中度哮喘给予小剂量布地奈德福莫特罗干粉吸入剂与茶碱缓释片联合治疗效果分析.docVIP

中度哮喘给予小剂量布地奈德福莫特罗干粉吸入剂与茶碱缓释片联合治疗效果分析.doc

  1. 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
  2. 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  3. 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  4. 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  5. 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  6. 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  7. 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
中度哮喘给予小剂量布地奈德福莫特罗干粉吸入剂与茶碱缓释片联合治疗效果分析

中度哮喘给予小剂量布地奈德福莫特罗干粉吸入剂与茶碱缓释片联合治疗的效果分析   【摘要】 目的 研究小剂量布地奈德福莫特罗干粉吸入剂联合茶碱缓释片治疗中度哮喘患者的临床效果。方法 58例中度哮喘患者, 依据入院时间先后将患者分为观察组和对照组, 各29例。对照组给予小剂量布地奈德福莫特罗干粉吸入剂联合酮替芬分散片治疗, 观察组给予小剂量布地奈德福莫特罗干粉吸入剂联合茶碱缓释片治疗, 比较两组治疗效果及肺功能情况。结果 观察组患者治疗总有效率为96.6%, 显著高于对照组的75.9%, 差异有统计学意义(P0.05)。治疗后观察组患者第一秒用力呼气容积(FEV1)、FEV1/用力肺活量的比值(FEV1%)明显优于对照组, 差异有统计学意义(P0.05)。结论 小剂量布地奈德福莫特罗干粉吸入剂联合茶碱缓释片治疗中度哮喘患者效果显著, 能有效控制患者病情并改善其肺功能指标, 值得临床推广。   【关键词】 中度哮喘;布地奈德福莫特罗干粉吸入剂;茶碱缓释片;酮替芬   DOI:10.14163/j.cnki.11-5547/r.2018.02.046   Effect analysis of low-dose budesonide formoterol powder inhalation combined with theophylline sustained-release tablets in the treatment of moderate asthma DIAO Zhen-hua, DUAN Cai-rao. Department of Respiratory Medicine, Shenzhen Longgang District Second People’s Hospital, Shenzhen 518112, China   【Abstract】 Objective To study the clinical effect of low-dose budesonide formoterol powder inhalation combined with theophylline sustained-release tablets in the treatment of patients with moderate asthma.   Methods A total of 58 patients with moderate asthma were divided by admission order into observation group and control group, with 29 cases in each group. The control group received low-dose budesonide formoterol powder inhalation combined with ketotefen dispersible tablet, and the observation group received low-dose budesonide formoterol powder inhalation combined with theophylline sustained-release tablets. Comparison were made on treatment efficacy and pulmonary function between two groups. Results The observation group had obviously higher total treatment effective rate as 96.6% than 75.9% in the control group, and the difference was statistically significant (P0.05). After treatment, the observation group had obviously better forced expiratory volume in   1 second (FEV1), FEV1 / forced vital capacity (FEV1%) than the control group, and their difference was statistically significant (P0.05). Conclusion Low-dose budesonide formoterol powder inhalation and theophylline sustained-release

文档评论(0)

fangsheke66 + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档