Breast cancer treatment experiences of Latinas in Los Angeles County

Am J Public Health. 2005 Dec;95(12):2225-30. doi: 10.2105/AJPH.2004.057950. Epub 2005 Oct 27.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Breast Neoplasms* / radiotherapy
  • Breast Neoplasms* / surgery
  • Carcinoma, Ductal, Breast
  • Carcinoma, Intraductal, Noninfiltrating
  • Data Collection
  • Female
  • Hispanic Americans*
  • Humans
  • Los Angeles
  • Middle Aged
  • Odds Ratio
  • Outcome Assessment, Health Care
  • Patient Satisfaction*
  • Prospective Studies
  • Surveys and Questionnaires