[儿童腺样体肥大的睡眠结构改变]。

Xiaowen Zhang, Yuan Li, Zhaotong Huang, Gehua Zhang, Xian Liu, Jin Ye
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引用次数: 0

摘要

目的:儿童腺样体肥大伴口呼吸、打鼾、夜咳等阻塞性表现。然而,睡眠结构在AH儿童中定义不清,这是本研究的目的。方法:采用计算机辅助诊断系统记录多导睡眠图(PSG)。根据Rechtschaffen制定的标准进行人工睡眠评分。47例患有腺扁桃体肥大(AH)的儿童采用PSG诊断,并与正常儿童PSG结果进行比较。结果:(1)与正常儿童相比,AH组I期明显增高;4 + / - 9.3) % vs (7.9 + / - 6.8) % (P < 0.01),下降阶段II: (41.8 + / - 9.7) % vs (46.7 + / - 7.6) % (P < 0.01);增加δ(26.2 + / - 10.6)% vs (23.3 + / - 8.7) % (P > 0.05);REM期明显下降:(7.7 +/- 4.9)% vs (27.3 +/- 5.6)% (P < 0.01);NREM占83.33%;(2) AH组唤醒指数(ARI)升高,分别为32.8 +/- 26.03 vs 18.3 +/- 12.2 (P < 0.05);(3) REM潜伏期为(157.1 +/- 71.4)min,约为正常儿童的2倍。结论:AH患儿睡眠结构异常。频繁的从睡眠中唤醒的脑电图可能导致明显的睡眠断裂,但深度睡眠是足够的。需要进一步的研究来确定睡眠结构异常是否会影响生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Sleep architecture changes in children with adenoidal hypertrophy].

Objective: Adenoidal hypertrophy in children is associated with obstructive manifestations like mouth breathing, snoring, night cough. However, the sleep architecture is poorly defined in children with AH, which is this studies for.

Method: A computer-assistant diagnostic system was used for polysomnography (PSG) recording. Sleep was scored manually according to the standard set by Rechtschaffen. 47 children with adenotonsillar hypertrophy (AH) were defined by PSG and compared with normal children PSG results.

Result: (1) Compared with normal children, AH group had increased stage I: (15. 4 +/- 9.3)% vs (7.9 +/- 6.8)% (P < 0.01) and decreased stage II: (41.8 +/- 9.7)% vs (46.7 +/- 7.6)% (P < 0.01); increased Delta (26.2 +/- 10.6)% vs (23.3 +/- 8.7) % (P > 0.05); obviously decreased in REM: (7.7 +/- 4.9)% vs (27.3 +/- 5.6)% (P < 0.01); NREM (83.33%) was increasingly; (2) AH group had increased Arousal Index(ARI) 32.8 +/- 26.03 vs 18.3 +/- 12.2 (P < 0.05); (3) The latent period of REM was (157.1 +/- 71.4) min and about two times long as normal children.

Conclusion: Sleep architecture is abnormal in children with AH. Frequent electroencephalogram arousals from sleep may result in significant sleep fragmentation,but the deep sleep is sufficient. Further studies are needed to determine whether abnormalities in sleep architecture contribute to quality of life.

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