Family Medicine, Univeristy of Washington, Seattle, WA, USA.
Health and Community Science, University of Exeter, Exeter, UK.
BMJ Open. 2023 Oct 29;13(10):e073886. doi: 10.1136/bmjopen-2023-073886.
This study has two objectives: first, to explore the diagnostic experiences of black/African American (BAA) patients with lung cancer to pinpoint pitfalls, suboptimal experiences and instances of discrimination leading to disparities in outcomes compared with patients of other ethnic backgrounds, especially white patients. The second objective is to identify the underlying causes contributing to health disparities in the diagnosis of lung cancer among BAA patients.
We employed a phenomenological research approach, guiding in-depth interviews with patients self-identifying as BAA diagnosed with lung cancer, as well as caregivers, healthcare professionals and community advocates knowledgeable about BAA experiences with lung cancer. We performed thematic analysis to identify experiences at patient, primary care and specialist levels. Contributing factors were identified using the National Institute of Minority Health and Health Disparities (NIMHD) health disparity model.
From March to November 2021, we conducted individual interviews with 19 participants, including 9 patients/caregivers and 10 providers/advocates. Participants reported recurring and increased pain before seeking treatment, treatment for non-cancer illnesses, delays in diagnostic tests and referrals, poor communication and bias when dealing with specialists and primary care providers. Factors contributing to suboptimal experiences included reluctance by insurers to cover costs, provider unwillingness to conduct comprehensive testing, provider bias in recommending treatment, high healthcare costs, and lack of healthcare facilities and qualified staff to provide necessary support. However, some participants reported positive experiences due to their insurance, availability of services and having an empowered support structure.
BAA patients and caregivers encountered suboptimal experiences during their care. The NIMHD model is a useful framework to organise factors contributing to these experiences that may be leading to health disparities. Additional research is needed to fully capture the extent of these experiences and identify ways to improve BAA patient experiences in the lung cancer diagnosis pathway.
本研究有两个目的:首先,探索非裔美国(BAA)肺癌患者的诊断经历,以发现导致与其他族裔背景(尤其是白种人)患者相比,结局存在差异的陷阱、不佳的体验和歧视实例。第二个目的是确定导致 BAA 患者肺癌诊断中健康差异的潜在原因。
我们采用了现象学研究方法,指导自认为患有肺癌的 BAA 患者以及照顾者、了解 BAA 肺癌经历的医疗保健专业人员和社区倡导者进行深入访谈。我们进行了主题分析,以确定患者、初级保健和专科医生层面的经历。使用国家少数民族健康和健康差异研究所(NIMHD)健康差异模型确定促成因素。
2021 年 3 月至 11 月,我们对 19 名参与者进行了个体访谈,其中包括 9 名患者/照顾者和 10 名提供者/倡导者。参与者报告在寻求治疗前反复出现并加剧疼痛、治疗非癌症疾病、诊断测试和转诊延迟、与专科医生和初级保健提供者沟通不畅和存在偏见。导致体验不佳的因素包括保险公司不愿支付费用、提供者不愿进行全面检查、提供者在推荐治疗方面存在偏见、医疗保健费用高、以及缺乏医疗设施和合格人员提供必要支持。然而,一些参与者报告说,由于他们的保险、服务的可用性和拥有一个赋权的支持结构,他们有积极的体验。
BAA 患者和照顾者在护理过程中经历了不佳的体验。NIMHD 模型是组织导致这些体验的因素的有用框架,这些因素可能导致健康差异。需要进一步研究以充分了解这些体验的程度,并确定改善 BAA 患者在肺癌诊断途径中的体验的方法。