Experiences of first trimester antenatal screening in a one-stop clinic

2008 ◽  
Vol 16 (3) ◽  
pp. 156-159 ◽  
Author(s):  
Gillian Lewando Hundt ◽  
J Sandall ◽  
K Spencer ◽  
B Heyman ◽  
C Williams ◽  
...  
2005 ◽  
Vol 61 (9) ◽  
pp. 1983-1992 ◽  
Author(s):  
Clare Williams ◽  
Jane Sandall ◽  
Gillian Lewando-Hundt ◽  
Bob Heyman ◽  
Kevin Spencer ◽  
...  

2002 ◽  
Vol 48 (3) ◽  
pp. 473-483 ◽  
Author(s):  
Qiu-Ping Qin ◽  
Michael Christiansen ◽  
Kim Pettersson

Abstract Background: Screening for Down syndrome in the first trimester by a combination of fetal nuchal translucency thickness and maternal serum pregnancy-associated plasma protein A (PAPP-A) and free β-human chorionic gonadotropin has been shown to be effective and efficient. We aimed to develop a fast point-of-care assay that could be placed in one-stop clinics for the measurement of PAPP-A. Methods: We developed a two-site, one-step assay that uses two monoclonal antibodies (mAbs) to PAPP-A, based on a dry-reagent, all-in-one immunoassay concept with a stable fluorescent lanthanide chelate and time-resolved fluorometry. One antibody (mAb 10E1) was biotinylated, and the other (mAb 234-5) was europium-labeled, both via the ε-amino groups of surface lysine residues. The assay was performed on an AIO immunoanalyzer at 36 °C in single, streptavidin-coated microtitration wells that contained the dry reagents. PAPP-A, either in free or complexed form, was detected by the antibodies used. Results: The assay procedure required 20 min and used 10 μL of sample. The calibration curve was linear from 5 to 10 000 mIU/L. The detection limit was 0.5 mIU/L. Intra- and interassay imprecision (CV) was ≤4.3% and 8.3%, respectively, for whole blood, plasma, or serum samples. Recovery was 93–96% for serum, 95–108% for heparin-derived whole blood, and 98–103% for heparin-derived plasma. Parallelism was observed in all three matrices. Results correlated [slope = 0.85 (confidence interval, 0.82–0.87); intercept = −33 (confidence interval, −58 to −9); Sy|x = 85 mIU/L; r = 0.991; n = 100] with those obtained by a Delfia assay. Heparin did not affect the assay, but EDTA markedly reduced PAPP-A values. PAPP-A was stable at 4 °C for at least 18 days in serum and for 8 days in heparin-derived whole blood or plasma. Conclusions: The present assay appears suited for use in one-stop clinics for screening for Down syndrome in the first trimester, with results available within 1 h.


Midwifery ◽  
2017 ◽  
Vol 47 ◽  
pp. 15-21 ◽  
Author(s):  
Maarit Nykänen ◽  
Katri Vehviläinen-Julkunen ◽  
Reija Klemetti

2018 ◽  
Vol 25 (3) ◽  
pp. 114-118
Author(s):  
Drahomira Springer ◽  
Jaroslav Loucky ◽  
Pavel Tesner ◽  
David Cutka ◽  
David Stejskal ◽  
...  

Objective In the Czech Republic, over 97% of all pregnant women undergo some type of antenatal screening for Down’s syndrome. In about 95% of cases with a confirmed fetal chromosomal abnormality, the pregnancy is terminated. The most commonly used test is the first trimester combined test. We investigated the impact of implementing an integrated sequential test to improve the detection of Down’s syndrome pregnancies. Methods Data on the incidence of congenital defects, number of births, and affected pregnancies terminated are recorded in the National Registry of Congenital Anomalies. Anonymous data on cases of Down’s syndrome diagnosed antenatally or postnatally between 2010 and 2015 in one of the large antenatal care centers were analyzed. Results There were 600 diagnoses of Down’s syndrome (5.7 per 1000 births), 90% of which were made antenatally. Of antenatally detected cases, 80% were indicated for diagnostic procedure by multimarker screening results. In the multimarker screen positive group, 75% cases were first trimester positive and 25% second trimester positive (most of these had positive integrated test results). Among Down’s syndrome cases indicated for antenatal diagnosis by multimarker screening results 6.25% (n = 26) were first trimester negative, and became positive after integration with the second trimester screening results. Conclusions Results from five major Czech antenatal centers confirm that an integrated sequential test would detect 80–85% of Down’s syndrome fetuses in the first trimester and at least an extra 5–10% of Down’s syndrome pregnancies in the second trimester of pregnancy. These are important data that should be considered in implementing the national antenatal screening program.


2007 ◽  
Vol 30 (4) ◽  
pp. 377-377
Author(s):  
J. M. Johnson ◽  
R. Kohut ◽  
R. Simrose ◽  
D. Dewey ◽  
G. Connors ◽  
...  
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