利用右心室等容松弛时间估计肺动脉收缩压升高

A. Arke, P. M. Babu, A. Borkar
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引用次数: 0

摘要

超声心动图估计肺动脉高压(PH)在没有三尖瓣反流(TR)仍然是一个挑战。多普勒组织成像(DTI)测量的等容松弛时间(IVRT)是估计PH的有效方法。本研究旨在评估右心室(RV) IVRT预测PH的可行性和准确性。我们对90例连续怀疑或已知患有肺动脉高压(PH)的患者进行了分析性横断面研究。利用伯努利方程利用TR射流速度评估sPAP。采用组织多普勒成像计算RV - IVRT。在90例连续患者中,49例(54.4%)为女性,平均年龄为48 +/- 14岁,平均收缩压(sPAP)为68.25+/- 29.15 mmHg。RV平均IVRT为67.29±22.2 msec。我们发现,IVRT与肺收缩压之间有很强的相关性(r = 0.69, P < 0.0001), 43 ms的临界值预测sPAP升高(≥39 mm Hg)的敏感性和特异性分别为89%和93%。然而,在RV功能障碍和RA平均压力升高的情况下,这种相关性降低。用DTI法计算IVRT是一种简单可行的方法。它与sPAP有很好的相关性。它是一种有用的超声心动图参数,可用于筛选有PH风险的患者,监测疾病进展和PH治疗效果,特别是在没有TR的患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimation of Elevated Systolic Pulmonary Artery Pressure Using Right Ventricular Isovolumic Relaxation Time
Echocardiographic estimation of pulmonary hypertension (PH) in absence of tricuspid regurgitation (TR) remains a challenge. Isovolumic relaxation time (IVRT) measured by Doppler tissue imaging (DTI) can be a useful method to estimate PH. This study was designed to evaluate the feasibility and accuracy of the right ventricle (RV) IVRT for predicting PH. We conducted an analytical cross-sectional study in 90 consecutive patients suspected or known to have pulmonary hypertension (PH). sPAP was assessed using TR jet velocity using a Bernoulli’s equation. RV IVRT was calculated using tissue Doppler imaging. Out of the 90 consecutive patients [49 (54.4%) were female, mean age was 48 +/- 14 years and mean systolic pulmonary aretry pressure (sPAP) was 68.25+/- 29.15 mmHg. Mean RV IVRT was 67.29 ± 22.2 msec. We found a strong correlation between IVRT and systolic pulmonary pressure (r = 0.69, P < 0.0001) and a cutoff of 43 ms showed a sensitivity and specificity of 89% and 93%, respectively, for the prediction of elevated sPAP (≥39 mm Hg). However, this correlation reduces in the presence of RV dysfunction and elevated mean RA pressure. The calculation of IVRT by DTI is a simple and feasible method. It correlates well with sPAP. It is a useful echocardiographic parameter as a screening in patients at risk for PH, monitoring the disease progression and the effect of the treatment for PH, especially in patients with absent TR.
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