Open AccessClinical whole‐exome sequencing results impact medical management
Author(s) -
Niguidula Nancy,
Alamillo Christina,
Shahmirzadi Mowlavi Layla,
Powis Zöe,
Cohen Julie S.,
Farwell Hagman Kelly D.
Publication year - 2018
Publication title -
molecular genetics and genomic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 29
ISSN - 2324-9269
DOI - 10.1002/mgg3.484
Subject(s) - exome sequencing , medicine , exome , genetic testing , pediatrics , mutation , genetics , biology , gene
Background Clinical diagnostic whole‐exome sequencing (WES) is a powerful tool for patients with undiagnosed genetic disorders. To demonstrate the clinical utility, we surveyed healthcare providers (HCP) about changes in medical management and treatment, diagnostic testing, reproductive planning, and use of educational services subsequent to WES testing. Methods For a period of 18 months, an 18‐question survey was sent to HCPs attached to the WES reports. We analyzed the molecular diagnosis, patient clinical features, and the medical management changes reported in the returned surveys. Results A total of 62 (2.2% of 2,876) surveys were returned, consisting of 37.1% patients with a positive or likely positive pathogenic alteration, 51.6% negative results, 9.7% uncertain findings, and 1 patient (1.6%) with a novel candidate finding. Overall, 100% of the HCPs of patients with positive or likely positive WES results ( n = 23) and HCPs of patients with uncertain WES results ( n = 6) responded positively to one of the 18 queries. Of note, 37.5% of the HCPs of patients with negative WES results ( n = 32) responded positively to at least one query. Conclusion Overall, these data clearly demonstrate the clinical utility of WES by demonstrating the impact on medical management irrespective of the exome result.