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Dose related effects of salbutamol and ipratropium bromide on airway calibre and reactivity in subjects with asthma.

机译:沙丁胺醇和异丙托溴铵对哮喘患者气道口径和反应性的剂量相关影响。

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摘要

The relationship between change in airway calibre and change in airway reactivity after administration of bronchodilator drugs has been investigated by comparing the effect of increasing doses of inhaled salbutamol and ipratropium bromide on the forced expiratory volume in one second (FEV1), specific airways conductance (sGaw), and the dose of histamine causing a 20% fall in FEV1 (PD20) in six subjects with mild asthma. On each of 10 occasions measurements were made of baseline FEV1, sGaw, and PD20 after 15 minutes' rest, and followed one hour later, when the FEV1 had returned to baseline, by a single nebulised dose of salbutamol (placebo, 5, 30, 200 and 1000 micrograms) or ipratropium (placebo, 5, 30, 200 and 1000 micrograms) given in random order. Measurements of FEV1, sGaw, and PD20 were repeated 15 minutes after salbutamol and 40 minutes after ipratropium. Salbutamol and ipratropium caused a similar dose related increase in FEV1 and sGaw, with a mean increase after the highest doses of 0.76 and 0.69 litres for FEV1 and 1.15 and 0.96 s-1 kPa-1 for sGaw. Salbutamol also caused a dose related increase in PD20 to a maximum of 2.87 (95% confidence interval 2.18-3.55) doubling doses of histamine after the 1000 micrograms dose, but ipratropium bromide caused no significant change in PD20 (maximum increase 0.24 doubling doses, 95% confidence interval -0.73 to 1.22). Thus bronchodilatation after salbutamol was associated with a significantly greater change in airway reactivity than a similar amount of bronchodilatation after ipratropium bromide. This study shows that the relation between change in airway reactivity and bronchodilatation is different for two drugs with different mechanisms of action, suggesting that change in airway calibre is not a major determinant of change in airway reactivity with bronchodilator drugs.
机译:通过比较吸入沙丁胺醇和异丙托溴铵吸入剂量增加对一秒钟的呼气量(FEV1),比气道电导率(sGaw)的影响,研究了支气管扩张药给药后气道口径变化与气道反应性变化之间的关系。 ),以及导致6名轻度哮喘患者FEV1(PD20)下降20%的组胺剂量。休息15分钟后,每10次测量一次基线FEV1,sGaw和PD20,然后在1小时后,当FEV1返回基线时,用一次雾化剂量的沙丁胺醇(安慰剂,5、30, 200和1000微克)或异丙托溴铵(安慰剂,5、30、200和1000微克)以随机顺序给予。沙丁胺醇后15分钟和异丙托铵后40分钟重复进行FEV1,sGaw和PD20的测量。沙丁胺醇和异丙托铵引起FEV1和sGaw的剂量相关增加相似,FEV1最高剂量为0.76和0.69升,sGaw为1.15和0.96 s-1 kPa-1时,平均增加。沙丁胺醇在1000毫克剂量后还导致PD20的剂量相关增加至最大2.87(95%置信区间2.18-3.55)组胺加倍剂量,但是异丙托溴铵不会导致PD20发生显着变化(最大增加0.24倍剂量95) %置信区间-0.73至1.22)。因此,沙丁胺醇后的支气管扩张与异丙托溴铵后的类似量的支气管扩张相比,气道反应性的变化明显更大。这项研究表明,对于两种作用机理不同的药物,气道反应性变化与支气管扩张之间的关系是不同的,这表明气道口径的变化并不是支气管扩张药引起的气道反应性变化的主要决定因素。

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