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Qualitative Study of Latino Cancer Patient Perspectives on Care Access and Continuity in a Rural, U.S.-Mexico Border Region

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Abstract

Access to quality cancer care for cancer patients living in the rural U.S.-Mexico border region is complex due to common binational health care-seeking behaviors and regional socio-economic and cultural characteristics. But little is known about the challenges border dwelling residents face when navigating their cancer care systems. In-depth interviews were conducted with 22 cancer patients in Southern California. Thematic analysis was applied to identify patterns of meaning in the data. Emerging themes were: (1) delays in cancer care coordination: (a) poor coordination of cancer care (b) U.S. and cross-border discordance in cancer diagnosis; (2) regional shortage of cancer specialists; and (3) financial hardship. Findings revealed that care needs distinctly involved care coordination in/outside of the patient’s community and bi-national care coordination. In addition to local solutions to improve cancer coordination through community-based partnerships, efforts to bridge care in a two-nation context are also imperative.

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Correspondence to Eunjeong Ko.

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We would like to declare that there is no conflict of interest for all authors.

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All study participants signed the informed consent and this study was approved by the San Diego State University Institutional Review Board.

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Ko, E., Zúñiga, M.L., Palomino, H. et al. Qualitative Study of Latino Cancer Patient Perspectives on Care Access and Continuity in a Rural, U.S.-Mexico Border Region. J Immigrant Minority Health 20, 674–679 (2018). https://doi.org/10.1007/s10903-017-0605-5

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  • DOI: https://doi.org/10.1007/s10903-017-0605-5

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