Improving genetic testing utilization in a tertiary care neonatal intensive care unit through quality improvement

There is an increasing recognition of the importance of diagnosing genetic conditions with an ever‐growing list of genetic testing options. However, most providers do not have formal genetics training, which makes choosing the most appropriate test to order challenging. Our project sought to improve...

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Veröffentlicht in:American journal of medical genetics. Part A 2024-12, Vol.194 (12), p.e63834-n/a
Hauptverfasser: Jacobsmeyer, Andrew T., Buitrago‐Mogollon, Talia L., White, Blanche, Charles, Jasmyne‐Rian, Clarke‐Pounder, Jessica P., Amador, Jodi, Carter, Lauren B.
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Sprache:eng
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Zusammenfassung:There is an increasing recognition of the importance of diagnosing genetic conditions with an ever‐growing list of genetic testing options. However, most providers do not have formal genetics training, which makes choosing the most appropriate test to order challenging. Our project sought to improve cytogenetic testing utilization in a tertiary care neonatal intensive care unit (NICU) through utilizing quality improvement techniques, specifically the Model for Improvement framework with rapid Plan‐Do‐Study‐Act cycles. Our project utilized various interventions including the implementation of a NICU genetic testing algorithm. Interventions demonstrated improvement in all areas, specifically a 92% reduction in unnecessary cytogenetic testing with improvement in the diagnostic rate. Our work also resulted in a 59% decrease in charges with an estimated projected savings of $21,000 per year. Quality improvement can minimize redundancies and inefficiencies in genetic testing in a Level IV NICU in a large tertiary care children's hospital and result in substantial cost‐savings.
ISSN:1552-4825
1552-4833
1552-4833
DOI:10.1002/ajmg.a.63834