Patient COUNTS: A pilot navigation program for Asian American cancer patients.

IF 2.4 4区 心理学 Q1 ETHNIC STUDIES
Janet N Chu, Janice Y Tsoh, Salma Shariff-Marco, Laura Allen, Debora Oh, Mei-Chin Kuo, Ching Wong, Hoan Bui, Junlin Chen, Angeline Truong, Katarina Wang, Andrea Hwang, Feng Ming Li, Carmen Ma, Scarlett L Gomez, Tung T Nguyen
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Abstract

Many Asian American cancer patients face barriers to cancer care but little is known about their navigational needs. We designed and implemented a pilot study to provide culturally- and linguistically-appropriate navigation for Asian American cancer patients. We recruited Asian American adults age 21+ years, who spoke English, Cantonese, Mandarin, or Vietnamese, with newly diagnosed, stage I-III colorectal, liver, or lung cancer in the Northern California Bay Area. Participants were assigned a language-concordant patient navigator, who provided support and resources over 6 months. Surveys were administered at baseline, 3-, and 6-months to assess sociodemographic characteristics, healthcare access, quality of life (FACT-G), and cancer care needs. Participants' mean age was 65 years (range 38-81); 62% were men, 67% spoke Chinese, and 75% reported limited English proficiency. Forty-two percent of participants had lung, 38% colorectal, and 21% liver cancer. Of 24 participants who enrolled, 67% completed the program and 75% completed standard of care cancer treatment. The average total FACT-G score was 72.6 (SD 17) at baseline, 68.0 (SD 20) at 3 months, and 69.9 (SD 22) at 6 months. All participants reported that the program was culturally appropriate and would recommend it. Asian American cancer patients in a patient navigation program reported lower quality of life compared to the general adult cancer population. Even with navigation, 75% of participants reported completing standard of care treatment. While participants were satisfied with the program, more research is needed to address the quality of cancer care Asian American cancer patients receive.

患者重要:针对亚裔美国人癌症患者的试点导航计划。
许多美籍亚裔癌症患者面临癌症治疗的障碍,但对他们的导航需求却知之甚少。我们设计并实施了一项试点研究,为美籍亚裔癌症患者提供文化和语言上适宜的导航。我们在北加州湾区招募了 21 岁以上、讲英语、粤语、普通话或越南语的亚裔成人,他们都是新诊断的 I-III 期结直肠癌、肝癌或肺癌患者。参与者被指派了一名语言一致的患者导航员,由其在 6 个月内提供支持和资源。在基线、3 个月和 6 个月时进行了调查,以评估社会人口特征、医疗保健获取途径、生活质量(FACT-G)和癌症护理需求。参与者的平均年龄为 65 岁(38-81 岁不等);62% 为男性,67% 讲中文,75% 表示英语水平有限。42%的参与者患有肺癌,38%患有结肠直肠癌,21%患有肝癌。在 24 名参加者中,67% 的人完成了项目,75% 的人完成了标准癌症治疗。FACT-G 的平均总分基线为 72.6 分(标准差 17 分),3 个月时为 68.0 分(标准差 20 分),6 个月时为 69.9 分(标准差 22 分)。所有参与者都认为该项目符合他们的文化背景,并愿意推荐该项目。与普通成年癌症患者相比,参加患者导航计划的亚裔癌症患者的生活质量较低。即使有了导航,仍有 75% 的参与者表示完成了标准护理治疗。虽然参与者对该项目表示满意,但还需要进行更多的研究,以了解亚裔美国癌症患者所接受的癌症护理的质量。
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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来源期刊
CiteScore
3.40
自引率
6.70%
发文量
57
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