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囊性纤维化急性加重期治疗后夜间血氧饱和度的变化。

Changes in nocturnal oximetry after treatment of exacerbations in cystic fibrosis.

作者信息

Allen M B, Mellon A F, Simmonds E J, Page R L, Littlewood J M

机构信息

Department of Respiratory Medicine, St James's University Hospital, Leeds.

出版信息

Arch Dis Child. 1993 Aug;69(2):197-201. doi: 10.1136/adc.69.2.197.

DOI:10.1136/adc.69.2.197
PMID:8215520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1029456/
Abstract

Sleep related arterial oxygen desaturation has been described in clinically stable young adults with cystic fibrosis. The incidence and severity of nocturnal oxygen desaturation in children during infective exacerbations and the changes that occur with treatment were examined. Forty five children with proved cystic fibrosis, median age 8.9 years, admitted to the Regional Cystic Fibrosis Unit underwent clinical evaluation, spirometry, and measurement of peak flow and nocturnal oxygen saturation on admission and after 10 days' treatment. There was a significant improvement in all the above measurements, with the averaged overnight saturation changing from a mean (SD) 92.7 (2.7)% to 94.3 (2.0)%, mean (SE) difference 1.58 (0.37). The time spent with a saturation 4% or more below their clinic value showed a marked improvement from 122 (152) minutes on the first night to 21 (30.7) on the second, mean (SE) difference 101 (22.4). Eight young children could not perform pulmonary function tests, all desaturated on the admission night. Nocturnal hypoxaemia is a common finding in young cystic fibrosis patients during infective exacerbations but improves with treatment. Overnight oximetry is simple to perform, well tolerated, and identifies patients with marked nocturnal desaturation.

摘要

睡眠相关的动脉血氧饱和度下降已在临床状况稳定的囊性纤维化青年患者中有所描述。研究人员对儿童感染性加重期夜间血氧饱和度下降的发生率和严重程度以及治疗过程中发生的变化进行了检查。45名确诊为囊性纤维化的儿童,年龄中位数为8.9岁,入住地区囊性纤维化治疗中心,在入院时和治疗10天后接受了临床评估、肺功能测定、峰值流量测量和夜间血氧饱和度测量。上述所有测量结果均有显著改善,平均夜间饱和度从平均(标准差)92.7(2.7)%变为94.3(2.0)%,平均(标准误)差异为1.58(0.37)。血氧饱和度低于其门诊值4%或更多的时间显示出明显改善,从第一晚的122(152)分钟降至第二晚的21(30.7)分钟,平均(标准误)差异为101(22.4)。8名幼儿无法进行肺功能测试,入院当晚均出现血氧饱和度下降。夜间低氧血症在囊性纤维化患儿感染性加重期很常见,但治疗后会有所改善。夜间血氧饱和度监测操作简单,耐受性好,可识别出夜间血氧饱和度显著下降的患者。

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引用本文的文献

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The heart in cystic fibrosis.囊性纤维化中的心脏
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2
Nocturnal oximetry in infants with cystic fibrosis.囊性纤维化婴儿的夜间血氧饱和度测定
Arch Dis Child. 2001 Jan;84(1):50-54. doi: 10.1136/adc.84.1.50.
3
Tolerance, pharmacokinetics and efficacy of once daily amikacin for treatment of Pseudomonas aeruginosa pulmonary exacerbations in cystic fibrosis patients.每日一次使用阿米卡星治疗囊性纤维化患者铜绿假单胞菌肺部加重的耐受性、药代动力学及疗效
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本文引用的文献

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The systematic evaluation of the chest radiograph in cystic fibrosis.囊性纤维化患者胸部X光片的系统评估
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PULMONARY HYPERTENSION AND COR PULMONALE IN CYSTIC FIBROSIS OF THE PANCREAS.胰腺囊性纤维化中的肺动脉高压与肺源性心脏病
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Hemoglobin desaturation: its occurrence during sleep in patients with cystic fibrosis.血红蛋白氧饱和度降低:在囊性纤维化患者睡眠期间的发生情况。
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Is anti-Pseudomonas therapy warranted in acute respiratory exacerbations in children with cystic fibrosis?囊性纤维化患儿急性呼吸道加重期是否需要进行抗假单胞菌治疗?
J Pediatr. 1980 Jul;97(1):144-7. doi: 10.1016/s0022-3476(80)80155-7.
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The cardiovascular system in cystic fibrosis.囊性纤维化中的心血管系统。
Pediatrics. 1982 Nov;70(5):728-41.
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Ventilation and oxygenation changes during sleep in cystic fibrosis.囊性纤维化患者睡眠期间的通气与氧合变化
Chest. 1983 Oct;84(4):388-93. doi: 10.1378/chest.84.4.388.