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Being Fully Present: Gains Patients Attribute to a Telephone-Delivered Parenting Program for Child-Rearing Mothers With Cancer.全情投入:接受电话育儿模式的癌症患儿母亲对其的认可。
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Family Stress in Pediatric Critical Care.儿科重症监护中的家庭压力
J Pediatr Nurs. 2017 Jan-Feb;32:32-40. doi: 10.1016/j.pedn.2016.10.007. Epub 2016 Nov 21.
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Experiencing Support During Needle-Related Medical Procedures: A Hermeneutic Study With Young Children (3-7Years).在与针头相关的医疗程序中体验支持:一项针对幼儿(3至7岁)的诠释学研究。
J Pediatr Nurs. 2016 Nov-Dec;31(6):667-677. doi: 10.1016/j.pedn.2016.06.004. Epub 2016 Jul 11.
4
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Daily Sleep Patterns, Sleep Quality, and Sleep Hygiene Among Parent-Child Dyads of Young Children Newly Diagnosed With Juvenile Idiopathic Arthritis and Typically Developing Children.新诊断为幼年特发性关节炎的幼儿与发育正常儿童的亲子二元组的每日睡眠模式、睡眠质量和睡眠卫生
J Pediatr Psychol. 2016 Jul;41(6):651-60. doi: 10.1093/jpepsy/jsw007. Epub 2016 Mar 19.
6
A recurring rollercoaster ride: a qualitative study of the emotional experiences of parents of children with juvenile idiopathic arthritis.一场反复的过山车之旅:对幼年特发性关节炎患儿家长情感体验的定性研究
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The experience of taking methotrexate for juvenile idiopathic arthritis: results of a cross-sectional survey with children and young people.青少年特发性关节炎患者服用甲氨蝶呤的体验:一项针对儿童和青少年的横断面调查结果
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The Contribution of Parent and Family Variables to the Well-Being of Youth With Arthritis.父母及家庭因素对患关节炎青少年幸福感的影响
J Fam Nurs. 2015 Nov;21(4):579-616. doi: 10.1177/1074840715601475. Epub 2015 Aug 29.
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Procedural pain and patient-reported side effects with weekly injections of subcutaneous methotrexate in children with rheumatic disorders.风湿性疾病患儿每周皮下注射甲氨蝶呤的操作疼痛及患者报告的副作用
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在黑暗中挣扎以帮助我的孩子:父母照顾幼年特发性关节炎幼儿的经历。

Struggling in the Dark to Help My Child: Parents' Experience in Caring for a Young Child with Juvenile Idiopathic Arthritis.

作者信息

Yuwen Weichao, Lewis Frances M, Walker Amy J, Ward Teresa M

机构信息

Nursing and Healthcare Leadership, University of Washington Tacoma, Tacoma, WA, United States.

Family and Child Nursing, University of Washington, Seattle, WA, United States.

出版信息

J Pediatr Nurs. 2017 Nov-Dec;37:e23-e29. doi: 10.1016/j.pedn.2017.07.007. Epub 2017 Aug 1.

DOI:10.1016/j.pedn.2017.07.007
PMID:28778610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5681389/
Abstract

PURPOSE

The purpose of this study is to describe parents' experiences in caring for 2-5-year-old children with juvenile idiopathic arthritis (JIA).

DESIGN AND METHODS

A qualitative study using single-occasion in-depth interviews was conducted. Nine parents (eight mothers and one father) were interviewed in-person or via telephone. Data were analyzed using inductive content analysis. Methods used to protect the trustworthiness of study results included maintenance of an audit trail, peer debriefing, and member checks.

RESULTS

The core construct Struggling in the Dark to Help My Child explained parents' experience in six domains: not knowing, trying to reach out in the dark, feeling my child's pain, working out the kinks to stay on top to manage, feeling drained by the whole process, and being hard on the entire household. Parents struggled with the unknown, searched for resources, witnessed their child's suffering without knowing how to help, and tried every possible way to stay on top of the child's illness and treatment, even when they felt drained physically and emotionally. JIA not only consumed their lives, but also affected the entire family, including the siblings and spouse, and the relationships among family members.

CONCLUSION AND IMPLICATIONS

Findings highlight the day-to-day lived challenges parents face when caring for a young child with JIA. Healthcare providers including nurses need to assess the particular needs of an ill child and parents as well as the impact of the illness on the physical and psychosocial health of the entire family so that proper resources can be provided.

摘要

目的

本研究旨在描述父母照顾2至5岁幼年特发性关节炎(JIA)患儿的经历。

设计与方法

采用单次深度访谈进行定性研究。对9名家长(8名母亲和1名父亲)进行了面对面或电话访谈。采用归纳性内容分析法对数据进行分析。用于保护研究结果可信度的方法包括保持审计追踪、同行汇报和成员核对。

结果

“在黑暗中挣扎以帮助我的孩子”这一核心构念解释了父母在六个领域的经历:一无所知、在黑暗中努力寻求帮助、感受孩子的痛苦、解决难题以掌控局面、在整个过程中感到疲惫不堪以及对整个家庭要求苛刻。父母们与未知作斗争,寻找资源,目睹孩子的痛苦却不知如何帮助,想尽一切办法掌控孩子的病情和治疗,即使他们在身体和情感上都感到疲惫不堪。幼年特发性关节炎不仅消耗了他们的生活,还影响了整个家庭,包括兄弟姐妹和配偶,以及家庭成员之间的关系。

结论与启示

研究结果凸显了父母在照顾幼年特发性关节炎患儿时面临的日常实际挑战。包括护士在内的医疗保健提供者需要评估患病儿童及其父母的特殊需求,以及疾病对整个家庭身心健康的影响,以便提供适当的资源。