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Designed & Managed by
Dr. Joseph Vettukattil

me
Consultant Congenital Cardiologist, Southampton University Hospital, UK

 

Assessing AV valve regurgitation: MR

Real Time Three-Dimensional Color Doppler Echocardiographic Characterization of Regurgitant Orifice Area in Children with Mitral Regurgitation.

 

We use colour 3D MPR to define the effective regurgitant orifice area in quantifying mitral regurgitation  in children, and to derive indices for assessing mitral regurgitation

Study protocol

All patients referred for evaluation of MR had Standard 2-D assessment
3-D assessment from the routine clinics. No sedation and images acquired like any transthoracic echo

Age/height/weight, clinical symptoms recorded.

Images were acquired using Phillips Sonos 7500/ IE33 using 4 MHz X4 transducer/ X3-1 transducer.
Full volume dataset of mitral valve and Full volume colour Doppler data set - MR were acquired.
Analysis performed with Q lab version-4.1

 

Severity of clinical symptoms were scored 1-3. 2-D echocardiographic findings were sored mild, moderate or severe (1-3) Pulmonary venous hypertension was scored from (1-3) using CXR by an experienced cardiac radiologist blinded to the clinical or echocardiographic findings.

Total clinical score was tabulated as Mild- 0-3, Moderate- 4-6, Severe > 7

 

mrmpr1

Alignment of MPR planes along the regurgitant jet to obtain vena contracta area

 

 

vaamvaa

Method of MPR for measuring mitral valve annulus area in systole and diastole.

 

 

roagraph

The venacontracta area measured by MPR. Note the variation in the shape of venacontracta. Measuring the width shows enormous variation in diameter at different points, making the 2D venacontracta measurement unreliable.

The graph on the right shows clinical severity score plotted against venacontracta area indexed to body surface area

The inter observer variability was 0.966 and Intra observer variability was 0.952

Conclusion: Regurgitant orifice area as assessed by VCA indexed to body surface area gives the best correlation to the clinical severity of MR. This is highly reproducible and useful for monitoring the severity of MR in children

 

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