Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children
Published 2022 View Full Article
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Title
Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children
Authors
Keywords
Children, Cost-benefit, Cost-effectiveness, Genomics, Rare diseases
Journal
GENETICS IN MEDICINE
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2022-02-16
DOI
10.1016/j.gim.2022.01.013
References
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Related references
Note: Only part of the references are listed.- Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment
- (2021) Ilias Goranitis et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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- (2021) Nathaly M. Sweeney et al. npj Genomic Medicine
- Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children’s hospitals demonstrates improved clinical outcomes and reduced costs of care
- (2021) David Dimmock et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementation
- (2021) Linda S. Franck et al. JOURNAL OF PEDIATRICS
- Rapid genomic testing for critically ill children: time to become standard of care?
- (2021) Zornitza Stark et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments
- (2020) Ilias Goranitis et al. GENETICS IN MEDICINE
- The leadership behaviors needed to implement clinical genomics at scale: a qualitative study
- (2020) Stephanie Best et al. GENETICS IN MEDICINE
- Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
- (2020) et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate
- (2020) Lauren S. Akesson et al. HUMAN MUTATION
- Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates
- (2019) Samantha Ayres et al. Journal of Genetic Counseling
- Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care
- (2019) Zornitza Stark et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit—successes and challenges
- (2019) Alison M. Elliott et al. EUROPEAN JOURNAL OF PEDIATRICS
- The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders
- (2019) Nick Dragojlovic et al. GENETICS IN MEDICINE
- Meeting the challenges of implementing rapid genomic testing in acute pediatric care
- (2018) Zornitza Stark et al. GENETICS IN MEDICINE
- Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization
- (2018) Lauge Farnaes et al. npj Genomic Medicine
- Genomic sequencing in acutely ill infants: what will it take to demonstrate clinical value?
- (2018) Scott D. Grosse et al. GENETICS IN MEDICINE
- Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children
- (2018) Lamia Mestek-Boukhibar et al. JOURNAL OF MEDICAL GENETICS
- Valuation of Health and Nonhealth Outcomes from Next-Generation Sequencing: Approaches, Challenges, and Solutions
- (2018) Dean A. Regier et al. VALUE IN HEALTH
- Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement
- (2017) Zornitza Stark et al. GENETICS IN MEDICINE
- Model Transparency and Validation
- (2012) David M. Eddy et al. MEDICAL DECISION MAKING
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