Counseling for non-invasive prenatal testing (NIPT): What pregnant women may want to know

Ultrasound in Obstetrics and Gynecology

Volumn 44, Issue 1, 2014, Pages 1-5

  Oepkes, D ^a   Yaron, Y ^b   Kozlowski, P ^c   Rego De Sousa, M J ^d   Bartha, J L ^e   Van Den Akker, E S ^f   Dornan, S M ^g   Krampl Bettelheim, E ^h   Schmid, M ^h   Wielgos, M ⁱ   Cirigliano, V ^j   Di Renzo, G C ^k   Cameron, A ^l   Calda, P ^m   Tabor, A ⁿ  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b TEL AVIV UNIVERSITY   (Israel)

^c Praenatal Medizin und Genetik   (Germany)

^d Immunochemotherapy Department   (Portugal)

^e HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^f ONZE LIEVE VROUWE GASTHUIS   (Netherlands)

^g ROYAL MATERNITY HOSPITAL   (United Kingdom)

^h MEDICAL UNIVERSITY OF VIENNA   (Austria)

ⁱ MEDICAL UNIVERSITY OF WARSAW   (Poland)

^j UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^k UNIVERSITY OF PERUGIA   (Italy)

^l SOUTHERN GENERAL HOSPITAL   (United Kingdom)

^m CHARLES UNIVERSITY   (Czech Republic)

ⁿ Rigshospitalet   (Denmark)

more..

Author keywords

[No Author keywords available]

Indexed keywords

FEMALE; GENETIC COUNSELING; GENETIC SCREENING; HUMAN; MATERNAL SERUM SCREENING TEST; PATIENT EDUCATION; PREGNANCY; PROCEDURES;

FEMALE; GENETIC COUNSELING; GENETIC TESTING; HUMANS; MATERNAL SERUM SCREENING TESTS; PATIENT EDUCATION AS TOPIC; PREGNANCY;

EID: 84903754633     PISSN: 09607692     EISSN: 14690705     Source Type: Journal    
DOI: 10.1002/uog.13394     Document Type: Note

References (13)

1. Mersy E, Smits LJ, van Winden LA, de Die-Smulders CE,; South-East Netherlands NIPT Consortium, Paulussen AD, Macville MV, Coumans AB, Frints SG,. Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012. Hum Reprod Update 2013; 19: 318-329.
2. Gil MM, Akolekar R, Quezada MS, Bregant B, Nicolaides KH,. Analysis of cell-free DNA in maternal blood in screening for aneuploidies: meta-analysis. Fetal Diagn Ther 2014 Feb 8. [Epub ahead of print]
3. Nicolaides KH, Syngelaki A, Ashoor G, Birdir C, Touzet G,. Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population. Am J Obstet Gynecol 2012; 207: 374. e1-6.
4. Fairbrother G, Johnson S, Musci TJ, Song K,. Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population. Prenat Diagn 2013; 33: 580-583.
5. Song Y, Liu C, Qi H, Zhang Y, Bian X, Liu J,. Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population. Prenat Diagn 2013; 33: 700-706.
6. Gil MM, Quezada MS, Bregant B, Ferraro M, Nicolaides KH,. Implementation of maternal blood cell-free DNA testing in early screening for aneuploidies. Ultrasound Obstet Gynecol 2013; 42: 34-40.
7. Bianchi DW, Parker RL, Wentworth J, Madankumar R, Saffer C, Das AF, Craig JA, Chudova DI, Devers PL, Jones KW, Oliver K, Rava RP, Sehnert AJ,; CARE Study Group. DNA sequencing versus standard prenatal aneuploidy screening. N Engl J Med 2014; 370: 799-808.
8. Ferres MA, Hui L, Bianchi DW,. Antenatal noninvasive DNA testing: clinical experience and impact. Am J Perinatol 2014 Mar 28. [E pub ahead of print]
9. Ekelund CK, Jørgensen FS, Petersen OB, Sundberg K, Tabor A,; Danish Fetal Medicine Research Group. Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study. BMJ 2008; 337: a2547.
10. Evans MI, Henry GP, Miller WA, Bui TH, Snijders RJ, Wapner RJ, Miny P, Johnson MP, Peakman D, Johnson A, Nicolaides K, Holzgreve W, Ebrahim SA, Babu R, Jackson L,. International, collaborative assessment of 146,000 prenatal karyotypes: expected limitations if only chromosome-specific probes and fluorescent in-situ hybridization are used. Hum Reprod 1999; 14: 1213-1216.
11. Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, Savage M, Platt LD, Saltzman D, Grobman WA, Klugman S, Scholl T, Simpson JL, McCall K, Aggarwal VS, Bunke B, Nahum O, Patel A, Lamb AN, Thom EA, Beaudet AL, Ledbetter DH, Shaffer LG, Jackson L,. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med 2012; 367: 2175-2184.
12. Bernhardt BA, Kellom K, Barbarese A, Faucett WA, Wapner RJ,. An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing. J Genet Couns 2014 Feb 27. [Epub ahead of print]
13. Petersen OB, Vogel I, Ekelund C, Hyett J, Tabor A; Danish Fetal Medicine Study Group; Danish Clinical Genetics Study Group. Potential diagnostic consequences of applying non-invasive prenatal testing: population-based study from a country with existing first-trimester screening. Ultrasound Obstet Gynecol 2014; 43: 265-271.