Literature DB >> 21706514

Detection rate of quadruple-marker screening determined by clinical follow-up and registry data in the statewide California program, July 2007 to February 2009.

Niloufar Neely Kazerouni1, Robert J Currier, Monica Flessel, Sara Goldman, Colin Hennigan, Christina Hodgkinson, Fred Lorey, Linda Malm, Corinna Tempelis, Marie Roberson.   

Abstract

OBJECTIVE: To evaluate the efficiency of California's quadruple-marker screening program and construct receiver-operating characteristic (ROC) curves.
METHODS: This study included the screening records of 552 941 women during July 2007 to February 2009. The screen-positive women received clinical follow-up services at state-approved centers. We used the California Chromosome Defect Registry which includes clinical, laboratory, and demographic data from the prenatal diagnostic centers, cytogenetic laboratories, hospitals, and prenatal care providers. Risk calculations, screen-positive rates (SPRs), detection rates (DRs) for chromosomal abnormalities, and 95% confidence intervals (95% CIs) were determined. ROC curves comparing the quadruple-marker to triple-marker screening were constructed.
RESULTS: The DR and SPR for trisomy 21 (N = 827) during the quadruple-marker time period were 75.7% (95% CI 72.8-78.6%) and 3.75% (95% CI 3.70-3.80%) compared with 77.4% (95% CI 75.0-79.7%) and 5.4% during the triple-marker phase. The DRs were 78.2% (95% CI 75.0-81.4%) with ultrasound dating and 66.9% (95% CI 59.7-74.0%) for last-menstrual-period-dated pregnancies. For trisomy 18, triploidy, and trisomy 13, the DRs were 84.3, 95.7, and 43.5%, respectively.
CONCLUSIONS: The DR for trisomy 21 in California's statewide quadruple-marker screening is very similar to the Program's previously reported DR using triple-marker screening. However, this was achieved at a lower SPR, demonstrating improved screening performance.
Copyright © 2011 John Wiley & Sons, Ltd.

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Year:  2011        PMID: 21706514     DOI: 10.1002/pd.2802

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  6 in total

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Review 2.  Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.

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Journal:  Cochrane Database Syst Rev       Date:  2017-11-10

3.  Early pregnancy prediction of gestational diabetes mellitus risk using prenatal screening biomarkers in nulliparous women.

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Journal:  Diabetes Res Clin Pract       Date:  2020-04-06       Impact factor: 5.602

4.  A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.

Authors:  Hongyan Chai; Autumn DiAdamo; Brittany Grommisch; Fang Xu; Qinghua Zhou; Jiadi Wen; Maurice Mahoney; Allen Bale; James McGrath; Michele Spencer-Manzon; Peining Li; Hui Zhang
Journal:  Front Genet       Date:  2019-11-20       Impact factor: 4.599

5.  Triploidy and Routine Combined First Trimester Pregnancy Screening.

Authors:  Mitra Eftekhariyazdi; Ali Khaligh; Behnaz Suizi; Maryam Naghibi Nasab; Davood Zare-Abdollahi
Journal:  Avicenna J Med Biotechnol       Date:  2019 Jan-Mar

6.  Performance of a universal prenatal screening program incorporating cell-free fetal DNA analysis in Ontario, Canada.

Authors:  Shelley D Dougan; Nan Okun; Kara Bellai-Dussault; Lynn Meng; Heather E Howley; Tianhua Huang; Jessica Reszel; Andrea Lanes; Mark C Walker; Christine M Armour
Journal:  CMAJ       Date:  2021-08-03       Impact factor: 8.262

  6 in total

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