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Listening in the shadows: The experience of living with chronic illnesses for medically uninsured individuals.

机译:在阴影中聆听:没有医疗保险的个人患有慢性病的经历。

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There are over 45 million medically uninsured individuals in the United States and 90 million individuals with chronic illnesses. And, as the profession of pharmacy moves towards the provision of pharmaceutical care, a patient-centered practice, it is important to gain an understanding of patients' medication and illness experiences as well as the socioeconomic context that affects a patient's care, like uninsurance. The illness experience literature is extensive in medicine and nursing, however, the exploration of marginalized groups like the uninsured is largely missing. The number of uninsured has been increasing both nationally as well as in the state of Minnesota. The awareness of the uninsured has occurred primarily through national surveys with a limited understanding of the experience for those who live it. This study explores the experience of living with chronic illnesses for uninsured individuals. The methodology is hermeneutic phenomenology with the use of in-depth, unstructured interviews. The participants include eleven adults, twenty-seven to sixty-four years of age, each with at least two chronic illnesses and uninsured for a period from one to twenty-seven years. Additionally, over one hundred individuals responded to the recruitment flier and offer insight into the meanings of illness and uninsurance. The interviews were audio taped, transcribed and subsequently analyzed for themes. The analysis and interpretation of the data uncovered the following: (1) The experience of uninsurance was primarily a fear of the unknown. (2) The chronic illness experience included themes divided into the chronic illness course, lived body in illness and access, care and providers. (3) The essence of the medication experience was expressed as variations on control. This study challenges the assumptions about the uninsured and offers a deeper understanding of the medication experience. Additionally, this study adds to the illness experience literature, specifically offering an understanding of the uninsured individual's illness experience. The findings also reveal ethical implications important for clinical researchers whose subjects are uninsured. Lastly, this research provides health care practitioners with valuable information to provide patient-centered care to medically uninsured individuals.
机译:在美国,有超过4500万没有医疗保险的个体和9000万患有慢性病的个体。并且,随着药学专业朝着以患者为中心的药学服务的方向发展,重要的是要了解患者的用药和疾病经历以及影响患者护理的社会经济环境,例如保险。关于疾病的经验文献在医学和护理领域非常广泛,但是,对于像未保险者这样的边缘化群体的探索却大为缺失。全国范围内以及明尼苏达州的未投保人数都在增加。对未参保者的意识主要是通过全国性调查而获得的,对那些生活在其中的人的经验知之甚少。这项研究探索了没有保险的个人患有慢性病的经验。该方法是诠释学现象学,使用了深入的,非结构化的访谈。参与者包括11名成年人,年龄在27岁至64岁之间,每个成年人至少患有两种慢性疾病,并且没有保险,年龄为1至27岁。此外,一百多位员工对招聘信息做出了回应,并深入了解了疾病和非保险的含义。采访录音,录制和随后分析主题。对数据的分析和解释揭示了以下几点:(1)没有保险的经历主要是对未知的恐惧。 (2)慢性病的经历包括主题,分为慢性病课程,生病的身体和获取,护理和提供者。 (3)用药经验的实质表示为对照的变化。这项研究挑战了有关未投保者的假设,并提供了对用药经验的更深刻理解。此外,该研究增加了疾病经验文献,特别是提供了对未参保个体疾病经验的理解。该发现还揭示了伦理学意义,对受试者没有保险的临床研究者很重要。最后,这项研究为医疗保健从业人员提供了宝贵的信息,以为没有医疗保险的个人提供以患者为中心的护理。

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