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埃塞俄比亚先天性心脏病患儿的照料者如何获取并使用医疗保健系统?

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

作者信息

Choi Sugy, Shin Heesu, Heo Jongho, Gedlu Etsegenet, Nega Berhanu, Moges Tamirat, Bezabih Abebe, Park Jayoung, Kim Woong-Han

机构信息

Department of Health Law, Policy & Management, Boston University School of Public Health, Boston, MA, USA.

Program in Global Surgery and Implementation Science, JW LEE Center for Global Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.

出版信息

BMC Health Serv Res. 2021 Feb 1;21(1):110. doi: 10.1186/s12913-021-06083-2.

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.

摘要

背景

手术可以矫正先天性心脏缺陷,但由于缺乏转诊系统、财政资源、人力资源以及手术和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具有挑战性且复杂。本研究调查了患有先天性心脏病的儿童的照料者在获取医疗保健系统和小儿心脏手术方面的经历。

方法

在埃塞俄比亚的一家教学医院进行了一项定性研究。我们对10例接受心脏手术的先天性心脏病患儿的13名照料者进行了半结构化访谈。我们还进行了病历审查以进行三角互证和核实。访谈用阿姆哈拉语进行,然后翻译成英语。数据根据诠释性主题分析原则进行分析,并参考候选资格框架。

结果

访谈得出以下四点观察结果:(a)大多数在医疗机构出生的患者在出生时被诊断出患有先天性心脏病,但对于那些在家中出生的患者,先天性心脏病的发现要晚得多;(b)许多患者在到大医院就医之前经历过误诊;(c)诊断后,患者等待手术的时间超过一年;(d)一旦能够安排手术日期,照料者会感到焦虑和乐观。在寻求治疗的过程中,照料者遇到了经济困难,在分散的医疗服务体系中挣扎,并且体验到了较差的服务质量。

结论

获得治疗的延迟主要是由于缺乏对先天性心脏病的早期识别以及经济困难,这与低效和无序的医疗保健系统有关。有费用减免措施来帮助低收入儿童获得医疗服务或药物,但申请信息并不容易获取。长途旅行等间接成本也造成了这一挑战。总体而言,必须改善地区级筛查和医疗保健工作人员的状况。

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