Key result
Mitral valve area estimation using 3D PISA showed strong correlation with 3D planimetry (rho=0.78, P<0.0001) and better agreement than 2D methods (mean difference -0.03 cm2).
Why the study?
Does 3D PISA improve the accuracy of mitral valve area estimation compared to 2D methods in patients with rheumatic mitral stenosis?
Observational (n=27)
Does 3D PISA improve the accuracy of mitral valve area estimation compared to 2D methods in patients with rheumatic mitral stenosis?
Effect estimate: rho=0.78
p-value: p=<.0001
3D PISA is a feasible and more accurate method for estimating mitral valve area in rheumatic mitral stenosis compared to conventional 2D echocardiographic methods.
May support 3D PISA for MVA estimation in rheumatic MS; leaves open need for prospective validation before practice change.
Purpose Management of patients with mitral stenosis ( MS ) depends heavily on the accurate quantification of mitral valve area ( MVA ) using echocardiography. All currently used two‐dimensional (2D) methods have limitations. Estimation of MVA using the proximal isovelocity surface area ( PISA ) method with real time three‐dimensional (3D) echocardiography may circumvent those limitations. We aimed to evaluate the accuracy of 3D direct measurement of PISA in the estimation of MVA . Methods Twenty‐seven consecutive patients (median age of 63 years; 77.8% females) with rheumatic MS were prospectively studied. Transthoracic and transesophageal echocardiography with 2D and 3D acquisitions were performed on the same day. The reference method for MVA quantification was valve planimetry after 3D‐volume multiplanar reconstruction. A semi‐automated software was used to calculate the 3D flow convergence volume. Results Compared to MVA estimation using 3D planimetry, 3D PISA showed the best correlation (rho=0.78, P <.0001), followed by pressure half‐time ( PHT : rho=0.66, P <.001), continuity equation ( CE : rho=0.61, P =.003), and 2D PISA (rho=0.26, P =.203). Bland‐Altman analysis revealed a good agreement for MVA estimation with 3D PISA (mean difference −0.03 cm 2 ; limits of agreement ( LOA ) −0.40–0.35), in contrast to wider LOA for 2D methods: CE (mean difference 0.02 cm 2 , LOA −0.56–0.60); PHT (mean difference 0.31 cm 2 , LOA −0.32–0.95); 2D PISA (mean difference −0.03 cm 2 , LOA −0.92–0.86). Conclusions MVA estimation using 3D PISA was feasible and more accurate than 2D methods. Its introduction in daily clinical practice seems possible and may overcome technical limitations of 2D methods.
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Sampaio et al. (2017) conducted an observational in rheumatic mitral stenosis (n=27). 3D proximal isovelocity surface area (PISA) vs. 2D methods and 3D planimetry was evaluated on Correlation of MVA estimation with 3D planimetry (rho=0.78, p=<.0001). Mitral valve area estimation using 3D PISA showed strong correlation with 3D planimetry (rho=0.78, P<0.0001) and better agreement than 2D methods (mean difference -0.03 cm2).
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