Clinical characteristics of eosinophilic asthma exacerbations

被引:16
|
作者
Bjerregaard, Asger [1 ,2 ,3 ]
Laing, Ingrid A. [2 ,3 ]
Backer, Vibeke [1 ]
Fally, Markus [1 ]
Khoo, Siew-Kim [2 ,3 ]
Chidlow, Glenys [5 ]
Sikazwe, Chisha [4 ,5 ]
Smith, David W. [2 ,4 ,5 ]
Le Souef, Peter [3 ]
Porsbjerg, Celeste [1 ]
机构
[1] Bispebjerg Hosp, Resp Res Unit, Bispebjerg Bakke 23, DK-2400 Copenhagen, Denmark
[2] Univ Western Australia, Telethon Kids Inst, Perth, WA, Australia
[3] Univ Western Australia, Sch Paediat & Child Hlth, Perth, WA, Australia
[4] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA, Australia
[5] PathWest Lab Med Western Australia, Dept Microbiol, Perth, WA, Australia
关键词
acute asthma; eosinophils; phenotypes; sputum; viral infection; SPUTUM CELL COUNTS; INFLAMMATION; MEPOLIZUMAB; PHENOTYPES; AIRWAYS; SCORE; FLOW;
D O I
10.1111/resp.12905
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background and objective: Airway eosinophilia is associated with an increased risk of asthma exacerbations; however, the impact on the severity of exacerbations is largely unknown. We describe the sputum inflammatory phenotype during asthma exacerbation and correlate it with severity and treatment response. Methods: Patients presenting to hospital with an asthma exacerbation were recruited during a 12-month period and followed up after 4 weeks. Induced sputum was collected at both visits. Patients underwent spirometry, arterial blood gas analysis, fractional exhaled nitric oxide analysis, white blood cell counts and a screening for common respiratory viruses and bacteria. An eosinophilic exacerbation (EE) was defined as having sputum eosinophils >= 3% and a non-eosinophilic exacerbation as < 3% (NEE). Results: A total of 47 patients were enrolled; 37 (79%) had successful sputum induction at baseline, of whom 43% had sputum eosinophils >= 3% (EE). Patients with EE had a significantly lower forced expiratory volume in 1 s (FEV1) % predicted (70.8%, P = 0.03) than patients with NEE (83.6%). Furthermore, EE patients were more likely to require supplemental oxygen during admission (63% vs 14%, P = 0.002). The prevalence of respiratory viruses was the same in EE and NEE patients (44% vs 52%, P = 0.60), as was bacterial infection (6% vs 14%, P = 0.44). Fractional expiratory nitric oxide (FeNO) correlated with sputum %-eosinophils (rho = 0.57, P < 0.001), and predicted airway eosinophilia with a sensitivity of 86% and a specificity of 70%. Conclusion: Our findings suggest that eosinophilic asthma exacerbations may be clinically more severe than NEEs, supporting the identification of these higher risk patients for specific interventions.
引用
收藏
页码:295 / 300
页数:6
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