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Machine learning applications on neonatal sepsis treatment: a scoping review.

O'Sullivan, C; Tsai, DH-T; Wu, IC-Y; Boselli, E; Hughes, C; Padmanabhan, D; Hsia, Y (2023) Machine learning applications on neonatal sepsis treatment: a scoping review. BMC Infect Dis, 23 (1). p. 441. ISSN 1471-2334 https://doi.org/10.1186/s12879-023-08409-3
SGUL Authors: Wu, Chang-Yen

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Abstract

INTRODUCTION: Neonatal sepsis is a major cause of health loss and mortality worldwide. Without proper treatment, neonatal sepsis can quickly develop into multisystem organ failure. However, the signs of neonatal sepsis are non-specific, and treatment is labour-intensive and expensive. Moreover, antimicrobial resistance is a significant threat globally, and it has been reported that over 70% of neonatal bloodstream infections are resistant to first-line antibiotic treatment. Machine learning is a potential tool to aid clinicians in diagnosing infections and in determining the most appropriate empiric antibiotic treatment, as has been demonstrated for adult populations. This review aimed to present the application of machine learning on neonatal sepsis treatment. METHODS: PubMed, Embase, and Scopus were searched for studies published in English focusing on neonatal sepsis, antibiotics, and machine learning. RESULTS: There were 18 studies included in this scoping review. Three studies focused on using machine learning in antibiotic treatment for bloodstream infections, one focused on predicting in-hospital mortality associated with neonatal sepsis, and the remaining studies focused on developing machine learning prediction models to diagnose possible sepsis cases. Gestational age, C-reactive protein levels, and white blood cell count were important predictors to diagnose neonatal sepsis. Age, weight, and days from hospital admission to blood sample taken were important to predict antibiotic-resistant infections. The best-performing machine learning models were random forest and neural networks. CONCLUSION: Despite the threat antimicrobial resistance poses, there was a lack of studies focusing on the use of machine learning for aiding empirical antibiotic treatment for neonatal sepsis.

Item Type: Article
Additional Information: © The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Keywords: Antibiotic, Antimicrobial Resistance, Bloodstream Infection, Machine Learning, Neonate, Adult, Infant, Newborn, Humans, Neonatal Sepsis, Sepsis, Anti-Bacterial Agents, Gestational Age, Hydrolases, Machine Learning, Humans, Sepsis, Hydrolases, Anti-Bacterial Agents, Gestational Age, Adult, Infant, Newborn, Machine Learning, Neonatal Sepsis, Neonate, Bloodstream Infection, Machine Learning, Antibiotic, Antimicrobial Resistance, 0605 Microbiology, 1103 Clinical Sciences, 1108 Medical Microbiology, Microbiology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: BMC Infect Dis
ISSN: 1471-2334
Language: eng
Dates:
DateEvent
29 June 2023Published
20 June 2023Accepted
Publisher License: Creative Commons: Attribution 4.0
PubMed ID: 37386442
Web of Science ID: WOS:001020885200001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/115601
Publisher's version: https://doi.org/10.1186/s12879-023-08409-3

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