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Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management

BACKGROUND: Dengue fever (DF) outbreaks present regionally specific epidemiological and clinical characteristics. In certain medium-sized cities (100 000–250 000 inhabitants) of São Paulo State, Brazil, and after reaching an incidence of 150 cases/100 000 inhabitants (“epidemiological threshold”), c...

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Autores principales: dos Santos Carmo, Andréia Moreira, Suzuki, Rodrigo Buzinaro, Riquena, Michele Marcondes, Eterovic, André, Sperança, Márcia Aparecida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011355/
https://www.ncbi.nlm.nih.gov/pubmed/27593529
http://dx.doi.org/10.1186/s40249-016-0177-y
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author dos Santos Carmo, Andréia Moreira
Suzuki, Rodrigo Buzinaro
Riquena, Michele Marcondes
Eterovic, André
Sperança, Márcia Aparecida
author_facet dos Santos Carmo, Andréia Moreira
Suzuki, Rodrigo Buzinaro
Riquena, Michele Marcondes
Eterovic, André
Sperança, Márcia Aparecida
author_sort dos Santos Carmo, Andréia Moreira
collection PubMed
description BACKGROUND: Dengue fever (DF) outbreaks present regionally specific epidemiological and clinical characteristics. In certain medium-sized cities (100 000–250 000 inhabitants) of São Paulo State, Brazil, and after reaching an incidence of 150 cases/100 000 inhabitants (“epidemiological threshold”), clinical diagnosis indicated dengue virus (DENV) infection. During this period, other seasonally infectious diseases with symptoms and physical signs mimicking DF can simultaneously occur, with the consequential overcrowding of health care facilities as the principal drawbacks. Confirmation of clinical diagnosis of DF with serological tests may help in avoiding faulty diagnosis in patients, who might later undergo dengue hemorrhagic fever (DHF) and the dengue-shock syndrome (DSS). Furthermore, demographic and hematological profiles of patients are useful in detecting specific early characteristics associated to DF, DHF and DSS. METHODS: From March to June, 2007, 456 patients from Marilia in northwest São Paulo State who had only been diagnosed for DF by clinical criteria, underwent serologic testing for non-structural 1 (NS1) DENV antigens. Individual results were used in comparative analysis according to demographic (gender, age) and hematological (leukocyte and platelet counts, percentage of atypical lymphocytes) profiles. Temporal patterns were evaluated by subdividing data according to time of initial attendance, using recorded variables as predictors of DENV infection in logistic regression models and ROC curves. RESULTS: Serologic DENV detection was positive in 70.6 % of the patients. Lower leukocyte and platelet counts were the most important factors in predicting DENV infection (respective medians DENV + = 3 715 cells/ml and DENV- = 6 760 cells/ml, and DENV + = 134 896 cells/ml and DENV- = 223 872 cells/ml). Furthermore, all demographic and hematological profiles presented a conservative temporal pattern throughout this long-lasting outbreak. CONCLUSIONS: As consistency throughout the epidemic facilitated defining the conservation pattern throughout the early stages, this was useful for improving management during the remaining period. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40249-016-0177-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-50113552016-09-06 Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management dos Santos Carmo, Andréia Moreira Suzuki, Rodrigo Buzinaro Riquena, Michele Marcondes Eterovic, André Sperança, Márcia Aparecida Infect Dis Poverty Research Article BACKGROUND: Dengue fever (DF) outbreaks present regionally specific epidemiological and clinical characteristics. In certain medium-sized cities (100 000–250 000 inhabitants) of São Paulo State, Brazil, and after reaching an incidence of 150 cases/100 000 inhabitants (“epidemiological threshold”), clinical diagnosis indicated dengue virus (DENV) infection. During this period, other seasonally infectious diseases with symptoms and physical signs mimicking DF can simultaneously occur, with the consequential overcrowding of health care facilities as the principal drawbacks. Confirmation of clinical diagnosis of DF with serological tests may help in avoiding faulty diagnosis in patients, who might later undergo dengue hemorrhagic fever (DHF) and the dengue-shock syndrome (DSS). Furthermore, demographic and hematological profiles of patients are useful in detecting specific early characteristics associated to DF, DHF and DSS. METHODS: From March to June, 2007, 456 patients from Marilia in northwest São Paulo State who had only been diagnosed for DF by clinical criteria, underwent serologic testing for non-structural 1 (NS1) DENV antigens. Individual results were used in comparative analysis according to demographic (gender, age) and hematological (leukocyte and platelet counts, percentage of atypical lymphocytes) profiles. Temporal patterns were evaluated by subdividing data according to time of initial attendance, using recorded variables as predictors of DENV infection in logistic regression models and ROC curves. RESULTS: Serologic DENV detection was positive in 70.6 % of the patients. Lower leukocyte and platelet counts were the most important factors in predicting DENV infection (respective medians DENV + = 3 715 cells/ml and DENV- = 6 760 cells/ml, and DENV + = 134 896 cells/ml and DENV- = 223 872 cells/ml). Furthermore, all demographic and hematological profiles presented a conservative temporal pattern throughout this long-lasting outbreak. CONCLUSIONS: As consistency throughout the epidemic facilitated defining the conservation pattern throughout the early stages, this was useful for improving management during the remaining period. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40249-016-0177-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-05 /pmc/articles/PMC5011355/ /pubmed/27593529 http://dx.doi.org/10.1186/s40249-016-0177-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
dos Santos Carmo, Andréia Moreira
Suzuki, Rodrigo Buzinaro
Riquena, Michele Marcondes
Eterovic, André
Sperança, Márcia Aparecida
Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
title Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
title_full Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
title_fullStr Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
title_full_unstemmed Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
title_short Maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
title_sort maintenance of demographic and hematological profiles in a long-lasting dengue fever outbreak: implications for management
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011355/
https://www.ncbi.nlm.nih.gov/pubmed/27593529
http://dx.doi.org/10.1186/s40249-016-0177-y
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