Gao Peng, Gibson Peter G, Zhang Jie, He Xiaoyan, Hao Yuqiu, Li Ping, Liu Huan
Department of Respiratory Medicine, The Second Affiliated Hospital of Jilin University, Changchun, Jilin, China.
Clin Respir J. 2013 Jan;7(1):101-9. doi: 10.1111/j.1752-699X.2012.00291.x. Epub 2012 Apr 23.
Induced sputum is a non-invasive method, and a useful tool to evaluate inflammatory cells and mediators in the airway lumen in the setting of acute exacerbation of chronic obstructive pulmonary disease (AECOPD). However, the inhalation of hypertonic saline solution to induce sputum may cause a bronchoconstrictive response, so it is important to evaluate the success and safety of sputum induction (SI).
The aims of this study were to assess the safety and efficacy of SI in adults with AECOPD.
Eighty-three AECOPD subjects and 26 healthy controls underwent a modified SI. The outcome measures included fall in lung function during induction and success of SI.
Adults hospitalized with AECOPD had moderate to very severe airflow obstruction. SI was successful in over 80% of subjects. The percentage decrease in forced expiratory volume in 1s (FEV1 ) from baseline by the Global initiative for Chronic Obstructive Lung Disease (GOLD) category was median 1.2(interquartile range, 0.5-3.3)(GOLD II), 2.3(1.3-3.2)(GOLD III), 5.2(3.3-8.6)(GOLD IV) and 1.4(0.5-3.2)(control), respectively. A fall in FEV1 of >20% occurred in only one subject with AECOPD who was in GOLD category III. The decrease in percentage of FEV1 from baseline was greatest in the second stage of induction, and correlated with that of the final stage (r=0.589; P=0.01). The fall in FEV1 during induction increased with GOLD category (P<0.05).
SI can be safely and successfully performed in patients with moderate to very severe chronic obstructive pulmonary disease who experience an exacerbation using this modified induction protocol. The early decrease in FEV1 can be used to predict the maximum fall.
诱导痰是一种非侵入性方法,是评估慢性阻塞性肺疾病急性加重期(AECOPD)时气道腔内炎症细胞和介质的有用工具。然而,吸入高渗盐溶液诱导痰液可能会引起支气管收缩反应,因此评估痰液诱导(SI)的成功率和安全性很重要。
本研究旨在评估SI在成年AECOPD患者中的安全性和有效性。
83名AECOPD受试者和26名健康对照者接受了改良的SI。观察指标包括诱导过程中肺功能的下降情况和SI的成功率。
因AECOPD住院的成年人存在中度至非常严重的气流受限。超过80%的受试者SI成功完成1秒用力呼气容积(FEV1)较基线水平下降的百分比,根据慢性阻塞性肺疾病全球倡议(GOLD)分级,GOLD II级患者中位数为1.2(四分位间距为0.5-3.3),GOLD III级患者为2.3(1.3-3.2),GOLD IV级患者为5.2(3.3-8.6),对照组为1.4(0.5-3.2)仅1名GOLD III级的AECOPD受试者FEV1下降超过20%诱导第二阶段FEV1较基线水平下降的百分比最大,且与最后阶段相关(r=0.589;P=0.01)诱导过程中FEV1的下降随GOLD分级增加而增加(P<0.05)。
使用这种改良的诱导方案,SI可在中度至非常严重的慢性阻塞性肺疾病急性加重期患者中安全、成功地进行FEV1的早期下降可用于预测最大下降幅度。