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Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion

Patients with both serous effusion and eosinophilia are rarely reported and geographically distributed; their early diagnosis is difficult. According to the ultimate diagnosis, patients (≤14 years) in West China Second hospital with serous effusion and eosinophilia were divided into two groups inclu...

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Autores principales: Miao, Ruixue, Zhu, Yu, Wang, Zhiling, Luo, Shuanghong, Wan, Chaomin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440094/
https://www.ncbi.nlm.nih.gov/pubmed/32243388
http://dx.doi.org/10.1097/MD.0000000000019625
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author Miao, Ruixue
Zhu, Yu
Wang, Zhiling
Luo, Shuanghong
Wan, Chaomin
author_facet Miao, Ruixue
Zhu, Yu
Wang, Zhiling
Luo, Shuanghong
Wan, Chaomin
author_sort Miao, Ruixue
collection PubMed
description Patients with both serous effusion and eosinophilia are rarely reported and geographically distributed; their early diagnosis is difficult. According to the ultimate diagnosis, patients (≤14 years) in West China Second hospital with serous effusion and eosinophilia were divided into two groups including a parasitic group and a non-parasitic group. Clinical data were collected and analyzed between the two groups. Subsequently, significant measurement indicators were evaluated by receiver operating characteristic (ROC) curve to explore the optimal cut-off points for the most appropriate sensitivity and specificity. A total of 884 patients were diagnosed with serous effusion and 61 of them displayed co-morbidity with eosinophilia during enrolled time. Among 61 patients, 34 patients had parasitic infection and 27 had non-parasitic diseases. There were statistical difference in effusion position, the levels of white blood cell count (WBC), eosinophil (EOS), EOS%, C-reactive protein (CRP) between parasitic group and non-parasitic group. ROC curve demonstrated that the areas under the curve of EOS count and EOS% were >80%, and the corresponding optimal cut-off values were 1.71 × 10(9)/L and 25.6% for distinguishing between parasitic and non-parasitic infections in our patients. This study provided a quantified index for potentially quick and convenient indicators of pediatric patients presenting with both eosinophilia and effusion. Eosinophils were helpful to improve the initial diagnosis with awareness of parasitic diseases. For the cases with EOS > 1.71 × 10(9)/L or EOS% > 25.6%, parasitic infection should be considered and serological tests are recommended in our region.
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spelling pubmed-74400942020-09-04 Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion Miao, Ruixue Zhu, Yu Wang, Zhiling Luo, Shuanghong Wan, Chaomin Medicine (Baltimore) 4900 Patients with both serous effusion and eosinophilia are rarely reported and geographically distributed; their early diagnosis is difficult. According to the ultimate diagnosis, patients (≤14 years) in West China Second hospital with serous effusion and eosinophilia were divided into two groups including a parasitic group and a non-parasitic group. Clinical data were collected and analyzed between the two groups. Subsequently, significant measurement indicators were evaluated by receiver operating characteristic (ROC) curve to explore the optimal cut-off points for the most appropriate sensitivity and specificity. A total of 884 patients were diagnosed with serous effusion and 61 of them displayed co-morbidity with eosinophilia during enrolled time. Among 61 patients, 34 patients had parasitic infection and 27 had non-parasitic diseases. There were statistical difference in effusion position, the levels of white blood cell count (WBC), eosinophil (EOS), EOS%, C-reactive protein (CRP) between parasitic group and non-parasitic group. ROC curve demonstrated that the areas under the curve of EOS count and EOS% were >80%, and the corresponding optimal cut-off values were 1.71 × 10(9)/L and 25.6% for distinguishing between parasitic and non-parasitic infections in our patients. This study provided a quantified index for potentially quick and convenient indicators of pediatric patients presenting with both eosinophilia and effusion. Eosinophils were helpful to improve the initial diagnosis with awareness of parasitic diseases. For the cases with EOS > 1.71 × 10(9)/L or EOS% > 25.6%, parasitic infection should be considered and serological tests are recommended in our region. Wolters Kluwer Health 2020-04-03 /pmc/articles/PMC7440094/ /pubmed/32243388 http://dx.doi.org/10.1097/MD.0000000000019625 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4900
Miao, Ruixue
Zhu, Yu
Wang, Zhiling
Luo, Shuanghong
Wan, Chaomin
Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
title Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
title_full Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
title_fullStr Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
title_full_unstemmed Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
title_short Distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
title_sort distinguishment of parasite-infected children from pediatric inpatients with both eosinophilia and effusion
topic 4900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440094/
https://www.ncbi.nlm.nih.gov/pubmed/32243388
http://dx.doi.org/10.1097/MD.0000000000019625
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