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Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients
OBJECTIVE: The current study aimed to know procalcitonin levels in patients with metastatic tumor, and to discover the cut-off point for sepsis in this population. A cross-sectional study was conducted with patients with solid tumor. Sepsis and systemic inflammation response syndrome (SIRS) were ide...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791197/ https://www.ncbi.nlm.nih.gov/pubmed/29382396 http://dx.doi.org/10.1186/s13104-018-3204-1 |
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author | Aziz, Segal Abdul Nelwan, Erni Juwita Sukrisman, Lugyanti Suhendro, Suhendro |
author_facet | Aziz, Segal Abdul Nelwan, Erni Juwita Sukrisman, Lugyanti Suhendro, Suhendro |
author_sort | Aziz, Segal Abdul |
collection | PubMed |
description | OBJECTIVE: The current study aimed to know procalcitonin levels in patients with metastatic tumor, and to discover the cut-off point for sepsis in this population. A cross-sectional study was conducted with patients with solid tumor. Sepsis and systemic inflammation response syndrome (SIRS) were identified using clinical, laboratory, and microbiological criteria. The cut-off point was determined using receiver operating characteristic (ROC) curve. RESULTS: A total of 112 subjects enrolled in this study, 51% male, mean age 47.9 ± 12.47 years. Among 71 (63.4%) patients who had metastasis, 36 (32.1%) had sepsis and 6 (5.3%) experienced SIRS. In the absence of sepsis, the procalcitonin levels were significantly higher in patients with metastatic tumor compared to those without [0.25 ng/mL (0.07–1.76) vs. 0.09 ng/mL (0.03–0.54); p < 0.001]. The ROC curve showed that levels of procalcitonin for sepsis in metastatic solid tumors were in the area under curve (AUC) [0.956; CI 0.916–0.996]. Cut-off point of procalcitonin for sepsis was 1.14 ng/mL, Sn 86%, and Sp 88%. Thus, the results show that metastatic tumor affects the patients’ procalcitonin level, even in the absence of sepsis. The cut-off point of procalcitonin level for diagnosing sepsis in the meta-static solid tumor was higher compared to the standard value. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3204-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5791197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57911972018-02-08 Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients Aziz, Segal Abdul Nelwan, Erni Juwita Sukrisman, Lugyanti Suhendro, Suhendro BMC Res Notes Research Note OBJECTIVE: The current study aimed to know procalcitonin levels in patients with metastatic tumor, and to discover the cut-off point for sepsis in this population. A cross-sectional study was conducted with patients with solid tumor. Sepsis and systemic inflammation response syndrome (SIRS) were identified using clinical, laboratory, and microbiological criteria. The cut-off point was determined using receiver operating characteristic (ROC) curve. RESULTS: A total of 112 subjects enrolled in this study, 51% male, mean age 47.9 ± 12.47 years. Among 71 (63.4%) patients who had metastasis, 36 (32.1%) had sepsis and 6 (5.3%) experienced SIRS. In the absence of sepsis, the procalcitonin levels were significantly higher in patients with metastatic tumor compared to those without [0.25 ng/mL (0.07–1.76) vs. 0.09 ng/mL (0.03–0.54); p < 0.001]. The ROC curve showed that levels of procalcitonin for sepsis in metastatic solid tumors were in the area under curve (AUC) [0.956; CI 0.916–0.996]. Cut-off point of procalcitonin for sepsis was 1.14 ng/mL, Sn 86%, and Sp 88%. Thus, the results show that metastatic tumor affects the patients’ procalcitonin level, even in the absence of sepsis. The cut-off point of procalcitonin level for diagnosing sepsis in the meta-static solid tumor was higher compared to the standard value. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3204-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-30 /pmc/articles/PMC5791197/ /pubmed/29382396 http://dx.doi.org/10.1186/s13104-018-3204-1 Text en © The Author(s) 2018 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 Note Aziz, Segal Abdul Nelwan, Erni Juwita Sukrisman, Lugyanti Suhendro, Suhendro Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
title | Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
title_full | Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
title_fullStr | Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
title_full_unstemmed | Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
title_short | Higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
title_sort | higher cut-off serum procalcitonin level for sepsis diagnosis in metastatic solid tumor patients |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791197/ https://www.ncbi.nlm.nih.gov/pubmed/29382396 http://dx.doi.org/10.1186/s13104-018-3204-1 |
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