Classification and pathophysiology of pulmonary hypertension

J. R. Sysol, R. F. Machado
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引用次数: 32

Abstract

Pulmonary hypertension is a fatal disease of multiple etiologies that is estimated to affect over 100 million people worldwide. The disease is defined hemodynamically as a mean pulmonary artery pressure ≥ 25 mmHg at rest. Despite important advances in our understanding of the pathobiology of this disease and improvements in patient management, outcomes are still poor and no curative treatments are currently available. The complex nature of this disease requires detailed clinical evaluation for accurate diagnosis and treatment. Recent advances in clinical recognition, classification, and understanding of the underlying pathological processes in pulmonary hypertension have led to improved diagnostic testing and therapeutic options for patients. A hallmark of pulmonary hypertension is an increased pulmonary vascular resistance which leads to progressive elevations in pulmonary artery pressure, resulting in compensatory right ventricular hypertrophy and, ultimately, heart failure. Clinically, these pulmonary vascular changes initially present as nonspecific symptoms, including unexplained dyspnea on exertion, fatigue, chest pain, and syncope. Signs of right ventricular dysfunction are also frequently present. Common pathogenic features of pulmonary hypertension include sustained pulmonary vasoconstriction, vascular remodeling of the small pulmonary arteries, in situ thrombosis, and increased vascular wall stiffness, resulting in increased pulmonary arterial pressure due to increased pulmonary vascular resistance. Despite improvements in clinical classification and understanding of the underlying pathogenic mechanisms of pulmonary hypertension, current therapies are limited to supportive care and targeting pulmonary vasoconstriction. There remains a need to identify novel therapeutic targets in this disease. This review provides a succinct overview of the clinical classification and pathophysiology of PH that can be used as a reference by physicians and physician-scientists.

Abstract Image

肺动脉高压的分型及病理生理
肺动脉高压是一种多种病因的致命疾病,据估计全世界有超过1亿人受到影响。该疾病的血流动力学定义为静息时平均肺动脉压≥25 mmHg。尽管我们对这种疾病的病理生物学和患者管理的理解取得了重要进展,但结果仍然很差,目前尚无治愈性治疗方法。这种疾病的复杂性需要详细的临床评估才能准确诊断和治疗。近年来,在肺动脉高压的临床认识、分类和对其病理过程的理解方面取得了进展,从而改善了患者的诊断测试和治疗选择。肺动脉高压的一个特征是肺血管阻力增加,导致肺动脉压进行性升高,导致代偿性右心室肥厚,最终导致心力衰竭。临床上,这些肺血管病变最初表现为非特异性症状,包括运动时不明原因的呼吸困难、疲劳、胸痛和晕厥。右心室功能障碍的迹象也经常出现。肺动脉高压的常见致病特征包括持续的肺血管收缩,肺动脉小动脉血管重塑,原位血栓形成,血管壁硬度增加,由于肺血管阻力增加导致肺动脉压力升高。尽管临床分类和对肺动脉高压潜在致病机制的了解有所改善,但目前的治疗仅限于支持性护理和针对肺血管收缩的治疗。仍然需要确定这种疾病的新的治疗靶点。本文综述了PH的临床分类和病理生理学的简要概述,可作为医生和医学家的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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