Noninvasive Assessment of Pulmonary Vascular Resistance by Doppler Echocardiography

被引:136
作者
Abbas, Amr E. [1 ,2 ]
Franey, Laura M. [1 ]
Marwick, Thomas [3 ]
Maeder, Micha T. [4 ,5 ,6 ]
Kaye, David M. [4 ,5 ]
Vlahos, Antonios P. [7 ]
Serra, Walter [8 ]
Al-Azizi, Karim [9 ]
Schiller, Nelson B. [10 ]
Lester, Steven J. [11 ]
机构
[1] Beaumont Hlth Syst, Dept Cardiol, Royal Oak, MI 48073 USA
[2] Oakland Univ, William Beaumont Sch Med, Rochester, MI 48063 USA
[3] Menzies Res Inst Tasmania, Hobart, Tas, Australia
[4] Baker IDI Heart & Diabet Inst, Melbourne, Vic, Australia
[5] Alfred Hosp, Ctr Heart, Melbourne, Vic, Australia
[6] Kantonsspital, Div Cardiol, St Gallen, Switzerland
[7] Univ Ioannina, Div Pediat Cardiol, GR-45110 Ioannina, Greece
[8] Univ Hosp, Cardiopulm Dept, Parma, Italy
[9] St Joseph Mercy Oakland, Dept Internal Med, Pontiac, MI USA
[10] Univ San Francisco, San Francisco, CA 94117 USA
[11] Mayo Clin, Div Cardiovasc Dis, Scottsdale, AZ USA
关键词
Pulmonary vascular resistance; Doppler echocardiography; Pulmonary hypertension; CONGENITAL HEART-DISEASE; CORONARY-ARTERY-DISEASE; SYSTEMIC-SCLEROSIS; HYPERTENSION; PRESSURE; ECHO; ACCURACY; FAILURE; FLOW;
D O I
10.1016/j.echo.2013.06.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The ratio of tricuspid regurgitation velocity (TRV) to the time-velocity integral of the right ventricular outflow tract (TVIRVOT) has been studied as a reliable measure to distinguish elevated from normal pulmonary vascular resistance (PVR). The equation TRV/TVIRVOT x 10 + 0.16 (PVRecho) has been shown to provide a good noninvasive estimate of PVR. However, its role in patients with significantly elevated PVR (> 6 Wood units [WU]) has not been conclusively evaluated. The aim of this study was to establish the validity of the TRV/TVIRVOT ratio as a correlate of PVR. The role of TRV/TVIRVOT was also compared with that of a new ratio, TRV2/TVIRVOT, in patients with markedly elevated PVR (> 6 WU). Methods: Data from five validation studies using TRV/TVIRVOT as an estimate of PVR were compared with invasive PVR measurements (PVRcath). Multiple linear regression analyses were generated between PVRcath and both TRV/TVIRVOT and TRV2/TVIRVOT. Both PVRecho and a new derived regression equation based on TRV2/TVIRVOT: 5.19 x TRV2/TVIRVOT - 0.4 (PVRecho2) were compared with PVRcath using Bland-Altman analysis. Logistic models were generated, and cutoff values for both TRV/TVIRVOT and TRV2/TVIRVOT were obtained to predict PVR > 6 WU. Results: One hundred fifty patients remained in the final analysis. Linear regression analysis between PVRcath and TRV/TVIRVOT revealed a good correlation (r = 0.76, P <.0001, Z = 0.92). There was a better correlation between PVRcath and TRV2/TVIRVOT (r = 0.79, P <.0001, Z = -0.01) in the entire cohort as well as in patients with PVR > 6 WU. Moreover, PVRecho2 compared better with PVRcath than PVRecho using Bland-Altman analysis in the entire cohort and in patients with PVR > 6 WU. TRV2/TVIRVOT and TRV/TVIRVOT both predicted PVR > 6 WU with good sensitivity and specificity. Conclusions: TRV/TVIRVOT is a reliable method to identify patients with elevated PVR. In patients with TRV/TVIRVOT > 0.275, PVR is likely > 6 WU, and PVRecho2 derived from TRV2/TVIRVOT provides an improved noninvasive estimate of PVR compared with PVRecho.
引用
收藏
页码:1170 / 1177
页数:8
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