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Original Articles

Neonatal hypoglycemia algorithms improve hospital outcomes

, , , ORCID Icon, &
Pages 2278-2285 | Received 24 Jan 2020, Accepted 17 Jun 2020, Published online: 20 Jul 2020
 

Abstract

Objective

Neonatal hypoglycemia is a common diagnosis for which management strategies vary. Our goal was to implement hypoglycemia algorithms (HGA) to streamline management of neonatal hypoglycemia within our hospital system and improve outcomes related to promoting the mother-infant dyad and decreasing hospital costs.

Patients and methods

A retrospective cohort study analyzed data on 4,666 asymptomatic infants at risk for hypoglycemia and born at two, large, community hospitals between 2010 and 2016. The first algorithm (HGA1) was created in 2012 and subsequently updated (HGA2) in 2014 to include the use of dextrose gel. Infants were separated into three groups by epoch: pre-HGA (2010–2011), HGA1 (2012–2013), and HGA2 (2014–2016). Outcomes between groups were then analyzed. Cost savings were calculated using linear regression.

Results

Compared with the pre-HGA group, the HGA1 group had decreased intravenous dextrose use (3.9 vs. 2.5%, p < .001). Compared with the HGA1 group, the HGA2 group had decreased intravenous dextrose use (2.5 vs. 1.0%, p < .001) and increased breastfeeding rates (88.4% vs. 86.7%, p = .003). Neonatal intensive care unit admission rates decreased when comparing the pre-HGA group with the HGA2 group (10.6% vs 9.4%, p = .03). Length of stay was overall unchanged. Total cost savings were approximately $222 per case.

Conclusions

By implementing HGA1 and providing resources to unify care for asymptomatic infants at risk for hypoglycemia, short-term outcomes in our hospital system improved. By updating HGA2 to include the use of dextrose gel, the advantages gained by HGA1 were maintained and further enhanced. Overall cost of care was reduced.

Author contribution

Dr. Plummer assisted in study design, analyzed and interpreted data, drafted the initial manuscript, and reviewed and revised the manuscript.

Ms. Ninkovic and Ms. Rees coordinated and supervised data collection, aided in acquisition of data, carried out analysis and interpretation of data, and reviewed and revised the manuscript.

Dr. Rao and Dr. Bendel reviewed the manuscript and revised it critically for important intellectual content.

Dr. Stepka conceptualized and designed the study, analyzed and interpreted data, and reviewed and revised the manuscript.

All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

Acknowledgements

Thank you to Sally Wallstrom, CRN, Carmen G. Henke, NNP, Nancy Fahim, MD for their significant contributions to the design and implementation of the clinical process models. Thank you to Paul James for his assistance with the cost analysis.

Disclosure statement

No potential conflict of interest was reported by the author(s).

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