Division of Pediatrics, "F. Del Ponte" Hospital, University of Insubria, 21100 Varese, Italy.
Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, 37134 Verona, Italy.
Int J Environ Res Public Health. 2020 May 18;17(10):3531. doi: 10.3390/ijerph17103531.
Upper airway abnormalities increase the risk of pediatric morbidity in infants. A multidisciplinary approach to obstructive sleep apnea syndrome (OSAS) poses challenges to clinical practice. The incidence and causes of OSA are poorly studied in children under 2 years of age. To fill this gap, we performed this retrospective observational study to determine the causes of obstructive sleep apnea (OSA) in children admitted to our hospital between January 2016 and February 2018, after a brief unexplained event (BRUE) or for OSA. We reviewed the medical charts of 82 patients (39 males; BRUE n = 48; OSAS n = 34) and divided them into two age groups: < 1 year old (1-12 months; n = 59) and >1 year old (>12-24 months; n = 23). Assessment included nap polysomnography, multichannel intraluminal impedance-pH, and nasopharyngoscopy. Sleep disordered breathing was comparable between the two groups. Omega-shaped epiglottis, laryngomalacia, and nasal septum deviation were more frequent in the younger group, and nasal congestion in older group. Tonsillar and adenoidal hypertrophy was more frequent in the older group, while laryngomalacia and gastroesophageal reflux was more frequent in the younger group. Tonsil and adenoid size were associated with grade of apnea-hypopnea index severity in the older group, and laryngomalacia and gastroesophageal reflux in the younger group. The main causes of respiratory sleep disorders differ in children before or after age 1 year. Our findings have potential clinical utility for assessing the pathophysiology of obstructive sleep disordered breathing in patients less than 2 years old.
上呼吸道异常会增加婴儿患儿科疾病的风险。阻塞性睡眠呼吸暂停综合征(OSAS)的多学科方法对临床实践提出了挑战。2 岁以下儿童中 OSA 的发病率和病因尚未得到充分研究。为了填补这一空白,我们进行了这项回顾性观察研究,以确定我们医院收治的因短暂性不明原因事件(BRUE)或 OSA 而入院的儿童发生阻塞性睡眠呼吸暂停(OSA)的原因。我们回顾了 82 名患者(39 名男性;BRUE 组 48 例;OSAS 组 34 例)的病历,并将他们分为两个年龄组:<1 岁(1-12 个月;n=59)和>1 岁(>12-24 个月;n=23)。评估包括午睡多导睡眠图、多通道腔内阻抗-pH 监测和鼻咽镜检查。两组的睡眠呼吸障碍相当。在年龄较小的组中,Ω形会厌、喉软骨软化和鼻中隔偏曲更为常见,而在年龄较大的组中,鼻塞更为常见。在年龄较大的组中,扁桃体和腺样体肥大更为常见,而在年龄较小的组中,喉软骨软化和胃食管反流更为常见。在年龄较大的组中,扁桃体和腺样体大小与呼吸暂停低通气指数严重程度分级相关,而在年龄较小的组中,与喉软骨软化和胃食管反流相关。1 岁前和 1 岁后儿童呼吸睡眠障碍的主要原因不同。我们的研究结果对评估 2 岁以下患者阻塞性睡眠呼吸障碍的病理生理学具有潜在的临床应用价值。