Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. (December 2017)
- Record Type:
- Journal Article
- Title:
- Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. (December 2017)
- Main Title:
- Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray
- Authors:
- Hayeems, Robin
Bhawra, Jasmin
Tsiplova, Kate
Meyn, M.
Monfared, Nasim
Bowdin, Sarah
Stavropoulos, D.
Marshall, Christian
Basran, Raveen
Shuman, Cheryl
Ito, Shinya
Cohn, Iris
Hum, Courtney
Girdea, Marta
Brudno, Michael
Cohn, Ronald
Scherer, Stephen
Ungar, Wendy - Abstract:
- Abstract The clinical use of whole-genome sequencing (WGS) is expected to alter pediatric medical management. The study aimed to describe the type and cost of healthcare activities following pediatric WGS compared to chromosome microarray (CMA). Healthcare activities prompted by WGS and CMA were ascertained for 101 children with developmental delay over 1 year. Activities following receipt of non-diagnostic CMA were compared to WGS diagnostic and non-diagnostic results. Activities were costed in 2016 Canadian dollars (CDN). Ongoing care accounted for 88.6% of post-test activities. The mean number of lab tests was greater following CMA than WGS (0.55 vs. 0.09;p = 0.007). The mean number of specialist visits was greater following WGS than CMA (0.41 vs. 0;p = 0.016). WGS results (diagnostic vs. non-diagnostic) modified the effect of test type on mean number of activities (p < 0.001). The cost of activities prompted by diagnostic WGS exceeded $557CDN for 10% of cases. In complex pediatric care, CMA prompted additional diagnostic investigations while WGS prompted tailored care guided by genotypic variants. Costs for prompted activities were low for the majority and constitute a small proportion of total test costs. Optimal use of WGS depends on robust evaluation of downstream care and cost consequences.
- Is Part Of:
- European journal of human genetics. Volume 25:Number 12(2017)
- Journal:
- European journal of human genetics
- Issue:
- Volume 25:Number 12(2017)
- Issue Display:
- Volume 25, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 25
- Issue:
- 12
- Issue Sort Value:
- 2017-0025-0012-0000
- Page Start:
- 1303
- Page End:
- 1312
- Publication Date:
- 2017-12
- Subjects:
- Human genetics -- Periodicals
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://www.nature.com/ejhg/index.html ↗
https://www.karger.com/Journal/Home/224162 ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41431-017-0020-3 ↗
- Languages:
- English
- ISSNs:
- 1018-4813
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.730020
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11056.xml