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学校护士在镰状细胞病循证管理方面的教育需求。

Educational Needs of School Nurses Regarding the Evidence-Based Management of Sickle Cell Disease.

机构信息

Cincinnati Comprehensive Sickle Cell Center, Division of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA.

出版信息

Int J Environ Res Public Health. 2021 Nov 5;18(21):11641. doi: 10.3390/ijerph182111641.

DOI:10.3390/ijerph182111641
PMID:34770153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8582712/
Abstract

Sickle cell disease (SCD) is a rare blood disorder that can have life-threatening complications. This presents a challenge for school nurses who may have had limited experience managing complications in the school setting. This study assessed the experience, self-reported knowledge, confidence and ability of school nurses in managing SCD in the school-setting and identified continuing educational needs and preferences. This study used a qualitative, descriptive approach. A survey was previously administered to over 400 school nurses who worked in K-12 schools in Ohio. Those participants who reported experience with managing SCD were invited to participate in a focus group or semi-structured interview. Data were interpreted using thematic analysis strategy. Four overarching themes emerged from the data: (1) perceived lack of support and resources, (2) self-reported lack of knowledge about SCD, (3) importance of partnerships with parents, and (4) need for continuing education and networking with other school nurses. Easily accessible, educational interventions, along with peer networking, can be designed to improve school nurse knowledge and confidence levels in managing SCD. These types of on-demand interventions are important as many school nurses reported infrequent exposure to students with SCD.

摘要

镰状细胞病(SCD)是一种罕见的血液疾病,可能会导致危及生命的并发症。这对学校护士来说是一个挑战,因为他们可能在学校环境中处理并发症的经验有限。本研究评估了学校护士在学校环境中管理 SCD 的经验、自我报告的知识、信心和能力,并确定了继续教育的需求和偏好。本研究采用定性、描述性方法。之前对俄亥俄州 K-12 学校的 400 多名学校护士进行了调查。那些报告有管理 SCD 经验的参与者被邀请参加焦点小组或半结构化访谈。使用主题分析策略对数据进行解释。数据中出现了四个总体主题:(1)缺乏支持和资源的感觉,(2)自我报告的 SCD 知识不足,(3)与家长建立伙伴关系的重要性,(4)需要继续教育和与其他学校护士建立联系。可以设计易于获取的教育干预措施以及同行网络,以提高学校护士管理 SCD 的知识和信心水平。这些按需干预措施很重要,因为许多学校护士报告说很少接触到患有 SCD 的学生。

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本文引用的文献

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School Professionals' Knowledge and Beliefs About Youth With Chronic Illness.学校专业人员对慢性病青少年的知识和信念。
J Sch Health. 2018 Aug;88(8):615-623. doi: 10.1111/josh.12646.
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Translating sickle cell guidelines into practice for primary care providers with Project ECHO.通过“知识转化协作网络”(ECHO)项目将镰状细胞病指南应用于初级医疗服务提供者的实践中。
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The possible impact of teachers and school nurses on the lives of children living with sickle cell disease.教师和学校护士对患有镰状细胞病儿童生活的潜在影响。
J Sch Health. 2011 May;81(5):219-22. doi: 10.1111/j.1746-1561.2011.00582.x.
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School nurse case management for children with chronic illness: health, academic, and quality of life outcomes.针对慢性病患儿的学校护士病例管理:健康、学业及生活质量成果。
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