and complexities of multidisciplinary cancer care.


2021 ◽  
Vol 4 (8) ◽  
pp. e2119929
Author(s):  
Ana I. Velazquez ◽  
Jessica H. Hayward ◽  
Blake Gregory ◽  
Niharika Dixit

2019 ◽  
Vol 229 (4) ◽  
pp. S159
Author(s):  
Kristin N. Kelly ◽  
Emily Ryon ◽  
Ahkeel Allen ◽  
Dido Franceschi ◽  
Mecker Moller ◽  
...  

2011 ◽  
Vol 22 (6) ◽  
pp. 925-929 ◽  
Author(s):  
J. M. Timmers ◽  
G. J. den Heeten ◽  
E. M. Adang ◽  
J. D. Otten ◽  
A. L. Verbeek ◽  
...  

Author(s):  
Kristin N. Kelly ◽  
Alexandra Hernandez ◽  
Sina Yadegarynia ◽  
Emily Ryon ◽  
Dido Franceschi ◽  
...  

2019 ◽  
Vol 1 (2) ◽  
pp. 84-91
Author(s):  
Jonathan V Nguyen ◽  
Martha H Thomas

Abstract The majority of our hereditary breast cancer genes incur not only an increased risk for breast cancer but for other malignancies as well. Knowing whether an individual carries a pathogenic variant in a hereditary breast cancer gene can affect not only screening for the patient but for his or her family members as well. Identifying and appropriately testing individuals via multigene panels allows for risk reduction and early surveillance in at-risk individuals. Radiologists can serve as first-line identifiers of women who are at risk of having an inherited predisposition to breast cancer because they are interacting with all women receiving routine screening mammograms, and collecting family history suggestive of the presence of a mutation. We outline here the 11 genes associated with high breast cancer risk discussed in the National Comprehensive Cancer Network Genetic/Familial High-Risk: Breast and Ovarian (version 3.2019) as having additional breast cancer screening recommendations outside of annual mammography to serve as a guide for breast cancer screening and risk reduction, as well as recommendations for surveillance of nonbreast cancers.


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