Kidane Samuel, Shamebo Semay Desta, Ntaganda Edmond, Petroze Robin T, McNatt Zahirah, Wong Rex, Rabideau Melany
Bill and Joyce Cummings Institute of Global Health, University of Global Health Equity, Butaro, Rwanda.
Department of Surgery, Centre Hospitalier Universitaire de Kigali, Kigali, Rwanda.
PLOS Glob Public Health. 2022 Jun 15;2(6):e0000439. doi: 10.1371/journal.pgph.0000439. eCollection 2022.
Pediatric surgery is a crucial pillar of health equity but is often not prioritized in the global health agenda, especially in low-and middle-income countries. Gastroschisis (GS) is a type of structural congenital anomaly that can be treated through surgical interventions. In Rwanda, neonatal surgical care is only available in one hospital. The experience of parents of children born with gastroschisis has not been previously studied in Rwanda. The objective of this study was to explore the lived experiences of parents of children diagnosed with GS in Rwanda. A qualitative study using a semi-structured interview guide was conducted. Parents who had children with gastroschisis and were discharged alive from the hospital in Rwanda were interviewed by trained data collectors, from May to July 2021. Data were transcribed, translated, and then coded using a structured code-book. Thematic analysis was conducted with the use of Dedoose software. Sixteen parents participated in the study. Five themes emerged from the data. They were: "GS diagnosis had a significant emotional impact on the parents", "Parents were content with the life-saving medical care provided for their children despite some dissatisfaction due to the delayed initiation of care and shortage of medications", "GS care was accompanied by financial challenges", "support systems were important coping mechanisms" and "the impact of GS care extended into the post-discharge period". Having a newborn with GS was an emotional journey. The lack of pre-knowledge about the condition created a shock to the parents. Parents found support from their faith and other parents with similar experiences. The experiences with the care received were mostly positive. The overall financial burden incurred from the medical treatment and indirect costs was high and extended beyond the hospital stay. Strengthening prenatal and hospital services, providing peer, spiritual and financial support could enhance the parents' experience.
小儿外科是卫生公平的关键支柱,但在全球卫生议程中往往未被列为优先事项,尤其是在低收入和中等收入国家。腹裂(GS)是一种结构性先天性异常,可通过手术干预进行治疗。在卢旺达,只有一家医院提供新生儿外科护理。此前尚未在卢旺达对腹裂患儿父母的经历进行过研究。本研究的目的是探讨卢旺达被诊断为GS的患儿父母的生活经历。采用半结构化访谈指南进行了一项定性研究。2021年5月至7月,经过培训的数据收集人员对在卢旺达有腹裂患儿且已出院存活的父母进行了访谈。数据被转录、翻译,然后使用结构化编码手册进行编码。使用Dedoose软件进行了主题分析。16名父母参与了该研究。数据中出现了五个主题。它们是:“GS诊断对父母产生了重大情感影响”、“尽管由于护理开始延迟和药物短缺存在一些不满,但父母对为其子女提供的挽救生命的医疗护理感到满意”、“GS护理伴随着经济挑战”、“支持系统是重要的应对机制”以及“GS护理的影响延伸到出院后时期”。生下患有GS的新生儿是一段充满情感的历程。对该病缺乏预先了解给父母带来了震惊。父母从他们的信仰和其他有类似经历的父母那里获得了支持。所接受护理的经历大多是积极的。医疗治疗和间接成本产生的总体经济负担很高,并且超出了住院期间。加强产前和医院服务、提供同伴、精神和经济支持可以改善父母的体验。