Literature DB >> 30756437

Diagnostic and service impact of genomic testing technologies in a neonatal intensive care unit.

Natalie B Tan1, Tiong Yang Tan1,2, Melissa M Martyn3, Ravi Savarirayan1,2, David J Amor1,2, Amanda Moody4, Susan M White1,2, Zornitza Stark1,2,3.   

Abstract

AIM: To investigate the diagnostic and service impact of chromosomal microarray and whole exome sequencing (WES) in a neonatal intensive care unit (NICU).
METHODS: This was a retrospective medical record review of NICU patients referred for genetics consultation at three time points over a 9-year period at a single centre to determine referral indications, genetic consultation outcomes and time to diagnosis.
RESULTS: The number of NICU patients referred for genetics consultation increased from 44 in 2007 to 95 in 2015. The proportion of NICU patients suspected of having a genetic condition following clinical geneticist assessment remained stable, averaging 5.3% of all admissions. The proportion of patients receiving a confirmed diagnosis rose from 21% in 2007 to 53% in 2015, with a shift from primarily chromosomal abnormalities to a broad range of monogenic disorders, increasingly diagnosed by WES as a first-tier test. The average age at diagnosis in 2015 was 19 days (range 12-38 days) for chromosomal abnormalities and 138 days (range 10-309 days) for monogenic conditions.
CONCLUSIONS: The adoption of new genetic technologies at our centre has increased the proportion of patients receiving a confirmed genetic diagnosis. This study provides important benchmark data to measure further improvements as turn-around times for genomic testing decrease.
© 2019 Paediatrics and Child Health Division (The Royal Australasian College of Physicians).

Entities:  

Keywords:  diagnostic yield; exome sequencing; microarray; neonatal intensive care unit

Mesh:

Year:  2019        PMID: 30756437     DOI: 10.1111/jpc.14398

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN: 1034-4810            Impact factor:   1.954


  6 in total

1.  Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing.

Authors:  Stephen F Kingsmore; Audrey Henderson; Mallory J Owen; Michelle M Clark; Christian Hansen; David Dimmock; Christina D Chambers; Laura L Jeliffe-Pawlowski; Charlotte Hobbs
Journal:  NPJ Genom Med       Date:  2020-11-02       Impact factor: 8.617

Review 2.  Rapid genomic testing for critically ill children: time to become standard of care?

Authors:  Zornitza Stark; Sian Ellard
Journal:  Eur J Hum Genet       Date:  2021-11-08       Impact factor: 4.246

3.  Perspectives of United States neonatologists on genetic testing practices.

Authors:  Monica H Wojcik; Maya C Del Rosario; Pankaj B Agrawal
Journal:  Genet Med       Date:  2022-03-15       Impact factor: 8.864

4.  Expanding the genotypes and phenotypes for 19 rare diseases by exome sequencing performed in pediatric intensive care unit.

Authors:  Juan Liu; Yu Zheng; Jiaotian Huang; Desheng Zhu; Ping Zang; Zhenqing Luo; Yongjia Yang; Yu Peng; Zhenghui Xiao; Yimin Zhu; Xiulan Lu
Journal:  Hum Mutat       Date:  2021-08-15       Impact factor: 4.700

5.  Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing.

Authors:  Stephen F Kingsmore; Audrey Henderson; Mallory J Owen; Michelle M Clark; Christian Hansen; David Dimmock; Christina D Chambers; Laura L Jeliffe-Pawlowski; Charlotte Hobbs
Journal:  NPJ Genom Med       Date:  2020-11-02       Impact factor: 8.617

Review 6.  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

  6 in total

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