Tiotropium bromide

被引:59
作者
Gross, NJ [1 ]
机构
[1] Hines VA Hosp, Hines, IL USA
关键词
acute exacerbations of COPD; adverse effects; antocholinergic agent; bronchodilators; COPD; quality of life; tiotropium bromide; transition dyspnea index;
D O I
10.1378/chest.126.6.1946
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Tiotropium bromide is a novel, inhaled, once-daily anticholinergic bronchodilator that has recently been approved in the United States for use in patients with COPD. Its unique feature is the persistence of bronchodilation for > 24 h due to prolonged M, muscarinic receptor blockade. Tiotropium provides significant improvement in spirometry and lung volumes. Clinically relevant outcomes such as the relief of dyspnea, improvement in the quality of life (health status), and reductions in the frequency and severity of acute exacerbations have been consistently obtained with tiotropium in clinical trials. In head-to-head trials, tiotropium administered once daily resulted in bronchodilation (peak, trough, and area under the curve) that was statistically superior to ipratropium administered four times daily and salmeterol administered twice daily. Clinical outcomes (dyspnea, quality of life, exacerbation frequency) were numerically but not always statistically better with tiotropium than salmeterol. Long-term studies of the combination of tiotropium with adrenergic agents, methylxanthines, or inhaled corticosteroids have not been reported in full. Several I-year studies demonstrate that the only significant side effect of tiotropium was dryness of the mouth, which occurred in approximately 10 to 16% of patients; it is well tolerated by patients and safe.
引用
收藏
页码:1946 / 1953
页数:8
相关论文
共 48 条
[1]  
BRIGGS D, 2002, CHEST, V122, pS140
[2]   Health outcomes following treatment for six months with once daily tiotropium compared with twice daily salmeterol in patients with COPD [J].
Brusasco, V ;
Hodder, R ;
Miravitlles, M ;
Korducki, L ;
Towse, L ;
Kesten, S .
THORAX, 2003, 58 (05) :399-404
[3]   Effect of tiotropium bromide on circadian variation in airflow limitation in chronic obstructive pulmonary disease [J].
Calverley, PMA ;
Lee, A ;
Towse, L ;
van Noord, J ;
Witek, TJ ;
Kelsen, S .
THORAX, 2003, 58 (10) :855-860
[4]   A long-term evaluation of once-daily inhaled tiotropium in chronic obstructive pulmonary disease [J].
Casaburi, R ;
Mahler, DA ;
Jones, PW ;
Wanner, A ;
San Pedro, G ;
ZuWallack, RL ;
Menjoge, SS ;
Serby, CW ;
Witek, T .
EUROPEAN RESPIRATORY JOURNAL, 2002, 19 (02) :217-224
[5]   Improvement in resting inspiratory capacity and hyperinflation with tiotropium in COPD patients with increased static lung volumes [J].
Celli, B ;
ZuWallack, R ;
Wang, S ;
Kesten, S .
CHEST, 2003, 124 (05) :1743-1748
[6]   Outcomes following acute exacerbation of severe chronic obstructive lung disease [J].
Connors, AF ;
Dawson, NV ;
Thomas, C ;
Harrell, FE ;
Desbiens, N ;
Fulkerson, WJ ;
Kussin, P ;
Bellamy, P ;
Goldman, L ;
Knaus, WA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (04) :959-967
[7]   Muscarinic acetylcholine receptors and airway diseases [J].
Coulson, FR ;
Fryer, AD .
PHARMACOLOGY & THERAPEUTICS, 2003, 98 (01) :59-69
[8]   Assessment of patient performance of the HandiHaler® compared with the metered dose inhaler four weeks after instruction [J].
Dahl, R ;
Backer, V ;
Ollgaard, B ;
Gerken, F ;
Kesten, S .
RESPIRATORY MEDICINE, 2003, 97 (10) :1126-1133
[9]   Tiotropium (Spiriva™):: Mechanistical considerations and clinical profile in obstructive lung disease [J].
Disse, B ;
Speck, GA ;
Rominger, KL ;
Witek, TJ ;
Hammer, R .
LIFE SCIENCES, 1999, 64 (6-7) :457-464
[10]   BA 679 BR, A NOVEL LONG-ACTING ANTICHOLINERGIC BRONCHODILATOR [J].
DISSE, B ;
REICHL, R ;
SPECK, G ;
TRAUNECKER, W ;
ROMINGER, KL ;
HAMMER, R .
LIFE SCIENCES, 1993, 52 (5-6) :537-544