Speltz Matthew L, Collett Brent R, Wallace Erin R, Kapp-Simon Kathleen
Seattle, Wash.; and Chicago, Ill.
From the Department of Psychiatry and Behavioral Sciences, University of Washington; the Center for Child Health, Behavior, and Development, Seattle Children's Research Institute; the Cleft-Craniofacial Center, Shriner's Hospital for Children; and the Craniofacial Center, Department of Surgery, University of Illinois at Chicago.
Plast Reconstr Surg. 2016 Aug;138(2):435-445. doi: 10.1097/PRS.0000000000002383.
Previous research has observed higher than average rates of behavior problems in school-age children with single-suture craniosynostosis. However, most studies used a single informant (mothers) and did not include comparison groups to control for sociodemographic factors.
The authors gave standardized behavior checklists to the mothers, fathers, and teachers of 179 elementary school children with single-suture craniosynostosis and 183 controls. We used linear regression to compare children with and without single-suture craniosynostosis on continuous measures of adjustment, and logistic regression to compare the proportions of children who scored above a well-established clinical threshold based on the report of one or more informants. All analyses were adjusted for demographic confounds (age, sex, socioeconomic status, maternal intelligence quotient).
Cases received higher average behavior problem scores than controls from all informants. However, differences were small in magnitude (0.01 to 0.2 SD; p = 0.12 to p = 0.96). Thirty-three percent of children with single-suture craniosynostosis were rated above a clinical threshold by one or more informants, compared with 21 percent of controls (adjusted odds ratio, 1.67; p = 0.04). Among cases, children with metopic synostosis had the highest level of observed behavior problems (41 percent greater than threshold); those with sagittal synostosis had the lowest level (29 percent).
The authors observed little difference in average ratings of behavior problems between children with and without single-suture craniosynostosis. However, children with single-suture craniosynostosis were more likely to score above a clinical threshold than unaffected controls. No specific areas of maladjustment were associated with case status or location of suture fusion.
CLINICAL QUESTION/LEVEL OF EVIDENCE: Risk, II.
先前的研究发现,患有单缝颅缝早闭的学龄儿童出现行为问题的几率高于平均水平。然而,大多数研究仅采用单一信息提供者(母亲),且未设置对照组以控制社会人口统计学因素。
作者向179名患有单缝颅缝早闭的小学生及183名对照儿童的母亲、父亲和教师发放了标准化行为清单。我们采用线性回归,比较患有和未患有单缝颅缝早闭儿童在连续调整指标上的差异;采用逻辑回归,比较基于一名或多名信息提供者报告,得分高于既定临床阈值的儿童比例。所有分析均对人口统计学混杂因素(年龄、性别、社会经济地位、母亲智商)进行了调整。
所有信息提供者给出的结果均显示,病例组儿童的平均行为问题得分高于对照组。然而,差异幅度较小(0.01至0.2标准差;p值为0.12至0.96)。一名或多名信息提供者将33%的单缝颅缝早闭儿童评定为高于临床阈值,而对照组这一比例为21%(调整优势比为1.67;p = 0.04)。在病例组中,额缝早闭儿童的行为问题水平最高(比阈值高41%);矢状缝早闭儿童的行为问题水平最低(比阈值高29%)。
作者观察到,患有和未患有单缝颅缝早闭的儿童在行为问题平均评分上差异不大。然而,患有单缝颅缝早闭的儿童比未受影响的对照组更有可能得分高于临床阈值。未发现特定的适应不良领域与病例状态或缝融合位置相关。
临床问题/证据水平:风险,II级。