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原发性纤毛运动障碍和囊性纤维化患儿与健康对照者的多次呼吸冲洗和肺量测定比较。

Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls.

机构信息

University of Washington, Seattle, Washington.

Washington University School of Medicine, St. Louis, Missouri.

出版信息

Ann Am Thorac Soc. 2020 Sep;17(9):1085-1093. doi: 10.1513/AnnalsATS.201905-375OC.

Abstract

In cystic fibrosis (CF), the lung clearance index (LCI), derived from multiple breath washout (MBW), is more sensitive in detecting early lung disease than FEV; MBW has been less thoroughly evaluated in young patients with primary ciliary dyskinesia (PCD). Our objectives were ) to evaluate the sensitivity of MBW and spirometry for the detection of mild lung disease in young children with PCD and CF compared with healthy control (HC) subjects and ) to compare patterns of airway obstruction between disease populations. We used a multicenter, single-visit, observational study in children with PCD and CF with a forced expiratory volume in 1 second (FEV) greater than 60% predicted and HC subjects, ages 3-12 years. Nitrogen MBW and spirometry were performed and overread for acceptability. χ and Kruskall-Wallis tests compared demographics and lung function measures between groups, linear regression evaluated the effect of disease state, and Spearman's rank correlation coefficient compared the LCI and spirometric measurements. Twenty-five children with PCD, 49 children with CF, and 80 HC children were enrolled, among whom 17 children with PCD (68%), 36 children with CF (73%), and 53 (66%) HC children performed both acceptable spirometry and MBW; these children made up the analytic cohort. The median age was 9.0 years (interquartile range [IQR], 6.8-11.1). The LCI was abnormal (more than 7.8) in 10 of 17 (59%) patients with PCD and 21 of 36 (58%) patients with CF, whereas FEV was abnormal in three of 17 (18%) patients with PCD and six of 36 (17%) patients with CF. The LCI was significantly elevated in patients with PCD and CF compared with HC subjects (ratio of geometric mean vs. HC: PCD 1.27; 95% confidence interval [CI], 1.15-1.39; and CF 1.24; 95% CI, 1.15-1.33]). Children with PCD had lower midexpiratory-phase forced expiratory flow % predicted compared with children with CF (62% [IQR, 50-78%] vs. 85% [IQR, 68-99%];  = 0.05). LCI did not correlate with FEV. The LCI is more sensitive than FEV in detecting lung disease in young patients with PCD, similar to CF. LCI holds promise as a sensitive endpoint for the assessment of early PCD lung disease.

摘要

在囊性纤维化 (CF) 中,源自多次呼吸冲洗 (MBW) 的肺清除指数 (LCI) 比 FEV 更能敏感地检测早期肺疾病;MBW 在原发性纤毛运动障碍 (PCD) 的年轻患者中评估得不够充分。我们的目标是)评估 MBW 和肺活量计在检测与健康对照 (HC) 受试者相比,年轻 PCD 和 CF 患者轻度肺疾病的敏感性)比较疾病人群之间气道阻塞的模式。我们使用多中心、单次就诊、观察性研究,纳入了年龄在 3-12 岁之间 FEV 大于 60%预计值的 PCD 和 CF 患儿和 HC 受试者。进行了氮 MBW 和肺活量计检查,并进行了可接受性复查。组间比较采用 χ 和 Kruskal-Wallis 检验,比较人口统计学和肺功能指标,线性回归评估疾病状态的影响,Spearman 秩相关系数比较 LCI 和肺活量计测量值。共纳入 25 名 PCD 患儿、49 名 CF 患儿和 80 名 HC 患儿,其中 17 名 PCD 患儿(68%)、36 名 CF 患儿(73%)和 53 名(66%)HC 患儿同时进行了可接受的肺活量计和 MBW 检查;这些患儿构成了分析队列。中位年龄为 9.0 岁(四分位距 [IQR],6.8-11.1)。17 名 PCD 患儿中有 10 名(59%)和 36 名 CF 患儿中有 21 名(58%)的 LCI 异常(大于 7.8),而 17 名 PCD 患儿中有 3 名(18%)和 36 名 CF 患儿中有 6 名(17%)的 FEV 异常。与 HC 受试者相比,PCD 和 CF 患者的 LCI 显著升高(几何均数比与 HC:PCD 1.27;95%置信区间 [CI],1.15-1.39;和 CF 1.24;95% CI,1.15-1.33])。与 CF 患儿相比,PCD 患儿的中期呼气流量 %预计值较低(62%[IQR,50-78%]与 85%[IQR,68-99%];=0.05)。LCI 与 FEV 无相关性。LCI 比 FEV 更能敏感地检测年轻 PCD 患者的肺疾病,与 CF 相似。LCI 有望成为评估早期 PCD 肺疾病的敏感终点。

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