文献速递慢阻肺急性加重

支气管扩张症的肺功能与气流受限:两项独立队列的病例对照研究

Pulmonary function and airflow limitation in bronchiectasis: a case-control study of two independent cohorts
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该研究分析了一个多中心支气管扩张症登记队列和健康体检队列,比较支气管扩张症患者与对照的肺功能。结果显示支气管扩张症患者气流受限比例更高,且支气管扩张症是气流受限的独立危险因素。病变累及肺叶数多、吸烟和铜绿假单胞菌定植与肺功能更差相关。

要点

  • 支气管扩张症患者气流受限患病率显著高于无支气管扩张症者。
  • 吸烟、病变范围广和铜绿假单胞菌定植与肺功能恶化相关。
  • 支气管扩张症是气流受限的独立危险因素。

核心结论

  • 支气管扩张症是气流受限的独立危险因素。
  • 病变严重程度、吸烟和铜绿假单胞菌定植均与肺功能恶化相关。

研究设计与样本

  • 病例对照研究,纳入一个多中心支气管扩张症登记队列和一个健康体检队列。
  • 支气管扩张症登记队列共768例。

主要发现

  • 健康体检队列中,支气管扩张症患者气流受限患病率高于无支气管扩张症者(17.3% vs 8.1%,p<0.001)。
  • 有吸烟史的支气管扩张症患者FEV1、FEV1/FVC和FVC值最低,气流受限患病率最高。
  • 支气管扩张症登记队列中,累及肺叶数更多和铜绿假单胞菌定植者肺功能参数更差。
  • 多因素logistic回归显示支气管扩张症与气流受限独立相关(OR 2.22,95% CI 1.75至2.82)。

关键数值与推荐

  • 气流受限定义为FEV1/FVC<0.7。
  • 支气管扩张症严重程度按累及肺叶数分类。
  • 健康体检队列中支气管扩张症患者气流受限患病率为17.3%,无支气管扩张症者为8.1%(p<0.001)。
  • 支气管扩张症与气流受限独立相关:OR 2.22(95% CI 1.75至2.82)。

临床怎么用

  • 对支气管扩张症患者应常规评估肺功能,关注气流受限。
  • 对有吸烟史、病变范围广或铜绿假单胞菌定植的支气管扩张症患者应加强肺功能监测。

以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。

原文

Background Bronchiectasis is a respiratory disease structurally characterised by irreversible airway dilatation. Functional impairments are also implicated in bronchiectasis, but the detailed changes in pulmonary function and the impact of clinical factors are yet to be examined. We analysed pulmonary function in patients with bronchiectasis based on their clinical features. Methods Two study cohorts—a multicentre bronchiectasis registry and health check-up examinees—were analysed. Airflow limitation was defined as forced expiratory volume in 1 s (FEV 1 )/forced vital capacity (FVC) <0.7, and bronchiectasis severity was categorised using the number of involved lobes. Results Among 13 589 health check-up examinees, 606 (4.5%) had bronchiectasis; airflow limitation was more prevalent in those with bronchiectasis than in those without (17.3% vs 8.1%, p<0.001). Ever-smokers with bronchiectasis had the lowest FEV 1 , FEV 1 /FVC and FVC values, and the highest prevalence of airflow limitation. In the bronchiectasis registry (n=768), lung function parameters were worse in those with more involved lobes and Pseudomonas colonisation. Multivariable logistic regression analysis showed that bronchiectasis was independently associated with airflow limitation (OR 2.22 (95% CI 1.75 to 2.82)). Conclusions Bronchiectasis is an independent risk factor for airflow limitation, and disease severity, smoking and Pseudomonas colonisation were each associated with worsening in pulmonary function.

来源:BMJ Open Respiratory Research,查看原文。版权归原作者所有。

引用

  1. BMJ Open Respiratory Research:Pulmonary function and airflow limitation in bronchiectasis: a case-control study of two independent cohorts

供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。