Cargando…

333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days

BACKGROUND: Fever in infants 1–90 days of age is common. Bacterial meningitis (BM) is a rare, potentially fatal infection that may occur in well-appearing febrile infants (FI). Our objectives were to identify infants with BM in a large population of well-appearing FI and evaluate factors associated...

Descripción completa

Detalles Bibliográficos
Autores principales: Blaschke, Anne J, Korgenski, E Kent, Byington, Carrie L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255642/
http://dx.doi.org/10.1093/ofid/ofy210.344
_version_ 1783373989456904192
author Blaschke, Anne J
Korgenski, E Kent
Byington, Carrie L
author_facet Blaschke, Anne J
Korgenski, E Kent
Byington, Carrie L
author_sort Blaschke, Anne J
collection PubMed
description BACKGROUND: Fever in infants 1–90 days of age is common. Bacterial meningitis (BM) is a rare, potentially fatal infection that may occur in well-appearing febrile infants (FI). Our objectives were to identify infants with BM in a large population of well-appearing FI and evaluate factors associated with the diagnosis of BM in this population. METHODS: The Intermountain Healthcare System (IHS) is comprised of 22 hospitals across Utah and Idaho and includes Primary Children’s Hospital, the only pediatric hospital in a catchment of 400,000 miles(2). IHS has a care process model for the well-appearing FI. We queried the IHS EHR from July 1, 2004 to September 30, 2016 and captured data on age, laboratory testing, and outcomes. Diagnosis of BM required positive CSF culture. RESULTS: We identified 21,135 FI episodes; 54 infants (0.26%) had a diagnosis of BM. Gram-negative organisms predominated in FI 1–28 days [15/24 (63%)] and caused 28/54 (52%) cases overall (Figure 1). FI 1–28 days were significantly more likely to have BM than those 29–90 days (0.41% vs. 0.20%; RR 2.11, 95% CI 1.24–3.61). Laboratory screening showed abnormal white blood cell count in 63% of FI 1–28 days with BM and 50% of FI 29–90 days (P = 0.42); bands were abnormal in 33% and 47% respectively (P = 0.41); urinalysis was abnormal in 21% and 11% (P = 0.42). CSF profile was performed and interpretable in 48/54 (89%); CSF pleocytosis was present in 30/48 [(63%; 15/21 (71%) 1–28 days and 15/27 (56%) P = 0.34]. Nine of 54 (17%) FI with BM would not have been considered “high-risk” based on laboratory criteria alone. Of FI with BM, only 31/54 (57%) had bacteremia with the same organism [17/24 (71%) in those 1–28 days; and 14/30 (47%) in those 29–90 days; P = 0.099]. CONCLUSION: BM is rare and challenging to predict in well-appearing FI. Abnormal screening laboratory values identified 83% of FI with BM. Awaiting blood culture results before performing lumbar puncture would potentially miss 40%. Age was the only predictor for BM risk in our cohort. DISCLOSURES: A. J. Blaschke, BIoFire Diagnostics, LLC: I have intellectual property licensed to BioFire through the University of Utah, Independent Contractor and Investigator, Consulting fee and Licensing agreement or royalty. C. L. Byington, BIoFire Diagnostics, LLC: I have intellectual property licensed to BioFire through the University of Utah, Licensing agreement or royalty.
format Online
Article
Text
id pubmed-6255642
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-62556422018-11-28 333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days Blaschke, Anne J Korgenski, E Kent Byington, Carrie L Open Forum Infect Dis Abstracts BACKGROUND: Fever in infants 1–90 days of age is common. Bacterial meningitis (BM) is a rare, potentially fatal infection that may occur in well-appearing febrile infants (FI). Our objectives were to identify infants with BM in a large population of well-appearing FI and evaluate factors associated with the diagnosis of BM in this population. METHODS: The Intermountain Healthcare System (IHS) is comprised of 22 hospitals across Utah and Idaho and includes Primary Children’s Hospital, the only pediatric hospital in a catchment of 400,000 miles(2). IHS has a care process model for the well-appearing FI. We queried the IHS EHR from July 1, 2004 to September 30, 2016 and captured data on age, laboratory testing, and outcomes. Diagnosis of BM required positive CSF culture. RESULTS: We identified 21,135 FI episodes; 54 infants (0.26%) had a diagnosis of BM. Gram-negative organisms predominated in FI 1–28 days [15/24 (63%)] and caused 28/54 (52%) cases overall (Figure 1). FI 1–28 days were significantly more likely to have BM than those 29–90 days (0.41% vs. 0.20%; RR 2.11, 95% CI 1.24–3.61). Laboratory screening showed abnormal white blood cell count in 63% of FI 1–28 days with BM and 50% of FI 29–90 days (P = 0.42); bands were abnormal in 33% and 47% respectively (P = 0.41); urinalysis was abnormal in 21% and 11% (P = 0.42). CSF profile was performed and interpretable in 48/54 (89%); CSF pleocytosis was present in 30/48 [(63%; 15/21 (71%) 1–28 days and 15/27 (56%) P = 0.34]. Nine of 54 (17%) FI with BM would not have been considered “high-risk” based on laboratory criteria alone. Of FI with BM, only 31/54 (57%) had bacteremia with the same organism [17/24 (71%) in those 1–28 days; and 14/30 (47%) in those 29–90 days; P = 0.099]. CONCLUSION: BM is rare and challenging to predict in well-appearing FI. Abnormal screening laboratory values identified 83% of FI with BM. Awaiting blood culture results before performing lumbar puncture would potentially miss 40%. Age was the only predictor for BM risk in our cohort. DISCLOSURES: A. J. Blaschke, BIoFire Diagnostics, LLC: I have intellectual property licensed to BioFire through the University of Utah, Independent Contractor and Investigator, Consulting fee and Licensing agreement or royalty. C. L. Byington, BIoFire Diagnostics, LLC: I have intellectual property licensed to BioFire through the University of Utah, Licensing agreement or royalty. Oxford University Press 2018-11-26 /pmc/articles/PMC6255642/ http://dx.doi.org/10.1093/ofid/ofy210.344 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Blaschke, Anne J
Korgenski, E Kent
Byington, Carrie L
333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days
title 333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days
title_full 333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days
title_fullStr 333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days
title_full_unstemmed 333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days
title_short 333. Meningitis in Well-Appearing Febrile Infants Aged 1–90 Days
title_sort 333. meningitis in well-appearing febrile infants aged 1–90 days
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255642/
http://dx.doi.org/10.1093/ofid/ofy210.344
work_keys_str_mv AT blaschkeannej 333meningitisinwellappearingfebrileinfantsaged190days
AT korgenskiekent 333meningitisinwellappearingfebrileinfantsaged190days
AT byingtoncarriel 333meningitisinwellappearingfebrileinfantsaged190days