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500 D. Maulik<br />

Fig. 33.20. Echocardiogram shows simultaneous<br />

interrogation of the mitral<br />

flow (MF) and aortic outflow (AO). Top:<br />

Placement of the Doppler sample in<br />

the left ventricular chamber just distal<br />

to the tricuspid orifice encompassing<br />

the mitral flow and aortic outflow. LA<br />

left atrium, LV left ventricle<br />

veform from any fetal artery reflects the ventricular<br />

rhythm. On the other hand, insonation of the inferior<br />

vena cava or pulmonary vein and of the tricuspid or<br />

mitral flow tracts will yield the atrial rhythm. The<br />

use of Doppler velocimetry of the inferior vena cava<br />

for assessing fetal arrhythmia is discussed in Chap. 27.<br />

To assess the synchronicity of the atrial and ventricular<br />

rhythms, Doppler sample volume can be<br />

placed and extended to encompass both atrial and<br />

ventricular flows. It is accomplished by placing the<br />

sample volume appropriately in the ventricular chamber<br />

and extending it to include the atrial flow into<br />

the ventricle and the ventricular outflow. The tricuspid<br />

or mitral waveform reveals the atrial rhythm, and<br />

the pulmonary or aortic outflow indicates the ventricular<br />

rhythm (Fig. 33.20). An alternative approach,<br />

described by Chan and colleagues [45], involves placing<br />

the Doppler sample volume in the lower abdomen<br />

to encompass the aorta and the inferior vena cava,<br />

generating the ventricular and atrial rates, respectively.<br />

In this location the two vessels lie in close<br />

proximity and therefore are accessible to interrogation<br />

by an extended sample volume.<br />

In addition to rhythm determination, Doppler echocardiographic<br />

modalities allow assessment of hemodynamic<br />

changes associated with an abnormal rhythm.<br />

Moreover, color Doppler echocardiography is supplemental<br />

to 2D imaging for identifying any associated cardiac<br />

structural malformations. This point is clinically<br />

important, as the presence of malformations in conjunction<br />

with arrhythmia signifies a worse prognosis.<br />

Spectral Doppler may be particularly helpful for elucidating<br />

the hemodynamic pathophysiology of fetal<br />

cardiac arrhythmias. In our initial report [46] we noted<br />

that during an ectopic beat the right ventricular stroke<br />

volume may be reduced by 60%. Subsequent investigations<br />

have substantially expanded the application of<br />

Doppler sonography for studying the hemodynamic effects<br />

of fetal cardiac arrhythmia. Lingman and MarsÆ—l<br />

[47] observed that the systolic rising slope and peak<br />

value of the maximum aortic velocity were significantly<br />

increased during the first beat after the compensatory<br />

pause in fetuses with supraventricular extrasystole; this<br />

observation confirmed the Frank-Starling phenomenon<br />

in the fetus and was corroborated by Reed and coworkers<br />

[48], who reported cardiac Doppler flow<br />

changes during fetal arrhythmias in 54 fetuses with gestational<br />

ages of 21±41 weeks. During the postextrasystolic<br />

beats, time velocity integrals rose by 43% across<br />

the tricuspid orifice and 41% across the mitral orifice.<br />

Kanzaki and associates [49] investigated fetal cardiac<br />

arrhythmia with pulsed-wave Doppler sonography<br />

and observed characteristic inferior vena caval flow<br />

patterns with each arrhythmic condition. These patterns<br />

could be explained by the atrial and ventricular<br />

contraction characteristics. Furthermore, inferior vena<br />

caval flow components during sinus rhythm could be<br />

explained by the events of the cardiac cycle. Distinctive<br />

flow velocity patterns were observed for each arrhythmic<br />

condition. The most remarkable finding with all<br />

the arrhythmic conditions was the high-velocity reverse<br />

flow caused by atrial systole with closed tricuspid<br />

valve or tricuspid regurgitation. This subject is discussed<br />

in depth in Chap. 27.<br />

Premature Atrial Contractions<br />

As indicated in Table 33.9, premature atrial contractions<br />

(PACs) are the most common form of fetal cardiac<br />

arrhythmia. The condition is also known as at-

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