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首页> 外文期刊>Lung >Volumetric Capnography for the Evaluation of Pulmonary Disease in Adult Patients with Cystic Fibrosis and Noncystic Fibrosis Bronchiectasis
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Volumetric Capnography for the Evaluation of Pulmonary Disease in Adult Patients with Cystic Fibrosis and Noncystic Fibrosis Bronchiectasis

机译:容量二氧化碳图评估成年囊性纤维化和非囊性纤维化支气管扩张症患者的肺部疾病

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摘要

This study was designed to use volumetric capnography to evaluate the breathing pattern and ventilation inhomogeneities in patients with chronic sputum production and bronchiectasis and to correlate the phase 3 slope of the capnographic curve to spirometric measurements. Twenty-four patients with cystic fibrosis (CF) and 21 patients with noncystic fibrosis idiopathic bronchiectasis (BC) were serially enrolled. The diagnosis of cystic fibrosis was based on the finding of at least two abnormal sweat chloride concentrations (iontophoresis sweat test). The diagnosis of bronchiectasis was made when the patient had a complaint of chronic sputum production and compatible findings at high-resolution computed tomography (HRCT) scan of the thorax. Spirometric tests and volumetric capnography were performed. The 114 subjects of the control group for capnographic variables were nonsmoker volunteers, who had no respiratory symptoms whatsoever and no past or present history of lung disease. Compared with controls, patients in CF group had lower SpO2 (P < 0.0001), higher respiratory rates (RR) (P < 0.0001), smaller expiratory volumes normalized for weight (VE/kg) (P < 0.028), smaller expiratory times (Te) (P < 0.0001), and greater phase 3 Slopes normalized for tidal volume (P3Slp/VE) (P < 0.0001). Compared with controls, patients in the BC group had lower SpO2 (P < 0.0001), higher RR (P < 0.004), smaller VE/kg (P < 0.04), smaller Te (P < 0.007), greater P3Slp/VE (P < 0.0001), and smaller VCO2 (P < 0.0002). The pooled data from the two patient groups compared with controls showed that the patients had lower SpO2 (P < 0.0001), higher RR (P < 0.0001), smaller VE/kg (P < 0.05), smaller Te (P < 0.0001), greater P3Slp/VE (P < 0.0001), and smaller VCO2 (P < 0.0003). All of the capnographic and spirometric variables evaluated showed no significant differences between CF and BC patients. Spirometric data in this study reveals that the patients had obstructive defects with concomitant low vital capacities and both groups had very similar abnormalities. The capnographic variables in the patient group suggest a restrictive respiratory pattern (greater respiratory rates, smaller expiratory times and expiratory volumes, normal peak expiratory flows). Both groups of patients showed increased phase III slopes compared with controls, which probably indicates the presence of diffuse disease of small airways in both conditions leading to inhomogeneities of ventilation.
机译:这项研究旨在使用容积二氧化碳分析来评估慢性痰液生成和支气管扩张患者的呼吸模式和通气不均匀性,并将二氧化碳分析曲线的3期斜率与肺活量测定法相关联。连续招募了24例囊性纤维化(CF)患者和21例非囊性纤维化特发性支气管扩张(BC)患者。囊性纤维化的诊断是基于至少发现两个异常的汗液氯化物浓度异常(离子电渗疗法汗液测试)。支气管扩张的诊断是在患者对慢性痰产生有抱怨并在胸部高分辨计算机断层扫描(HRCT)扫描中发现相符的发现时做出的。进行肺活量测试和容积二氧化碳图。二氧化碳分析对照组的114名受试者是不吸烟的志愿者,他们没有呼吸道症状,也没有过去或现在的肺病史。与对照组相比,CF组患者的SpO 2 较低(P <0.0001),呼吸频率(RR)较高(P <0.0001),呼气量按体重归一化(V E < / sub> / kg)(P <0.028),较小的呼气时间(Te)(P <0.0001)和较大的第3阶段坡度,已将潮气量归一化(P3Slp / V E )(P <0.0001 )。与对照组相比,BC组患者的SpO 2 较低(P <0.0001),RR较高(P <0.004),V E / kg较小(P <0.04) ),较小的Te(P <0.007),较大的P3Slp / V E (P <0.0001)和较小的VCO 2 (P <0.0002)。两组患者与对照组相比的汇总数据显示,患者的SpO 2 较低(P <0.0001),RR较高(P <0.0001),V E 较小/ kg(P <0.05),较小的Te(P <0.0001),较大的P3Slp / V E (P <0.0001)和较小的VCO 2 (P <0.0003) 。评估的所有二氧化碳图和肺量计变量均显示CF和BC患者之间无显着差异。这项研究的肺活量测定数据表明,患者存在阻塞性缺陷,伴随着低肺活量,并且两组患者的异常情况非常相似。患者组中的二氧化碳描记变量表明呼吸模式受限(较大的呼吸频率,较小的呼气时间和呼气量,正常的呼气峰值流量)。两组患者的III期斜率均高于对照组,这可能表明在两种情况下都存在小气道弥漫性疾病,导致通气不均匀。

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