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收到的信息:非裔美国女性与乳腺癌筛查。

Message Received: African American Women and Breast Cancer Screening.

作者信息

Passmore Susan Racine, Williams-Parry Kester F, Casper Erica, Thomas Stephen B

机构信息

1 University of Maryland, College Park, MD, USA.

出版信息

Health Promot Pract. 2017 Sep;18(5):726-733. doi: 10.1177/1524839917696714. Epub 2017 Mar 23.

Abstract

African American women are more likely than other women to be diagnosed with breast cancer at a young age, to be diagnosed at a late stage, and to die from the disease. Yet we see evidence of irregular screening and follow-up. Previous research on psychosocial factors influencing decisions to screen reveals barriers: fear, fatalistic perceptions of cancer, inaccurate perceptions of risk, and associations with stigma. The current qualitative research with, largely, insured African American women ( n = 26), health navigators ( n = 6), and community stakeholders ( n = 24) indicates both positive and negative factors influencing decision making. The women in our sample believe in the value of early detection and are motivated to screen in response to encouragement from health providers. However, they also report several factors that contribute to their decisions to delay or not screen. These include (1) perceptions that the health community itself is confused about the need for screening, (2) perceptions that White women are the priority population for breast cancer, (3) family roles that prohibit self-care and encourage secrecy, and (4) fear of diagnosis. Participants report not feeling included in national-level health promotion campaigns. It is argued that African American women, in particular, may benefit from more nuanced health information about their risk.

摘要

非裔美国女性比其他女性更有可能在年轻时被诊断出患有乳腺癌,在晚期被诊断出,以及死于这种疾病。然而,我们看到了筛查和后续跟进不规律的证据。先前关于影响筛查决策的社会心理因素的研究揭示了一些障碍:恐惧、对癌症的宿命论看法、对风险的不准确认知以及与耻辱感的关联。目前针对主要为参保非裔美国女性(n = 26)、健康导航员(n = 6)和社区利益相关者(n = 24)的定性研究表明,存在影响决策的积极和消极因素。我们样本中的女性相信早期检测的价值,并在医疗服务提供者的鼓励下有进行筛查的动力。然而,她们也报告了一些导致她们决定推迟或不进行筛查的因素。这些因素包括:(1)认为医疗界本身对筛查的必要性感到困惑;(2)认为白人女性是乳腺癌的优先人群;(3)家庭角色限制自我护理并鼓励保密;(4)对诊断的恐惧。参与者表示感觉自己没有被纳入国家级健康促进活动。有人认为,非裔美国女性尤其可能从更细致入微的关于她们风险的健康信息中受益。

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