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识别左心发育不全综合征患儿家庭父母支持方面的差距。

Identifying gaps in parental support for families of children with hypoplastic left heart syndrome.

机构信息

Nursing Department, St. Catherine University, St. Paul, MN, USA.

Wanek Program for Hypoplastic Left Heart Syndrome, Mayo Clinic, Rochester, MN, USA.

出版信息

Cardiol Young. 2022 Feb;32(2):215-222. doi: 10.1017/S1047951121001736. Epub 2021 May 10.

DOI:10.1017/S1047951121001736
PMID:33966677
Abstract

PURPOSE

The purpose of this study is to identify gaps in support for parents of children with Hypoplastic Left Heart Syndrome.

DESIGN AND METHODS

Using a mixed-methods approach, the researchers first studied the parental and care team experience through interviews of Hypoplastic Left Heart Syndrome mothers and members of the inter-professional care team and then conducted an international survey of 690 Hypoplastic Left Heart Syndrome primary caregivers to validate the qualitative findings.

RESULTS

Parental and care team interviews revealed three main gaps in parental support, including lack of open communication, unrealistic parental expectations, and unclear inter-professional team roles. Survey results found that parents whose children were diagnosed with Hypoplastic Left Heart Syndrome after birth indicated significant dissatisfaction with the care team's open communication and welcoming of feedback (p = 0.008). As parents progress through the stages of surgical intervention, they also indicate significant dissatisfaction with the care team's anticipation of parental emotional needs and provision of coping resources (p = 0.003).

CONCLUSIONS

Parental support interventions should focus on providing resources to help parents cope, helping the care team model open communication, and welcoming feedback on the parental experience.

PRACTICE IMPLICATIONS

Interventions should be piloted with parents who are in the later stages of the surgical intervention timeline or whose children were diagnosed after birth as they are the populations who perceived the least support within this study.

摘要

目的

本研究旨在确定左心发育不全综合征患儿父母支持方面的差距。

设计和方法

研究人员采用混合方法,首先通过对左心发育不全综合征患儿母亲和跨专业护理团队成员进行访谈,研究了父母和护理团队的经验,然后对 690 名左心发育不全综合征主要照顾者进行了国际调查,以验证定性研究结果。

结果

父母和护理团队访谈揭示了父母支持方面的三个主要差距,包括缺乏开放的沟通、不切实际的父母期望和不明确的跨专业团队角色。调查结果发现,那些孩子在出生后被诊断出患有左心发育不全综合征的父母对护理团队的开放沟通和欢迎反馈表示出明显的不满(p=0.008)。随着父母经历手术干预的各个阶段,他们也对护理团队对父母情感需求的预测和应对资源的提供表示出明显的不满(p=0.003)。

结论

父母支持干预措施应侧重于提供资源帮助父母应对,帮助护理团队树立开放沟通的榜样,并欢迎对父母体验的反馈。

实践意义

应在处于手术干预时间轴后期的父母或其孩子在出生后被诊断出的父母中试行干预措施,因为他们是在这项研究中感知到支持最少的人群。

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Perceived family-centered care and post-traumatic stress in parents of infants cared for in the paediatric cardiac intensive care unit.父母感知的以家庭为中心的护理与儿科心脏重症监护病房患儿父母的创伤后应激
Nurs Crit Care. 2024 Sep;29(5):1059-1066. doi: 10.1111/nicc.13094. Epub 2024 May 30.
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Life situation of a caregiver of a child with congenital heart defect and/or other cardiac problems: structure and preliminary validation of a new questionnaire.
先天性心脏病和/或其他心脏问题患儿照料者的生活状况:一份新问卷的结构与初步验证
Front Psychol. 2023 Jun 15;14:1194031. doi: 10.3389/fpsyg.2023.1194031. eCollection 2023.