Circulation Journal
Online ISSN : 1347-4820
Print ISSN : 1346-9843
ISSN-L : 1346-9843
Letters to the Editor
Pulmonary Vascular Resistance in Patients With Pulmonary Hypertension: Importance of the Quadratic Velocity-Pressure Relationship – Reply –
Stéphane DoutreleauMatthieu CanuetIrina EnachePaola Di MarcoAnne Charloux
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2016 Volume 80 Issue 12 Pages 2563-2564

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We thank Dr Abbas for his critical reading of our paper recently published in the Journal.1 A number of articles have been published by Abbas and others on both the non-invasive determination and the prognostic value of pulmonary vascular resistance (PVR) in patients with pulmonary hypertension (PH).26 All of them noted a reduced accuracy and precision of PVR determined on echocardiography (PVRECHO), especially in patients with PVR >6 Wood units (WU). Most studies also determined cut-offs for normal or elevated PVR but, to the best of our knowledge, no equation was deemed to be suitable for an accurate and precise determination of absolute PVR.

Dr Abbas suggested that the use of the updated equation would have been more precise and accurate.2 The aim of the study was to compare several equations. We chose the initial equation published in 2003 (TRV/RVOTTVI×10)7 because it is used daily in echocardiographic laboratories in France. We tested other equations (including the one noted) but, given that the results were similar for the PVR calculations, we reported only some of them.

The cut-offs <0.175 and >0.275 for the tricuspid regurgitation velocity/right ventricle outflow tract velocity-time integral (TRV/RVOTTVI) ratio were used to repartition the original subjects, to distinguish PH with normal from elevated PVR (Figure 1). The majority of patients (65.2%) with TRV/RVOTTVI <0.175 had PVR >2 WU. For patients with TRV/RVOTTVI 0.175–0.275 (n=48), the use of the original equation (TRV/RVOTTVI×10) was globally poor (r=0.38, P=0.01; Figure 2), with a constant underestimation of PVR when the average (PVRRHC+PVRECHO) increased. Only 12 patients had TRV/RVOTTVI >0.275 (Figure 3). For those particular patients, PVRRHC was >6 WU in 8 of the 12 patients (66.7%). The equation TRV2/RVOTTVI×5, however, was not precise enough to calculate PVR, giving an underestimation when the average (PVRRHC+PVRECHO) increased. In the present subjects, TRV/RVOTTVI <0.175 was not suitable to exclude PVR >2 WU. TRV/RVOTTVI >0.275 was more sensitive and more accurately predicted elevated PVR >6 WU, but neither of the two equations was sufficiently accurate and precise with the echocardiography data.

Figure 1.

Repartition of the subjects according to tricuspid regurgitation velocity/right ventricle outflow tract velocity-time integral (TRV/RVOTTVI). PVR, pulmonary vascular resistance.

Figure 2.

(Left) Correlation between pulmonary vascular resistance (PVR) determined on right heart catheterization (PVRRHC) or echocardiography (PVRECHO), and (Right) Bland-Altman analysis of PVRECHO and PVRRHC in patients with tricuspid regurgitation velocity/right ventricle outflow tract velocity-time integral (TRV/RVOTTVI) 0.175–0.275. Red dotted lines, 95% limit of agreement. Continuous line, positive relationship between the two parameters.

Figure 3.

(Left) Correlation between pulmonary vascular resistance (PVR) determined on right heart catheterization (PVRRHC) or echocardiography (PVRECHO), and (Right) Bland-Altman analysis of PVRECHO and PVRRHC in patients with tricuspid regurgitation velocity/right ventricle outflow tract velocity-time integral (TRV/RVOTTVI) >0.275. Red dotted lines, 95% limit of agreement. Continuous line, positive relationship between the two parameters.

But is the determination of absolute PVR so important? We believe that it is, and in the last European guidelines, PVR (cut-off=3 WU) was included in the hemodynamic definition of pulmonary arterial hypertension.8 If, however, the variations in PVRECHO are similar (ie, in the same direction and with the same amplitude) to the changes in PVRRHC (regardless of the absolute value), echocardiography could play a more important role in the follow-up of PH. Further longitudinal studies with multiple assessments of both PVRECHO and PVRRHC are required.

  • Stéphane Doutreleau, MD, PhD
  • Matthieu Canuet, MD
  • Irina Enache, MD, PhD
  • Paola Di Marco, MD, PhD
  • Anne Charloux, MD, PhD
  • Department of Physiology, INSERM U1042, Grenoble (S.D.);
  • Department of Pneumology (M.C.),
  • Department of Physiology (I.E., P.D.M., A.C.), New Hospital, Strasbourg, France

(Released online November 9, 2016)

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© 2016 THE JAPANESE CIRCULATION SOCIETY
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