American Indian Community Leader and Provider Views of Needs and Barriers to Colorectal Cancer Screening.

Christine Makosky Daley, Aimee S James, Melissa Filippi, Maria Weir, Stacy Braiuca, Baljit Kaur, Won S Choi, K Allen Greiner
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Abstract

Colorectal cancer is a great concern for the American Indian/Alaska Native (AI/AN) community, as incidence and mortality rates remain high and screening rates stay low. We conducted interviews with community leaders (n=13) and with providers from the Indian Health Service (IHS), tribal clinics, and urban safety-net clinics (n=17) in Northeast Kansas and the Kansas City Metro Area to determine their understanding of needs and barriers to colorectal cancer screening among American Indians. Using a community-based participatory research (CBPR) approach for this pilot study, community leaders and providers identified similar needs, including: culturally-appropriate education about colorectal cancer and screenings, the potential use of Native elders as patient navigators, and an emphasis on preventive care, particularly through the IHS. Barriers included culturally specific issues such as historic mistrust and gender roles. Other barriers are similar to members of other ethnic groups, such as cost, transportation, fear, and repulsion toward the screening process.

美国印第安社区领导人和提供者对结直肠癌筛查的需求和障碍的看法。
结直肠癌是美国印第安人/阿拉斯加原住民(AI/AN)社区非常关注的问题,因为发病率和死亡率仍然很高,而筛查率仍然很低。我们对社区领导人(n=13)和来自堪萨斯州东北部和堪萨斯城都会区的印第安人健康服务(IHS)、部落诊所和城市安全网诊所(n=17)的提供者进行了访谈,以确定他们对美国印第安人结直肠癌筛查的需求和障碍的理解。在这项试点研究中,社区领导人和提供者采用基于社区的参与式研究(CBPR)方法,确定了类似的需求,包括:在文化上适当地进行有关结直肠癌和筛查的教育,潜在地利用土著老年人作为患者导航,以及强调预防保健,特别是通过IHS。障碍包括文化上的具体问题,如历史上的不信任和性别角色。其他障碍与其他族裔成员类似,如成本、交通、恐惧和对筛选过程的排斥。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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