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Embarking on a treatment journey: Experiences of caregivers of young children with craniofacial microsomia

Stock, Nicola; Johns, Alexis; McWilliams, Danielle; Rahman, Muhammad; Costa, Bruna; Crerand, Canice; Magee, Leanne; Hotton, Matthew; Feragen, Kristin; Tumblin, Melissa; Schefer, Amy; Drake, Amelia; Heike, Carrie

Authors

Alexis Johns

Danielle McWilliams

Muhammad Rahman

Bruna Costa

Canice Crerand

Leanne Magee

Matthew Hotton

Kristin Feragen

Melissa Tumblin

Amy Schefer

Amelia Drake

Carrie Heike



Abstract

Caregiver psychosocial adjustment can be impacted by their children’s early treatment for craniofacial microsomia (CFM). A deeper understanding of caregiver early experiences is needed to advance family-centered clinical care. This study aimed to describe the range of caregiver experiences of CFM care for their young children to inform recommendations for providers. As part of the ‘Craniofacial Microsomia: Accelerating Research and Education’ (CARE) program, health histories and narrative interviews were completed with a national sample of U.S. caregivers (N=42) of children with CFM aged 3-17 years (mean=10.1, SD = 4.5). Interviews (average 71 minutes) were in English (n=30) or Spanish (n=12) and primarily with mothers (93%). Thematic analysis was used to describe early care experiences. By age three, 91% of children were diagnosed with hearing loss, 64% had participated in early developmental services, 38% had undergone at least one surgery, and 24% used hearing aids. Caregivers’ experiences fit within themes of: 1) Burden of Care; 2) Adaptation; 3) Perceived Quality of Care; 4) Child’s Physical Health; and 5) Early Surgical Interventions. CFM care in early childhood presented challenges for caregivers, which may be mitigated by healthcare providers reducing burdens of care, coordinating care, building trust, increasing CFM and hearing education, instilling hope, assisting with hearing aid access, referring to early interventions, screening for caregiver distress, linking caregivers to support services, promoting coping and social support, and preparing families thoroughly for surgeries.

Journal Article Type Article
Acceptance Date Jun 4, 2025
Deposit Date Jun 5, 2025
Print ISSN 1049-2275
Electronic ISSN 1536-3732
Publisher Lippincott, Williams & Wilkins
Peer Reviewed Peer Reviewed
Keywords Visible difference; craniofacial; caregivers; treatment; psychosocial
Public URL https://uwe-repository.worktribe.com/output/14546709