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Multicentre external validation of the Neonatal Healthcare-associated infectiOn Prediction (NeoHoP) score: a retrospective case-control study.

Lloyd, LG; Dramowski, A; Bekker, A; Ballot, DE; Ferreyra, C; Gleeson, B; Nana, T; Sharland, M; Velaphi, SC; Wadula, J; et al. Lloyd, LG; Dramowski, A; Bekker, A; Ballot, DE; Ferreyra, C; Gleeson, B; Nana, T; Sharland, M; Velaphi, SC; Wadula, J; Whitelaw, A; van Weissenbruch, MM (2024) Multicentre external validation of the Neonatal Healthcare-associated infectiOn Prediction (NeoHoP) score: a retrospective case-control study. BMJ Paediatr Open, 8 (1). ISSN 2399-9772 https://doi.org/10.1136/bmjpo-2024-002748
SGUL Authors: Sharland, Michael Roy

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Abstract

BACKGROUND AND OBJECTIVES: Neonatal mortality due to severe bacterial infections is a pressing global issue, especially in low-middle-income countries (LMICs) with constrained healthcare resources. This study aims to validate the Neonatal Healthcare-associated infectiOn Prediction (NeoHoP) score, designed for LMICs, across diverse neonatal populations. METHODS: Prospective data from three South African neonatal units in the Neonatal Sepsis Observational (NeoOBS) study were analysed. The NeoHoP score, initially developed and validated internally in a South African hospital, was assessed using an external cohort of 573 sepsis episodes in 346 infants, focusing on different birth weight categories. Diagnostic metrics were evaluated, including sensitivity, specificity, positive predictive value and area under the receiver operating characteristic curve. RESULTS: The external validation cohort displayed higher median birth weight and gestational age compared with the internal validation cohort. A significant proportion were born before reaching healthcare facilities, resulting in increased sepsis evaluation, and diagnosed healthcare-associated infections (HAIs). Gram-negative infections predominated, with fungal infections more common in the external validation cohort.The NeoHoP score demonstrated robust diagnostic performance, with 92% specificity, 65% sensitivity and a positive likelihood ratio of 7.73. Subgroup analysis for very low birth weight infants produced similar results. The score's generalisability across diverse neonatal populations was evident, showing comparable performance across different birth weight categories. CONCLUSION: This multicentre validation confirms the NeoHoP score as a reliable 'rule-in' test for HAI in neonates, regardless of birth weight. Its potential as a valuable diagnostic tool in LMIC neonatal units addresses a critical gap in neonatal care in low-resource settings.

Item Type: Article
Additional Information: © Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Keywords: neonatology, Humans, Infant, Newborn, Cross Infection, Female, Case-Control Studies, Retrospective Studies, Male, South Africa, Neonatal Sepsis, Intensive Care Units, Neonatal, ROC Curve, Birth Weight, Sensitivity and Specificity, Gestational Age, Predictive Value of Tests, Infant Mortality, Humans, Cross Infection, Birth Weight, Infant Mortality, Sensitivity and Specificity, Case-Control Studies, Retrospective Studies, Predictive Value of Tests, ROC Curve, Gestational Age, Infant, Newborn, Intensive Care Units, Neonatal, South Africa, Female, Male, Neonatal Sepsis, neonatology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: BMJ Paediatr Open
ISSN: 2399-9772
Language: eng
Dates:
DateEvent
1 October 2024Published
11 September 2024Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDFIND, Diagnosis for allUNSPECIFIED
UNSPECIFIEDSouth African Medical Research Councilhttp://dx.doi.org/10.13039/501100001322
PubMed ID: 39353711
Web of Science ID: WOS:001324919000001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116919
Publisher's version: https://doi.org/10.1136/bmjpo-2024-002748

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