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J Am Coll Cardiol, 2004; 44:133-137, doi:10.1016/j.jacc.2004.03.038
© 2004 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: VALVULAR HEART DISEASE

Quantification of stenotic mitral valve area with magnetic resonance imaging and comparison with Doppler ultrasound

Shiow Jiuan Lin, MS*, Peggy A. Brown, RDCS*, Mary P. Watkins, RT*, Todd A. Williams, RT*, Katherine A. Lehr, BSN*, Wei Liu, MS{dagger}, Gregory M. Lanza, MD, PhD*, Samuel A. Wickline, MD*{dagger} and Shelton D. Caruthers, PhD*{dagger}{ddagger},*

* Cardiovascular Division, Washington University School of Medicine, St. Louis, Missouri, USA
{dagger} Department of Biomedical Engineering, Washington University, St. Louis, Missouri, USA
{ddagger} Philips Medical Systems, Best, Netherlands

Manuscript received December 10, 2003; revised manuscript received February 26, 2004, accepted March 23, 2004.

* Reprint requests and correspondence: Dr. Shelton D. Caruthers, Cardiovascular Division, Washington University School of Medicine, Campus Box 8086, 660 South Euclid Avenue, St. Louis, Missouri 63110, USA.
scaruthers{at}cmrl.wustl.edu

OBJECTIVES: The purpose of this study was to evaluate the reliability of the pressure half-time (PHT) method for estimating mitral valve areas (MVAs) by velocity-encoded cardiovascular magnetic resonance (VE-CMR) and to compare the method with paired Doppler ultrasound.

BACKGROUND: The pressure half-time Doppler echocardiography method is a practical technique for clinical evaluation of mitral stenosis. As CMR continues evolving as a routine clinical tool, its use for estimating MVA requires thorough evaluation.

METHODS: Seventeen patients with mitral stenosis underwent echocardiography and CMR. Using VE-CMR, MVA was estimated by PHT method. Additionally, peak E and peak A velocities were defined. Interobserver repeatability of VE-CMR was evaluated.

RESULTS: By Doppler, MVAs ranged from 0.87 to 4.49 cm2; by CMR, 0.91 to 2.70 cm2, correlating well between modalities (r = 0.86). The correlation coefficient for peak E and peak A between modalities was 0.81 and 0.89, respectively. Velocity-encoded CMR data analysis provided robust, repeatable estimates of peak E, peak A, and MVA (r = 0.99, 0.99, and 0.96, respectively).

CONCLUSIONS: Velocity-encoded cardiovascular magnetic resonance can be used routinely as a robust tool to quantify MVA via mitral flow velocity analysis with PHT method.

Abbreviations and Acronyms
  AF = atrial fibrillation
  CMR = cardiovascular magnetic resonance
  MS = mitral stenosis
  MVA = mitral valve area
  PHT = pressure half-time
  ROI = region of interest
  VENC = velocity encoding (maximum) value




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