Nair N, Townley R G, Bewtra A, Nair C K
Chest. 1984 Oct;86(4):515-8. doi: 10.1378/chest.86.4.515.
This prospective study was undertaken to evaluate the safety of nifedipine, a calcium channel blocking agent, on 60 subjects with asthma, chronic obstructive pulmonary disease (COPD), angina, and normal subjects. All subjects received nifedipine, 20 mg, sublingually. Spirometry was done pre-drug administration and every 20 minutes after for two hours. Parameters measured were forced vital capacity (FVC), forced expiratory volume in one second (FEV1), and forced expiratory flow at 25 percent to 75 percent of total volume (FEF25-75%). Subjects with asthma and COPD were also given nifedipine 20 mg three times daily, orally for two weeks, and tested biweekly during this period. All bronchodilators, beta-blockers, and long acting nitrates were withheld for five half-lives of the drug prior to test day. There was no adverse effect on the pulmonary function. We found a statistically significant improvement (p less than 0.05) in FEV1 after nifedipine. There was no tachyphylaxis at the end of two weeks. Nifedipine is safe in patients with asthma and/or chronic bronchitis.
本前瞻性研究旨在评估钙通道阻滞剂硝苯地平对60例哮喘、慢性阻塞性肺疾病(COPD)、心绞痛患者以及正常受试者的安全性。所有受试者均舌下含服20 mg硝苯地平。在给药前及给药后每20分钟进行一次肺功能测定,持续两小时。测定的参数包括用力肺活量(FVC)、一秒用力呼气容积(FEV1)以及占总量25%至75%时的用力呼气流量(FEF25 - 75%)。哮喘和COPD患者还口服20 mg硝苯地平,每日三次,持续两周,并在此期间每两周进行一次检测。在测试日前,所有支气管扩张剂、β受体阻滞剂和长效硝酸盐类药物均停用该药的五个半衰期。对肺功能无不良影响。我们发现硝苯地平给药后FEV1有统计学显著改善(p < 0.05)。两周结束时未出现快速耐受性。硝苯地平对哮喘和/或慢性支气管炎患者是安全的。