Continuity of Care for the Child With Spina Bifida

Christina Von Colln-Appling, Lauren E. Stoltzfus, Megan A. Infanti Mraz
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Abstract

Spina bifida (SB), the second most common congenital birth defect in North America, is characterized by inadequate closure of spinal canal (Lindsay, 2014). SB leads to permanent and irreversible damage to the nervous system and spinal cord. Children diagnosedwith SB can develop a variety of conditions including bowel and bladder dysfunction, conditions that impact skin integrity, neurological and learning complications, respiratory track problems, and functional limitations (Lindsay, 2014). It is important for school administrators, school nurses, teachers, and the multidisciplinary medical team to have knowledge regarding SB and subsequent limitations of SB to ensure that all children receive the proper care and education (KennedyKrieger Institute, 2009). Adaptations and modifications to the learning environment will be individualized based on the child's needs. The purpose of this article is to present holistic care at the elementary, middle, and high school phases for children with SB. This article will review the importance of the multidisciplinary process to foster autonomy and independence of the child with SB so they can thrive in the school system and community.
脊柱裂患儿护理的连续性
脊柱裂(SB)是北美第二常见的先天性出生缺陷,其特征是椎管闭合不足(Lindsay,2014)。SB会对神经系统和脊髓造成永久性和不可逆的损伤。被诊断患有SB的儿童可能会出现多种疾病,包括肠和膀胱功能障碍、影响皮肤完整性的疾病、神经和学习并发症、呼吸系统问题和功能限制(Lindsay,2014)。学校管理人员、学校护士、教师和多学科医疗团队必须了解SB及其后续限制,以确保所有儿童都能得到适当的照顾和教育(KennedyKrieger研究所,2009年)。对学习环境的适应和修改将根据孩子的需求进行个性化。本文旨在介绍SB儿童在小学、初中和高中阶段的整体护理。本文将回顾多学科过程对培养SB儿童自主性和独立性的重要性,以便他们能够在学校系统和社区中茁壮成长。
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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