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Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
- Source :
- Italian Journal of Pediatrics, Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-8 (2017)
- Publication Year :
- 2017
- Publisher :
- Biomed Central, 2017.
-
Abstract
- The rapid advancement of next-generation sequencing (NGS) technology and the decrease in costs for whole-exome sequencing (WES) and whole-genome sequening (WGS), has prompted its clinical application in several fields of medicine. Currently, there are no specific guidelines for the use of NGS in the field of neonatal medicine and in the diagnosis of genetic diseases in critically ill newborn infants. As a consequence, NGS may be underused with reduced diagnostic success rate, or overused, with increased costs for the healthcare system. Most genetic diseases may be already expressed during the neonatal age, but their identification may be complicated by nonspecific presentation, especially in the setting of critical clinical conditions. The differential diagnosis process in the neonatal intensive care unit (NICU) may be time-consuming, uncomfortable for the patient due to repeated sampling, and ineffective in reaching a molecular diagnosis during NICU stay. Serial gene sequencing (Sanger sequencing) may be successful only for conditions for which the clinical phenotype strongly suggests a diagnostic hypothesis and for genetically homogeneous diseases. Newborn screenings with Guthrie cards, which vary from country to country, are designed to only test for a few dozen genetic diseases out of the more than 6000 diseases for which a genetic characterization is available. The use of WES in selected cases in the NICU may overcome these issues. We present an intersociety document that aims to define the best indications for the use of WES in different clinical scenarios in the NICU. We propose that WES is used in the NICU for critically ill newborn infants when an early diagnosis is desirable to guide the clinical management during NICU stay, when a strong hypothesis cannot be formulated based on the clinical phenotype or the disease is genetically heterogeneous, and when specific non-genetic laboratory tests are not available. The use of WES may reduce the time for diagnosis in infants during NICU stay and may eventually result in cost-effectiveness.
- Subjects :
- 0301 basic medicine
Male
Neonatal intensive care unit
Disease
Review
030105 genetics & heredity
Pediatrics
Whole Exome Sequencing
Neonate
Neonatal
Outcome Assessment, Health Care
Diagnosis
Policy Making
Exome sequencing
Sanger sequencing
Genome
lcsh:RJ1-570
Perinatology and Child Health
Settore MED/38
Intensive Care Units
Italy
Whole-exome sequencing
Practice Guidelines as Topic
symbols
WES
Female
Human
Diagnosi
NICU
medicine.medical_specialty
Mendelian
03 medical and health sciences
symbols.namesake
Outcome Assessment (Health Care)
Neonatal Screening
Genetic
Intensive Care Units, Neonatal
Exome Sequencing
medicine
WGS
Pediatrics, Perinatology and Child Health
Humans
Genetic Testing
Intensive care medicine
Settore MED/06 - ONCOLOGIA MEDICA
Genetic heterogeneity
Critically ill
business.industry
Genome, Human
Infant, Newborn
Infant
lcsh:Pediatrics
Newborn
Infant newborn
030104 developmental biology
Differential diagnosis
business
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Italian Journal of Pediatrics, Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-8 (2017)
- Accession number :
- edsair.doi.dedup.....b3f5bb4c34c3e2ab8530519642fcb0df