Long-acting bronchodilators in cystic fibrosis

被引:20
作者
Colombo, JL [1 ]
机构
[1] Univ Nebraska, Med Ctr, Omaha, NE 68198 USA
关键词
bronchodilators in CF; mucociliary clearance; beta-adrenergic agonists;
D O I
10.1097/00063198-200311000-00010
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of review Over 80% of patients with cystic fibrosis (CF) have bronchodilator therapy prescribed, yet bronchodilator use in CF remains controversial. The development of long-acting beta-agonist drugs for clinical use has provided additional rationale for considering bronchodilator therapy in CF. This paper will review recent developments in bronchodilator use in CF patients, with emphasis on the long-acting beta agonists. Recent findings It is reported that 50 to 60% of CF patients demonstrate significant intermittent airway hyperreactivity in response to bronchodilators or challenges. The beta-agonist drugs are the most commonly prescribed bronchodilators. Several mechanisms may be implicated in therapeutic response of CF patients to bronchodilators including direct smooth muscle relaxation, increased mucociliary clearance, direct effects on inflammatory cells and bacterial adherence, and possible direct effects on CF transmembrane conductance regulator (CFTR) function. Several recent studies have shown improved outcomes with long-acting bronchodilators. Summary In spite of the widespread use of bronchodilators, there are very few long-term studies of their effects in CF patients. However, there are clearly clinical benefits in certain situations. Further research into the most appropriate utilization of these medications to improve outcomes in patients with CF would be helpful.
引用
收藏
页码:504 / 508
页数:5
相关论文
共 21 条
[1]  
APPLETON S, 2003, COCHRANE LIB, V2
[2]   CF asthma: what is it and what do we do about it? [J].
Balfour-Lynn, IM ;
Elborn, JS .
THORAX, 2002, 57 (08) :742-748
[3]  
Bennett William D., 2002, Journal of Allergy and Clinical Immunology, V110, pS291, DOI 10.1067/mai.2002.129704
[4]   β2 adrenoceptor gene polymorphisms in cystic fibrosis lung disease [J].
Büscher, R ;
Eilmes, KJ ;
Graseman, H ;
Torres, B ;
Knauer, N ;
Sroka, K ;
Insel, PA ;
Ratjen, F .
PHARMACOGENETICS, 2002, 12 (05) :347-353
[5]  
CROPP JC, 1996, AM J MED, V100, pS19
[6]   Effectiveness and tolerability of high-dose salmeterol in cystic fibrosis [J].
Hordvik, NL ;
Sammut, PH ;
Judy, CG ;
Colombo, JL .
PEDIATRIC PULMONOLOGY, 2002, 34 (04) :287-296
[7]   The effects of albuterol on the lung function of hospital ed patients with cystic fibrosis [J].
Hordvik, NL ;
Sammut, PH ;
Judy, CC ;
Strizek, SJ ;
Colombo, JL .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (01) :156-160
[8]   Treatment of severe small airways disease in children with cystic fibrosis: Alternatives to corticosteroids [J].
Jaffe A. ;
Balfour-Lynn I.M. .
Pediatric Drugs, 2002, 4 (6) :381-389
[9]   Factors influencing outcomes in cystic fibrosis - A center-based analysis [J].
Johnson, C ;
Butler, SM ;
Konstan, MW ;
Morgan, W ;
Wohl, MEB .
CHEST, 2003, 123 (01) :20-27
[10]  
König P, 1998, PEDIATR PULM, V25, P32, DOI 10.1002/(SICI)1099-0496(199801)25:1<32::AID-PPUL3>3.0.CO