Safety of bronchial thermoplasty in patients with severe refractory asthma

被引:102
作者
Pavord, Ian D. [1 ]
Thomson, Neil C. [2 ]
Niven, Robert M. [3 ,4 ]
Corris, Paul A. [5 ]
Chung, Kian Fan [6 ]
Cox, Gerard [7 ]
Armstrong, Brian [8 ]
Shargill, Narinder S. [9 ]
Laviolette, Michel [10 ]
机构
[1] Glenfield Gen Hosp, Univ Hosp Leicester NHS Trust, Leicester LE3 9QP, Leics, England
[2] Univ Glasgow, Gartnavel Gen Hosp, Glasgow, Lanark, Scotland
[3] Univ S Manchester Hosp, Manchester M20 8LR, Lancs, England
[4] Univ Manchester, Manchester, Lancs, England
[5] Newcastle Univ, Freeman Hosp, Dept Resp Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[6] Univ London Imperial Coll Sci Technol & Med, Royal Brompton Hosp, London, England
[7] McMaster Univ, St Josephs Healthcare, Hamilton, ON, Canada
[8] QST Consultat Ltd, Allendale, MI USA
[9] Asthmatx, Sunnyvale, CA USA
[10] Univ Laval, Quebec Heart & Lung Inst, Quebec City, PQ, Canada
关键词
TREATMENT REGIMENS TENOR; LUNG-FUNCTION; SEVERE EXACERBATIONS; RESEARCH-PROGRAM; NATURAL-HISTORY; DECLINE; EPIDEMIOLOGY; OUTCOMES; HEALTH; TRIAL;
D O I
10.1016/j.anai.2013.05.002
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
Background: Patients with severe refractory asthma treated with bronchial thermoplasty (BT), a bronchoscopic procedure that improves asthma control by reducing excess airway smooth muscle, were followed up for 5 years to evaluate long-term safety of this procedure. Objectives: To assess long-term safety of BT for 5 years. Methods: Patients with asthma aged 18 to 65 years requiring high-dose inhaled corticosteroids (ICSs) (> 750 mu g/d of fluticasone propionate or equivalent) and long-acting beta(2)-agonists (LABAs) (at least 100 mg/d of salmeterol or equivalent), with or without oral prednisone (< 30 mg/d), leukotriene modifiers, theophylline, or other asthma controller medications were enrolled in the Research in Severe Asthma (RISA) Trial. Patients had a prebronchodilator forced expiratory volume in 1 second of 50% or more of predicted, demonstrated methacholine airway hyperresponsiveness, had uncontrolled symptoms despite taking maintenance medication, abstained from smoking for 1 year or greater, and had a smoking history of less than 10 pack-years. Results: Fourteen patients (of the 15 who received active treatment in the RISA Trial) participated in the long-term follow-up study for 5 years. The rate of respiratory adverse events (AEs per patient per year) was 1.4, 2.4, 1.7, and 2.4, respectively, in years 2 to 5 after BT. There was a decrease in hospitalizations and emergency department visits for respiratory symptoms in each of years 1, 2, 3, 4, and 5 compared with the year before BT treatment. Measures of lung function showed no deterioration for 5 years. Conclusion: Our findings suggest that BT is safe for 5 years after BT in patients with severe refractory asthma. (C) 2013 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:402 / 407
页数:6
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