Division of Plastic and Maxillofacial Surgery, 5150Children's Hospital Los Angeles, Los Angeles, CA, USA.
Center for Child Health, Behavior, and Development, 145793Seattle Children's Research Institute, Seattle, WA, USA.
Cleft Palate Craniofac J. 2021 Jan;58(1):42-53. doi: 10.1177/1055665620947987. Epub 2020 Aug 12.
The study aim was to assess behavioral adjustment in preschool children with and without craniofacial microsomia (CFM).
Multisite cohort study of preschoolers with CFM ("cases") or without CFM ("controls").
Mothers (89%), fathers (9%), and other caregivers (2%) of 161 preschoolers.
Child Behavior Check List (CBCL 1.5-5); linear regressions with standardized effect sizes (ES) adjusted for sociodemographic confounds.
Child Behavior Check Lists for 89 cases and 72 controls (average age 38.3 ± 1.9 months). Children were male (54%), white (69%), and of Latino ethnicity (47%). Cases had microtia with mandibular hypoplasia (52%), microtia only (30%), or other CFM-associated features (18%). Nearly 20% of cases had extracranial anomalies. Composite CBCL scores were in the average range compared to test norms and similar for cases and controls. On the subscales, cases' parents reported higher Anxious/Depressed scores (ES = 0.35, = .04), Stress Problems (ES = 0.40, = .04), Anxiety Problems (ES = 0.34, = .04), and Autism Spectrum Problems (ES = 0.41, = .02); however, the autism subscale primarily reflected speech concerns. Among cases, more problems were reported for children with extracranial anomalies and certain phenotypic categories with small ES.
Behavioral adjustment of preschoolers with CFM was comparable to peers. However, parental reports reflected greater concern for internalizing behaviors; thus, anxiety screening and interventions may benefit children with CFM. Among cases, more problems were reported for those with more complex presentations of CFM. Craniofacial microsomia-related speech problems should be distinguished from associated psychosocial symptoms during developmental evaluations.
本研究旨在评估颅面小颌畸形(CFM)患儿与无 CFM 患儿的行为调整情况。
多中心队列研究,纳入 CFM 患儿(“病例组”)和无 CFM 患儿(“对照组”)的学龄前儿童。
161 名学龄前儿童的母亲(89%)、父亲(9%)和其他照顾者(2%)。
儿童行为检查表(CBCL 1.5-5);经社会人口统计学混杂因素调整后的标准化效应量(ES)的线性回归。
89 例病例组和 72 例对照组的儿童行为检查表(平均年龄 38.3±1.9 个月)。患儿中,男性占 54%,白人占 69%,拉丁裔占 47%。病例组包括小耳伴下颌发育不全(52%)、小耳畸形(30%)或其他 CFM 相关特征(18%)。近 20%的病例存在颅外异常。复合 CBCL 评分与测试常模相比处于平均范围,且病例组和对照组间相似。在子量表上,病例组的父母报告其患儿存在更高的焦虑/抑郁评分(ES=0.35,P=.04)、压力问题评分(ES=0.40,P=.04)、焦虑问题评分(ES=0.34,P=.04)和自闭症谱系问题评分(ES=0.41,P=.02);然而,自闭症子量表主要反映了言语问题。在病例组中,存在颅外异常和某些表型类别的患儿报告的问题更多,但其 ES 值较小。
CFM 患儿的行为调整与同龄人相当。然而,父母报告反映出对患儿内在行为的更大担忧;因此,焦虑筛查和干预可能有益于 CFM 患儿。在病例组中,存在更复杂 CFM 表现的患儿报告的问题更多。在发育评估中,应将 CFM 相关的言语问题与相关的心理社会症状区分开来。