One-stop clinic for assessment of risk for trisomy 21 at 11-14 weeks: a prospective study of 15 030 pregnancies
- PMID: 12230441
- DOI: 10.1046/j.1469-0705.2002.00808.x
One-stop clinic for assessment of risk for trisomy 21 at 11-14 weeks: a prospective study of 15 030 pregnancies
Abstract
Objective: To evaluate the performance of a one-stop clinic for assessment of risk (OSCAR) for trisomy 21 by a combination of maternal age, fetal nuchal translucency (NT) thickness and maternal serum free beta-human chorionic gonadotropin (hCG) and pregnancy-associated plasma protein-A (PAPP-A) at 11-14 weeks of gestation.
Method: Screening for trisomy 21 was carried out by OSCAR in 15 030 singleton pregnancies with live fetuses at 11-14 weeks. The estimated risk for trisomy 21 was calculated, and the women were counseled regarding this risk and the option of invasive testing or expectant management. Follow-up of the outcome of all pregnancies was carried out. The detection and false-positive rates for different risk cut-offs were calculated.
Results: Fetal NT and maternal serum free beta-hCG and PAPP-A were successfully measured in all cases. Pregnancy outcome, including karyotype results or the birth of a phenotypically normal baby, was obtained from 14 383 cases. The median maternal age of these cases was 34 (range 15-49) years and in 6768 (47.1%) the age was 35 years or greater. The median gestation at screening was 12 (range 11-14) weeks and the median fetal crown-rump length was 64 (range 45-84) mm. The estimated risk for trisomy 21 based on maternal age, fetal NT and maternal serum free beta-hCG and PAPP-A was 1 in 300 or greater in 6.8% (967 of 14 240) normal pregnancies, in 91.5% (75 of 82) of those with trisomy 21 and in 88.5% (54 of 61) of those with other chromosomal defects. For a fixed false-positive rate of 5% the respective detection rates of screening for trisomy 21 by maternal age alone, maternal age and serum free beta-hCG and PAPP-A, maternal age and fetal NT, and by maternal age, fetal NT and maternal serum biochemistry were 30.5%, 59.8%, 79.3% and 90.2%, respectively.
Conclusion: Screening for trisomy 21 by a combination of maternal age, fetal NT and maternal serum biochemistry at 11-14 weeks can be provided in an OSCAR setting and is associated with a detection rate of about 90% for a false-positive rate of 5%.
Similar articles
-
Screening for trisomy 21 by fetal tricuspid regurgitation, nuchal translucency and maternal serum free beta-hCG and PAPP-A at 11 + 0 to 13 + 6 weeks.Ultrasound Obstet Gynecol. 2006 Feb;27(2):151-5. doi: 10.1002/uog.2699. Ultrasound Obstet Gynecol. 2006. PMID: 16388509
-
Multicenter study of first-trimester screening for trisomy 21 in 75 821 pregnancies: results and estimation of the potential impact of individual risk-orientated two-stage first-trimester screening.Ultrasound Obstet Gynecol. 2005 Mar;25(3):221-6. doi: 10.1002/uog.1860. Ultrasound Obstet Gynecol. 2005. PMID: 15736186
-
Prospective validation of first-trimester combined screening for trisomy 21.Ultrasound Obstet Gynecol. 2009 Jul;34(1):14-8. doi: 10.1002/uog.6412. Ultrasound Obstet Gynecol. 2009. PMID: 19526452
-
First-trimester ultrasound and biochemical markers of aneuploidy and the prediction of impending fetal death.Ultrasound Obstet Gynecol. 2006 Oct;28(5):637-43. doi: 10.1002/uog.3809. Ultrasound Obstet Gynecol. 2006. PMID: 16952214 Review.
-
One-stop clinic for assessment of risk of chromosomal defects at 12 weeks of gestation.J Matern Fetal Neonatal Med. 2002 Jul;12(1):9-18. doi: 10.1080/jmf.12.1.9.18. J Matern Fetal Neonatal Med. 2002. PMID: 12422904 Review.
Cited by
-
Distribution of nuchal translucency thickness at 11 to 14 weeks of gestation in a normal Turkish population.Turk J Med Sci. 2021 Feb 26;51(1):90-94. doi: 10.3906/sag-2001-48. Turk J Med Sci. 2021. PMID: 32777901 Free PMC article.
-
The assessment of combined first trimester screening in women of advanced maternal age in an Asian cohort.Singapore Med J. 2015 Jan;56(1):47-52. doi: 10.11622/smedj.2015009. Singapore Med J. 2015. PMID: 25640099 Free PMC article.
-
Assessemnt of nasal bone in first trimester screening for chromosomal abnormalities in Khuzestan.Iran J Reprod Med. 2014 May;12(5):321-6. Iran J Reprod Med. 2014. PMID: 25031576 Free PMC article.
-
The associations of nuchal translucency and fetal abnormalities; significance and implications.J Clin Diagn Res. 2013 May;7(5):936-41. doi: 10.7860/JCDR/2013/5888.2989. Epub 2013 Mar 20. J Clin Diagn Res. 2013. PMID: 23814750 Free PMC article.
-
First Trimester Maternal Serum Screening Using Biochemical Markers PAPP-A and Free β-hCG for Down Syndrome, Patau Syndrome and Edward Syndrome.Indian J Clin Biochem. 2013 Jan;28(1):3-12. doi: 10.1007/s12291-012-0269-9. Epub 2012 Oct 12. Indian J Clin Biochem. 2013. PMID: 24381414 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous