Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos

Detalhes bibliográficos
Autor(a) principal: Costa, Flávia Oliveira da
Data de Publicação: 2013
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFS
Texto Completo: https://ri.ufs.br/handle/riufs/3807
Resumo: Infection is the major complication for neutropenic patients, and cause of morbidity and mortality. Clinical signs are nonspecific and fever may be a late marker for the early use of antibiotics, which may complicate the prognosis. The approaches of most protocols focus on adult patients. Thus, to improve safety in the clinical approach in pediatric neutropenic patients, this work was performed in order to evaluate biomarkers involved in the inflammatory response in pediatric patients. In the period 2010 to 2012 were included 70 children with neutropenia with neutrophil count ≤ 1000 cells / mm ³, 35 pediatric patients with visceral leishmaniasis (VL) and 35 patients with onco-hematological disease, ranging in age from 0 to 18, from the oncology service of the Hospital Emergency ward Segipe and Pediatrics Diseases, University Hospital of Sergipe. Serum levels of biomarkers were evaluated following: Interferon gamma (IFN-γ), interleukin-5 (IL-5), interleukin-6 (IL-6), interleukin-10 (IL-10), lactate, ultrasensitive CRP (hsCRP), nprocalcitonina (PCT) and Tumor Necrosis Factor-α (TNF-α). The results showed that the average of the groups was no significant difference with biomarkers IFN-γ, IL-10 and TNF-α with p <0.001, IL-5 and p = 0.020, p = 0.002 with lactate and p = 0.011 PCT The hsCRP and IL-6 did not show statistical significance. Correlating CAN groups with the average of biomarkers, there was no statistical significance. This study suggests that biomarkers biomarkers that IFN-γ, IL-5, IL-10, lactate, procalcitonin and TNF-α, laboratory values showed a significant difference between the group of patients neutropenic patients with LV disease and onco- hematologic, this is not happening with the results presented by biomarkers IL-6 and hsCRP, leading us to observe that although the groups have in common neutropenia, interpretation of these biomarkers should be performed separately for each group. Except for lactate and procalcitonin, all other biomarkers showed increased results when comparing the mean of the two groups, which leads us to conclude that studies with larger numbers of subjects are important to verify the use of IFN-γ biomarkers, IL- 5, IL-6, IL-10 and TNF-α in the diagnosis of infection in neutropenic patients.
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spelling Costa, Flávia Oliveira dahttp://lattes.cnpq.br/7360890887517177Silva, Angela Maria dahttp://lattes.cnpq.br/75297369139213522017-09-26T12:17:35Z2017-09-26T12:17:35Z2013-02-05COSTA, Flávia Oliveira da. Evaluation of biomarkers in pediatric patients with leishmaniosis and onco-hematological. 2013. 77 f. Dissertação (Mestrado em Ciências da Saúde) - Universidade Federal de Sergipe, Aracaju, 2013.https://ri.ufs.br/handle/riufs/3807Infection is the major complication for neutropenic patients, and cause of morbidity and mortality. Clinical signs are nonspecific and fever may be a late marker for the early use of antibiotics, which may complicate the prognosis. The approaches of most protocols focus on adult patients. Thus, to improve safety in the clinical approach in pediatric neutropenic patients, this work was performed in order to evaluate biomarkers involved in the inflammatory response in pediatric patients. In the period 2010 to 2012 were included 70 children with neutropenia with neutrophil count ≤ 1000 cells / mm ³, 35 pediatric patients with visceral leishmaniasis (VL) and 35 patients with onco-hematological disease, ranging in age from 0 to 18, from the oncology service of the Hospital Emergency ward Segipe and Pediatrics Diseases, University Hospital of Sergipe. Serum levels of biomarkers were evaluated following: Interferon gamma (IFN-γ), interleukin-5 (IL-5), interleukin-6 (IL-6), interleukin-10 (IL-10), lactate, ultrasensitive CRP (hsCRP), nprocalcitonina (PCT) and Tumor Necrosis Factor-α (TNF-α). The results showed that the average of the groups was no significant difference with biomarkers IFN-γ, IL-10 and TNF-α with p <0.001, IL-5 and p = 0.020, p = 0.002 with lactate and p = 0.011 PCT The hsCRP and IL-6 did not show statistical significance. Correlating CAN groups with the average of biomarkers, there was no statistical significance. This study suggests that biomarkers biomarkers that IFN-γ, IL-5, IL-10, lactate, procalcitonin and TNF-α, laboratory values showed a significant difference between the group of patients neutropenic patients with LV disease and onco- hematologic, this is not happening with the results presented by biomarkers IL-6 and hsCRP, leading us to observe that although the groups have in common neutropenia, interpretation of these biomarkers should be performed separately for each group. Except for lactate and procalcitonin, all other biomarkers showed increased results when comparing the mean of the two groups, which leads us to conclude that studies with larger numbers of subjects are important to verify the use of IFN-γ biomarkers, IL- 5, IL-6, IL-10 and TNF-α in the diagnosis of infection in neutropenic patients.A infecção constitui a maior complicação para o paciente neutropênico, sendo causa de morbidade e mortalidade. Sinais clínicos são inespecíficos e febre pode ser um marcador tardio para início do uso de antibióticos, podendo complicar o prognóstico. As abordagens da maioria dos protocolos focam-se em pacientes adultos. Desta forma, para reforçar a segurança na abordagem clínica em pacientes neutropênicos pediátricos, foi realizado este trabalho com o objetivo de avaliar os biomarcadores envolvidos na resposta inflamatória em pacientes pediátricos. No período de 2010 a 2012 foram incluidos 70 crianças portadoras de neutropenia, com contagem de neutrófilos ≤ 1000 cel/mm³, sendo 35 pacientes pediatricos portadores de Leishmaniose visceral(LV) e 35 portadores de doença onco-hematológica , com idade variando de 0 a 18 anos, oriundos do serviço de oncologia do Hospital de Urgência de Sergipe e da enfermaria de Pediatria do Hospital Universitário de Sergipe. Os níveis séricos dos seguintes biomarcadores foram avaliados: Interferon gamma (IFN-γ), Interleucina-5(IL-5), interleucina-6(IL-6), interleucina-10(IL-10), lactato, Proteina C Reativa ultrassensível(PCR-US),procalcitonina(PCT) e Fator de Necrose Tumoral alfa(TNF-α) . Os resultados mostraram que na média dos grupos estudados houve diferença significativa com os biomarcadores IFN-γ, IL-10 e TNF-α com p <0,001, IL-5 com p=0,020, lactato com p=0,002 e PCT com p=0,011 A PCR-US e a IL-6 não apresentaram estatiscamente significância. Correlacionando a CAN dos grupos com a média dos biomarcadores, não foi observado significancia estatística. Este trabalho sugere que os biomarcadores que os biomarcadores IFN-γ, IL-5, IL-10, lactato, procalcitonina e TNF-α, apresentaram valores laboratoriais com diferença significativa entre o grupo de pacientes neutropênicos portadores de LV e doença onco-hematológica, o mesmo não acontecendo com os resultados apresentados pelos biomarcadores IL-6 e a PCR-US, levando-nos a observar que apesar dos grupos terem a neutropenia em comum, a interpretação destes biomarcadores deve ser realizada de forma distinta para cada grupo. Excetuando-se o lactato e a procalcitonina, todos os demais biomarcadores apresentaram resultados aumentados quando comparadas as médias dos dois grupos, fato que nos faz concluir que estudos com um número maior de indivíduos são importantes para verificar o uso dos biomarcadores IFN-γ, IL-5, IL-6, IL-10 e TNF-α no diagnóstico de infecção em pacientes neutropênicos.application/pdfporUniversidade Federal de SergipePós-Graduação em Ciências da SaúdeUFSBRBiomarcadoresCriançasLeishmaniose visceralNeutropeniaOnco-hematologiaNeutropeniaBiomarkersChildVisceral leishmaniasisOnco-hematologyCNPQ::CIENCIAS DA SAUDEAvaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicosEvaluation of biomarkers in pediatric patients with leishmaniosis and onco-hematologicalinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSinstname:Universidade Federal de Sergipe (UFS)instacron:UFSTEXTFLAVIA_OLIVEIRA_COSTA.pdf.txtFLAVIA_OLIVEIRA_COSTA.pdf.txtExtracted texttext/plain132187https://ri.ufs.br/jspui/bitstream/riufs/3807/2/FLAVIA_OLIVEIRA_COSTA.pdf.txta957350b1b45b2e3358e157f54b8e3f0MD52THUMBNAILFLAVIA_OLIVEIRA_COSTA.pdf.jpgFLAVIA_OLIVEIRA_COSTA.pdf.jpgGenerated Thumbnailimage/jpeg1362https://ri.ufs.br/jspui/bitstream/riufs/3807/3/FLAVIA_OLIVEIRA_COSTA.pdf.jpgf88fe111c3b018d71725aee11198fb86MD53ORIGINALFLAVIA_OLIVEIRA_COSTA.pdfapplication/pdf927736https://ri.ufs.br/jspui/bitstream/riufs/3807/1/FLAVIA_OLIVEIRA_COSTA.pdfc23cd0deb5e0afe20b9777174f5614d9MD51riufs/38072020-05-26 10:42:43.174oai:ufs.br:riufs/3807Repositório InstitucionalPUBhttps://ri.ufs.br/oai/requestrepositorio@academico.ufs.bropendoar:2020-05-26T13:42:43Repositório Institucional da UFS - Universidade Federal de Sergipe (UFS)false
dc.title.por.fl_str_mv Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
dc.title.alternative.eng.fl_str_mv Evaluation of biomarkers in pediatric patients with leishmaniosis and onco-hematological
title Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
spellingShingle Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
Costa, Flávia Oliveira da
Biomarcadores
Crianças
Leishmaniose visceral
Neutropenia
Onco-hematologia
Neutropenia
Biomarkers
Child
Visceral leishmaniasis
Onco-hematology
CNPQ::CIENCIAS DA SAUDE
title_short Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
title_full Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
title_fullStr Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
title_full_unstemmed Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
title_sort Avaliação de biomarcadores em pacientes pediátricos neutropênicos com leishmaniose visceral e onco-hematológicos
author Costa, Flávia Oliveira da
author_facet Costa, Flávia Oliveira da
author_role author
dc.contributor.author.fl_str_mv Costa, Flávia Oliveira da
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/7360890887517177
dc.contributor.advisor1.fl_str_mv Silva, Angela Maria da
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7529736913921352
contributor_str_mv Silva, Angela Maria da
dc.subject.por.fl_str_mv Biomarcadores
Crianças
Leishmaniose visceral
Neutropenia
Onco-hematologia
topic Biomarcadores
Crianças
Leishmaniose visceral
Neutropenia
Onco-hematologia
Neutropenia
Biomarkers
Child
Visceral leishmaniasis
Onco-hematology
CNPQ::CIENCIAS DA SAUDE
dc.subject.eng.fl_str_mv Neutropenia
Biomarkers
Child
Visceral leishmaniasis
Onco-hematology
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS DA SAUDE
description Infection is the major complication for neutropenic patients, and cause of morbidity and mortality. Clinical signs are nonspecific and fever may be a late marker for the early use of antibiotics, which may complicate the prognosis. The approaches of most protocols focus on adult patients. Thus, to improve safety in the clinical approach in pediatric neutropenic patients, this work was performed in order to evaluate biomarkers involved in the inflammatory response in pediatric patients. In the period 2010 to 2012 were included 70 children with neutropenia with neutrophil count ≤ 1000 cells / mm ³, 35 pediatric patients with visceral leishmaniasis (VL) and 35 patients with onco-hematological disease, ranging in age from 0 to 18, from the oncology service of the Hospital Emergency ward Segipe and Pediatrics Diseases, University Hospital of Sergipe. Serum levels of biomarkers were evaluated following: Interferon gamma (IFN-γ), interleukin-5 (IL-5), interleukin-6 (IL-6), interleukin-10 (IL-10), lactate, ultrasensitive CRP (hsCRP), nprocalcitonina (PCT) and Tumor Necrosis Factor-α (TNF-α). The results showed that the average of the groups was no significant difference with biomarkers IFN-γ, IL-10 and TNF-α with p <0.001, IL-5 and p = 0.020, p = 0.002 with lactate and p = 0.011 PCT The hsCRP and IL-6 did not show statistical significance. Correlating CAN groups with the average of biomarkers, there was no statistical significance. This study suggests that biomarkers biomarkers that IFN-γ, IL-5, IL-10, lactate, procalcitonin and TNF-α, laboratory values showed a significant difference between the group of patients neutropenic patients with LV disease and onco- hematologic, this is not happening with the results presented by biomarkers IL-6 and hsCRP, leading us to observe that although the groups have in common neutropenia, interpretation of these biomarkers should be performed separately for each group. Except for lactate and procalcitonin, all other biomarkers showed increased results when comparing the mean of the two groups, which leads us to conclude that studies with larger numbers of subjects are important to verify the use of IFN-γ biomarkers, IL- 5, IL-6, IL-10 and TNF-α in the diagnosis of infection in neutropenic patients.
publishDate 2013
dc.date.issued.fl_str_mv 2013-02-05
dc.date.accessioned.fl_str_mv 2017-09-26T12:17:35Z
dc.date.available.fl_str_mv 2017-09-26T12:17:35Z
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dc.identifier.citation.fl_str_mv COSTA, Flávia Oliveira da. Evaluation of biomarkers in pediatric patients with leishmaniosis and onco-hematological. 2013. 77 f. Dissertação (Mestrado em Ciências da Saúde) - Universidade Federal de Sergipe, Aracaju, 2013.
dc.identifier.uri.fl_str_mv https://ri.ufs.br/handle/riufs/3807
identifier_str_mv COSTA, Flávia Oliveira da. Evaluation of biomarkers in pediatric patients with leishmaniosis and onco-hematological. 2013. 77 f. Dissertação (Mestrado em Ciências da Saúde) - Universidade Federal de Sergipe, Aracaju, 2013.
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