Derivation of a clinical-based model to detect invasive bacterial infections in febrile infants.
Derivation of a clinical-based model to detect invasive bacterial infections in febrile infants.
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DOI:
10.1002/jhm.12956
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发表时间:
2022-11
影响因子:
2.6
通讯作者:
Fiscella, Kevin A.
中科院分区:
文献类型:
--
作者:
Yaeger, Jeffrey P.;Jones, Jeremiah;Ertefaie, Ashkan;Caserta, Mary T.;Fiscella, Kevin A.
Febrile infants are at risk for invasive bacterial infections (IBIs) (i.e. bacteremia and bacterial meningitis) which, when undiagnosed, may have devastating consequences. Current IBI predictive models rely on serum biomarkers which may not provide timely results and may be difficult to obtain in low-resource settings. To derive a clinical-based IBI predictive model for febrile infants.. This is a cross-sectional study of infants brought to two pediatric emergency departments from January 2011-December 2018. Inclusion criteria were age 0–90 days, temperature ≥38°C, and documented gestational age, fever duration and illness duration. To detect IBIs, we used regression and ensemble machine learning models and evidence-based predictors (i.e. sex, age, chronic medical condition, gestational age, appearance, maximum temperature, fever duration, illness duration, cough status, and urinary tract inflammation). We up-weighted infants with IBIs 8-fold and used 10-fold cross-validation to avoid overfitting. We calculated area-under-the-receiver operating characteristic curve (AUC), prioritizing a high sensitivity to identify the optimal cut-point to estimate sensitivity and specificity. Of 2,311 febrile infants, 39 had an IBI (1.7%). Median age was 54 days (IQR 35–71). The AUC was 0.819 (95% CI 0.762, 0.868). The predictive model achieved a sensitivity of 0.974 (0.800, 1.00) and specificity of 0.530 (0.484, 0.575). Findings suggest a clinical-based model can detect IBIs in febrile infants, performing similarly to serum biomarker-based models. This model may improve health equity by enabling clinicians to estimate IBI risk in any setting. Future studies should prospectively validate findings across multiple sites and investigate performance by age.
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影响因子:
5.1
作者:
DAGAN, R;POWELL, KR;MENEGUS, MA
通讯作者:
MENEGUS, MA
影响因子:
8
作者:
Levine, DA;Platt, SL;Kuppermann, N
通讯作者:
Kuppermann, N
影响因子:
8
作者:
Pantell, Robert H.;Roberts, Kenneth B.;Woods, Charles R., Jr.
通讯作者:
Woods, Charles R., Jr.
影响因子:
--
作者:
Pantell, Robert H;Roberts, Kenneth B;Pantell, Matthew S
通讯作者:
Pantell, Matthew S
DOI:
10.1007/978-3-030-50420-5_41
发表时间:
2020-05-22
期刊:
Computational Science – ICCS 2020
影响因子:
--
作者:
Mnich K;Kitlas Golińska A;Polewko-Klim A;Rudnicki WR
通讯作者:
Rudnicki WR