视网膜母细胞瘤儿童:诊断公告、困难及家长经验

A. Kachouchi, N. Albab, M. Berghalout, S. belghmaidi, J. Hakam, I. Adali, I. Hajji, F. Manoudi, A. Moutaouakil, F. Asri
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引用次数: 1

摘要

视网膜母细胞瘤是一种视网膜癌性肿瘤。这是一种罕见的疾病,在法国,每年每1.5万到2万名新生儿中就有1名患有此病。在摩洛哥,在卡萨布兰卡儿科眼科进行的一项为期2年零3个月的前瞻性研究中,视网膜母细胞瘤的年发病率估计为每年18例。癌症的诊断,像任何其他严重的疾病一样,在孩子和他的父母中引起强烈的内疚感。视网膜母细胞瘤的诊断公告仍然是一个困难和微妙的时刻,照顾者和家长。我们工作的目的是描述视网膜母细胞瘤儿童父母的经历,并评估这些儿童对其孩子的治疗和清晰度的满意程度。信息传播。材料和方法:我们对在摩洛哥马拉喀什穆罕默德六世眼科接受治疗的视网膜母细胞瘤儿童的父母进行了描述性横断面研究,研究时间为2016年3月至2017年3月一年。本研究采用问卷调查的方式收集家长的数据,旨在评估家长在以下方面的感受和体验:公告结构、信任氛围、形式化个性化支持的建议。结果:患儿确诊时平均年龄11个月,以男性为主,性别比为1.4。所有家庭都有一个生病的孩子。2例视网膜母细胞瘤为双侧。所有病例的手术治疗都是根治性的。75%的人认为医生能够找到正确的词语来宣布疾病,42%的人认为他找到了正确的词语。在诊断时,12个家庭中有11个认为他们从医疗保健专业人员那里得到了足够的倾听,75%的人认为倾听是相当充分的。所有的父母都报告说,医生对他们说的是关心和尊重,92%的人给出了极端积极的分数。66%的家庭表示接受了个性化护理计划。结论:本研究的结果将改善对儿童的整体照顾,并将家长所表达和感受到的困难融入照顾项目中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Child with Retinoblatoma: Diagnosis Announcement, Difficulties and Parent’s Experiences
Introduction: Retinoblastoma is a cancerous tumor of the retina. It is a rare pathology that affects each year, in France, one child out of 15,000 to 20,000 births. In Morocco, and in a prospective study conducted over 2 years and 3 months in the pediatric ophthalmology department in Casablanca, the annual incidence of retinoblastoma was estimated at 18 cases per year. The diagnosis of cancer, like any other serious illness, provokes an intense feeling of guilt in the child and in his parents. The retinoblastoma diagnosis announcement remains a difficult and delicate moment for caregivers and parents. The purpose of our work is to describe the experience of the parents of a child with retinoblastoma and to assess the degree of satisfaction of these children both for the treatment of their child and for clarity. information transmitted. Material and method: We conducted a descriptive cross-sectional study of the parents of children with retinoblastoma who received care in the ophthalmology department of Mohammed VI CHU Marrakech Morocco, and this over a period of one year from March 2016 to March 2017. The data is collected from parents with a questionnaire aimed to assess the parents' feelings and experiences around the following areas: the announcement structure, the climate of trust, proposal of formalizing personalized support. Results: The average age of children at the time of diagnosis is 11 months, with a male predominance, sex ratio is 1.4. All families had one sick child. Retinoblastoma was bilateral in two cases. The surgical treatment was radical in all cases. 75% felt that the doctor was able to find the right words to announce the disease, and 42% felt he found the right words. At the time of diagnosis, 11 out of 12 families felt that they had received sufficient listening from the healthcare professionals and 75% felt that listening was quite sufficient. All parents report that the doctor who made the announcement spoke to them with care and respect and 92% spoke on the extreme positive score. 66% of families report receiving a personalized care plan. Conclusion: The results of this study will improve the overall care provided to children and integrate the difficulties expressed and felt by parents to the care project.
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