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Changes in blood flow velocity waveforms following fetal blood sampling
C Zoppini1, D Brioschi, B Tassis
11st Department of Obstetrics and Gynecology, University of Milano, Italy.
Fetal Diagnosis and Therapy
|September 1, 1995
Summary
Fetal blood sampling temporarily reduces umbilical artery pulsatility, indicating altered fetal circulation. This response, likely due to vasoactive substances, is blunted in fetuses with acidemia or hypoxemia.
Area of Science:
- Perinatology
- Fetal Medicine
- Diagnostic Ultrasound
Background:
- Fetal blood sampling is a common diagnostic procedure.
- Understanding its effects on fetal circulation is crucial for accurate interpretation of results.
Purpose of the Study:
- To investigate the impact of fetal blood sampling on fetal arterial pulsatility indices.
- To explore potential mechanisms and influencing factors, including saline infusion and fetal acid-base status.
Main Methods:
- Pulsed Doppler ultrasound was used to measure pulsatility indices in the umbilical artery, aorta, and middle cerebral artery in 73 fetuses (18-37 weeks gestation).
- Measurements were taken before and after fetal blood sampling at either the placental cord insertion or intrahepatic vein.
- Fetuses were randomized into a control group (n=38) and a saline infusion group (n=35) to replace withdrawn blood volume.
Main Results:
- Umbilical artery pulsatility indices decreased significantly after blood sampling in both control (p=0.004) and saline groups (p=0.006).
- Middle cerebral artery velocity waveforms showed similar changes only in the control group (p=0.01).
- No significant changes were observed in aortic pulsatility indices or fetal heart rate. Acidemic/hypoxemic fetuses showed no modification in pulsatility indices.
Conclusions:
- Fetal blood sampling induces transient changes in fetal circulation, likely mediated by the release of vasoactive substances.
- The vasodilative response appears diminished in fetuses with acidemia or hypoxemia.
- Saline infusion did not prevent the observed changes in umbilical artery pulsatility.