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1.
J Matern Fetal Med ; 5(2): 70-3, 1996.
Article in English | MEDLINE | ID: mdl-8796771

ABSTRACT

The objective of this study was to evaluate a 2-year experience in a health maintenance organization with mid-trimester maternal serum screening with alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), and unconjugated estriol (UE) as a screen for fetal Down's syndrome. Women at 15-20 weeks gestation were offered triple marker screening. A patient-specific second trimester risk of 1:295 for Down's syndrome was used as a threshold for referral. Women at risk for trisomy 18 were identified by a protocol with fixed low cutoffs. The AFP threshold for referral for neural tube defects (NTD) was 2.0 multiples of the median (MoM). Patients at risk were offered ultrasonography, genetic counseling, and prenatal diagnosis. A total of 6,474 samples were drawn. The initial screen positive rate for Down's syndrome was 7.1%. After ultrasound evaluation, 351 (5.7%) of the remaining 6,197 women were still at risk for Down's syndrome. After genetic counseling, 292 (4.7%) women underwent prenatal diagnosis. Overall, 12 of 16 (75%) cases of Down's syndrome were detected antenatally by triple marker screening. Using AFP alone, only 3 of 14 (21%) cases of Down's syndrome in women under 35 years would have been detected. We detected 1 abnormal karyotype (including one 45, X) for every 22 amniocenteses performed for abnormal Down's syndrome screening. For trisomy 18, 13 women (0.2%) were at risk and, of these, 3 cases were diagnosed. All 6 cases of NTD during the study period were detected by AFP after identifying 3.8% of women as at risk. In conclusion, in the setting of a health maintenance organization where abnormal screening tests were managed by a single referral center, triple marker screening was effective not only for screening for fetal Down's syndrome, but also for trisomy 18 and NTD.


Subject(s)
Chorionic Gonadotropin/blood , Down Syndrome/diagnosis , Estriol/blood , Prenatal Diagnosis , alpha-Fetoproteins/analysis , Amniocentesis , Biomarkers/blood , Chromosome Aberrations , Chromosomes, Human, Pair 18 , Down Syndrome/prevention & control , Female , Genetic Counseling , Health Maintenance Organizations , Humans , Karyotyping , Mass Screening , Pregnancy , Reproducibility of Results , Trisomy , Ultrasonography, Prenatal
2.
Am J Obstet Gynecol ; 163(3): 818-23, 1990 Sep.
Article in English | MEDLINE | ID: mdl-2403162

ABSTRACT

The division between "normal" and low Apgar scores is based largely on data obtained from term newborns and may not apply to the premature infant. Umbilical artery pH has been suggested as a better indicator of intrapartum asphyxia. We examined the charts of 558 infants with birth weights less than or equal to 2500 gm with respect to umbilical artery pH, 5-minute Apgar scores, and birth weight percentiles. A positive correlation between birth weight and 5-minute Apgar score was noted. No such relationship existed between birth weight and umbilical artery pH. Within birth weight groups, small-for-gestational-age infants have higher Apgar scores and lower umbilical artery pH values than their appropriate-for-gestational age counterparts.


Subject(s)
Apgar Score , Birth Weight , Fetal Blood/analysis , Infant, Low Birth Weight , Blood Gas Analysis , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Reference Values , Umbilical Arteries
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