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慢性阻塞性肺疾病急性加重期患者规范化痰诱导安全性的初步研究
引用本文:曾勉,吴健锋,谢灿茂,严英硕,陈冬梅,禤建美. 慢性阻塞性肺疾病急性加重期患者规范化痰诱导安全性的初步研究[J]. 中华结核和呼吸杂志, 2005, 28(4): 238-241
作者姓名:曾勉  吴健锋  谢灿茂  严英硕  陈冬梅  禤建美
作者单位:1. 510080 广州,中山大学附属第一医院呼吸内科
2. 510080 广州,中山大学附属第一医院 细菌室
基金项目:广东省自然科学基金资助项目(04009385),广东省医学科研基金资助项目(A2004188)
摘    要:目的探讨慢性阻塞性肺疾病急性加重期(AECOPD)患者进行高渗盐水痰诱导的安全性。方法制定规范化操作流程,对22例重度、极重度AECOPD患者进行痰诱导,在诱导过程中严密监测患者第一秒用力呼气容积(FEV1)和脉搏容积血氧饱和度(SpO2)的变化。结果22例AECOPD患者在诱导前SpO2为(93.8±0.9)%,结束时SpO2为(91.7±0.8)%,较基础值下降了(2.1±0.4)%(P<0.01),结束后10min,SpO2恢复至基础值水平;诱导前FEV1为(0.70±0.19)L,结束时为(0.62±0.17)L,FEV1较基础值下降了(12.3±3.1)%(P=0.027),结束后10min,FEV1恢复至基础值水平。共有19例患者渡过了整个痰诱导过程,成功率为86%。结论在严密监控下,使用规范化的痰诱导流程,痰诱导法对AECOPD患者是一种比较安全的方法。

关 键 词:慢性阻塞性肺疾病 急性加重期 痰诱导 规范化 安全性 步研究 COPD患者 用力呼气容积 SpO2 FEV1 血氧饱和度 高渗盐水 操作流程 极重度 AE 诱导法 下降 水平 恢复
修稿时间:2004-07-13

Safety of sputum induction in subjects with acute exacerbations of chronic obstructive pulmonary disease
ZENG Mian,WU Jian-feng,XIE Can-mao,YAN Ying-shuo,CHEN Dong-mei,XUAN Jian-mei. Safety of sputum induction in subjects with acute exacerbations of chronic obstructive pulmonary disease[J]. Chinese journal of tuberculosis and respiratory diseases, 2005, 28(4): 238-241
Authors:ZENG Mian  WU Jian-feng  XIE Can-mao  YAN Ying-shuo  CHEN Dong-mei  XUAN Jian-mei
Affiliation:Department of Respiratory Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.
Abstract:OBJECTIVE: To evaluate the safety of sputum induction in subjects with acute exacerbations of chronic obstructive pulmonary disease (AECOPD). METHODS: Twenty-two patients with AECOPD were enrolled in the study. All subjects inhaled a mist of 3% hypertonic saline solution and the forced expiratory volume in one second (FEV(1)) and pulse oxygen saturation (SpO(2)) were measured during the procedure. RESULTS: A significant fall in SpO(2) and FEV(1) was found during sputum induction by inhalation of 3% hypertonic saline solution. Mean decline in SpO(2) during sputum induction was (2.1 +/- 0.4)% (P < 0.01) and recovered within 10 min after cessation of sputum induction. Mean decline in FEV(1) during sputum induction was (12.3 +/- 3.1)% (P = 0.027), an absolute fall of (0.11 +/- 0.03) L, and the FEV(1) returned to the baseline in all subjects within 10 min after cessation of sputum induction. The sputum induction was successful in 19 of the 22 (86%) patients. CONCLUSION: The use of a standardized sputum induction protocol is relatively safe in sampling the lower airways in patients with AECOPD.
Keywords:Pulmonary disease  chronic obstructive  Acute exacerbations  Sputum induction  Safety
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