首页 | 本学科首页   官方微博 | 高级检索  
     

茶碱缓释胶囊对轻中度阻塞型睡眠呼吸暂停低通气综合征的影响
引用本文:寿志南,陈敏,卢红燕,香松林. 茶碱缓释胶囊对轻中度阻塞型睡眠呼吸暂停低通气综合征的影响[J]. 临床肺科杂志, 2016, 0(10): 1788-1790. DOI: 10.3969/j.issn.1009-6663.2016.10.013
作者姓名:寿志南  陈敏  卢红燕  香松林
作者单位:贵阳市第一人民医院呼吸内科, 贵州 贵阳,550004
基金项目:贵阳市卫生局科学技术计划项目(2013筑卫科技合同字第创20号)
摘    要:目的观察轻中度阻塞型睡眠呼吸暂停低通气综合征(OSAHS)患者口服氨茶碱前后睡眠参数变化情况。方法随机选择60例经多导睡眠图(PSG)监测确诊的轻中度OSAHS患者,入选对象随机分成A、B两组,A组30例,给予口服茶碱缓释胶囊0.2/晚,B组30例,给予安慰剂口服。比较未给药、口服茶碱后、口服安慰剂后睡眠监测指标变化情况,包括:睡眠呼吸暂停低通气指数(apnea hypopnea index,AHI)、最低夜间血氧饱和度(LSaO_2)、平均夜间血氧饱和度(MSaO_2)、SaO_290%时间、睡眠呼吸障碍最长时间,同时监测茶碱血药浓度,观察药物不良反应发生情况。结果 (1)口服茶碱后LSaO_2:90.4%±2.1%,MSaO_2:92.2%±1.5%,SaO_290%时间(34.3±10.2)秒,睡眠呼吸障碍最长时间(25.0±2.3)秒,较未给药LSaO_2:86.2%±2.6%,MSaO_2:89.1%±1.8%,SaO_290%时间(45.1±18.6)秒,睡眠呼吸障碍最长时间(32.0±5.0)秒及给予安慰剂后LSaO_2:85.3%±3.8%,MSaO_2:90.8%±2.6%,SaO_290%时间(39.2±19.8)秒,睡眠呼吸障碍最长时间(31.0±3.4)秒,均有显著差异(P0.017)。但AHI改变无统计学差异。口服安慰剂与未给药时比较,睡眠监测指标差异无统计学意义。(2)口服茶碱缓释胶囊,观察药物不良反应发生1例,表现为恶心,监测茶碱血药浓度在安全范围,停药后症状缓解。结论轻中度OSAHS睡前口服茶碱缓释胶囊安全有效,可缩短睡眠呼吸障碍最长时间,改善夜间LSaO_2、MSaO_2、SaO_290%时间。

关 键 词:阻塞型睡眠呼吸暂停低通气综合征  茶碱  血药浓度  治疗药物监测

Effect of aminophylline on mild to moderate obstruction sleep apnea hypopnea syndrome
Abstract:Objective To observe the change of sleep parameters with oral aminophylline patients with mild or moderate obstructive sleep apnea hypopnea syndrome(OSAHS). Methods 60 patients with mild to moderate OSAHS diagnosed by PSG monitoring were randomly divided into two groups. The group A was given oral theophylline sustained release capsules 0. 2 / night,and the group B was given oral placebo. The sleep monitoring indexes were compared in oral theophylline,oral placebo and without medicine,such as AHI,LSaO2 ,MSaO2 ,the time of SaO2 less than 90% ,the longest time of sleep disordered breathing events in patients with OSAHS. At the same time,the-ophylline blood drug concentration was monitored,and the incidence of adverse drug reactions was observed. Results After oral theophylline,the value of LSaO2 was 90. 4% ± 2. 1% ,MSaO2 was 92. 2% ± 1. 5% ,the time of SaO2 less than 90% was(34. 3 ± 10. 2)s,and the longest time of sleep disordered breathing events was(25. 0 ± 2. 3)s. Before treatment,the value of LSaO2 was 86. 2% ± 2. 6% ,MSaO2 was 89. 1% ± 1. 8% ,the time of SaO2 less than 90% was(45. 1 ± 18. 6)s,and the longest time of sleep disordered breathing events was(32. 0 ± 5. 0)s. After oral placebo,LSaO2 was 85. 3% ± 3. 8% ,MSaO2 was 90. 8% ± 2. 6% ,the time of SaO2 less than 90% was(39. 2 ± 19. 8)s,and the longest time of sleep disordered breathing events was(31. 0 ± 3. 4)s. There was no significant difference in AHI between the two groups. There was one case of adverse drug reaction occurred after oral theophyl-line,characterized by nausea. The monitoring of theophylline serum concentration was in a safe range,after with-drawal symptom relief. Conclusion Theophylline sustained release capsules can significantly improve LSaO2 , MSaO2 ,the time of SaO2 less than 90% and the longest time of sleep disordered breathing events,which is safe and effective for patients with mild to moderate OSAHS.
Keywords:obstructive sleep apnea hypopnea syndrome  theophylline  serum concentration  therapeutic drug monitoring
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号