Diagnosing early-onset neonatal sepsis in low-resource settings: development of a multivariable prediction model

被引:7
作者
Neal, Samuel R. [1 ]
Fitzgerald, Felicity [2 ]
Chimhuya, Simba [3 ]
Heys, Michelle [1 ,4 ]
Cortina-Borja, Mario [1 ]
Chimhini, Gwendoline [3 ]
机构
[1] UCL Great Ormond St Inst Child Hlth, Populat Policy & Practice, London, England
[2] UCL Great Ormond St Inst Child Hlth, Infect Immun & Inflammat, London, England
[3] Univ Zimbabwe, Child & Adolescent Hlth Unit, Harare, Zimbabwe
[4] UCL Great Ormond St Inst Child Hlth, Populat Policy & Practice, London WC1N 1EH, England
基金
英国惠康基金;
关键词
Global Health; Infectious Disease Medicine; Intensive Care Units; Neonatal; Neonatology; Sepsis; MANAGEMENT;
D O I
10.1136/archdischild-2022-325158
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ObjectiveTo develop a clinical prediction model to diagnose neonatal sepsis in low-resource settings. DesignSecondary analysis of data collected by the Neotree digital health system from 1 February 2019 to 31 March 2020. We used multivariable logistic regression with candidate predictors identified from expert opinion and literature review. Missing data were imputed using multivariate imputation and model performance was evaluated in the derivation cohort. SettingA tertiary neonatal unit at Sally Mugabe Central Hospital, Zimbabwe. PatientsWe included 2628 neonates aged <72 hours, gestation >= 32(+0) weeks and birth weight >= 1500 g. InterventionsParticipants received standard care as no specific interventions were dictated by the study protocol. Main outcome measuresClinical early-onset neonatal sepsis (within the first 72 hours of life), defined by the treating consultant neonatologist. ResultsClinical early-onset sepsis was diagnosed in 297 neonates (11%). The optimal model included eight predictors: maternal fever, offensive liquor, prolonged rupture of membranes, neonatal temperature, respiratory rate, activity, chest retractions and grunting. Receiver operating characteristic analysis gave an area under the curve of 0.74 (95% CI 0.70-0.77). For a sensitivity of 95% (92%-97%), corresponding specificity was 11% (10%-13%), positive predictive value 12% (11%-13%), negative predictive value 95% (92%-97%), positive likelihood ratio 1.1 (95% CI 1.0-1.1) and negative likelihood ratio 0.4 (95% CI 0.3-0.6). ConclusionsOur clinical prediction model achieved high sensitivity with low specificity, suggesting it may be suited to excluding early-onset sepsis. Future work will validate and update this model before considering implementation within the Neotree.
引用
收藏
页码:608 / 615
页数:8
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