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Sonography, a complementary examination to alpha‐fetoprotein testing for fetal neural tube defects.
Author(s) -
Hashimoto B E,
Mahony B S,
Filly R A,
Golbus M S,
Anderson R L,
Callen P W
Publication year - 1985
Publication title -
journal of ultrasound in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 91
eISSN - 1550-9613
pISSN - 0278-4297
DOI - 10.7863/jum.1985.4.6.307
Subject(s) - medicine , amniocentesis , amniotic fluid , obstetrics , fetus , ultrasound , neural tube , alpha fetoprotein , prenatal diagnosis , neural tube defect , ultrasonography , pregnancy , gestation , radiology , embryo , genetics , hepatocellular carcinoma , biology , microbiology and biotechnology
Neural tube defects (NTDs) are among the most common congenital anomalies in the United States, with an estimated prevalence of 16 per 10,000 births. The measurement of amniotic fluid alpha‐fetoprotein (AF‐AFP) concentration has been used to detect NTDs since the early 1970s. When the AF‐AFP concentration is elevated, ultrasonography is commonly used to confirm the presence of a NTD. In this study, patient charts, amniocentesis records, and ultrasound reports from a three‐year period were reviewed. The 97 fetuses identified as being at high risk for NTDs were divided into four groups: those with high AF‐AFP concentrations (Groups 1 and 2, with from 3 to 5 standard deviations (SD) above the mean and with more than 5 SD above the mean, respectively): those referred from other institutions because of suspicious sonographic results (Group 3); and those at risk because of a previous sibling with a NTD (Group 4). Ultrasonography was 100 per cent sensitive and 100 per cent specific in diagnosing NTDs. Thus, in pregnancies with an elevated AF‐AFP concentration, ultrasonography can reliably identify normal fetuses as well as differentiate between those with NTDs and those with other congenital anomalies. Also, since AF‐AFP concentrations decline after 20 weeks' gestation, ultrasonography may be a better test than a repeat amniocentesis in equivocal cases of AF‐AFP elevation.