Koumis Tina, Samuel Sheeba
International Drug Information Center, Arnold & Marie Schwartz College of Pharmacy and HealthSciences, Long Island University, Brooklyn, New York 11201, USA.
Clin Ther. 2005 Apr;27(4):377-92. doi: 10.1016/j.clinthera.2005.04.006.
Tiotropium bromide is a new inhaled anticholinergic agent approved for once-daily, long-term maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease (COPD).
This article reviews the pharmacology, pharmacokinetic and pharmacodynamic properties, clinical efficacy, tolerability, and cost of tiotropium therapy in patients with COPD.
The MEDLINE (1966-October 2004), Iowa Drug Information Service (1966-October 2004), and International Pharmaceutical Abstracts (1970-November 2004) databases were searched for original research and review articles published in English. The search terms were tiotropium, Ba 679 BR, and HandiHaler. Reference lists from these articles were also consulted, as was selected information provided by the manufacturer of tiotropium. All relevant identified studies were included in the review, with preference given to Phase II/III trials. Pharmacoeconomic studies were limited to those conducted in the United States.
Tiotropium is a nonselective anticholinergic agent that exhibits kinetic receptor selectivity for the muscarinic M1 and M3 receptors. After inhalation, tiotropium has an onset of action within 30 minutes, a peak effect within 3 to 4 hours, and a > or = 24-hour duration of action that allows once-daily dosing. In clinical trials, patients receiving tiotropium 18 microg QD had significant improvements in trough, peak, and mean forced expiratory volume in 1 second (FEV1), dyspnea, and health-related quality of life, as well as fewer COPD exacerbations and hospitalizations, compared with patients receiving placebo and ipratropium (all, P < 0.05). Improvement in FEV1 was also significantly greater in patients who received tiotropium compared with those who received salmeterol (P < 0.05), although the number of exacerbations and extent of health resource use were comparable between groups. Dry mouth was the most commonly reported adverse effect. One analysis found tiotropium to be cost-effective compared with ipratropium.
Tiotropium offers several advantages over ipratropium in the management of COPD. Long-term (> 1 year) studies are necessary to determine the impact of tiotropium on disease progression and life expectancy.
噻托溴铵是一种新型吸入性抗胆碱能药物,已被批准用于慢性阻塞性肺疾病(COPD)相关支气管痉挛的每日一次长期维持治疗。
本文综述了噻托溴铵治疗COPD患者的药理学、药代动力学和药效学特性、临床疗效、耐受性及成本。
检索MEDLINE(1966年 - 2004年10月)、爱荷华州药物信息服务(1966年 - 2004年10月)和国际药学文摘(1970年 - 2004年11月)数据库中以英文发表的原始研究和综述文章。检索词为噻托溴铵、Ba 679 BR和HandiHaler。还查阅了这些文章的参考文献列表以及噻托溴铵制造商提供的选定信息。所有相关的已识别研究均纳入综述,并优先选择II/III期试验。药物经济学研究仅限于在美国进行的研究。
噻托溴铵是一种非选择性抗胆碱能药物,对毒蕈碱M1和M3受体表现出动力学受体选择性。吸入后,噻托溴铵起效时间在30分钟内,3至4小时达到峰值效应,作用持续时间≥24小时,允许每日一次给药。在临床试验中,与接受安慰剂和异丙托溴铵的患者相比,接受每日一次18微克噻托溴铵的患者在1秒用力呼气容积(FEV1)的谷值、峰值和平均值、呼吸困难及健康相关生活质量方面有显著改善,COPD急性加重和住院次数也更少(所有P < 0.05)。与接受沙美特罗的患者相比,接受噻托溴铵的患者FEV1改善也更显著(P < 0.05),尽管两组之间急性加重次数和卫生资源使用程度相当。口干是最常报告的不良反应。一项分析发现,与异丙托溴铵相比,噻托溴铵具有成本效益。
在COPD管理方面,噻托溴铵比异丙托溴铵有多个优势。需要进行长期(>1年)研究以确定噻托溴铵对疾病进展和预期寿命的影响。