Nursing care for patients with rare diseases on the example of patients with Alternating Hemiplegia of Childhood

M. Pazdur
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Abstract

Introduction: Rare diseases are those which occur in 1 person in 2000. Usually they are genetically conditioned. They also comprise diseases which appear as a result of metabolic, immunological defects, infections and uncommon cancers. Development of science, especially genetics prompted discovery of new gene’s mutations. One of them is a mutation of ATP1A3 which alternating hemiplegia of childhood. It is a disease whose manifestations appear in early childhood and are unpredictable. Strokes can be hemiplegic or tetraplegic. Sometimes they are accompanied by problems with swallowing and breathing. The aim of the thesis was to compare 2 different cases of patients suffering from AHC, to show problems connected with taking care of them in bio-psycho-socio-spiritual dimensions and to present a model of care on the example of Dorothey Orem’s theory. Material and methods: The comparative method used in the work compares two cases of patients. It is a quality work. Techniques of interview, observation, measurement and documentation analysis were also applied. An interview questionnaire containing 13 questions and an observation conducted in everyday circumstances made it possible to show care problems of patients with AHC. The research was carried out from March 2018 to May 2018. Two cases were juxtaposed: a 10-year-old girl and a 34-year-old man. Results and conclusions: Patients who suffer from rare diseases have restricted access to diagnosis, cure, rehabilitation and social assistance. They often grapple with lack of understanding on the part of society and medical staff who do not have enough knowledge about this issue. By comparing 2 cases it was proved that care problems of these patients are very complicated and vary depending on age, type of stroke, intensity, duration of the disease and family’s and society’s support. The care system of Dorothey Orem seems to be the best one.
罕见病患者的护理——以儿童交替性偏瘫患者为例
简介:罕见病是指2000年1人发病的疾病。通常它们是由基因决定的。它们还包括由于代谢、免疫缺陷、感染和罕见癌症而出现的疾病。科学的发展,特别是遗传学的发展促进了新基因突变的发现。其中之一是ATP1A3基因突变导致儿童偏瘫。这是一种疾病,其症状出现在儿童早期,是不可预测的。中风可以是偏瘫或四肢瘫痪。有时还伴有吞咽和呼吸困难。这篇论文的目的是比较两种不同的AHC患者的情况,以显示在生物心理社会精神方面照顾他们的问题并以Dorothey Orem的理论为例提出一个护理模式。材料与方法:本研究采用比较法对两例患者进行比较。这是一部高质量的作品。采用访谈、观察、测量、文献分析等方法。一份包含13个问题的访谈问卷和在日常环境中进行的观察,可以显示AHC患者的护理问题。该研究于2018年3月至2018年5月进行。两例并列:一名10岁女孩和一名34岁男子。结果与结论:罕见病患者获得诊断、治疗、康复和社会援助的机会有限。他们经常与社会和医务人员缺乏理解作斗争,他们对这个问题没有足够的了解。通过对两例病例的比较,证明该类患者的护理问题非常复杂,且因年龄、脑卒中类型、强度、病程以及家庭和社会的支持而有所不同。Dorothey Orem的护理体系似乎是最好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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