Alexis L. Johns
Embarking on a treatment journey: Experiences of caregivers of young children with craniofacial microsomia
Johns, Alexis L.; Stock, Nicola; McWilliams, Danielle; Rahman, Muhammad; Costa, Bruna; Crerand, Canice E.; Magee, Leanne; Hotton, Matthew; Feragen, Kristin B.; Tumblin, Melissa; Schefer, Amy; Drake, Amelia F.; Heike, Carrie L.
Authors
Dr Nicola Stock Nicola2.Stock@uwe.ac.uk
Associate Professor of Psychology
Danielle McWilliams
Muhammad Rahman
Bruna Costa
Canice E. Crerand
Leanne Magee
Matthew Hotton
Kristin B. Feragen
Melissa Tumblin
Amy Schefer
Amelia F. Drake
Carrie L. 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 US caregivers (N=42) of children with CFM aged 3 to 17 years (mean=10.1, SD=4.5). Interviews (average 71 min) 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 3, 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 health care 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 |
Online Publication Date | Jul 7, 2025 |
Deposit Date | Jun 5, 2025 |
Publicly Available Date | Jul 8, 2026 |
Journal | Journal of Craniofacial Surgery |
Print ISSN | 1049-2275 |
Electronic ISSN | 1536-3732 |
Publisher | Lippincott, Williams & Wilkins |
Peer Reviewed | Peer Reviewed |
DOI | https://doi.org/10.1097/scs.0000000000011643 |
Keywords | Visible difference; craniofacial; caregivers; treatment; psychosocial |
Public URL | https://uwe-repository.worktribe.com/output/14546709 |
Files
This file is under embargo until Jul 8, 2026 due to copyright reasons.
Contact Nicola2.Stock@uwe.ac.uk to request a copy for personal use.
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