特发性肺动脉高压患者的右心室表型。

IF 6.4 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Heart and Lung Transplantation Pub Date : 2024-06-26 DOI:10.1016/j.healun.2024.06.003
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引用次数: 0

摘要

背景:右心室(RV)成像在肺动脉高压(PAH)患者的风险分层中并没有明确的作用。我们测试了一个假设,即超声心动图得出的表型描述了不同程度的右心室重塑和功能障碍,可为当前的风险分层工具提供额外的预后信息:2005年1月至2021年12月期间确诊的年龄≥18岁的连续发病PAH患者接受临床评估、右心导管检查和标准超声心动图检查。结合简单的超声心动图变量,先验地定义了四种表型,分别代表不同程度的 RV 扩张和 RV-肺动脉(PA)耦合:表型1:右心室轻度扩张,RV-PA耦合保留(152例患者);表型2:右心室轻度扩张,RV-PA耦合不良(143例患者);表型3:右心室严重扩张,RV-PA耦合保留(201例患者);表型4:右心室严重扩张,RV-PA耦合不良,伴有或不伴有严重三尖瓣反流(519例患者)。风险分层基于ESC/ERS三层模型和REVEAL 2.0评分:所有风险组均存在这些表型。值得注意的是,无论患者的ESC/ERS风险分层如何,表型4都与死亡几率增加2倍相关(HR 2.1,95% C.I.1.6-2.8,p结论:描述 RV 重塑和功能障碍的超声心动图表型可提供独立于临床定义的 PAH 患者风险之外的预后信息。
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Right ventricular phenotyping in incident patients with idiopathic pulmonary arterial hypertension

Background

Right ventricular (RV) imaging has not a definite role in risk stratification of pulmonary arterial hypertension (PAH) patients. We tested the hypothesis that echocardiography-derived phenotypes, depicting different degrees of RV remodeling and dysfunction, may provide additional prognostic information to current risk stratification tools.

Methods

Consecutive incident PAH patients aged ≥18 years, diagnosed between January 2005 and December 2021, underwent clinical assessment, right heart catheterization, standard echocardiography. Simple echocardiographic variables were combined in order to define a priori four phenotypes representing different degrees of RV dilatation and RV-pulmonary arterial (PA) coupling: Phenotype 1 with mildy dilated right ventricle and preserved RV-PA coupling (n = 152 patients); phenotype 2 with mildly dilated right ventricle and poor RV-PA coupling (n = 143 patients); phenotype 3 with severely dilated right ventricle and preserved RV-PA coupling (n = 201 patients); phenotype 4 with severely dilated right ventricle and poor RV-PA coupling, with or without severe tricuspid regurgitation (n = 519 patients). Risk stratification was based on the European Society of Cardiology/European Respiratory Society (ESC/ERS) 3-strata model and Registry to Evaluate Early and Long-Term PAH disease Management (REVEAL) 2.0 score.

Results

These phenotypes were present in all risk groups. Notably, regardless of the ESC/ERS risk stratum assigned to the patient, phenotype 4 was associated with a 2-fold increase of the odds of death (HR 2.1, 95% CI 1.6–2.8, p < 0.001), while phenotype 1 was associated with a 71% reduction in the odds of dying (HR 0.29, 95% CI 0.18–0.47, p < 0.001).

Conclusions

Echocardiography-derived phenotypes describing RV remodeling and dysfunction may provide prognostic information which is independent of and additional to the clinically defined risk in incident PAH patients.

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来源期刊
CiteScore
10.10
自引率
6.70%
发文量
1667
审稿时长
69 days
期刊介绍: The Journal of Heart and Lung Transplantation, the official publication of the International Society for Heart and Lung Transplantation, brings readers essential scholarly and timely information in the field of cardio-pulmonary transplantation, mechanical and biological support of the failing heart, advanced lung disease (including pulmonary vascular disease) and cell replacement therapy. Importantly, the journal also serves as a medium of communication of pre-clinical sciences in all these rapidly expanding areas.
期刊最新文献
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