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Severe pertussis infection: A clinicopathological study

We aimed to investigate the clinicopathological features of pertussis in children admitted to a tertiary-care university hospital in Brazil. This was a retrospective cohort study of all pediatric hospital admissions with pertussis from January 1, 2008 to December 31, 2014. We also reported the autop...

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Autores principales: Palvo, Fernando, Fabro, Alexandre Todorovic, Cervi, Maria Célia, Aragon, Davi Casale, Ramalho, Fernando Silva, Carlotti, Ana Paula de Carvalho Panzeri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728762/
https://www.ncbi.nlm.nih.gov/pubmed/29310361
http://dx.doi.org/10.1097/MD.0000000000008823
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author Palvo, Fernando
Fabro, Alexandre Todorovic
Cervi, Maria Célia
Aragon, Davi Casale
Ramalho, Fernando Silva
Carlotti, Ana Paula de Carvalho Panzeri
author_facet Palvo, Fernando
Fabro, Alexandre Todorovic
Cervi, Maria Célia
Aragon, Davi Casale
Ramalho, Fernando Silva
Carlotti, Ana Paula de Carvalho Panzeri
author_sort Palvo, Fernando
collection PubMed
description We aimed to investigate the clinicopathological features of pertussis in children admitted to a tertiary-care university hospital in Brazil. This was a retrospective cohort study of all pediatric hospital admissions with pertussis from January 1, 2008 to December 31, 2014. We also reported the autopsy findings in children who died. Fifty-five patients admitted to the hospital over the study period had laboratorial confirmation of Bordetella pertussis infection, 17 (30.9%) needed pediatric intensive care unit (PICU) admission and 6 (10.9%) died. All patients who died were younger than 60 days old and unvaccinated for pertussis; 50% of them had coinfection with respiratory syncytial virus. Leukocyte count ≥40,000/mm(3) at hospital admission was an independent risk factor for PICU admission. Mean heart rate during hospitalization ≥160 bpm was an independent risk factor for death. A cut-off point of 41,200 leukocytes/mm(3) at hospital admission had sensitivity of 64.7% and specificity of 89.5% to predict PICU admission (area under the curve 0.75) and sensitivity of 100% and specificity of 81.6% to predict death (area under the curve 0.93). Autopsy showed medial thickening of small pulmonary arteries in 80% of patients who had pulmonary hypertension; intravascular aggregates of leukocytes or pulmonary thrombosis were not observed. Immunohistochemical staining of tissue samples obtained at autopsy identified B pertussis and respiratory syncytial virus in pulmonary and extra-pulmonary sites. Marked leukocytosis at presentation was associated with morbidity and mortality in children hospitalized with pertussis. Implementation of preventive strategies is crucial to diminish the incidence of the disease, especially in young unimmunized infants.
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spelling pubmed-57287622017-12-20 Severe pertussis infection: A clinicopathological study Palvo, Fernando Fabro, Alexandre Todorovic Cervi, Maria Célia Aragon, Davi Casale Ramalho, Fernando Silva Carlotti, Ana Paula de Carvalho Panzeri Medicine (Baltimore) 4900 We aimed to investigate the clinicopathological features of pertussis in children admitted to a tertiary-care university hospital in Brazil. This was a retrospective cohort study of all pediatric hospital admissions with pertussis from January 1, 2008 to December 31, 2014. We also reported the autopsy findings in children who died. Fifty-five patients admitted to the hospital over the study period had laboratorial confirmation of Bordetella pertussis infection, 17 (30.9%) needed pediatric intensive care unit (PICU) admission and 6 (10.9%) died. All patients who died were younger than 60 days old and unvaccinated for pertussis; 50% of them had coinfection with respiratory syncytial virus. Leukocyte count ≥40,000/mm(3) at hospital admission was an independent risk factor for PICU admission. Mean heart rate during hospitalization ≥160 bpm was an independent risk factor for death. A cut-off point of 41,200 leukocytes/mm(3) at hospital admission had sensitivity of 64.7% and specificity of 89.5% to predict PICU admission (area under the curve 0.75) and sensitivity of 100% and specificity of 81.6% to predict death (area under the curve 0.93). Autopsy showed medial thickening of small pulmonary arteries in 80% of patients who had pulmonary hypertension; intravascular aggregates of leukocytes or pulmonary thrombosis were not observed. Immunohistochemical staining of tissue samples obtained at autopsy identified B pertussis and respiratory syncytial virus in pulmonary and extra-pulmonary sites. Marked leukocytosis at presentation was associated with morbidity and mortality in children hospitalized with pertussis. Implementation of preventive strategies is crucial to diminish the incidence of the disease, especially in young unimmunized infants. Wolters Kluwer Health 2017-12-01 /pmc/articles/PMC5728762/ /pubmed/29310361 http://dx.doi.org/10.1097/MD.0000000000008823 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 4900
Palvo, Fernando
Fabro, Alexandre Todorovic
Cervi, Maria Célia
Aragon, Davi Casale
Ramalho, Fernando Silva
Carlotti, Ana Paula de Carvalho Panzeri
Severe pertussis infection: A clinicopathological study
title Severe pertussis infection: A clinicopathological study
title_full Severe pertussis infection: A clinicopathological study
title_fullStr Severe pertussis infection: A clinicopathological study
title_full_unstemmed Severe pertussis infection: A clinicopathological study
title_short Severe pertussis infection: A clinicopathological study
title_sort severe pertussis infection: a clinicopathological study
topic 4900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728762/
https://www.ncbi.nlm.nih.gov/pubmed/29310361
http://dx.doi.org/10.1097/MD.0000000000008823
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