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How do caregivers of children with congenital heart diseases access and navigate the healthcare system in Ethiopia?

机译:如何在埃塞俄比亚获得和导航医疗保健系统的儿童的护理人员如何访问和导航

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Abstract Background Surgery can correct congenital heart defects, but disease management in low- and middle-income countries can be challenging and complex due to a lack of referral system, financial resources, human resources, and infrastructure for surgical and post-operative care. This study investigates the experiences of caregivers of children with CHD accessing the health care system and pediatric cardiac surgery. Methods A qualitative study was conducted at a teaching hospital in Ethiopia. We conducted semi-structured interviews with 13 caregivers of 10 patients with CHD who underwent cardiac surgery. We additionally conducted chart reviews for triangulation and verification. Interviews were conducted in Amharic and then translated into English. Data were analyzed according to the principles of interpretive thematic analysis, informed by the candidacy framework. Results The following four observations emerged from the interviews: (a) most patients were diagnosed with CHD at birth if they were born at a health care facility, but for those born at home, CHD was discovered much later (b) many patients experienced misdiagnoses before seeking care at a large hospital, (c) after diagnosis, patients were waiting for the surgery for more than a year, (d) caregivers felt anxious and optimistic once they were able to schedule the surgical date. During the care-seeking journey, caregivers encountered financial constraints, struggled in a fragmented delivery system, and experienced poor service quality. Conclusions Delayed access to care was largely due to the lack of early CHD recognition and financial hardships, related to the inefficient and disorganized health care system. Fee waivers were available to assist low-income children in gaining access to health services or medications, but application information was not readily available. Indirect costs like long-distance travel contributed to this challenge. Overall, improvements must be made for district-level screening and the health care workforce.
机译:摘要背景手术可以纠正先天性心脏缺陷,但由于缺乏推荐制度,财政资源,人力资源和外科手术后护理的基础设施,低收入和中等收入国家的疾病管理可能是挑战性和复杂的。本研究调查了CHD访问医疗保健系统和儿科心脏手术的儿童护理人员的经验。方法在埃塞俄比亚的教学院进行定性研究。我们对13例CHD接受心脏手术的CHD患者进行了半结构化访。我们还在进行三角测量和验证的情况下进行了图表评论。采访是在Amharic进行的,然后翻译成英文。根据候选框架告知,根据解释性专题分析的原则进行分析数据。结果采访中出现了以下四次观察结果:(a)大多数患者在出生时被诊断出患有CHD,如果他们出生在医疗机构,但对于在家出生的人,CHD被发现很多(b)许多患者经历了误诊在在大型医院寻求护理之前,(c)诊断后,患者正在等待一年多的手术,(d)护理人员一旦他们能够安排手术日期,就会感到焦虑和乐观。在寻求追求旅程中,护理人员遇到了财政限制,在分散的交付系统中挣扎,经历了不良的服务质量。结论由于缺乏早期CHD认可和金融困难,延迟了护理机会主要是缺乏与效率低下和混乱的医疗保健系统相关的。收取豁免可用于协助低收入儿童获得卫生服务或药物的获得,但申请信息并不容易获得。像长途旅行一样的间接成本导致这一挑战。总体而言,必须对地区级筛查和医疗保健劳动力进行改进。

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