Azithromycin for prevention of exacerbations in non-cystic fibrosis bronchiectasis (EMBRACE): a randomised, double-blind, placebo-controlled trial

被引:407
|
作者
Wong, Conroy [1 ]
Jayaram, Lata [4 ]
Karalus, Noel [5 ]
Eaton, Tam
Tong, Cecilia [2 ]
Hockey, Hans [6 ]
Milne, David [7 ]
Fergusson, Wendy [8 ]
Tuffery, Christine [5 ]
Sexton, Paul [8 ]
Storey, Louanne [3 ]
Ashton, Toni [9 ]
机构
[1] Middlemore Hosp, Dept Resp Med, Counties Manukau Dist Hlth Board, Auckland 2025, New Zealand
[2] Middlemore Hosp, Counties Manukau Dist Hlth Board, Ctr Clin Res & Effect Practice, Auckland 2025, New Zealand
[3] Middlemore Hosp, Counties Manukau Dist Hlth Board, Dept Microbiol, Auckland 2025, New Zealand
[4] Monash Med Ctr, Dept Resp Med, Clayton, Vic 3168, Australia
[5] Waikato Hosp, Waikato Dist Hlth Board, Dept Resp Med, Hamilton, New Zealand
[6] Biometr Matters Ltd, Hamilton, New Zealand
[7] Auckland City Hosp, Auckland Dist Hlth Board, Dept Radiol, Auckland, New Zealand
[8] Auckland City Hosp, Auckland Dist Hlth Board, Dept Resp Med, Auckland, New Zealand
[9] Univ Auckland, Sch Populat Hlth, Auckland 1, New Zealand
来源
LANCET | 2012年 / 380卷 / 9842期
关键词
LONG-TERM; PSEUDOMONAS-AERUGINOSA; CHILDREN; PARAMETERS; MACROLIDES; THERAPY;
D O I
10.1016/S0140-6736(12)60953-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Azithromycin is a macrolide antibiotic with anti-inflammatory and immunomodulatory properties. We tested the hypothesis that azithromycin would decrease the frequency of exacerbations, increase lung function, and improve health-related quality of life in patients with non-cystic fibrosis bronchiectasis. Methods We undertook a randomised, double-blind, placebo-controlled trial at three centres in New Zealand. Between Feb 12, 2008, and Oct 15, 2009, we enrolled patients who were 18 years or older, had had at least one pulmonary exacerbation requiring antibiotic treatment in the past year, and had a diagnosis of bronchiectasis defined by high-resolution CT scan. We randomly assigned patients to receive 500 mg azithromycin or placebo three times a week for 6 months in a 1: 1 ratio, with a permuted block size of six and sequential assignment stratified by centre. Participants, research assistants, and investigators were masked to treatment allocation. The coprimary endpoints were rate of event-based exacerbations in the 6-month treatment period, change in forced expiratory volume in 1 s (FEV1) before bronchodilation, and change in total score on St George's respiratory questionnaire (SGRQ). Analyses were by intention to treat. This study is registered with the Australian New Zealand Clinical Trials Registry, number ACTRN12607000641493. Findings 71 patients were in the azithromycin group and 70 in the placebo group. The rate of event-based exacerbations was 0.59 per patient in the azithromycin group and 1.57 per patient in the placebo group in the 6-month treatment period (rate ratio 0.38, 95% CI 0.26-0.54; p<0.0001). Prebronchodilator FEV1 did not change from baseline in the azithromycin group and decreased by 0.04 L in the placebo group, but the difference was not significant (0.04 L, 95% CI -0.03 to 0.12; p=0.251). Additionally, change in SGRQ total score did not differ between the azithromycin (-5.17 units) and placebo groups (-1.92 units; difference -3.25, 95% CI -7.21 to 0.72; p=0.108). Interpretation Azithromycin is a new option for prevention of exacerbations in patients with non-cystic fibrosis bronchiectasis with a history of at least one exacerbation in the past year.
引用
收藏
页码:660 / 667
页数:8
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