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1-3型小儿脊髓性肌萎缩症的多导睡眠图检查结果

Polysomnography findings in pediatric spinal muscular atrophy types 1-3.

作者信息

Chacko Archana, Sly Peter D, Gauld Leanne

机构信息

Queensland Children's Hospital, Brisbane, Australia; Centre for Child Health Research, University of Queensland, Brisbane, Australia.

Centre for Child Health Research, University of Queensland, Brisbane, Australia.

出版信息

Sleep Med. 2020 Apr;68:124-130. doi: 10.1016/j.sleep.2019.12.004. Epub 2019 Dec 24.

Abstract

BACKGROUND

Sleep disordered breathing (SDB) causes sleep disturbance and daytime symptoms in children with neuromuscular disorders. Although polysomnography (PSG) findings are well described in many neuromuscular disorders, there are limited reports from children with spinal muscular atrophy (SMA). The aim of this study was to determine the sleep architecture and breathing characteristics and non-invasive ventilation (NIV) use in our pediatric SMA cohort.

METHODS

We conducted a cross-sectional cohort study of all children with SMA in Queensland, Australia. Children were Nusinersen naïve and had a full diagnostic PSG in 2018. The PSG was scored and reported by a single pediatric sleep physician in accordance with American Academy of Sleep Medicine Criteria (2012).

RESULTS

In sum, 31 children (18 males), Six with Type 1, 16 with Type 2 and nine with Type 3, aged 0.25-18.8 years old were studied. SDB was seen in each SMA type and was more pronounced during rapid eye movement (REM) sleep. Type 1: all patients exhibited SDB, three (50%) with central sleep apnea (CSA) and three (50%) with mixed disease. Type 2: five (31%) had CSA, one (6%) mixed disease, seven (44%) had early SDB and three (19%) had normal sleep breathing. Type 3: four (44%) children had CSA and five had early SDB. No child exhibited obstructive sleep apnea (OSA) alone.Starting NIV significantly reduced mean total PSG Apnea-Hypopnea Index (AHI) scores from a grouped mean of 15.4 events per hour (SD ± 14.6; 95% CI 6.1-24.7) to 4.0 events per hour (SD ± 4.2, 95% CI 1.2-6.5, p = 0.01).

CONCLUSION

SDB is common in children with SMA and was present in all types. CSA was the most common disorder; with mixed SDB also present in type 1 and 2 SMA.

摘要

背景

睡眠呼吸障碍(SDB)会导致神经肌肉疾病患儿出现睡眠障碍和日间症状。尽管多导睡眠图(PSG)检查结果在许多神经肌肉疾病中已有详细描述,但关于脊髓性肌萎缩症(SMA)患儿的相关报道却很有限。本研究的目的是确定我们儿科SMA队列中的睡眠结构、呼吸特征以及无创通气(NIV)的使用情况。

方法

我们对澳大利亚昆士兰州所有SMA患儿进行了一项横断面队列研究。这些患儿未使用过诺西那生,于2018年接受了全面的诊断性PSG检查。PSG由一位儿科睡眠医生按照美国睡眠医学学会标准(2012年)进行评分和报告。

结果

总共研究了31名儿童(18名男性),其中6名1型、16名2型和9名3型,年龄在0.25至18.8岁之间。各型SMA患儿均存在SDB,且在快速眼动(REM)睡眠期间更为明显。1型:所有患者均表现出SDB,3例(50%)为中枢性睡眠呼吸暂停(CSA),3例(50%)为混合型疾病。2型:5例(31%)有CSA,1例(6%)为混合型疾病,7例(44%)有早期SDB,3例(19%)睡眠呼吸正常。3型:4例(44%)儿童有CSA,5例有早期SDB。没有儿童单独表现出阻塞性睡眠呼吸暂停(OSA)。开始使用NIV后,平均总PSG呼吸暂停低通气指数(AHI)评分从每小时15.4次事件的分组平均值(标准差±14.6;95%置信区间6.1 - 24.7)显著降低至每小时4.0次事件(标准差±4.2,95%置信区间1.2 - 6.5,p = 0.01)。

结论

SDB在SMA患儿中很常见,且各型均有。CSA是最常见的疾病类型;1型和2型SMA中也存在混合型SDB。

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