Farrell Christine, Balasubramanian Aparna, Hays Allison G, Hsu Steven, Rowe Steven, Zimmerman Stefan L, Hassoun Paul M, Mathai Stephen C, Mukherjee Monica
Division of Medicine, Johns Hopkins University, Baltimore, MD, United States.
Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, Baltimore, MD, United States.
Front Cardiovasc Med. 2022 Jan 18;8:794706. doi: 10.3389/fcvm.2021.794706. eCollection 2021.
Pulmonary hypertension (PH) is a clinical condition characterized by progressive elevations in mean pulmonary artery pressures and right ventricular dysfunction, associated with significant morbidity and mortality. For resting PH to develop, ~50-70% of the pulmonary vasculature must be affected, suggesting that even mild hemodynamic abnormalities are representative of advanced pulmonary vascular disease. The definitive diagnosis of PH is based upon hemodynamics measured by right heart catheterization; however this is an invasive and resource intense study. Early identification of pulmonary vascular disease offers the opportunity to improve outcomes by instituting therapies that slow, reverse, or potentially prevent this devastating disease. Multimodality imaging, including non-invasive modalities such as echocardiography, computed tomography, ventilation perfusion scans, and cardiac magnetic resonance imaging, has emerged as an integral tool for screening, classifying, prognosticating, and monitoring response to therapy in PH. Additionally, novel imaging modalities such as echocardiographic strain imaging, 3D echocardiography, dual energy CT, FDG-PET, and 4D flow MRI are actively being investigated to assess the severity of right ventricular dysfunction in PH. In this review, we will describe the utility and clinical application of multimodality imaging techniques across PH subtypes as it pertains to screening and monitoring of PH.
肺动脉高压(PH)是一种临床病症,其特征为平均肺动脉压逐渐升高以及右心室功能障碍,伴有显著的发病率和死亡率。要发生静息性PH,约50 - 70%的肺血管系统必须受到影响,这表明即使是轻微的血流动力学异常也代表着晚期肺血管疾病。PH的确诊基于右心导管检查所测量的血流动力学;然而,这是一项侵入性且资源消耗大的检查。早期识别肺血管疾病为通过实施减缓、逆转或潜在预防这种毁灭性疾病的治疗来改善预后提供了机会。多模态成像,包括超声心动图、计算机断层扫描、通气灌注扫描和心脏磁共振成像等非侵入性模态,已成为PH筛查、分类、预后评估及监测治疗反应的重要工具。此外,诸如超声心动图应变成像、三维超声心动图、双能CT、氟代脱氧葡萄糖正电子发射断层显像(FDG - PET)和四维血流磁共振成像(4D flow MRI)等新型成像模态正在积极研究中,以评估PH中右心室功能障碍的严重程度。在本综述中,我们将描述多模态成像技术在各类PH亚型中的应用及临床用途,因为它与PH的筛查和监测相关。