Waters K A, Everett F, Sillence D, Fagan E, Sullivan C E
Royal Prince Alfred Hospital Sleep Unit, Camperdown, Australia.
Arch Dis Child. 1993 Aug;69(2):191-6. doi: 10.1136/adc.69.2.191.
Overnight sleep studies were performed in 20 subjects with achondroplasia to document further the respiratory abnormalities present in this group. Somatosensory evoked potentials (SEPs) were recorded in 19 of the subjects to screen for the presence of brainstem abnormalities, which are one of the potential aetiological mechanisms. Fifteen children aged 1 to 14 years, and five young adults, aged 20 to 31 years were included. All had upper airway obstruction and 15 (75%) had a pathological apnoea index (greater than five per hour). Other sleep associated respiratory abnormalities, including partial obstruction, central apnoea, and abnormal electromyographic activity of accessory muscles of respiration, also showed a high prevalence. SEPs were abnormal in eight (42%), but there was no correlation between abnormal SEPs and apnoea during sleep, either qualitatively or quantitatively. A high prevalence of both sleep related respiratory abnormalities and abnormal SEPs in young subjects with achondroplasia was demonstrated. However, the sleep related respiratory abnormalities do not always result in significant blood gas disturbances or correlate with abnormal SEPs in this group.
对20名软骨发育不全患者进行了夜间睡眠研究,以进一步记录该组患者存在的呼吸异常情况。对其中19名受试者进行了体感诱发电位(SEP)记录,以筛查脑干异常情况,脑干异常是潜在的病因机制之一。研究纳入了15名年龄在1至14岁的儿童和5名年龄在20至31岁的年轻人。所有患者均存在上呼吸道阻塞,其中15名(75%)患者的病理性呼吸暂停指数(每小时大于5次)。其他与睡眠相关的呼吸异常,包括部分阻塞、中枢性呼吸暂停以及呼吸辅助肌的异常肌电图活动,也显示出高患病率。8名(42%)受试者的SEP异常,但睡眠期间SEP异常与呼吸暂停在定性或定量方面均无相关性。研究证实,年轻软骨发育不全患者睡眠相关呼吸异常和SEP异常的患病率均较高。然而,该组患者中睡眠相关呼吸异常并不总是导致显著的血气紊乱,也与SEP异常无相关性。