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

Author:

Jacobsmeyer Andrew T.1ORCID,Buitrago‐Mogollon Talia L.2,White Blanche2,Charles Jasmyne‐Rian2,Clarke‐Pounder Jessica P.3,Amador Jodi3,Carter Lauren B.4

Affiliation:

1. Division of Pediatric Hospital Medicine, Department of Pediatrics Atrium Health Levine Children's Hospital Charlotte North Carolina USA

2. Center for Advancing Pediatric Excellence Atrium Health Levine Children's Hospital Charlotte North Carolina USA

3. Division of Neonatology, Department of Pediatrics Atrium Health Levine Children's Hospital Charlotte North Carolina USA

4. Division of Medical Genetics, Department of Pediatrics Atrium Health Levine Children's Hospital Charlotte North Carolina USA

Abstract

AbstractThere 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.

Publisher

Wiley

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