Arnman K, Willén B, Borgström L, Conradson T B
Department of Medicine, County Hospital, Ystad, Sweden.
Ther Drug Monit. 1989;11(3):249-52. doi: 10.1097/00007691-198905000-00006.
Nine patients (3 women), aged 29-78 years, with acute asthma were treated with the antiasthma xanthine, enprofylline, in an open-design study without a reference drug. Enprofylline was administered intravenously (i.v.) over 2 h with an exponentially decreasing concentration. This alternative infusion system was found to be simple to handle. All patients but one reached a therapeutic plasma concentration of enprofylline within 20 min, but with a lower peak plasma, concentration as compared to what previously has been found with a conventional i.v. injection of the same amount of drug. The plasma concentration of enprofylline remained on a stable and therapeutic level over the 2-h observation period. The effect on lung function was comparable to that found in other controlled trials with enprofylline. A system for i.v. administration of drugs with an exponentially decreasing concentration as an alternative to manually given i.v. injections should be further evaluated.
在一项无对照药物的开放性研究中,对9例年龄在29至78岁之间的急性哮喘患者(3名女性)使用抗哮喘黄嘌呤类药物恩丙茶碱进行治疗。恩丙茶碱以指数递减浓度在2小时内静脉输注。发现这种替代输注系统易于操作。除1例患者外,所有患者在20分钟内均达到恩丙茶碱的治疗血浆浓度,但与先前相同剂量药物传统静脉注射相比,血浆峰值浓度较低。在2小时的观察期内,恩丙茶碱的血浆浓度保持在稳定的治疗水平。对肺功能的影响与其他恩丙茶碱对照试验中发现的效果相当。作为手动静脉注射的替代方法,以指数递减浓度静脉给药的系统应进一步评估。