Division of Pulmonary Medicine and Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan ROC.
School of Medicine, Chung Shan Medical University, Taichung, Taiwan ROC.
Ann Med. 2023 Dec;55(1):2228696. doi: 10.1080/07853890.2023.2228696.
Restrictive ventilatory defects and elevated pulmonary artery pressure (PAP) are common in patients with chronic heart failure (CHF) and those with interstitial lung disease (ILD). However, as oxyhemoglobin desaturation seldom occurs in stable CHF patients at peak exercise, we hypothesized that the pathophysiology may be different between them. This study aimed to investigate: (1) PAP and lung function at rest, (2) pulmonary gas exchange (PGX) and breathing patterns at peak exercise, (3) mechanisms of dyspnea at peak exercise in patients with CHF compared to healthy subjects and ILD patients.
We consecutively enrolled 83 participants (27 with CHF, 23 with ILD, and 33 healthy controls). The CHF and ILD groups had similar functional status. Lung function and cardiopulmonary exercise tests with Borg Dyspnea Score were performed. PAP was estimated using echocardiography. Resting lung function, PAP and peak exercise data in the CHF group were compared to the healthy and ILD groups. Correlation analysis was performed to elucidate the mechanisms of dyspnea in the CHF and ILD groups.
Compared to the healthy group, the CHF group had normal lung function, PAP at rest, and normal dyspnea score and PGX at peak exercise, whereas the ILD group had abnormal values compared to the CHF group. Dyspnea score was positively correlated with pressure gradient, lung expansion capabilities, and expiratory tidal flow in the CHF group (all < 0.05), but inversely correlated with inspiratory time-related variables in the ILD group (all < 0.05).
Normal lung function and PAP at rest, and dyspnea scores and PGX at peak exercise indicated that pulmonary hypertension and fibrosis were insignificant in the patients with CHF. The factors affecting dyspnea at peak exercise were different between the CHF and ILD groups. As the sample size in this study was small, large-scale studies are warranted to confirm our findings.
慢性心力衰竭(CHF)和间质性肺疾病(ILD)患者常出现限制性通气缺陷和肺动脉高压(PAP)。然而,由于稳定期 CHF 患者在运动峰值很少出现氧合血红蛋白饱和度降低,我们假设它们的病理生理学可能不同。本研究旨在探讨:(1)静息时的 PAP 和肺功能;(2)运动峰值时的肺气体交换(PGX)和呼吸模式;(3)与健康受试者和 ILD 患者相比,CHF 患者运动峰值时呼吸困难的机制。
我们连续纳入 83 名参与者(27 名 CHF 患者、23 名 ILD 患者和 33 名健康对照者)。CHF 和 ILD 组的功能状态相似。进行肺功能和心肺运动试验,同时记录 Borg 呼吸困难评分。使用超声心动图估计 PAP。将 CHF 组的静息肺功能、PAP 和运动峰值数据与健康组和 ILD 组进行比较。进行相关性分析以阐明 CHF 和 ILD 组呼吸困难的机制。
与健康组相比,CHF 组静息时肺功能、PAP 正常,运动峰值时呼吸困难评分和 PGX 正常,而 ILD 组与 CHF 组相比各项指标异常。CHF 组呼吸困难评分与压力梯度、肺扩张能力和呼气潮流量呈正相关(均 P<0.05),而与 ILD 组吸气时间相关变量呈负相关(均 P<0.05)。
静息时肺功能和 PAP 正常,运动峰值时呼吸困难评分和 PGX 正常,表明 CHF 患者的肺动脉高压和肺纤维化不明显。影响运动峰值时呼吸困难的因素在 CHF 和 ILD 组之间不同。由于本研究的样本量较小,需要进行大规模研究来证实我们的发现。