Hemodynamic Assessment



Hemodynamic Assessment


Robert M. Savage1

Lee K. Wallace2

Michael G. Licina2

Ahmad Adi2


1OUTLINE AUTHOR

2ORIGINAL CHAPTER AUTHORS





I. INTRODUCTION

The quantitative hemodynamic data discussed in this chapter can be obtained with the combination of two-dimensional (2D) echocardiography and Doppler echocardiography (Table 15-1). The accuracy of many of these Doppler-derived measurements has been validated in the cardiac catheterization laboratory using transthoracic echocardiography.1,2,3,4








TABLE 15.1 HEMODYNAMIC DATA OBTAINABLE WITH 2D DOPPLER ECHOCARDIOGRAPHY























































Volumetric measurements



Stroke volume



Cardiac output



Pulmonary-to-systemic flow ratio (Qp/Qs)



Regurgitant volume and fraction


Pressure gradients



Maximum gradient



Mean gradient


Valve area



Stenotic valve area



Regurgitant orifice area


Intracardiac and pulmonary artery pressures



Right ventricular systolic pressure



Pulmonary artery systolic pressure



Pulmonary artery mean pressure



Pulmonary artery diastolic pressure



Left atrial pressure



Left ventricular end-diastolic pressure


Ventricular dp/dt




II. DOPPLER MEASUREMENTS OF STROKE VOLUME AND CARDIAC OUTPUT


A. Stroke volume


1. The Hydraulic orifice formula

The flow rate of a fluid through a fixed orifice is directly proportional to the product of the cross-sectional area (CSA) of the orifice and the flow velocity of the fluid within the orifice (Fig. 15-1).

Flow rate (cm3 / s)=CSA (cm2)×flow velocity (cm / s)


2. The velocity-time integral

The acceleration and deceleration of blood flow velocity during the ejection period (or filling period) provide a distinct Doppler profile for a given orifice. The summation of velocities over the entire flow period is correctly called the VTI, although it is also commonly referred to as the TVI. The VTI is equal to the area bounded by the Doppler flow velocity profile and the zero velocity baseline (Fig. 15-2).


3. Calculation of stroke volume

SV can be calculated at many different locations within the heart or great vessels by using the appropriate Doppler velocity signal to determine the VTI at the same location that 2D imaging is used to determine CSA (Fig. 15-3).

SV (cm3) = CSA (cm2)×VTI (cm)

The VTI is usually measured with pulse wave Doppler; however, continuous wave Doppler may be utilized to determine the aortic valve VTI in the absence of subvalvular or supravalvular aortic obstruction.






FIGURE 15.1







FIGURE 15.2






FIGURE 15.3









TABLE 15.2 ASSUMPTIONS FOR ACCURATE DOPPLER STROKE VOLUME CALCULATIONS













1. Blood flow is laminar with a spatially flat flow velocity profile.


2. Measurements of the velocity-time integral and cross-sectional area (i.e., diameter) are made at the same time and at the same anatomic location.


3. The velocity-time integral measurement represents the average velocity-time integral (several measurements should be averaged for a patient in normal sinus rhythm, whereas 8-10 should be averaged for a patient in atrial fibrillation).


4. Cross-sectional area (i.e., diameter) measurement is accurate.


5. The velocity-time integral is measured with the Doppler beam parallel to blood flow (i.e., θ = 0 in the Doppler equation) in order to avoid underestimation.



4. Cross-sectional area

Most often the CSA of the “orifice” to be measured is assumed to be circular and thus can be calculated using the formula for the area of a circle (of radius r) after measuring the orifice diameter (D) in cm:

CSA (cm2) = II×r2 = II×(D / 2)2 = 0.785×D2


5. Assumptions in Doppler SV calculation (Table 15-2)


a. Laminar blood flow with a flat flow velocity profile

Blood flow is assumed to be laminar and the spatial flow velocity profile is assumed to be flat, as is generally the case in the LVOT (Fig. 15-4). The narrow band of velocities and smooth spectral signal obtained with pulsed wave Doppler are evidence of laminar flow in the great vessels and across normal cardiac valves. A flat flow velocity profile can be demonstrated by showing uniform velocities while moving the pulsed wave Doppler sample volume from side to side within the flow of interest from two orthogonal views.


b. Simultaneous CSA and VTI measurement at the same location

CSA and VTI measurements are assumed to be made at the same time and at the same anatomic location. Diameter is measured most
accurately when the ultrasound beam is perpendicular to the blood-tissue interface, while VTI is measured most accurately when the ultrasound beam is parallel to blood flow. Thus, diameter measurements and Doppler velocity profiles are usually not recorded from the same imaging plane. Efforts should be made to perform these measurements at the same anatomic location and in close sequence in order to minimize error in the calculated SV.






FIGURE 15.4


c. Average VTI measurement

The VTI used in calculating SV is assumed to represent the average VTI. Therefore, several measurements should be averaged for a patient in normal sinus rhythm, whereas 8 to 10 measurements should be averaged for a patient in atrial fibrillation, in order to most accurately estimate the average VTI.


d. Accurate CSA measurement

Changes in CSA during the flow period or deviations from an assumed geometry (usually circular) are inherent problems in Doppler SV calculations. Accurate determination of 2D measurements for calculation of CSA is essential. In the case of an assumed circular orifice, a small error in diameter measurement will result in a large error in the calculated CSA due to the quadratic relationship between the radius and area of a circle (i.e., CSA = II r2).


e. Accurate VTI measurement

The VTI is assumed to be recorded with the ultrasound beam parallel to the flow (i.e., the intercept angle θ = 0). In this case the velocities measured by Doppler are accurate based on a cosine θ = 1
in the Doppler equation (Fig. 15-5). However, as θ increases from 20 to 60 degrees, the error in the calculated Doppler velocity increases from 6% to 50% (Fig. 15-6). The highest velocity signal obtained (the loudest audio signal) will correlate with the most parallel alignment of the Doppler beam with blood flow.






FIGURE 15.5






FIGURE 15.6


B. Cardiac output


1. Calculation of cardiac output

CO can be estimated with 2D Doppler after determining a Doppler SV and measuring heart rate (HR)5:

CO (L / min) = SV (cm3) × (1 L / 1,000 cm3 × HR (bpm)

CO measurements performed with TEE, usually measured at the LVOT or aortic valve in the absence of aortic regurgitation, have been shown to correlate well with measurements made by thermodilution. Cardiac index (CI) can be calculated by dividing CO by body surface area (BSA):

CI (L /min /m2) = CO (L / min) / BSA (m2)


2. Preferred sites for CO calculation: LVOT and aortic valve


a. Laminar blood flow with a flat flow velocity profile

The acceleration of blood through the LVOT or aortic valve during systole favors laminar flow with a flat flow velocity profile, in contrast to the parabolic flow velocity profile present in the ascending aorta or pulmonary artery (PA).



b. Excellent views for CSA estimation

Multiplane TEE provides excellent views of the LVOT and aortic valve for accurate determinations of LVOT diameter and aortic valve CSA.


c. Little change in CSA

The LVOT is more circular and changes shape very little during the cardiac cycle when compared to the main PA or mitral valve. Measurements made at the main PA or mitral valve are less reliable than those made at the LVOT and aortic valve.6 Although the CSA of the aortic valve orifice changes dramatically throughout systole, the CSA of the aortic valve during midsystole can be used to provide a good estimate of transaortic SV by Doppler.


C. Data for LVOT stroke volume calculation


1. VTILVOT

The pulsed wave Doppler sample volume is placed in the LVOT just proximal to the aortic valve (˜1 cm) using either the transgastric long-axis view or the deep transgastric long-axis view for determination of the VTILVOT (Fig. 15-7A, B).


2. CSALVOT

The diameter (cm) of the LVOT is best obtained from the midesophageal long-axis view of the aortic valve (approximately 1 cm proximal to the valve) for determination of CSA using the formula for the area of a circle (Fig. 15-7C):

CSALVOT (cm2) = 0.785×DLVOT2






FIGURE 15.7







FIGURE 15.7 (CONTINUED)







FIGURE 15.8







FIGURE 15.8 (CONTINUED)


D. Data for transaortic valve stroke volume calculation


1. VTIAV

The continuous wave Doppler beam is placed through the aortic valve from either the transgastric long-axis view or the deep transgastric long-axis view for determination of the VTIAV (Fig. 15-8A, B).


2. CSAAV

Planimetry can be used to measure the area (cm2) of the aortic valve orifice during midsystole from a cine of the midesophageal short-axis view of the aortic valve (Fig. 15-8C).7 Alternatively, a cine of a “normal” aortic valve from the same midesophageal short-axis view is used to measure the side (S) in cm of the equilateral opening of the valve during midsystole (Fig. 15-8D). Several measurements may be made and then averaged in order to improve accuracy. The formula for the area of an equilateral triangle is then used to calculate the CSA of the aortic valve:

CSAAV (cm2) = 0.433×(S)2


E. Data for main PA stroke volume calculation


1. VTIPA

The pulsed wave Doppler sample volume is placed in the main PA using the upper esophageal short-axis view of the aortic arch (with the transducer rotated from 80 to 90 degrees) or the midesophageal shortaxis view of the aorta for determination of the VTIPA (Fig. 15-9A).


2. CSAPA

The diameter (cm) of the main PA is obtained from either view at the same location for determination of the CSA using the formula for the area of a circle (Fig. 15-9B, C):

CSAPV (cm2) = 0.785×DPA2







FIGURE 15.9



F. Data for RVOT stroke volume calculation


1. VTIRVOT

The RVOT may be visualized using a transgastric RV inflow-outflow view with the transducer rotated from 110 to 150 degrees and the probe turned to the right. The pulsed wave Doppler sample volume is placed in the RVOT just proximal to the pulmonic valve for determination of the VTIRVOT (Fig. 15-10A).






FIGURE 15.10



2. CSARVOT

The diameter (cm) of the RVOT is best obtained from the same view at the same location for determination of CSA using the formula for the area of a circle:

CSARVOT (cm2) = 0.785×DRVOT2

Alternatively, the diameter (cm) of the RVOT can be measured from the upper esophageal short-axis view of the aortic arch in some patients (Fig. 15-10B).


G. Data for transmitral stroke volume calculation


1. VTIMV

The pulsed wave Doppler sample volume is placed at the level of the mitral valve annulus using the midesophageal four-chamber view (alternatively, the midesophageal two-chamber view or midesophageal long-axis view may be used) for determination of the VTIMV (Fig. 15-11A, B).


2. CSAMV

While the mitral valve orifice is not truly elliptical during diastole, it is more elliptical than circular. The American Society of Echocardiography has concluded that assumption of a circular orifice has generally worked well for all valves other than the tricuspid in its document on Quantitation of Doppler Echocardiography.8 Nevertheless, it may be preferable to estimate the CSA of the mitral valve using the formula for an ellipse. The long and short diameters (cm) of the mitral valve annulus can be approximated using measurements from the midesophageal four-chamber and two-chamber views (Fig. 15-11C, D). The formula for an ellipse can then be used to calculate the CSA of the mitral valve:

CSAMV (cm2) = 0.785×D1 × D2


III. DOPPLER MEASUREMENT OF PULMONARY-TO-SYSTEMIC FLOW RATIO


A. Calculation of Qp/Qs

The ratio of pulmonic to systemic blood flow, Qp/Qs, usually indicates the magnitude of a shunt (i.e., atrial septal defect, ventricular septal defect, or patent pulmonary ductus arteriosus) and may be useful information in determining the need for surgery or the timing of surgery. Qp/Qs can be calculated once the systemic SV (measured at the LVOT or aortic valve) and pulmonic SV (measured at the PA or RVOT) have been determined9:

Qp / Qs = (SVPA × HR) / (SVLVOT × HR)



B. Limitations


1. Doppler SV measurement

Potential errors in the estimation of Qp/Qs are the same as for any Doppler determination of SV.


2. Propagation of errors

It should be noted that there is also the possibility of compounding calculated Doppler SV errors in the calculation of Qp/Qs with this formula (i.e., if SVPA is overestimated and SVLVOT is underestimated, then Qp/Qs may be significantly overestimated).






FIGURE 15.11







FIGURE 15.11 (CONTINUED)


3. Aortic regurgitation

In the presence of significant aortic regurgitation this calculation is not accurate and Qp/Qs will be underestimated.


IV. DOPPLER MEASUREMENT OF REGURGITANT VOLUME AND FRACTION


A. Volumetric method

RV is the volume of blood that flows backward through a regurgitant valve during one cardiac cycle. Conservation of mass says that the
SV delivered to the systemic circulation (SVSYSTEMIC) must equal the total forward SV across a regurgitant valve (SVTOTAL) minus the RV (Fig. 15-12):

SVSYSTEMIC = SVTOTAL-RV

or

RV=SVTOTAL-SVSYSTEMIC

The regurgitant fraction (RF) for any valve is calculated as the ratio of RV to total forward flow across the regurgitant valve expressed as a percentage:

RF (%) = (RV / SVTOTAL) × 100%


B. Assessment of mitral regurgitation


1. Calculation of RVMV

In mitral regurgitation, the SVTOTAL is the mitral inflow SV and the SVSYSTEMIC is the LVOT SV. Thus, the mitral valve RV can be estimated by subtracting the LVOT SV from the mitral valve inflow SV and then the mitral RF can be calculated (Fig. 15-13).10

RVMV = SVMVI-SVLVOT

RFMV (%) = (RVMV / SVMVI) × 100%


2. Limitations


a. Doppler SV measurement

Potential errors in the estimation of RVMV are the same as for any Doppler determination of SV.






FIGURE 15.12







FIGURE 15.13


b. Propagation of errors

It should be noted that there is also the possibility of compounding calculated Doppler SV errors in the calculation of RVMV with this formula.


c. Aortic regurgitation

In the presence of significant aortic regurgitation this calculation is not accurate and mitral RV will be underestimated.


C. Assessment of aortic regurgitation


1. Calculation of RVAV

In aortic regurgitation, the SVTOTAL is the LVOT forward SV and the SVSYSTEMIC is the mitral valve inflow SV. Thus, the aortic valve RV can be estimated by subtracting the mitral valve inflow SV from the LVOT forward SV and then aortic RF can be calculated (Fig. 15-14).10

RVAV – SVLVOT – SVMVI

RFav (%) = (RVAV / SVLVOT) × 100%


2. Limitations


a. Doppler SV measurement

Potential errors in the estimation of RVAV are the same as for any Doppler determination of SV.



b. Propagation of errors

It should be noted that there is also the possibility of compounding calculated Doppler SV errors in the calculation of RVAV with this formula.


c. Mitral regurgitation

In the presence of significant mitral regurgitation this calculation is not accurate and aortic RV will be underestimated.


D. Proximal convergence method


1. PISA concept

As blood flows toward a regurgitant orifice (i.e., mitral regurgitation), or in some cases a stenotic orifice (i.e., mitral stenosis), blood flow velocity increases with the formation of multiple concentric “isovelocity” shells (Fig. 15-15A, B).10,11 These “isovelocity” shells can be “seen” with color flow imaging (Fig. 15-16A, B) and have been termed proximal isovelocity surface areas (PISAs). The size of a PISA proximal to a regurgitant orifice can be altered by adjusting the Nyquist limit of the color flow map. As the negative aliasing velocity is reduced (in the case of mitral regurgitation), the transition from red to blue will occur farther from the regurgitant orifice resulting in a hemispheric shell with a larger radius (r). The instantaneous velocity of blood at the PISA is the same as the aliasing velocity on the color flow map.


2. PISA flow rate

The instantaneous flow rate through a PISA that is a hemispheric shell is equal to the product of the area of the PISA and the instantaneous velocity of blood at the PISA:

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May 26, 2016 | Posted by in CARDIOLOGY | Comments Off on Hemodynamic Assessment

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