Psychosocial and Health-Related Experiences of Individuals With Microtia and Craniofacial Microsomia and Their Families: Narrative Review Over 2 Decades

被引:9
|
作者
Johns, Alexis L. [1 ,2 ]
Stock, Nicola M. [3 ]
Costa, Bruna [3 ]
Billaud Feragen, Kristin [4 ]
Crerand, Canice E. [5 ]
机构
[1] Univ Southern Calif, Div Plast & Maxillofacial Surg, Childrens Hosp Los Angeles, Los Angeles, CA USA
[2] Univ Southern Calif, Keck Sch Med, Los Angeles, CA USA
[3] Univ West England, Ctr Appearance Res, Bristol, Avon, England
[4] Oslo Univ Hosp, Ctr Rare Disorders, Oslo, Norway
[5] Nationwide Childrens Hosp, Abigail Wexner Res Inst, Ctr Biobehav Hlth, Columbus, OH USA
来源
CLEFT PALATE CRANIOFACIAL JOURNAL | 2023年 / 60卷 / 09期
关键词
craniofacial microsomia; microtia; healthcare experiences; psychosocial adjustment; QUALITY-OF-LIFE; UNILATERAL HEARING-LOSS; EAR RECONSTRUCTION; AURICULAR RECONSTRUCTION; HEMIFACIAL MICROSOMIA; YOUNG-ADULTS; PSYCHOLOGICAL ADJUSTMENT; ACADEMIC-PERFORMANCE; ACHIEVING CONSENSUS; POROUS POLYETHYLENE;
D O I
10.1177/10556656221091699
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: This paper describes 20 years of microtia and craniofacial microsomia (CFM) psychosocial and healthcare studies and suggests directions for clinical care and research. Design: A narrative review of papers January 2000 to July 2021 related to psychosocial and healthcare experiences of individuals with microtia and CFM and their families. Results: Studies (N = 64) were mainly cross-sectional (69%), included a range of standardized measures (64%), and were with European (31%), American (27%), or multinational (23%) samples. Data were generally collected from both patients and caregivers (38%) or patient self-report (35%). Sample sizes were 11 to 25 (21%), 26 to 50 (19%), 51 to 100 (22%), or over 100 (38%). Studies addressed 5 primary topics: (1) Healthcare Experiences, including Medical Care, Hearing Loss/Amplification, Diagnostic Experiences, and Information Preferences; (2) Psychosocial Experiences, including Teasing, Behavioral Adjustment, Psychosocial Support, and Public Perception; (3) Neurocognitive Functioning and Academic Assistance; (4) Pre- and Post-Operative Psychosocial Outcomes of Ear Reconstruction/Canaloplasty; and (5) Quality of Life and Patient Satisfaction. Conclusions: Care involved multiple specialties and was often experienced as stressful starting at diagnosis. Psychosocial and neurocognitive functioning were generally in the average range, with possible risk for social and language concerns. Coping and resiliency were described into adulthood. Satisfaction and positive benefit of ear reconstruction/canaloplasty were high. Care recommendations include increasing: hearing amplification use, microtia and CFM knowledge among providers, efficient treatment coordination, psychosocial support, academic assistance, and advances to minimize surgical scarring. This broad literature overview informs clinical practice and research to improve psychosocial outcomes.
引用
收藏
页码:1090 / 1112
页数:23
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