Literature DB >> 23746553

Improving surveillance for hyperammonemia in the newborn.

Samantha A Vergano1, Jonathan M Crossette, Frederick C Cusick, Bimal R Desai, Matthew A Deardorff, Neal Sondheimer.   

Abstract

OBJECTIVE: Prompt ascertainment is crucial for the management of hyperammonemic infants. Because these patients are rare and recognition of hyperammonemia is often delayed, we designed and implemented an electronic medical record (EMR)-based tool to assist physicians in the detection of hyperammonemia.
METHODS: We retrospectively evaluated the hospitalizations of prior hyperammonemic infants to identify codable elements that could trigger an EMR-based warning. An alert was designed and implemented and its utilization was prospectively analyzed.
RESULTS: Blood gas studies were obtained universally and early in the retrospectively evaluated infants (x¯=26h before ammonia level). Prompting physicians to evaluate ammonia after ordering blood gas studies would have accelerated the initial ammonia order in 89% of retrospective cases. The alert has activated 184 times over the first six months of operation leading to 63 laboratory evaluations and detection of one hyperammonemic infant.
CONCLUSION: Implementation of an EMR-based warning system can improve surveillance for hyperammonemia in a susceptible population.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CMP; EMR; Electronic medical record; IEM; Infant; Screening; UCD; Urea cycle defect; comprehensive metabolic panel; electronic medical record; inborn error of metabolism; urea cycle disorder

Mesh:

Substances:

Year:  2013        PMID: 23746553      PMCID: PMC3755016          DOI: 10.1016/j.ymgme.2013.05.005

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


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