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Utility of linking survey and registry data to evaluate interventions and policies to address disparities in breast cancer survivorship among young women

Author

Listed:
  • Subramanian, Sujha
  • Jones, Madeleine
  • Tangka, Florence K.L.
  • Edwards, Patrick
  • Flanigan, Tim
  • Kaganova, Jenya
  • Smith, Kevin
  • Fairley, Temeika
  • Hawkins, Nikki A.
  • Rodriguez, Juan L.
  • Guy, Gery P.
  • Thomas, Cheryll C.

Abstract

There is limited research linking data sources to evaluate the multifactorial impacts on the quality of treatment received and financial burden among young women with breast cancer. To address this gap and support future evaluation efforts, we examined the utility of combining patient survey and cancer registry data.

Suggested Citation

  • Subramanian, Sujha & Jones, Madeleine & Tangka, Florence K.L. & Edwards, Patrick & Flanigan, Tim & Kaganova, Jenya & Smith, Kevin & Fairley, Temeika & Hawkins, Nikki A. & Rodriguez, Juan L. & Guy, Ger, 2021. "Utility of linking survey and registry data to evaluate interventions and policies to address disparities in breast cancer survivorship among young women," Evaluation and Program Planning, Elsevier, vol. 88(C).
    • Handle: RePEc:eee:epplan:v:88:y:2021:i:c:s0149718921000628
    DOI: 10.1016/j.evalprogplan.2021.101967
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    References listed on IDEAS

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    1. George, S. & Duran, N. & Norris, K., 2014. "A systematic review of barriers and facilitators to minority research participation among African Americans, Latinos, Asian Americans, and Pacific Islanders," American Journal of Public Health, American Public Health Association, vol. 104(2), pages 16-31.
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