Fish J E, Peterman V I
Respiration. 1979;37(4):201-7. doi: 10.1159/000194028.
We measured the effect of inhaled lidocaine on pulmonary function in 8 asthmatic subjects. Plethysmographic specific airways conductance (SGaw) and the 1-sec forced expired volume (FEV1) were measured before and after the inhalation of 2cm3 of lidocaine (4%). Responses were also measured after patients were pretreated with either aerosolized isoproterenol, aerosolized atropine, or intramuscular atropine. In response to lidocaine alone, we observed a 23.4 +/- (SE) 4.8% fall in FEV1 and a 64.1 +/-(SE)3.8% fall in SGaw (p is less than 0.001). These effects were reversed with aerosolized atropine or isoproterenol. After pretreatment with aerosolized atropine or isoproterenol, the bronchoconstrictor effect of lidocaine were either prevented or markedly reduced. The protective effects of intramuscular atropine varied in different subjects, but in general, aerosolized bronchodilators afforded better protection against the bronchoconstrictor effect of lidocaine. Although lidocaine is theoretically capable of blocking neurogenic reflexes in the lung, our studies indicate that this topical anesthetic agent produces untoward reflex-mediated bronchoconstriction in patients with asthma and hyperirritable airways.
我们测定了吸入利多卡因对8名哮喘患者肺功能的影响。在吸入2立方厘米4%的利多卡因前后,测量了体积描记法气道比传导率(SGaw)和1秒用力呼气容积(FEV1)。在患者接受雾化异丙肾上腺素、雾化阿托品或肌肉注射阿托品预处理后,也进行了反应测量。仅对利多卡因的反应中,我们观察到FEV1下降了23.4±(标准误)4.8%,SGaw下降了64.1±(标准误)3.8%(p<0.001)。这些效应可被雾化阿托品或异丙肾上腺素逆转。在雾化阿托品或异丙肾上腺素预处理后,利多卡因的支气管收缩效应被预防或显著降低。肌肉注射阿托品的保护作用在不同患者中有所不同,但总体而言,雾化支气管扩张剂对利多卡因的支气管收缩效应提供了更好的保护。尽管利多卡因理论上能够阻断肺内神经源性反射,但我们的研究表明,这种局部麻醉剂在哮喘患者和气道高反应性患者中会产生不良的反射介导的支气管收缩。