Uncontrolled asthma: A review of the prevalence, disease burden and options for treatment

被引:260
作者
Peters, Stephen P.
Ferguson, Gary
Deniz, Yamo
Reisner, Colin
机构
[1] Wake Forest Univ, Sch Med, Winston Salem, NC 27157 USA
[2] Pulm Res Inst SE Michigan, Livonia, MI USA
[3] Genentech Inc, San Francisco, CA USA
[4] Novartis Pharmaceut, E Hanover, NJ USA
关键词
asthma; anti-IgE; omalizumab; inhaled corticosteroids; long-acting beta(2)-agonists;
D O I
10.1016/j.rmed.2006.03.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An estimated 300 million people are affected by asthma worldwide and the burden is likely to rise substantially in the next few decades. Estimates of the prevalence of asthma range from 7% in France and Germany to 11% in the USA and 15-18% in the United Kingdom. Approximately 20% of these patients have severe asthma, of which 20% is inadequately controlled. Patients with inadequately controlled severe persistent asthma are at a particularly high risk of exacerbations, hospitalization and death, and often have severely impaired quality of life. Current management of asthma focuses on a stepwise approach tailored to disease severity. In addition to needing high-dose inhaled corticosteroids (ICS) and long-acting flagonists (LABAs), patients with severe persistent asthma often require additional controller medications, such as anti-leukotrienes, oral LABAs, oral corticosteroids and/or anti-IgE therapy. There is currently little evidence on which to base treatment decisions in patients with inadequately controlled severe persistent asthma already treated with ICS and LABAs. The anti-IgE monoclonal antibody omalizumab is the most recent addition to the list of treatment options for these patients and has been shown to reduce exacerbations and emergency visits and improve lung function, symptom scores and quality of life in patients with difficult-to-treat asthma whose symptoms remain inadequately controlled despite receiving ICS and LABAs. Comparative trials are needed to determine the merits of different treatments and strategies for patients with inadequately controlled severe persistent asthma and to identify patients likely to benefit from new treatment options. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1139 / 1151
页数:13
相关论文
共 79 条
[41]   Benefits of omalizumab as add-on therapy in patients with severe persistent asthma who are inadequately controlled despite best available therapy (GINA 2002 step 4 treatment):: INNOVATE [J].
Humbert, M ;
Beasley, R ;
Ayres, J ;
Slavin, R ;
Hébert, J ;
Bousquet, J ;
Beeh, KM ;
Ramos, S ;
Canonica, GW ;
Hedgecock, S ;
Fox, H ;
Blogg, M ;
Surrey, K .
ALLERGY, 2005, 60 (03) :309-316
[42]   The European Community Respiratory Health Survey: what are the main results so far? [J].
Janson, C ;
Anto, J ;
Burney, P ;
Chinn, S ;
de Marco, R ;
Heinrich, J ;
Jarvis, D ;
Kuenzli, N ;
Leynaert, B ;
Luczynska, C ;
Neukirch, F ;
Svanes, C ;
Sunyer, J ;
Wjst, M .
EUROPEAN RESPIRATORY JOURNAL, 2001, 18 (03) :598-611
[43]  
Juniper E F, 1998, Can Respir J, V5 Suppl A, p77A
[44]   Relationship between quality of life and clinical status in asthma: a factor analysis [J].
Juniper, EF ;
Wisniewski, ME ;
Cox, FM ;
Emmett, AH ;
Nielsen, KE ;
O'Byrne, PM .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (02) :287-291
[45]   Effect of SCH55700, a humanized anti-human interleukin-5 antibody, in severe persistent asthma - A pilot study 164/rccm.200206-5250C [J].
Kips, JC ;
O'Connor, BJ ;
Langley, SJ ;
Woodcock, A ;
Kerstjens, HAM ;
Postma, DS ;
Danzig, M ;
Cuss, F ;
Pauwels, RA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (12) :1655-1659
[46]   Perennial rhinitis: An independent risk factor for asthma in nonatopic subjects. Results from the European Community Respiratory Health Survey [J].
Leynaert, B ;
Bousquet, J ;
Neukirch, C ;
Liard, R ;
Neukirch, F .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 104 (02) :301-304
[47]   LONG-TERM PROGNOSIS OF NEAR-FATAL ASTHMA - A 6-YEAR FOLLOW-UP-STUDY OF 145 ASTHMATIC-PATIENTS WHO UNDERWENT MECHANICAL VENTILATION FOR A NEAR-FATAL ATTACK OF ASTHMA [J].
MARQUETTE, CH ;
SAULNIER, F ;
LEROY, O ;
WALLAERT, B ;
CHOPIN, C ;
DEMARCQ, JM ;
DUROCHER, A ;
TONNEL, AB .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (01) :76-81
[48]   The global burden of asthma: executive summary of the GINA Dissemination Committee Report [J].
Masoli, M ;
Fabian, D ;
Holt, S ;
Beasley, R .
ALLERGY, 2004, 59 (05) :469-478
[49]  
MCCOWAN C, 2002, EFFECT ASTHMA SEVERI, pA27
[50]  
MIRANDA C, 2001, J ALLERGY CLIN IMMUN, V107, P449