Whole exome sequencing (WES) has revolutionized the way we think about and diagnose epileptic encephalopathies. Multiple recent review articles discuss the benefits of WES and suggest various algorithms to follow for determining the etiology of epileptic encephalopathies. Incorporation of WES in these algorithms is leading to the discovery of new genetic diagnoses of early onset epileptic encephalopathies (EOEEs) at a rapid rate; however, WES is not yet a universally utilized diagnostic tool. Clinical WES may be underutilized due to provider discomfort in ordering the test or perceived costliness. At our hospital WES is not routinely performed for patients with EOEE due to limited insurance reimbursement. In fact for any patient with noncommercial insurance (Medicaid) the institution does not allow sending out WES as this is not "established"/"proven to be highly useful and cost effective"/"approved test" in patients with epilepsy. Recently, we performed WES on four patients from three families and identified novel mutations in known epilepsy genes in all four cases. These patients had State Medicaid as their insurance carrier and were followed up for several years for EOEE while being worked up using the traditional/approved testing methods. Following a recently proposed diagnostic pathway, we analyzed the cost savings (US dollars) that could be accrued if WES was performed earlier in the diagnostic odyssey. This is the first publication that addresses the dollar cost of traditional testing in EOEE as performed in these four cases versus WES and the potential cost savings.
Journal article
Reducing the Cost of the Diagnostic Odyssey in Early Onset Epileptic Encephalopathies
BioMed Research International, Vol.2016, pp.6421039-6421039
04/07/2016
DOI: 10.1155/2016/6421039
PMCID: PMC4875968
PMID: 27243033
Abstract
Details
- Title: Subtitle
- Reducing the Cost of the Diagnostic Odyssey in Early Onset Epileptic Encephalopathies
- Creators
- Charuta Joshi - University of IowaDiana L Kolbe - University of IowaM Adela Mansilla - University of IowaSara O MasonRichard J H Smith - University of IowaColleen A Campbell - University of Iowa
- Resource Type
- Journal article
- Publication Details
- BioMed Research International, Vol.2016, pp.6421039-6421039
- DOI
- 10.1155/2016/6421039
- PMID
- 27243033
- PMCID
- PMC4875968
- NLM abbreviation
- Biomed Res Int
- ISSN
- 2314-6141
- Number of pages
- 9
- Copyright
- Copyright © 2016 Charuta Joshi et al.
- Grant note
- name: University of Iowa Carver College of Medicine
- Language
- English
- Date published
- 04/07/2016
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Carver College of Medicine; Otolaryngology; Internal Medicine; Iowa Institute of Human Genetics
- Record Identifier
- 9983557323502771
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