纤维化间质性肺疾病的亚临床右室功能障碍:斑点追踪和三维超声心动图的联合评估

A. Canora, A. Buonauro, P. Dolce, C. Nicoletta, Giacomo Ghinassi, Emanuele Ciasullo, A. Zamparelli, M. Galderisi, M. Bocchino
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引用次数: 0

摘要

背景:对于间质性肺疾病(ILD)患者的亚临床右心室(RV)受累知之甚少。我们的研究旨在通过标准超声心动图和高级超声心动图评估这种临床情况下的早期右心室功能障碍。方法:60例纤维化性ILD患者,其中30例为特发性肺纤维化(IPF),无心力衰竭,20例为年龄和性别匹配的健康受试者,采用标准、斑点跟踪和实时右心室3D超声心动图。所有患者还进行了完整的肺功能检查。结果:ILD患者的收缩压(sPAP)明显高于对照组(IPF与无IPF之间无差异)(p结论:通过斑点追踪可以检测到ILD患者的亚临床RV功能障碍。尽管在非IPF患者中sPAP和3D RVEF相当,但RV GLS、RV SLS和RV LLS的损伤在IPF患者中更为突出,并且与气体传递呈负相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subclinical right ventricular dysfunction in fibrotic interstitial lung diseases: a combined assessment by speckle tracking and three-dimensional echocardiography
Background: Little is known about subclinical right ventricle(RV) involvement in interstitial lung disease (ILD)patients. Our study aimed at evaluating early RV dysfunction by standard and advanced echocardiography in this clinical scenario. Methods: Sixty fibrotic ILD patients, including 30 cases affected by idiopathic pulmonary fibrosis(IPF), without heart failure and 20 age- and sex-matched healthy subjects underwent standard, speckle tracking and real time 3D echocardiography of the right ventricle. All patients also performed complete lung function testing. Results: Systolic pulmonary arterial pressure (sPAP) was significantly higher in ILD patients (with no differences between IPF and no-IPF) than in controls (p Conclusions: A subclinical RV dysfunction is detectable by speckle tracking in ILD patients. The impairment of RV GLS, RV SLS and RV LLS is more prominent in IPF patients and inversely correlates with gas transfer, despite comparable sPAP and 3D RVEF in no-IPF cases.
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