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Elevated maternal serum alpha-fetoprotein caused by midtrimester amniocentesis: a prognostic factor
Obstetrics and Gynecology
|September 1, 1983
Summary
Ultrasonically guided amniocentesis can cause fetal-maternal bleeding, particularly with anterior placentas. This bleeding is linked to lower fetal birth weight, suggesting a potential hazard during pregnancy screening.
Area of Science:
- Maternal-Fetal Medicine
- Diagnostic Procedures
- Prenatal Screening
Background:
- Midtrimester amniocentesis is a common prenatal diagnostic procedure.
- Maternal serum alpha-fetoprotein (AFP) is a key biomarker in prenatal screening.
- Elevated AFP levels can indicate fetal abnormalities or complications.
Purpose of the Study:
- To investigate the incidence and implications of fetal-maternal bleeding following ultrasonically guided amniocentesis.
- To assess the correlation between amniocentesis-induced bleeding and placental location.
- To evaluate the impact of such bleeding on fetal birth weight and gestational age.
Main Methods:
- Prospective study of 247 patients undergoing midtrimester amniocentesis.
- Measurement of maternal serum alpha-fetoprotein (AFP) before and after the procedure.
- Correlation analysis of AFP elevation, placental location, and fetal birth weight.
Main Results:
- Amniocentesis induced significant AFP elevation (indicating fetal-maternal bleeding) in 21.0% of patients with pre-procedure AFP > 19 µg/L.
- This bleeding was significantly correlated with anterior placental location (P < .025).
- Patients experiencing bleeding had a significantly reduced mean fetal birth weight (3143 vs. 3385 g, P < .05).
Conclusions:
- Ultrasonically guided amniocentesis can pose a risk of fetal-maternal bleeding.
- Anterior placental location increases the likelihood of this complication.
- Amniocentesis-induced bleeding may negatively impact fetal growth, warranting consideration given its expanding indications.