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合并性肺纤维化和肺气肿:同居如何影响呼吸功能?

Combined pulmonary fibrosis and emphysema: How does cohabitation affect respiratory functions?

机构信息

Department of Chest Disease, Ankara University School of Medicine, Ankara, Turkey.

Department of Radiology, Ankara University School of Medicine, Ankara, Turkey.

出版信息

Adv Med Sci. 2019 Sep;64(2):285-291. doi: 10.1016/j.advms.2019.03.005. Epub 2019 Apr 1.

DOI:10.1016/j.advms.2019.03.005
PMID:30947142
Abstract

PURPOSE

Combined pulmonary fibrosis and emphysema (CPFE) has emerged as a new syndrome with characteristics of both fibrosis and emphysema. We determined the impacts of radiologic emphysema severity on pulmonary function tests (PFTs), exercise capacity and mortality.

PATIENTS AND METHODS

IPF patients (n = 110) diagnosed at the Chest Diseases Clinic between September 2013 and January 2016 were enrolled in the study and followed up until June 2017. Visual and digital emphysema scores, PFTs, pulmonary artery pressure (sPAP), 6-minute walking test, composite physiologic index (CPI), and survival status were recorded. Patients with emphysema and those with pure IPF were compared.

RESULTS

The CPFE-group had a significantly greater ratio of men(p < 0.001), lower BMI (p < 0.001), lower mean PaO (p = 0.005), higher mean sPAP (p = 0.014), and higher exercise desaturation (p < 0.001). The CPFE group had a significantly higher FVC(L)(p = 0.016), and lower FEV1/FVC ratio (p = 0.002), DLCO, and DLCO/VA ratio(p = 0.03 and p = 0.005, respectively). Lung volumes of the CPFE group had significantly higher VC(p = 0.017), FRC (p < 0.001), RV(p < 0.001), RV/TLC(p < 0.001), and TLC(p < 0.001). There were significant correlations between emphysema scores and FVC (L)(p = 0.01), FEV1/FVC(p = 0.001), DLCO (p = 0.003), VC(p = 0.014), FRC (L)(p < 0.001), RV(p < 0.001), TLC(p < 0.001), and RV/TLC (p < 0.001). Mortality rates were comparable between the two groups. CPI (p = 0.02) and sPAP (p = 0.01) were independent predictors of mortality in patients with CPFE.

CONCLUSIONS

The presence and severity of emphysema affects pulmonary function in IPF. Patients with CPFE have reduced diffusion capacity, more severe air trapping, worse muscle weakness, more severe exercise desaturation, and pulmonary hypertension. CPI and pulmonary hypertension are two independent risk factors for mortality in subjects with CPFE.

摘要

目的

肺纤维化合并肺气肿(CPFE)是一种具有纤维化和肺气肿特征的新综合征。我们确定了影像学肺气肿严重程度对肺功能测试(PFT)、运动能力和死亡率的影响。

方法

2013 年 9 月至 2016 年 1 月在胸科疾病诊所诊断为特发性肺纤维化(IPF)的患者(n=110)纳入研究,并随访至 2017 年 6 月。记录视觉和数字肺气肿评分、PFT、肺动脉压(sPAP)、6 分钟步行试验、综合生理指数(CPI)和生存状态。比较有肺气肿和单纯 IPF 的患者。

结果

CPFE 组男性比例显著更高(p<0.001)、BMI 更低(p<0.001)、平均 PaO 更低(p=0.005)、平均 sPAP 更高(p=0.014)、运动性血氧饱和度下降更明显(p<0.001)。CPFE 组 FVC(L)显著更高(p=0.016)、FEV1/FVC 比值显著更低(p=0.002)、DLCO 和 DLCO/VA 比值显著更低(p=0.03 和 p=0.005)。CPFE 组的肺容积 VC 显著更高(p=0.017)、FRC 显著更高(p<0.001)、RV 显著更高(p<0.001)、RV/TLC 显著更高(p<0.001)、TLC 显著更高(p<0.001)。肺气肿评分与 FVC(L)(p=0.01)、FEV1/FVC(p=0.001)、DLCO(p=0.003)、VC(p=0.014)、FRC(L)(p<0.001)、RV(p<0.001)、TLC(p<0.001)和 RV/TLC(p<0.001)显著相关。两组死亡率相当。CPI(p=0.02)和 sPAP(p=0.01)是 CPFE 患者死亡的独立预测因素。

结论

肺气肿的存在和严重程度影响 IPF 的肺功能。CPFE 患者弥散能力降低、空气潴留更严重、肌肉无力更严重、运动性血氧饱和度下降更明显、肺动脉压更高。CPI 和肺动脉高压是 CPFE 患者死亡的两个独立危险因素。

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