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超声心动图评估肺动脉高压右心功能参数的最佳组合。

Optimal combination of right ventricular functional parameters using echocardiography in pulmonary arterial hypertension.

机构信息

National Key Laboratory for Innovation and Transformation of Luobing Theory, Shandong University, Jinan, China.

The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education, Chinese National Health Commission and Chinese Academy of Medical Sciences, Jinan, China.

出版信息

ESC Heart Fail. 2024 Oct;11(5):2694-2706. doi: 10.1002/ehf2.14752. Epub 2024 Mar 15.

Abstract

AIMS

Novel echocardiographic parameters of right ventricular (RV) function, including speckle-tracking-derived, three-dimensional, and RV-pulmonary artery coupling parameters, have emerged for the evaluation of pulmonary arterial hypertension (PAH). The relative role of these parameters in the risk stratification of PAH patients is unclear. We compared the performance of multiple RV parameters and sought to establish an optimal model for identifying the risk profile of patients with PAH.

METHODS AND RESULTS

Comprehensive risk assessments were performed for 70 patients with PAH. The risk profile of every patient was determined based on the guideline recommendations. Conventional parameters, including fractional area change (FAC) and tricuspid annular plane systolic excursion (TAPSE), novel speckle-tracking-derived RV longitudinal strain (RVLS), and three-dimensional RV ejection fraction (3D-RVEF), were used to evaluate RV function. Pressure-strain loops were measured for the assessment of RV myocardial work, including RV global wasted work (RVGWW). RV-pulmonary artery coupling was assessed by indexing RV parameters to the estimated pulmonary artery systolic pressure (PASP). The median age was 34 (30-43) years, and 62 (88.6%) patients were female. Forty-five patients were classified into the low-risk group, while 25 patients were classified into the intermediate-high-risk group. Most RV parameters could be used to determine the risk profile and exhibited significantly improved diagnostic performance after indexing to PASP (including FAC/PASP, TAPSE/PASP, and 3D-RVEF/PASP). RVLS/PASP showed the best performance, with an area under the curve of 0.895. In multivariate analysis (Model 1), only RVGWW (>90.5 mmHg%), RVLS (> -16.7%), and TAPSE (<17.5 mm) remained significant (all P < 0.05). Model 1 outperformed every single RV parameter, with a significantly larger area under the curve (all P < 0.05). With PASP indexing in Model 2, RVLS/PASP > -0.275 [odds ratio (OR) 20.63, 95% confidence interval (CI) 4.62-92.11, P < 0.001] and RVGWW > 90.5 mmHg% (OR 6.17, 95% CI 1.37-27.76, P = 0.018) independently identified a higher risk profile. The addition of RVGWW to two models determined incremental value in identification (continuous net reclassification improvement 1.058, 95% CI 0.639-1.477, P < 0.001).

CONCLUSIONS

The combination models for RV function outperformed any single parameter in identifying the risk profile of patients with PAH. Comprehensive assessment of RV-pulmonary artery coupling using multiparametric methods is clinically meaningful in patients with PAH.

摘要

目的

新型超声心动图右心室(RV)功能参数,包括斑点追踪衍生的三维和 RV-肺动脉偶联参数,已用于评估肺动脉高压(PAH)。这些参数在 PAH 患者危险分层中的相对作用尚不清楚。我们比较了多种 RV 参数的性能,并试图建立一个最佳模型来识别 PAH 患者的风险特征。

方法和结果

对 70 例 PAH 患者进行了全面的风险评估。根据指南建议确定每位患者的风险特征。使用常规参数,包括分数面积变化(FAC)和三尖瓣环平面收缩期位移(TAPSE)、新型斑点追踪衍生 RV 纵向应变(RVLS)和三维 RV 射血分数(3D-RVEF)评估 RV 功能。测量压力-应变环评估 RV 心肌做功,包括 RV 整体浪费功(RVGWW)。通过将 RV 参数与估计的肺动脉收缩压(PASP)指数化来评估 RV-肺动脉偶联。中位年龄为 34(30-43)岁,62(88.6%)例患者为女性。45 例患者被分类为低危组,25 例患者被分类为中高危组。大多数 RV 参数可用于确定风险特征,并在索引至 PASP 后显示出明显改善的诊断性能(包括 FAC/PASP、TAPSE/PASP 和 3D-RVEF/PASP)。RVLS/PASP 表现最佳,曲线下面积为 0.895。多变量分析(模型 1)中,只有 RVGWW(>90.5mmHg%)、RVLS(>-16.7%)和 TAPSE(<17.5mm)仍然具有显著意义(均 P<0.05)。模型 1 优于每个单独的 RV 参数,曲线下面积显著增大(均 P<0.05)。在模型 2 中进行 PASP 指数化后,RVLS/PASP>-0.275[比值比(OR)20.63,95%置信区间(CI)4.62-92.11,P<0.001]和 RVGWW>90.5mmHg%(OR 6.17,95%CI 1.37-27.76,P=0.018)独立识别出更高的风险特征。将 RVGWW 加入到两个模型中,确定了识别的增量价值(连续净重新分类改善 1.058,95%CI 0.639-1.477,P<0.001)。

结论

RV 功能联合模型在识别 PAH 患者的风险特征方面优于任何单个参数。使用多参数方法综合评估 RV-肺动脉偶联在 PAH 患者中具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3c8/11424360/5b72c656b987/EHF2-11-2694-g002.jpg

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