Predicting Risk of Serious Bacterial Infections in Febrile Children in the Emergency Department

被引:51
|
作者
Irwin, Adam D. [1 ]
Grant, Alison [5 ]
Williams, Rhian [5 ]
Kolamunnage-Dona, Ruwanthi [2 ]
Drew, Richard J. [8 ,9 ]
Paulus, Stephane [6 ]
Jeffers, Graham [3 ]
Williams, Kim [5 ]
Breen, Rachel [4 ]
Preston, Jennifer [3 ]
Appelbe, Duncan [4 ]
Chesters, Christine [7 ]
Newland, Paul [7 ]
Marzouk, Omnia [5 ]
McNamara, Paul S. [3 ]
Diggle, Peter J. [1 ,10 ]
Carrol, Enitan D. [1 ]
机构
[1] Univ Liverpool, Inst Infect & Global Hlth, Liverpool, Merseyside, England
[2] Univ Liverpool, Dept Biostat, Liverpool, Merseyside, England
[3] Univ Liverpool, Inst Translat Med, Liverpool, Merseyside, England
[4] Univ Liverpool, Clin Trials Res Ctr, Liverpool, Merseyside, England
[5] Alder Hey Childrens Hosp NHS Fdn Trust, Dept Emergency, Liverpool, Merseyside, England
[6] Alder Hey Childrens Hosp NHS Fdn Trust, Dept Infect Dis, Liverpool, Merseyside, England
[7] Alder Hey Childrens Hosp NHS Fdn Trust, Dept Biochem, Liverpool, Merseyside, England
[8] Rotunda Hosp, Dept Microbiol, Dublin, Ireland
[9] Royal Coll Surgeons Ireland, Dept Microbiol, Dublin, Ireland
[10] Univ Lancaster, Ctr Hlth Informat Comp & Stat, Lancaster, England
基金
美国国家卫生研究院;
关键词
MENINGOCOCCAL DISEASE; HOSPITAL ADMISSIONS; TIME-TRENDS; ENGLAND; VALIDATION; DIAGNOSIS; IMPACT; MODEL;
D O I
10.1542/peds.2016-2853
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: Improving the diagnosis of serious bacterial infections (SBIs) in the children's abstract emergency department is a clinical priority. Early recognition reduces morbidity and mortality, and supporting clinicians in ruling out SBIs may limit unnecessary admissions and antibiotic use. METHODS: A prospective, diagnostic accuracy study of clinical and biomarker variables in the diagnosis of SBIs (pneumonia or other SBI) in febrile children <16 years old. A diagnostic model was derived by using multinomial logistic regression and internally validated. External validation of a published model was undertaken, followed by model updating and extension by the inclusion of procalcitonin and resistin. RESULTS: There were 1101 children studied, of whom 264 had an SBI. A diagnostic model discriminated well between pneumonia and no SBI (concordance statistic 0.84, 95% confidence interval 0.78-0.90) and between other SBIs and no SBI (0.77, 95% confidence interval 0.71-0.83) on internal validation. A published model discriminated well on external validation. Model updating yielded good calibration with good performance at both high-risk (positive likelihood ratios: 6.46 and 5.13 for pneumonia and other SBI, respectively) and low-risk (negative likelihood ratios: 0.16 and 0.13, respectively) thresholds. Extending the model with procalcitonin and resistin yielded improvements in discrimination. CONCLUSIONS: Diagnostic models discriminated well between pneumonia, other SBIs, and no SBI in febrile children in the emergency department. Improvements in the classification of nonevents have the potential to reduce unnecessary hospital admissions and improve antibiotic prescribing. The benefits of this improved risk prediction should be further evaluated in robust impact studies.
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页数:11
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