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 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.

Authors

Institutions

Publication Details

Journal
American Journal of Medical Genetics Part A
Published
2024-08-12
DOI
https://doi.org/10.1002/ajmg.a.63834
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Talia Buitrago-Mogollon, Andrew T. Jacobsmeyer, Jodi Amador, Jasmyne‐Rian Charles et al.
American Journal of Medical Genetics Part A
Genomics and Rare Diseases
article

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

Talia Buitrago-Mogollon, Andrew T. Jacobsmeyer, Jodi Amador, Jasmyne‐Rian Charles, Jessica P. Clarke‐Pounder, Blanche White, Lauren B. Carter
article en

Abstract

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.

American Journal of Medical Genetics Part AVol. 194(12)
Levine Children's Hospital (US)
Openalex Percentile: Top 85%
Genomics and Rare Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Improving genetic testing utilization in a tertiary care neonatal intensive care unit through quality improvement — Talia Buitrago-Mogollon, Andrew T. Jacobsmeyer, et al. · American Journal of Medical Genetics Part A (2024) | TGRS Research Map | TGRS