Performance of ultrasound, maternal serum screening and cell-free DNA for the detection of 22q11.2 deletion syndrome

2021 ◽  
Vol 132 ◽  
pp. S307-S308
Author(s):  
Kimberly Martin ◽  
Bo Jacobsson ◽  
Pe’er Dar ◽  
Fergal Malone ◽  
Ronald Wapner ◽  
...  
2007 ◽  
Vol 143A (4) ◽  
pp. 410-411 ◽  
Author(s):  
Michael L. Begleiter ◽  
Molly M. Lund ◽  
Andrea M. Atherton ◽  
Janda D. Buchholz ◽  
Holly H. Ardinger

Author(s):  
Amber Mathiesen ◽  
Kali Roy

This chapter provides information about a genetic counselor’s role in prenatal screening, including discussing and offering options to a patient, interpreting and providing results, or managing referrals based on abnormal results. It discusses how a screen is evaluated using sensitivity, specificity, positive predictive value, negative predictive value, and personal utility. It provides a detailed description of both maternal serum screening and cell-free DNA testing. The maternal serum screening discussion includes information on multiples of median, calculating risk, timing, pattern association, limitations, and follow-up. The review of cell-free DNA testing includes fetal fraction, methodology, test performance, limitations and considerations for testing, and follow-up. This chapter also provides a list of additional resources to use for cell-free DNA testing.


2016 ◽  
Vol 24 (3) ◽  
pp. 113-119 ◽  
Author(s):  
Geralyn M Lambert-Messerlian ◽  
Elizabeth E Eklund ◽  
Louis M Neveux ◽  
Glenn E Palomaki

2021 ◽  
pp. 096914132110316
Author(s):  
Nathalie Lepage ◽  
Philip Wyatt ◽  
Edward R Ashwood ◽  
Robert G Best ◽  
Thomas Long ◽  
...  

Objective To compile current usage of serum-based prenatal screening for Down syndrome in the United States and compare it with results from a similar 2011/2012 survey. Setting The College of American Pathologists maternal screening proficiency testing survey includes a supplemental question on the first of three yearly distributions. Methods Information regarding tests offered and the monthly number of pregnancies tested for US-based laboratories were reviewed. Results were stratified by size of laboratory, tests offered, and pregnancies tested. Findings were compared to an earlier survey. Results Fifty-six laboratories reported they will have screened 1,131,336 pregnancies in 2020. Of these, 36% are screened by stand-alone first trimester testing, 48% by stand-alone second trimester testing, and 16% using tests that integrate results from both trimesters. Eighty percent of all serum screens were provided by the five laboratories that performed the most screens (at least 50,000). These five performed similar proportions of first or second trimester screens (42.2% and 41.8%, respectively). Compared to eight years earlier, there are now 54% fewer laboratories. Pregnancies screened using the first trimester, second trimester, and integrated protocols were lower by 27%, 69%, and 72%, respectively. The serum screening activity in the US showed a 62% decrease from 2012 levels. During 2012–2020, the number of cell-free DNA tests increased from negligible to 1,492,332. Conclusions Maternal serum screening for common aneuploidies has changed significantly in eight years with fewer laboratories, a shift toward larger laboratories and a 2.5-fold reduction in pregnancies tested, likely due to the introduction of cell-free DNA screening.


2016 ◽  
Vol 37 (1) ◽  
pp. 53-60 ◽  
Author(s):  
Lorraine Dugoff ◽  
Michael T. Mennuti ◽  
Donna M. McDonald-McGinn

Author(s):  
Pe’er Dar ◽  
Bo Jacobson ◽  
Rebecca Clifton ◽  
Melissa Egbert ◽  
Fergal Malone ◽  
...  

2021 ◽  
pp. 096914132110099
Author(s):  
Jiazhen Chang ◽  
Qingwei Qi ◽  
Xiya Zhou ◽  
Yulin Jiang ◽  
Na Hao ◽  
...  

Objective To investigate the factors associated with cell-free DNA test failure, and the optimal subsequent management of these pregnancies. Methods This was a retrospective study of 27,363 singleton pregnancies undergoing cell-free DNA testing. Women with cell-free DNA test failure were divided into a high-risk group and a low-risk group according to their indications. The subsequent management and pregnancy outcomes of these women were followed up. Results The rate of cell-free DNA test failure at the first sampling was 1.49%, and 78.4% of failures were due to a low fetal fraction. Of the 66 women who refused any subsequent management, an adverse pregnancy outcome was seen in 5 cases, all belonging to the high-risk group. Of the 13 low-risk women who chose second-trimester maternal serum screening, all obtained a low-risk maternal serum screening result and an unaffected pregnancy outcome. A redraw was chosen by 171 women, which yielded a result in 75.4% and their pregnancy outcomes were unaffected; 42 women had an uninformative result again and received an amniocentesis. As 158 women had an amniocentesis after the first sampling, this procedure was offered in 200 cases altogether. Abnormal genetic testing results were shown in six (3%, 6/200) cases, all in the high-risk group. Conclusions High-risk pregnant women with cell-free DNA test failure are at increased risk of adverse pregnancy outcomes. A second sampling for cell-free DNA test or maternal serum screening might be suggested to low-risk women. Invasive prenatal diagnosis should be offered to the high-risk patients, especially those with a second cell-free DNA test failure.


Sign in / Sign up

Export Citation Format

Share Document