头影测量法评估完全诊断为OSA伴明显矢状骨畸形的儿童患者的颅面形态

Simona Pisacane, M. Carotenuto, F. d’Apuzzo, M. Vitale, V. Grassia, C. Flores‐Mir, L. Perillo
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引用次数: 3

摘要

研究目的:确定通过侧位头影测量法评估的正确诊断为阻塞性睡眠呼吸暂停(OSA)的儿童的颅面和鼻咽形态是否与根据矢状错牙合分层的不可能的OSA对照儿童不同,并评估是否与呼吸暂停低通气指数(AHI)的严重程度有关。材料和方法:根据儿童睡眠问卷(PSQ)的阴性结果,对22名夜间多导睡眠图(nPSG)诊断为OSA并已进行腺扁桃体切除术的儿童(平均8.8岁)和20名非睡眠呼吸暂停综合征儿童(平均9.2岁)的对照组(年龄、性别和矢状错牙合)的各种头影测量结果进行比较。结果:当AHI值较高(4.5和4mm)时,OSA儿童的Go Me和Ba^SN维度在统计学上显著增加,而根据OSA严重程度(3.5mm),II类样本的ANSPNS维度显著增加。根据OSA严重程度,III级患者之间的任何变量均未发现显著差异。与对照组相比,在II级OSA儿童中,腭平面与前颅底之间的角度和颅底弯曲的角度均显著降低(0.36和2.3mm)。此外,观察到上腺样体轮廓的厚度增加和上咽部的尺寸减小(3.2和2.1mm)。在III级中,较短的鼻咽骨具有统计学意义(3.2 mm)。结论:与不太可能的OSA组相比,OSA样本显示出一些不同的颅面特征。当考虑矢状错牙合时,这些差异的位置并不一致。
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Cephalometric Evaluation of Craniofacial Morphology in Pediatric Patients With Fully Diagnosed OSA With Distinct Sagittal Skeletal Malocclusions
Study Objectives: To establish whether craniofacial and nasopharyngeal morphology, assessed through lateral cephalometry, in children properly diagnosed with obstructive sleep apnea (OSA) differed from that of non-likely OSA control children stratified based on sagittal malocclusion and to evaluate if there is any association with apneahypopnea index (AHI) severity. Materials and Methods: Various cephalometric measurements were compared between 22 children (mean age 8.8) with nocturnal polysomnography (nPSG) diagnosed OSA that had already adeno-tonsillectomy and a control group of 20 nonlikely OSA children (mean age 9.2) based on a negative pediatric sleep questionnaire (PSQ) results matched for age, sex and sagittal malocclusion. Results: Statistically significant increases in Go-Me and Ba^SN dimensions were observed among OSA children when higher AHI values (4.5 and 4 mm), whereas ANSPNS dimension was significantly increased in the Class II sample according to OSA severity (3.5 mm). No significant differences were identified for any variables among Class III based on OSA severity. In comparison to controls, in Class II both the angle between palatal plane and anterior cranial base and the angle of the flexure of cranial base were significantly reduced in OSA children (0.36 and 2.3 mm). In addition, an increased thickness of the upper adenoid profile and a reduced dimension of upper pharynx were observed (3.2 and 2.1 mm). In Class III a shorter bony nasopharynx was statistically significant (3.2 mm). Conclusions: The OSA sample showed some distinct craniofacial features compared to a non-likely OSA group. These differences were not consistently located when sagittal malocclusion was considered.
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