Southall D P, Croft C B, Stebbens V A, Ibrahim H, Gurney A, Buchdahl R, Warner J O
Department of Paediatrics, Cardiothoracic Institute, Brompton Hospital, London, United Kingdom.
Eur J Pediatr. 1989 Jan;148(4):353-9. doi: 10.1007/BF00444133.
Six infants were referred with symptoms and clinical signs suggesting airway obstruction during sleep. In each case, overnight recordings of arterial oxygen saturation, respiratory movements and end tidal expired carbon dioxide (ETCO2) showed the presence of abnormal episodes of hypoxaemia related to partial or complete airway obstruction and associated with a specific pattern of the inspiratory movement waveforms. These events and patterns were not found on recordings from 20 age-matched healthy infants and young children. ETCO2 levels were also abnormally elevated in all six patients when asleep. Fiber-optic upper airway endoscopy excluded structural abnormalities, including significant tonsillar or adenoidal enlargement, but showed an intermittent dysfunctional inspiratory obstruction in the pharynx. Continuous positive airways pressure and tracheostomy were effective in treating this obstruction.
六名婴儿因出现提示睡眠期间气道阻塞的症状和临床体征而被转诊。在每例病例中,对动脉血氧饱和度、呼吸运动和呼气末二氧化碳(ETCO2)进行的夜间记录显示,存在与部分或完全气道阻塞相关的低氧血症异常发作,并伴有特定的吸气运动波形模式。在20名年龄匹配的健康婴幼儿的记录中未发现这些事件和模式。所有六名患者睡眠时的ETCO2水平也异常升高。纤维光学上气道内窥镜检查排除了结构异常,包括明显的扁桃体或腺样体肿大,但显示咽部存在间歇性功能性吸气性阻塞。持续气道正压通气和气管切开术对治疗这种阻塞有效。