Literature DB >> 29951719

Genetic Counselors' Perspectives About Cell-Free DNA: Experiences, Challenges, and Expectations for Obstetricians.

Patricia K Agatisa1, Mary Beth Mercer2, Marissa Coleridge3, Ruth M Farrell4,5.   

Abstract

The expansion of cell-free fetal DNA (cfDNA) screening for a larger and diverse set of genetic variants, in addition for use among the low-risk obstetric population, presents important clinical challenges for all healthcare providers involved in the delivery of prenatal care. It is unclear how to leverage the different members of the healthcare team to respond to these challenges. We conducted interviews with 25 prenatal genetic counselors to understand their experience with the continued expansion of cfDNA screening. Participants supported the use of cfDNA screening for the common autosomal aneuploidies, but noted some reservations for its use to identify fetal sex and microdeletions. Participants reported several barriers to ensuring that patients have the information and support to make informed decisions about using cfDNA to screen for these different conditions. This was seen as a dual-sided problem, and necessitated additional education interventions that addressed patients seeking cfDNA screening, and obstetricians who introduce the concepts of genetic risk and cfDNA to patients. In addition, participants noted that they have a professional responsibility to educate obstetricians about cfDNA so they can be prepared to be gatekeepers of counseling and education about this screening option for use among the general obstetric population.

Entities:  

Keywords:  Cell-free fetal DNA; Genetic counselors; Medical education; Patient education; Prenatal genetic testing

Mesh:

Substances:

Year:  2018        PMID: 29951719     DOI: 10.1007/s10897-018-0268-y

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  54 in total

1.  Genetic counselors' experience with cell-free fetal DNA testing as a prenatal screening option for aneuploidy.

Authors:  Julie M H Horsting; Stephen R Dlouhy; Katelyn Hanson; Kimberly Quaid; Shaochun Bai; Karrie A Hines
Journal:  J Genet Couns       Date:  2013-12-19       Impact factor: 2.537

2.  Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.

Authors:  Diana W Bianchi; Lawrence D Platt; James D Goldberg; Alfred Z Abuhamad; Amy J Sehnert; Richard P Rava
Journal:  Obstet Gynecol       Date:  2012-05       Impact factor: 7.661

3.  Noninvasive prenatal testing: the paradigm is shifting rapidly.

Authors:  Lyn S Chitty; Diana W Bianchi
Journal:  Prenat Diagn       Date:  2013-06       Impact factor: 3.050

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

Authors:  D Oepkes; Y Yaron; P Kozlowski; M J Rego de Sousa; J L Bartha; E S van den Akker; S M Dornan; E Krampl-Bettelheim; M Schmid; M Wielgos; V Cirigliano; G C Di Renzo; A Cameron; P Calda; A Tabor
Journal:  Ultrasound Obstet Gynecol       Date:  2014-07       Impact factor: 7.299

5.  Non-invasive prenatal testing: UK genetic counselors' experiences and perspectives.

Authors:  Elizabeth Alexander; Susan Kelly; Lauren Kerzin-Storrar
Journal:  J Genet Couns       Date:  2014-10-15       Impact factor: 2.537

6.  Noninvasive prenatal testing goes global.

Authors:  Subhashini Chandrasekharan; Mollie A Minear; Anthony Hung; Megan Allyse
Journal:  Sci Transl Med       Date:  2014-04-09       Impact factor: 17.956

7.  Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.

Authors:  H Zhang; Y Gao; F Jiang; M Fu; Y Yuan; Y Guo; Z Zhu; M Lin; Q Liu; Z Tian; H Zhang; F Chen; T K Lau; L Zhao; X Yi; Y Yin; W Wang
Journal:  Ultrasound Obstet Gynecol       Date:  2015-04-08       Impact factor: 7.299

8.  Best ethical practices for clinicians and laboratories in the provision of noninvasive prenatal testing.

Authors:  M A Allyse; L C Sayres; M Havard; J S King; H T Greely; L Hudgins; J Taylor; M E Norton; M K Cho; D Magnus; K E Ormond
Journal:  Prenat Diagn       Date:  2013-05-21       Impact factor: 3.050

9.  Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort.

Authors:  Eugene Pergament; Howard Cuckle; Bernhard Zimmermann; Milena Banjevic; Styrmir Sigurjonsson; Allison Ryan; Megan P Hall; Michael Dodd; Phil Lacroute; Melissa Stosic; Nikhil Chopra; Nathan Hunkapiller; Dennis E Prosen; Sallie McAdoo; Zachary Demko; Asim Siddiqui; Matthew Hill; Matthew Rabinowitz
Journal:  Obstet Gynecol       Date:  2014-08       Impact factor: 7.661

10.  A novel approach in pediatric telegenetic services: geneticist, pediatrician and genetic counselor team.

Authors:  Shobana Kubendran; Siddharthan Sivamurthy; Gerald Bradley Schaefer
Journal:  Genet Med       Date:  2017-04-27       Impact factor: 8.822

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  1 in total

1.  Receiving a prenatal diagnosis of Down syndrome by phone: a qualitative study of the experiences of pregnant couples.

Authors:  Stina Lou; Kathrine Carstensen; Ida Vogel; Lone Hvidman; Camilla Palmhøj Nielsen; Maja Lanther; Olav Bjørn Petersen
Journal:  BMJ Open       Date:  2019-03-13       Impact factor: 2.692

  1 in total

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