A Double-Blind Crossover Study Comparing the Safety and Efficacy of Three Weeks of Flu/Sal 250/50 bid Plus Albuterol 180 ug prn q4 hours to Flu/Sal 250/50 bid Plus Albuterol/Ipratropium Bromide 2 puffs prn q4 hours in Patients with Chronic Obstructive Pulmonary Disease

被引:7
作者
Balkissoon, Ron [1 ]
Make, Barry [1 ]
机构
[1] Natl Jewish Med & Res Ctr, Denver, CO 80206 USA
关键词
COPD; fluticasone; salmeterol; albuterol; atrouent; combination therapy;
D O I
10.1080/15412550802237408
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The Federal Drug Administration (FDA) approved the use of Fluticasone 250 mu g/Salmeterol 50 mu g 1 puff bid for maintenance therapy in patients with COPD associated with chronic bronchitis. Short-acting beta agonists (SABA) have been the recommended rescue medication; however, previous studies have shown that combination short-acting Albuterol (alb) /Ipratropium bromide (IB) has superior bronchodilator properties to albuterol alone in patients with COPD. The safety and efficacy of Albuterol compared to Albuterol/lpratropium bromide as rescue medicaticons for COPD patients on maintenance combination therapy of ICS/LABA has not been evaluated. Double-blind randomized crossover trial with COPD subjects receiving Fluticasone/Salmeterol 500 mu g/50 mu g (Flu/Sal) 1 puff twice daily and 2 puffs of Albuterol Sulfate (90 mu g micrograms per inhalation) or 2 puffs of Albuterol (90 mu g/puff and Ipratropium Bromide 18 mu g/puff. Either Albuterol Sulfate (90 micrograms/puff) or Alb (90 micrograms/puff)/IB used prn for 3 weeks before crossing over to the other rescue formulation. This is a non-inferiority study where safety and efficacy outcomes were serially assessed, including adverse events, Baseline (BDI)/Transition Dyspnea Index (TDI), St. George Respiratory Questionnaire (SGRQ), SF36, diary cards, 24-hour cardiac monitoring, potassium and glucose levels and other adverse events. Twenty subjects completed the study. The mean age was 62.5 (+/- 14.5); 12 were males. The mean baseline FEV(1) (range) was 1.12 L (0.56-1.67) or 40.6 (21-65)% predicted. There were no statistically significant differences between either rescue inhaler formulation with regard to measures neither of lung function or dyspnea nor in terms of safety parameters of cardiac monitoring, glucose and potassium levels and other adverse events. SABA and combination SABA/lpratropium bromide are equally safe and efficacious as rescue inhalers for patients on combination Fluticasone 500 mu g/Salmeterol 50 mu g.
引用
收藏
页码:221 / 227
页数:7
相关论文
共 19 条
[1]   Combined salmeterol and fluticasone in the treatment of chronic obstructive pulmonary disease: a randomised controlled trial [J].
Calverley, P ;
Pauwels, R ;
Vestbo, J ;
Jones, P ;
Pride, N ;
Gulsvik, A ;
Anderson, J ;
Maden, C .
LANCET, 2003, 361 (9356) :449-456
[2]   Salmeterol and fluticasone propionate and survival in chronic obstructive pulmonary disease [J].
Calverley, Peter M. A. ;
Anderson, Julie A. ;
Celli, Bartolome ;
Ferguson, Gary T. ;
Jenkins, Christine ;
Jones, Paul W. ;
Yates, Julie C. ;
Vestbo, Jorgen ;
Calverley, P. M. A. ;
Anderson, J. A. ;
Celli, B. ;
Ferguson, G. T. ;
Jenkins, C. ;
Jones, P. W. ;
Knobil, K. ;
Yates, J. C. ;
Vestbo, J. ;
Cherniack, R. ;
Similowski, T. ;
Cleland, J. ;
Whitehead, A. ;
Wise, R. ;
McGarvey, L. ;
John, M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (08) :775-789
[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]   SALMETEROL AND FORMOTEROL IN PARTIALLY REVERSIBLE SEVERE CHRONIC OBSTRUCTIVE PULMONARY-DISEASE - A DOSE-RESPONSE STUDY [J].
CAZZOLA, M ;
MATERA, MG ;
SANTANGELO, G ;
VINCIGUERRA, A ;
ROSSI, F ;
DAMATO, G .
RESPIRATORY MEDICINE, 1995, 89 (05) :357-362
[6]   A 6-month, placebo-controlled study comparing lung function and health status changes in COPD patients treated with tiotropium or salmeterol [J].
Donohue, JF ;
van Noord, JA ;
Bateman, ED ;
Langley, SJ ;
Lee, A ;
Witek, TJ ;
Kesten, S ;
Towse, L .
CHEST, 2002, 122 (01) :47-55
[7]   The combination of ipratropium and albuterol optimizes pulmonary function reversibility testing in patients with COPD [J].
Dorinsky, PM ;
Reisner, C ;
Ferguson, GT ;
Menjoge, SS ;
Serby, CW ;
Witek, TJ .
CHEST, 1999, 115 (04) :966-971
[8]  
DORINSKY PM, USE CHANGES SYMPTOMS, P31936
[9]   Cardiovascular safety of salmeterol in COPD [J].
Ferguson, GT ;
Funck-Brentano, C ;
Fischer, T ;
Darken, P ;
Reisner, C .
CHEST, 2003, 123 (06) :1817-1824
[10]   The efficacy and safety of fluticasone propionate (250 μg)/salmeterol (50 μg) combined in the diskus inhaler for the treatment of COPD [J].
Hanania, NA ;
Darken, P ;
Horstman, D ;
Reisner, C ;
Lee, B ;
Davis, S ;
Shah, T .
CHEST, 2003, 124 (03) :834-843