Literature DB >> 29266212

Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact.

J Wynn1, R Ottman2, J Duong3, A L Wilson4, P Ahimaz1, J Martinez1, R Rabin5, E Rosen5, R Webster6, C Au4, M T Cho4,7, C Egan4, E Guzman4, M Primiano4, J E Shaw4, R Sisson4, R L Klitzman8, P S Appelbaum8, U Lichter-Konecki1, K Anyane-Yeboa1, A Iglesias1, W K Chung1,9.   

Abstract

Clinical exome sequencing (CES) is increasingly being used as an effective diagnostic tool in the field of pediatric genetics. We sought to evaluate the parental experience, understanding and psychological impact of CES by conducting a survey study of English-speaking parents of children who had diagnostic CES. Parents of 192 unique patients participated. The parent's interpretation of the child's result agreed with the clinician's interpretation in 79% of cases, with more frequent discordance when the clinician's interpretation was uncertain. The majority (79%) reported no regret with the decision to have CES. Most (65%) reported complete satisfaction with the genetic counseling experience, and satisfaction was positively associated with years of genetic counselor (GC) experience. The psychological impact of CES was greatest for parents of children with positive results and for parents with anxiety or depression. The results of this study are important for helping clinicians to prepare families for the possible results and variable psychological impact of CES. The frequency of parental misinterpretation of test results indicates the need for additional clarity in the communication of results. Finally, while the majority of patients were satisfied with their genetic counseling, satisfaction was lower for new GCs, suggesting a need for targeted GC training for genomic testing.
© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  exome sequencing; genetic counseling; genomic medicine; parental experience; psychological impact

Mesh:

Year:  2018        PMID: 29266212      PMCID: PMC5899627          DOI: 10.1111/cge.13200

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  36 in total

1.  Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.

Authors:  Marian Reiff; Ellen Giarelli; Barbara A Bernhardt; Ebony Easley; Nancy B Spinner; Pamela L Sankar; Surabhi Mulchandani
Journal:  J Autism Dev Disord       Date:  2015-10

2.  Conceptualizing genetic counseling as psychotherapy in the era of genomic medicine.

Authors:  Jehannine Austin; Alicia Semaka; George Hadjipavlou
Journal:  J Genet Couns       Date:  2014-05-21       Impact factor: 2.537

3.  The nuanced negative: Meanings of a negative diagnostic result in clinical exome sequencing.

Authors:  Debra Skinner; Kelly A Raspberry; Martha King
Journal:  Sociol Health Illn       Date:  2016-08-19

4.  Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients.

Authors:  Heidi S Lumish; Hallie Steinfeld; Carrie Koval; Donna Russo; Elana Levinson; Julia Wynn; James Duong; Wendy K Chung
Journal:  J Genet Couns       Date:  2017-03-29       Impact factor: 2.537

5.  Depression in the U.S. household population, 2009-2012.

Authors:  Laura A Pratt; Debra J Brody
Journal:  NCHS Data Brief       Date:  2014-12

6.  Clinical exome sequencing for genetic identification of rare Mendelian disorders.

Authors:  Hane Lee; Joshua L Deignan; Naghmeh Dorrani; Samuel P Strom; Sibel Kantarci; Fabiola Quintero-Rivera; Kingshuk Das; Traci Toy; Bret Harry; Michael Yourshaw; Michelle Fox; Brent L Fogel; Julian A Martinez-Agosto; Derek A Wong; Vivian Y Chang; Perry B Shieh; Christina G S Palmer; Katrina M Dipple; Wayne W Grody; Eric Vilain; Stanley F Nelson
Journal:  JAMA       Date:  2014-11-12       Impact factor: 56.272

7.  Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling.

Authors:  R Z Hayeems; R Babul-Hirji; N Hoang; R Weksberg; C Shuman
Journal:  J Genet Couns       Date:  2015-08-12       Impact factor: 2.537

8.  Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.

Authors:  Kelly D Farwell; Layla Shahmirzadi; Dima El-Khechen; Zöe Powis; Elizabeth C Chao; Brigette Tippin Davis; Ruth M Baxter; Wenqi Zeng; Cameron Mroske; Melissa C Parra; Stephanie K Gandomi; Ira Lu; Xiang Li; Hong Lu; Hsiao-Mei Lu; David Salvador; David Ruble; Monica Lao; Soren Fischbach; Jennifer Wen; Shela Lee; Aaron Elliott; Charles L M Dunlop; Sha Tang
Journal:  Genet Med       Date:  2014-11-13       Impact factor: 8.822

9.  Illustrative case studies in the return of exome and genome sequencing results.

Authors:  Laura M Amendola; Denise Lautenbach; Sarah Scollon; Barbara Bernhardt; Sawona Biswas; Kelly East; Jessica Everett; Marian J Gilmore; Patricia Himes; Victoria M Raymond; Julia Wynn; Ragan Hart; Gail P Jarvik
Journal:  Per Med       Date:  2015       Impact factor: 2.512

10.  "What does it mean?": uncertainties in understanding results of chromosomal microarray testing.

Authors:  Marian Reiff; Barbara A Bernhardt; Surabhi Mulchandani; Danielle Soucier; Diana Cornell; Reed E Pyeritz; Nancy B Spinner
Journal:  Genet Med       Date:  2012-01-05       Impact factor: 8.822

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  15 in total

1.  The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease.

Authors:  Allyn McConkie-Rosell; Kelly Schoch; Jennifer Sullivan; Heidi Cope; Rebecca Spillmann; Christina G S Palmer; Loren Pena; Yong-Hui Jiang; Nicole Daniels; Nicole Walley; Khoon G Tan; Stephen R Hooper; Vandana Shashi
Journal:  Clin Genet       Date:  2019-10-08       Impact factor: 4.438

Review 2.  Patients' views on variants of uncertain significance across indications.

Authors:  Kristin Clift; Sarah Macklin; Colin Halverson; Jennifer B McCormick; Abd Moain Abu Dabrh; Stephanie Hines
Journal:  J Community Genet       Date:  2019-08-20

3.  Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: 2 approved, 2 approved with reservations].

Authors:  Celine Lewis; James Buchannan; Angus Clarke; Emma Clement; Bettina Friedrich; Jillian Hastings-Ward; Melissa Hill; Ruth Horn; Anneke M Lucassen; Chris Patch; Alexandra Pickard; Lauren Roberts; Saskia C Sanderson; Sarah L Lewell; Cecilia Vindrola-Padros; Monica Lakhanpaul
Journal:  NIHR Open Res       Date:  2021-11-22

4.  A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.

Authors:  Julie A Cakici; David P Dimmock; Sara A Caylor; Mary Gaughran; Christina Clarke; Cynthia Triplett; Michelle M Clark; Stephen F Kingsmore; Cinnamon S Bloss
Journal:  Am J Hum Genet       Date:  2020-11-05       Impact factor: 11.025

5.  Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies.

Authors:  Jill O Robinson; Julia Wynn; Barbara Biesecker; Leslie G Biesecker; Barbara Bernhardt; Kyle B Brothers; Wendy K Chung; Kurt D Christensen; Robert C Green; Amy L McGuire; M Ragan Hart; Ida Griesemer; Donald L Patrick; Christine Rini; David Veenstra; Angel M Cronin; Stacy W Gray
Journal:  Genet Med       Date:  2019-06-13       Impact factor: 8.822

Review 6.  Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.

Authors:  Alison M Elliott
Journal:  Cold Spring Harb Perspect Med       Date:  2020-03-02       Impact factor: 6.915

7.  Hope versus reality: Parent expectations of genomic testing.

Authors:  Katherine E Donohue; Siobhan M Dolan; Dana Watnick; Katie M Gallagher; Jacqueline A Odgis; Sabrina A Suckiel; Nehama Teitelman; Bruce D Gelb; Eimear E Kenny; Melissa P Wasserstein; Carol R Horowitz; Laurie J Bauman
Journal:  Patient Educ Couns       Date:  2021-01-29

8.  Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort.

Authors:  Joseph D Symonds; Sameer M Zuberi; Kirsty Stewart; Ailsa McLellan; Mary O'Regan; Stewart MacLeod; Alice Jollands; Shelagh Joss; Martin Kirkpatrick; Andreas Brunklaus; Daniela T Pilz; Jay Shetty; Liam Dorris; Ishaq Abu-Arafeh; Jamie Andrew; Philip Brink; Mary Callaghan; Jamie Cruden; Louise A Diver; Christine Findlay; Sarah Gardiner; Rosemary Grattan; Bethan Lang; Jane MacDonnell; Jean McKnight; Calum A Morrison; Lesley Nairn; Meghan M Slean; Elma Stephen; Alan Webb; Angela Vincent; Margaret Wilson
Journal:  Brain       Date:  2019-08-01       Impact factor: 13.501

Review 9.  The influence of social determinants of health on the genetic diagnostic odyssey: who remains undiagnosed, why, and to what effect?

Authors:  Yarden S Fraiman; Monica H Wojcik
Journal:  Pediatr Res       Date:  2020-09-15       Impact factor: 3.756

10.  Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions.

Authors:  Afiqah Yusuf; Iskra Peltekova; Tal Savion-Lemieux; Jennifer Frei; Ridha Joober; Jennifer Howe; Stephen W Scherer; Mayada Elsabbagh
Journal:  J Genet Couns       Date:  2020-09-06       Impact factor: 2.537

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