The life situation of a family with a chronically ill child and the family's experience of support provided by healthcare professionals in Finland

IF 2.1 4区 医学 Q2 NURSING
Hanna Seppänen MHSc , Anna-Maija Koivisto MSc , Jari Kylmä PhD , Tuija Leppäkoski PhD , Tarja Heino-Tolonen , Eija Paavilainen PhD
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引用次数: 0

Abstract

Background

Chronic illness in children elicits emotions within the family, impacts family bonds, and reshapes family dynamics. Support from healthcare professionals is vital for facilitating family adaptation. The aim of this study is to describe the life situation of Finnish families with a chronically ill child and to enhance understanding of the types of support the families perceive.

Methods

Data were collected in Finland as part of an international research project (2021−2023). 76 parents of chronically ill children completed an electronic survey. Analyses, conducted using IBM SPSS 29, included descriptive and inferential statistical methods. The ICE-FPSQ instrument assessed perceived support, generating composite variables for overall, emotional, and cognitive support. Association of background variables and adaptation with composite scores were examined using the Mann-Whitney U test.

Results

Life situation: Among respondents, 54.7 % (n = 41) reported that the illness strains their family, and 47.4 % (n = 36) noted it has changed them as a family. However, 81.5 % (n = 62) felt the experience improved their coping abilities.
Support from healthcare professionals: The median ICE-FPSQ composite score was 37 (n = 71, Q1 = 28, Q3 = 44; range: 14–70). For cognitive support, the median was 16 (Q1 = 12, Q3 = 18; range: 5–25), and for emotional support, it was 20 (Q1 = 14.3, Q3 = 26.5; range: 9–45). Mothers perceived receiving less support than fathers, and the child's hospitalization increased the perceived amount of support.

Conclusion

Chronic illness places a considerable burden on families. Healthcare professionals can support families in adapting to life with a child who has a chronic illness.
芬兰一个患有慢性病儿童的家庭的生活状况以及该家庭获得保健专业人员提供的支持的经验
儿童慢性疾病引发家庭内部的情绪,影响家庭关系,重塑家庭动态。医疗保健专业人员的支持对于促进家庭适应至关重要。本研究的目的是描述有慢性病儿童的芬兰家庭的生活状况,并加强对家庭所感知的支持类型的理解。作为国际研究项目(2021 - 2023)的一部分,数据在芬兰收集。76名患有慢性病儿童的父母完成了一份电子调查。使用IBM SPSS 29进行分析,包括描述性和推断性统计方法。ICE-FPSQ工具评估感知支持,生成整体、情感和认知支持的复合变量。使用Mann-Whitney U检验背景变量和适应性与综合得分的关联。结果生活状况:受访者中,54.7% (n = 41)的人认为疾病给家庭带来了压力,47.4% (n = 36)的人认为疾病改变了他们的家庭。然而,81.5% (n = 62)的人认为这段经历提高了他们的应对能力。医疗保健专业人员的支持:ICE-FPSQ综合评分中位数为37分(n = 71, Q1 = 28, Q3 = 44;范围:14 - 70)。认知支持的中位数为16 (Q1 = 12, Q3 = 18;范围:5-25),情感支持为20 (Q1 = 14.3, Q3 = 26.5;范围:9-45)。母亲感知到的支持比父亲少,而孩子的住院治疗增加了感知到的支持量。结论慢性疾病给家庭带来相当大的负担。医疗保健专业人员可以帮助家庭适应患有慢性疾病的孩子的生活。
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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来源期刊
CiteScore
3.70
自引率
8.30%
发文量
291
审稿时长
65 days
期刊介绍: Official Journal of the Society of Pediatric Nurses and the Pediatric Endocrinology Nursing Society (PENS) The Journal of Pediatric Nursing: Nursing Care of Children and Families (JPN) is interested in publishing evidence-based practice, quality improvement, theory, and research papers on a variety of topics from US and international authors. JPN is the official journal of the Society of Pediatric Nurses and the Pediatric Endocrinology Nursing Society. Cecily L. Betz, PhD, RN, FAAN is the Founder and Editor in Chief. Journal content covers the life span from birth to adolescence. Submissions should be pertinent to the nursing care needs of healthy and ill infants, children, and adolescents, addressing their biopsychosocial needs. JPN also features the following regular columns for which authors may submit brief papers: Hot Topics and Technology.
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