Fractional exhaled nitric oxide for the management of asthma in adults: a systematic review

被引:59
|
作者
Essat, Munira [1 ]
Harnan, Sue [1 ]
Gomersall, Tim [1 ]
Tappenden, Paul [1 ]
Wong, Ruth [1 ]
Pavord, Ian [2 ]
Lawson, Rod [3 ]
Everard, Mark L. [4 ]
机构
[1] Univ Sheffield, Sch Hlth & Related Res, 30 Regent St, Sheffield S1 4DA, S Yorkshire, England
[2] Univ Oxford, Nuffield Dept Med, Oxford, England
[3] Royal Hallamshire Hosp, Dept Resp Med, Sheffield, S Yorkshire, England
[4] Univ Western Australia, Princess Margaret Hosp, Sch Paediat & Child Hlth, Perth, WA, Australia
关键词
CLUSTER-RANDOMIZED-TRIAL; STRATEGIES; FENO;
D O I
10.1183/13993003.01882-2015
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The aim of this review was to evaluate the clinical effectiveness of fractional exhaled nitric oxide (FeNO) measured in a clinical setting for the management of asthma in adults. 13 electronic databases were searched and studies were selected against predefined inclusion criteria. Quality assessment was conducted using QUADAS-2. Class effect meta-analyses were performed. Six studies were included. Despite high levels of heterogeneity in multiple study characteristics, exploratory class effect meta-analyses were conducted. Four studies reported a wider definition of exacerbation rates (major or severe exacerbation) with a pooled rate ratio of 0.80 (95% CI 0.63-1.02). Two studies reported rates of severe exacerbations (requiring oral corticosteroid use) with a pooled rate ratio of 0.89 (95% CI 0.43-1.72). Inhaled corticosteroid use was reported by four studies, with a pooled standardised mean difference of -0.24 (95% CI -0.56-0.07). No statistically significant differences for health-related quality of life or asthma control were found. FeNO guided management showed no statistically significant benefit in terms of severe exacerbations or inhaled corticosteroid use, but showed a statistically significant reduction in exacerbations of any severity. However, further research is warranted to clearly define which management protocols (including cut-off points) offer best efficacy and which patient groups would benefit the most.
引用
收藏
页码:751 / 768
页数:18
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