| Literature DB >> 30139798 |
C Bleakley1,2,3,4,5,6,7, M Eskandari1,2,3,4,5,6,7, O Aldalati1,2,3,4,5,6,7, K Monschonas1,2,3,4,5,6,7, M Huang1,2,3,4,5,6,7, A Whittaker1,2,3,4,5,6,7, M J Monaghan1,2,3,4,5,6,7.
Abstract
The mitral valve orifice area (MVOA) is difficult to assess accurately by 2D echocardiography because of geometric assumptions, therefore 3D planimetry may offer advantages. We studied differences in MVOA measurements and prediction of clinical outcomes between 2D and 3D methods. Methods This was a head to head comparison of the most commonly used techniques to grade mitral stenosis (MS) by orifice area. 2D measurements (pressure half-time (PHT), planimetry) and 3D planimetry were performed retrospectively on patients with at least mild MS. The clinical primary endpoint was defined as a composite of MV balloon valvotomy, mitral valve repair or replacement (MVR), and/or acute heart failure (HF) admissions. Results 41 consecutive patients were included; the majority were female (35; 85.4%), average age 55 (17) years. Mean and peak MV gradients were 9.4 (4) mmHg and 19 (6) mmHg, respectively. 2D and 3D measures of MVOA differed significantly; mean 2D planimetry MVOA was 1.28 (0.40) cm2, mean 3D planimetry MVOA 1.15 (0.29) cm2 (p = 0.003). Mean PHT MVOA was 1.43 (0.44) cm2 (p = 0.046 and p < 0.001 in comparison to 2D and 3D planimetry methods, respectively). 3D planimetry reclassified 7 (17%) patients from mild to moderate MS, and 1 (2.4%) from moderate to severe. Overall, differences between the 2 methods were significant (X2, p < 0.001). Only cases graded as severe by 3D predicted the primary outcome measure compared with mild or moderate cases (odds ratio 5.7). Conclusion 3D planimetry in MS returns significantly smaller measurements, which in some cases results in the reclassification of severity. Routine use of 3D may significantly impact on the management of MS, with a degree of prediction of clinical outcomes.Year: 2018 PMID: 30139798 DOI: 10.1530/ERP-18-0031
Source DB: PubMed Journal: Echo Res Pract ISSN: 2055-0464