Navigating the Unique Challenges of Caregiving for Children with Rare Diseases: Are the Care Experiences of All Caregivers the Same? A Focus on Life-Limiting Rare Diseases

被引:0
|
作者
Walkowiak, Dariusz [1 ]
Domaradzki, Jan [2 ]
Mozrzymas, Renata [3 ]
Kaluzny, Lukasz [4 ]
Walkowiak, Jaroslaw [4 ]
机构
[1] Poznan Univ Med Sci, Dept Org & Management Hlth Care, PL-60356 Poznan, Poland
[2] Poznan Univ Med Sci, Dept Social Sci & Humanities, PL-60356 Poznan, Poland
[3] Reg Specialist Hosp, Res & Dev Ctr, PL-53413 Wroclaw, Poland
[4] Poznan Univ Med Sci, Dept Pediat Gastroenterol & Metab Dis, PL-60356 Poznan, Poland
关键词
rare diseases; caregivers; children with rare diseases; phenylketonuria; PKU; life-limiting rare diseases; FAMILY CAREGIVERS; NETWORK ANALYSIS; CHRONIC ILLNESS;
D O I
10.3390/jcm13154510
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Caregiving experiences in rare diseases (RDs) vary based on factors such as specific clinical entity, disease severity, the child's age, and available support and resources, leading to challenges that significantly impact caregivers' lives. This study investigates whether caregivers of children with different RDs encounter varied aspects of care. Methods: This study was conducted as a self-administered, anonymous, computer-assisted online survey, focusing on the challenges of caregiving for children with RDs. Questions covered aspects such as information availability on RDs, diagnostic processes, modern treatment accessibility, family physicians and specialists, the impact of caregiving on personal life, family dynamics, and financial challenges. To achieve our study objectives, we categorized caregivers of children with RDs into two groups to compare various aspects of caregiving: caregivers of children with phenylketonuria (PKU) (n = 175) and those caring for children with life-limiting rare diseases (LLRD) (n = 226). Results: Caregivers of children with LLRD reported greater emotional challenges, personal sacrifices, and financial burdens compared to caregivers of children with PKU. Significant differences included heightened emotional distress, more frequent conflicts, and lower assessments of healthcare support among LLRD caregivers. Although family support ratings were similar between the groups, perceptions of financial concerns and interactions with the healthcare system varied significantly. Conclusions: This study, representing the inaugural systematic comparison of specific caregiver cohorts overseeing children with RDs across a substantial sample size, provides valuable insights. The findings lay a crucial foundation for precisely tailoring assistance and support initiatives to meet the unique needs of caregivers facing various RDs in diverse contexts.
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页数:17
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