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156 K. MarsÏ—l<br />

Table 11.5. Follow-up study on neurologic and intellectual<br />

performance of 149 children at 7 years of age a<br />

Summary<br />

Variable<br />

Relative<br />

risk<br />

95%<br />

Confidence<br />

interval<br />

Significant Aortic BFC 3.64 1.25±10.54<br />

contribution Social group 2.82 1.12±7.07<br />

to total IQ £85<br />

Significant Aortic BFC 3.61 1.55±8.41<br />

contribution<br />

to minor neurologic<br />

dysfunction<br />

IQ, intelligence quotient; BFC, blood flow class.<br />

a Results of logistic regression analysis [101, 102].<br />

A combination of real-time scanning and pulsed Doppler<br />

velocimetry is required for Doppler ultrasound<br />

velocimetry of the fetal descending aorta. A combined<br />

linear array real-time/pulsed Doppler method makes<br />

it possible to estimate fetal aortic volume flow. However,<br />

the volume flow method is open to error and is<br />

therefore less suitable for application to the clinical<br />

situation. The waveform of the maximum velocities<br />

recorded from the fetal descending aorta reflects the<br />

impedance to flow in the placenta and the lower fetal<br />

body. The waveform is also influenced by other factors<br />

(e.g., fetal heart function). The aortic waveform<br />

can be characterized by various indices (e.g., the PI<br />

and the RI). In a situation of increased peripheral<br />

vascular resistance, the aortic diastolic velocities decrease<br />

and eventually disappear. In extreme cases reversed<br />

flow during diastole can be detected. The finding<br />

of absent or reversed aortic flow is associated<br />

with an adverse outcome of pregnancy. For practical<br />

application, a semiquantitative method (blood flow<br />

classes) has been designed to evaluate fetal aortic<br />

velocity waveforms. The BFC method emphasizes<br />

especially the appearance of the diastolic part of the<br />

waveform. When recording fetal aortic Doppler signals,<br />

caution must be taken to avoid periods of fetal<br />

breathing movements, which can profoundly influence<br />

the shape of the waveform. The values of waveform<br />

indices in the fetal aorta are also dependent on<br />

fetal heart rate and activity/behavioral states.<br />

In uncomplicated pregnancies the velocity waveform<br />

of the fetal descending aorta shows positive flow<br />

throughout the cardiac cycle, the proportion of diastolic<br />

flow being higher in the abdominal aorta than<br />

in the thoracic aorta. The PI values are stable during<br />

the last trimester of gestation, with a slight increase<br />

at term. The aortic mean velocity and the relative<br />

flow do not change significantly with gestational age<br />

during late pregnancy. About 50%±60% of the flow in<br />

the thoracic descending aorta supplies the placenta.<br />

In fetuses with a cardiac arrhythmia, aortic Doppler<br />

velocimetry can facilitate diagnosis of the arrhythmia,<br />

and the estimation of aortic flow can provide<br />

an early indication of imminent heart failure. In<br />

anemic isoimmunized fetuses, the mean aortic velocity<br />

is increased.<br />

Clinical studies of pregnancies with IUGR showed<br />

that examination of fetal aortic velocity waveforms<br />

can be used for fetal surveillance. The develoment of<br />

fetal hypoxia is associated with typical changes of the<br />

waveform: increased PI and absence or reversal of<br />

diastolic flow. These changes usually precede other<br />

signals of fetal distress. The predictive capacity of fetal<br />

aortic velocimetry is comparable to that of umbilical<br />

artery velocimetry with regard to IUGR and the<br />

development of fetal distress. As is the case for umbilical<br />

artery velocimetry, Doppler examination of the<br />

fetal descending aorta is suited for application as a<br />

secondary diagnostic test in high-risk pregnancies.<br />

Changes in the intrauterine aortic waveforms have<br />

been shown to be significantly correlated to the perinatal<br />

outcome and to the long-term postnatal neurologic<br />

and psychological development. Analysis of the<br />

fetal aortic flow velocity pattern can be applied, together<br />

with examination of other vessel areas, for a<br />

more detailed study of redistribution of flow in the<br />

presence of fetal hypoxia. Clinical management protocols<br />

based on such a concept should be tested in prospective<br />

randomized trials.<br />

References<br />

1. FitzGerald DE, Drumm J (1977) Non-invasive measurement<br />

of human fetal circulation using ultrasound: a<br />

new method. BMJ 2:1450±1451<br />

2. McCallum WD, Williams CB, Napel S, Diagle RE (1978)<br />

Fetal blood velocity waveforms. Am J Obstet Gynecol<br />

132:425±429<br />

3. Gill RW (1979) Pulsed Doppler with B-mode imaging<br />

for quantitative blood flow measurement. Ultrasound<br />

Med Biol 5:223±235<br />

4. Eik-Nes SH, Brubakk AO, Ulstein MK (1980) Measurement<br />

of human fetal blood flow. BMJ 2:283±284<br />

5. Eik-Nes SH, MarsÏ—l K, Brubbakk AO, Kristoffersen K,<br />

Ulstein M (1982) Ultrasonic measurements of human<br />

fetal blood flow. J Biomed Eng 4:28±36<br />

6. Jouppila P, Kirkinen P (1984) Increased vascular resistance<br />

in the descending aorta of the human fetus in<br />

hypoxia. Br J Obstet Gynaecol 91:853±856<br />

7. Eik-Nes SH, MarsÏ—l K, Kristoffersen K, Vernersson E<br />

(1981) Noninvasive Messung des fetalen Blutstromes<br />

mittels Ultraschall. Ultraschall Med 2:226±231<br />

8. Lindstræm K, MarsÏ—l K, Gennser G et al (1977) Device<br />

for monitoring fetal breathing movements. I. TD-recorder:<br />

a new system for recording the distance between<br />

two echo generating structures as a function of<br />

time. Ultrasound Med Biol 3:143±151

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