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Breast cancer treatment experiences of Latinas in Los Angeles County
Steven J Katz1, Paula M Lantz, Yvonne Paredes
1Department of Medicine, University of Michigan, Ann Arbor, MI 48109-0429, USA. skatz@umich.edu
Objective:
We examined breast cancer treatment experiences of and outcomes for Latinas in Los Angeles County.
Methods:
We conducted a population-based survey of women who were diagnosed with breast cancer between December 2001 and November 2002 (n=910) to evaluate the types of treatments received, communication with clinicians, and satisfaction.
Results:
About two thirds were non-Latina White, 18.8% were African American, and 18.9% were Latina (with 11.0% preferring English and 7.9% preferring Spanish). The rest indicated other ethnic groups. Latinas who preferred Spanish were more likely to experience a delay of 3 months or more from diagnosis to surgical treatment (36.4% vs 9.1% for non-Latina Whites, 18.6% for African Americans, and 12.7%, for other Latinas, P<.001). African Americans and Latinas who preferred Spanish had very low rates of reconstruction (13.8% and 9.2%, respectively, compared with 42.1% for Whites and 34.5% for Latinas who preferred English, P=.009). Latinas who preferred Spanish had the highest odds ratio for low satisfaction.
Conclusion:
Latinas who preferred Spanish received different treatments and perceived a different treatment experience than did other cultural groups.
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