Feasibility of testing bronchodilator responsiveness with glycopyrronium in obstructive airway diseases: the initial appraisal of the pilot experience

P. Bhattacharyya, D. Saha, S. Sengupta, Debkanya De
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引用次数: 2

Abstract

Background: The short onset of action of glycopyrronium bromide, makes it a suitable antimuscarinic agent to test bronchodilator-responsiveness in airway diseases. The objective of the study was to explore the feasibility of the testing so. Methods: Subjects with features of airflow obstruction (FEV1/FVC < 0.07) were given to inhale a 50-μg single dose of dry powder of glycopyrronium bromide immediately following standard salbutamol-induced bronchodilator reversibility. A repeat spirometry was done after 30 minutes and the changes noted. The impact of both the drugs on spirometric variables suggesting airflow obstruction (FEV1. FEV1/FVC, and FEF25-75) were assessed statistically. A salbutamol-reversibility of ≥12% and >200ml was noted to differentiate asthmatics from chronic obstructive pulmonary disease (COPD) patients. Result: In a total of 35 subjects (asthma-10, COPD-25) with moderate baseline airflow obstruction [FEV1/FVC: 0.57 ± 0.12 and FEV1 (%predicted) as 46.17 ± 15.21], there was global improvement across the spirometric variables to serial inhalation of salbutamol and glycopyrronium. The post salbutamol changes in FEV1 (absolute value) were significant (P = 0.0001) overall and also for both asthma and COPD. Following inhalation of glycopyrronium, the changes were again significant for overall (P = 0.0001), asthma (P = 0.0065), and COPD (P = 0.0001). The parallel change in FEF25-75 was, however, showing better reversibility in asthma (P = 0.0008) with salbutamol compared to COPD (P = 0.1846) and the reverse to glycopyrronium inhalation that results in better reversibility in COPD (P = 0.0085) compared to asthma (P = 0.0949). Conclusion: Testing the reversibility with glycopyrronium appears feasible and safe in obstructive airway disease. It induced add-on reversibility once used after standard salbutamol reversibility. The observation demands further evaluations.
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格隆在阻塞性气道疾病中测试支气管扩张剂反应性的可行性:飞行员经验的初步评估
背景:溴化格隆起效时间短,是检测气道疾病中支气管扩张剂反应性的合适抗毒蕈碱药物。本研究的目的是探索这种测试的可行性。方法:在标准沙丁胺醇诱导的支气管扩张剂可逆性之后,让具有气流阻塞特征(FEV1/FVC<0.07)的受试者立即吸入50μg单剂量的格隆溴化干粉。30分钟后进行重复肺活量测定,并记录变化。两种药物对肺活量测量变量的影响提示气流阻塞(FEV1。FEV1/FVC和FEF25-75)进行统计学评估。沙丁胺醇的可逆性≥12%且>200ml可区分哮喘患者和慢性阻塞性肺病(COPD)患者。结果:在总共35名患有中度基线气流阻塞的受试者(哮喘-10,COPD-25)中[FEV1/FVC:0.57 ± 0.12,FEV1(预测百分比)为46.17 ± 15.21],连续吸入沙丁胺醇和格隆的肺活量测量变量总体上有所改善。沙丁胺醇治疗后FEV1(绝对值)变化显著(P = 0.0001),并且还用于哮喘和COPD。吸入甘吡隆后,总体变化再次显著(P = 0.0001)、哮喘(P = 0.0065)和COPD(P = 0.0001)。然而,FEF25-75的平行变化在哮喘中显示出更好的可逆性(P = 0.0008)与COPD比较(P = 0.1846),并且与吸入甘吡隆相反,其在COPD中具有更好的可逆性(P = 0.0085)与哮喘(P = 0.0949)。结论:在阻塞性气道疾病中用格隆检测可逆性是可行和安全的。在标准沙丁胺醇可逆性之后使用时,它诱导了附加可逆性。观察结果需要进一步评估。
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