Dentino Kelley, Ganjawalla Karan, Inverso Gino, Mulliken John B, Padwa Bonnie L
Clinical Research Fellow, Harvard Medical School, Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA.
Dental Student, Harvard School of Dental Medicine, Boston, MA.
J Oral Maxillofac Surg. 2015 Dec;73(12 Suppl):S20-5. doi: 10.1016/j.joms.2015.04.017.
Midfacial hypoplasia is a characteristic feature of the syndromic craniosynostoses and predisposes these patients to developing obstructive sleep apnea (OSA). The purpose of this study was to identify anatomic factors associated with airway obstruction in patients with syndromic craniosynostoses.
This was a retrospective cohort study. The authors enrolled a study sample composed of patients with syndromic craniosynostoses. The predictor variables were age, gender, body mass index (BMI), syndromic diagnosis, and parameters of upper airway length and size measured on lateral cephalograms. To control for age, upper airway length was corrected for differences in patient height. The outcome variable was OSA status (present or absent). Descriptive, bivariate, and regression statistics were computed. For all analyses, a P value less than or equal to .05 was considered statistically significant.
The sample was composed of 50 patients with a mean age of 10.3 ± 0.6 years, 50% were boys, and 24 (48%) had OSA. Patients with and without OSA did not differ statistically in age, gender, BMI, or syndromic diagnosis. Those with OSA had increased upper airway length (P = .016), decreased posterior airway space (P = .001), and more severe midfacial retrusion (P = .022) compared to patients without OSA. After adjusting for covariates, the odds ratio for OSA was 32.9 in patients with an upper airway longer than 45.3 mm per meter of height (P = .018), and for every 1-mm decrease in posterior airway space, the risk of OSA increased by 30% (P = .022).
Patients with syndromic craniosynostosis and OSA have a longer upper airway, smaller posterior airway space, and more severe midfacial retrusion than those without OSA.
面中部发育不全是综合征性颅缝早闭的一个特征性表现,且使这些患者易患阻塞性睡眠呼吸暂停(OSA)。本研究的目的是确定与综合征性颅缝早闭患者气道阻塞相关的解剖学因素。
这是一项回顾性队列研究。作者纳入了由综合征性颅缝早闭患者组成的研究样本。预测变量包括年龄、性别、体重指数(BMI)、综合征诊断以及在头颅侧位片上测量的上气道长度和大小参数。为控制年龄因素,对上气道长度进行了患者身高差异校正。结果变量为OSA状态(存在或不存在)。计算了描述性、双变量和回归统计量。对于所有分析,P值小于或等于0.05被认为具有统计学意义。
样本由50例患者组成,平均年龄为10.3±0.6岁,50%为男性,24例(48%)患有OSA。患有和未患有OSA的患者在年龄、性别、BMI或综合征诊断方面无统计学差异。与未患有OSA的患者相比,患有OSA的患者上气道长度增加(P = 0.016),后气道间隙减小(P = 0.001),面中部后缩更严重(P = 0.022)。在对协变量进行调整后,上气道长度每米身高超过45.3 mm的患者发生OSA的比值比为32.9(P = 0.018),后气道间隙每减少1 mm,OSA风险增加30%(P = 0.022)。
与未患有OSA的患者相比,患有综合征性颅缝早闭和OSA的患者上气道更长,后气道间隙更小,面中部后缩更严重。