Budesonide Combined with Feilike Treatment in Clinical Effect of Pediatric Asthma

LI Ai; HE Deng-ke

doi:10.13422/j.cnki.syfjx.2014240207

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Budesonide Combined with Feilike Treatment in Clinical Effect of Pediatric Asthma

更新时间：2024-01-04

- Budesonide Combined with Feilike Treatment in Clinical Effect of Pediatric Asthma
- Chinese Journal of Experimental Traditional Medical Formulae Vol. 20, Issue 24, Pages: 207-209(2014)
- 作者机构：
- 作者简介：
- 基金信息：
- DOI：10.13422/j.cnki.syfjx.2014240207
  CLC： R725.6
- Published：2014
- 稿件说明：
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LI Ai, HE Deng-ke. Budesonide Combined with Feilike Treatment in Clinical Effect of Pediatric Asthma[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(24): 207-209.
DOI：

LI Ai, HE Deng-ke. Budesonide Combined with Feilike Treatment in Clinical Effect of Pediatric Asthma[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(24): 207-209. DOI： 10.13422/j.cnki.syfjx.2014240207.

摘要

目的: 探讨布地奈德联合肺力咳治疗小儿哮喘的临床效果. 方法: 对来本院诊治的80例患者入院资料进行分析

将其随机分为两组.对照组采用布地奈德混悬液治疗

实验组联合肺力咳治疗

比较两组治疗效果. 结果: 实验组95%治疗效果理想

高于对照组(80%)(P<0.05);实验组95%对本院治疗总体满意

高于对照组(P<0.05);实验组咳嗽缓解时间为(4.35±1.25) d

咳嗽消失时间为(8.99±2.17) d

平均治疗时间为(17.12±1.5) d

低于对照组(P<0.05);实验组治疗后一秒用力呼气容积(forced expiratory volume in one second

FEV1) 指标为(1.57±0.31) L、峰值呼气流速(PEF)为(3.82±0.37) L

FEV1/用力肺活量(FVC)指标为(83.54±0.62)%

高于对照组(P<0.05);实验组治疗后3例出现不良反应

不良反应率为7.5%

低于对照组22.5%(9/40)(P<0.05). 结论: 文章采用布地奈德联合肺力咳治疗效果理想

能够有效的改善患者症状

值得推广使用.

Abstract

Objective: To investigate the clinical effect of budesonide combined with Feilike in children with asthma. Method: In eighty cases of patients admitted to our hospital were analyzed

and were randomly divided into two groups. The control group using budesonide treatment

experimental group combined with Feilike treatment

treatment effects were compared between the two groups. The experimental group after treatment

3 cases of adverse reactions

adverse reaction rate of 7.5%

lower than that of the control group 22.5% (9/40)(P<0.05). Result: The ideal effect in treatment of experimental group was 95%

higher than that of the control group (80%) (P<0.05);the experimental group of 95% in our hospital for the overall satisfaction

higher than that of the control group(P<0.05);the experimental group cough relief time was (4.35±1.25) days

cough disappeared time was (8.99±2.17) days

the average treatment time for (17.12±1.5) days

lower than that of the control group (P<0.05);the experimental group after treatment for forced expiratory volume in one second(FEV1) index (1.57±0.31) L

peak expiratory flow (PEF) index (3.82±0.37) L

FEV1/forced vital capacity(FVC)index (83.54±0.62) %

higher than that of the control group (P<0.05). Conclusion: The higher incidence of asthma in children

mechanism of the disease is also more complex

incentives

and the lack of an ideal method to cure the disease

the clinical application of budesonide combined with Feilike ideal treatment effect

can effectively improve the symptoms of patients

is worthy to be popularized.

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