Division of Bioethics and Palliative Care, Department of Pediatrics (J.B.), University of Washington School of Medicine; Treuman Katz Center for Bioethics, Center for Clinical and Translational Research, Seattle Children's Research Institute, Seattle, Washington, USA.
Divisions of Pediatric Palliative and Supportive Care and Hospital Medicine (J.Y.), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
J Pain Symptom Manage. 2023 Dec;66(6):647-655. doi: 10.1016/j.jpainsymman.2023.08.025. Epub 2023 Sep 4.
Children with severe neurological impairment (SNI) make up nearly 50% of pediatric intensive care unit (PICU) admissions, yet little is known about their family caregiver experiences.
To examine how parents and family caregivers of children with SNI navigate stress during PICU admissions.
This qualitative single-center study used content and thematic networks analysis to evaluate data from 1:1 semistructured interviews conducted around the time of PICU discharge with parents and family caregivers of children with SNI to examine ways they navigate stress. Proportions of participants reporting each theme and subtheme were calculated.
Fifteen parents/family caregivers of 15 children with SNI participated. Children were a median of 8 years old (range 1-21 years) and the majority had congenital/chromosomal conditions leading to their neurologic condition (80%, n = 12). 20% of participants were fathers (n = 3) and 45% (n = 7) reported identifying as having a minority racial background. Themes included 1) self-activation, and 2) letting go and the majority (80%, n = 12) of parents reported using both self-activation and letting go strategies. Within each of these themes, 5 subthemes illustrated ways parents navigate stress. The most reported subthemes were advocating and showing up (53%, n = 8) and being supported by compassionate clinicians (67%, n = 10). Themes/subthemes were used to create recommended language to guide clinicians in supporting parents.
Parents and family caregivers of children with SNI employ various ways to navigate stress in the PICU. Themes from this study can be used to develop interventions that meet the psychosocial needs of parents and family caregivers of children with SNI during highly stressful times.
患有严重神经功能障碍(SNI)的儿童占儿科重症监护病房(PICU)入院人数的近 50%,但人们对其家庭照顾者的经历知之甚少。
研究 SNI 患儿的父母和家庭照顾者在 PICU 入院期间如何应对压力。
这是一项单中心的定性研究,使用内容和主题网络分析,评估了在 PICU 出院时对 15 名 SNI 患儿的父母和家庭照顾者进行的 1:1 半结构化访谈的数据,以研究他们应对压力的方式。计算了报告每个主题和子主题的参与者的比例。
15 名 SNI 患儿的 15 名父母/家庭照顾者参与了研究。患儿的中位年龄为 8 岁(范围 1-21 岁),大多数患儿因先天性/染色体疾病导致神经系统疾病(80%,n=12)。20%的参与者为父亲(n=3),45%(n=7)报告自己属于少数族裔背景。主题包括 1)自我激活,2)放手。大多数(80%,n=12)父母报告同时使用自我激活和放手策略。在每个主题中,都有 5 个子主题说明了父母应对压力的方式。报告最多的子主题是倡导和出现(53%,n=8)和得到富有同情心的临床医生的支持(67%,n=10)。这些主题/子主题可用于创建建议性语言,以指导临床医生在高压力时期为 SNI 患儿的父母和家庭照顾者提供支持。
SNI 患儿的父母和家庭照顾者采用各种方式在 PICU 中应对压力。本研究的主题可用于制定干预措施,以满足 SNI 患儿的父母和家庭照顾者在高压力时期的心理社会需求。