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The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation

The diagnostic value of procalcitonin and the prognostic role of PCT clearance remain unclear in neutropenic period after allogeneic hematopoietic stem cell transplantation introduction. This study evaluated 219 febrile neutropenic patients (116, retrospectively; 103, prospectively) who underwent al...

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Autores principales: Shan, Meng, Shen, Danya, Song, Tiemei, Xu, Wenyan, Qiu, Huiying, Chen, Suning, Han, Yue, Tang, Xiaowen, Miao, Miao, Sun, Aining, Wu, Depei, Xu, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082027/
https://www.ncbi.nlm.nih.gov/pubmed/35547733
http://dx.doi.org/10.3389/fimmu.2022.843067
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author Shan, Meng
Shen, Danya
Song, Tiemei
Xu, Wenyan
Qiu, Huiying
Chen, Suning
Han, Yue
Tang, Xiaowen
Miao, Miao
Sun, Aining
Wu, Depei
Xu, Yang
author_facet Shan, Meng
Shen, Danya
Song, Tiemei
Xu, Wenyan
Qiu, Huiying
Chen, Suning
Han, Yue
Tang, Xiaowen
Miao, Miao
Sun, Aining
Wu, Depei
Xu, Yang
author_sort Shan, Meng
collection PubMed
description The diagnostic value of procalcitonin and the prognostic role of PCT clearance remain unclear in neutropenic period after allogeneic hematopoietic stem cell transplantation introduction. This study evaluated 219 febrile neutropenic patients (116, retrospectively; 103, prospectively) who underwent allo-HSCT from April 2014 to March 2016. The area under the receiver operator characteristic curve (AUC) of PCT for detecting documented infection (DI) was 0.637, and that of bloodstream infection (BSI) was 0.811. In multivariate analysis, the inability to decrease PCT by more than 80% within 5–7 days after the onset of fever independently predicted poor 100-day survival following allo-HSCT (P = 0.036). Furthermore, the prognostic nomogram combining PCTc and clinical parameters showed a stable predictive performance, supported by the C-index of 0.808 and AUC of 0.813 in the primary cohort, and C-index of 0.691 and AUC of 0.697 in the validation cohort. This study demonstrated the diagnostic role of PCT in documented and bloodstream infection during the neutropenic period after allo-HSCT. PCTc might serve as a predictive indicator of post-HSCT 100-day mortality. A nomogram based on PCTc and several clinical factors effectively predicted the 100-day survival of febrile patients and may help physicians identify high-risk patients in the post-HSCT neutropenic period.
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spelling pubmed-90820272022-05-10 The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation Shan, Meng Shen, Danya Song, Tiemei Xu, Wenyan Qiu, Huiying Chen, Suning Han, Yue Tang, Xiaowen Miao, Miao Sun, Aining Wu, Depei Xu, Yang Front Immunol Immunology The diagnostic value of procalcitonin and the prognostic role of PCT clearance remain unclear in neutropenic period after allogeneic hematopoietic stem cell transplantation introduction. This study evaluated 219 febrile neutropenic patients (116, retrospectively; 103, prospectively) who underwent allo-HSCT from April 2014 to March 2016. The area under the receiver operator characteristic curve (AUC) of PCT for detecting documented infection (DI) was 0.637, and that of bloodstream infection (BSI) was 0.811. In multivariate analysis, the inability to decrease PCT by more than 80% within 5–7 days after the onset of fever independently predicted poor 100-day survival following allo-HSCT (P = 0.036). Furthermore, the prognostic nomogram combining PCTc and clinical parameters showed a stable predictive performance, supported by the C-index of 0.808 and AUC of 0.813 in the primary cohort, and C-index of 0.691 and AUC of 0.697 in the validation cohort. This study demonstrated the diagnostic role of PCT in documented and bloodstream infection during the neutropenic period after allo-HSCT. PCTc might serve as a predictive indicator of post-HSCT 100-day mortality. A nomogram based on PCTc and several clinical factors effectively predicted the 100-day survival of febrile patients and may help physicians identify high-risk patients in the post-HSCT neutropenic period. Frontiers Media S.A. 2022-04-25 /pmc/articles/PMC9082027/ /pubmed/35547733 http://dx.doi.org/10.3389/fimmu.2022.843067 Text en Copyright © 2022 Shan, Shen, Song, Xu, Qiu, Chen, Han, Tang, Miao, Sun, Wu and Xu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Shan, Meng
Shen, Danya
Song, Tiemei
Xu, Wenyan
Qiu, Huiying
Chen, Suning
Han, Yue
Tang, Xiaowen
Miao, Miao
Sun, Aining
Wu, Depei
Xu, Yang
The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation
title The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation
title_full The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation
title_fullStr The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation
title_full_unstemmed The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation
title_short The Clinical Value of Procalcitonin in the Neutropenic Period After Allogeneic Hematopoietic Stem Cell Transplantation
title_sort clinical value of procalcitonin in the neutropenic period after allogeneic hematopoietic stem cell transplantation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082027/
https://www.ncbi.nlm.nih.gov/pubmed/35547733
http://dx.doi.org/10.3389/fimmu.2022.843067
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