Fetal Hyperechogenic Bowel Following Intra-Amniotic Bleeding

OBJECTIVE: METHODS:We studied 726 patients undergoing secondtrimester amniocentesis for advanced maternal age. Three groups were identified according to the color of the amniotic fluid (AF) obtainedclear fluid, blood-stained fluid, and dark brown fluid. Two to 4 weeks after the amniocentesis, all pa...

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Veröffentlicht in:Obstetrics and gynecology (New York. 1953) 1994-06, Vol.83 (6), p.947-950
Hauptverfasser: SEPULVEDA, WALDO, HOLLINGSWORTH, JEAN, BOWER, SARAH, VAUGHAN, JANET I., FISK, NICHOLAS M.
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Sprache:eng
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Zusammenfassung:OBJECTIVE: METHODS:We studied 726 patients undergoing secondtrimester amniocentesis for advanced maternal age. Three groups were identified according to the color of the amniotic fluid (AF) obtainedclear fluid, blood-stained fluid, and dark brown fluid. Two to 4 weeks after the amniocentesis, all patients had a targeted ultrasound examination for the detection of fetal structural anomalies and markers of chromosomal abnormalities, which included a survey of the fetal bowel. The incidence of hyperechogenic bowel in each group was compared by Fisher exact test. P < .05 was considered significant. RESULTS:In 694 cases, the AF was clear (95%), in 20 blood-stained (3%), and in 12 dark brown (2%). Hyperechogenic bowel was detected in 14 fetuses with clear fluid (2%), in two with blood-stained fluid (10%), and in three with dark brown fluid (25%). Fetuses with proven intra-amniotic bleeding (ie, dark brown or blood-stained AF at amniocentesis) had a significantly higher incidence of hyperechogenic bowel compared to those with clear AF (five of 32 [15.6%] and 14 of 694 [2.0%], respectively; P < .001, 95% confidence interval for the difference in proportions 6.3-17.6%). CONCLUSIONS:Our study demonstrates that intra-amniotic bleeding is associated with an increased incidence of fetal hyperechogenic bowel at second-trimester ultrasound scans. This sonographic phenomenon may be due to the presence of blood in the fetal bowel caused by fetal swallowing of bloody AF. (Obstet Gynecol 1994;83:947-50)
ISSN:0029-7844
1873-233X
DOI:10.1097/00006250-199406000-00009