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Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation

Infectious complications are common and sometimes life threatening in patients with immune thrombocytopenia (ITP), mainly due to the immune-suppressive therapy. Recent evidence suggests a potential role of platelets in the inflammation process. In this clinical study, we further investigated the rol...

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Autores principales: Qu, Mingming, Liu, Qiang, Zhao, Hong-Guo, Peng, Jun, Ni, Heyu, Hou, Ming, Jansen, A. J. Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097778/
https://www.ncbi.nlm.nih.gov/pubmed/29777278
http://dx.doi.org/10.1007/s00277-018-3367-9
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author Qu, Mingming
Liu, Qiang
Zhao, Hong-Guo
Peng, Jun
Ni, Heyu
Hou, Ming
Jansen, A. J. Gerard
author_facet Qu, Mingming
Liu, Qiang
Zhao, Hong-Guo
Peng, Jun
Ni, Heyu
Hou, Ming
Jansen, A. J. Gerard
author_sort Qu, Mingming
collection PubMed
description Infectious complications are common and sometimes life threatening in patients with immune thrombocytopenia (ITP), mainly due to the immune-suppressive therapy. Recent evidence suggests a potential role of platelets in the inflammation process. In this clinical study, we further investigated the role of thrombocytopenia on infections in patients with primary ITP. We retrospectively evaluated data from the recently published large randomized clinical trial of a cohort of 195 patients with primary ITP, who were randomized for prednisone or high-dose dexamethasone. From 158 patients (81%), data on platelet count and infections within the first month of treatment were collected. In this period, 24% of the ITP patients had an infection. Patients with infection had significant lower platelet counts during the first month of treatment leading to a significant lower therapy response at 1 month and a significant longer hospital stay (14.0 versus 9.8 days). Additionally, Cox regression analysis showed that an increase in platelet count of 20 × 10(9)/L led to a reduction of 52% in infections in the next week, showing low platelet count is a significant risk factor for infection. Platelet transfusion led to an increase in platelet count in ITP patients without infection, but not in patients with infection. In conclusion, infections are common in patients with primary ITP leading to significant worse response rates and a longer hospital stay. Interestingly, low platelet count was independently correlated with an increased risk of infection.
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spelling pubmed-60977782018-08-24 Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation Qu, Mingming Liu, Qiang Zhao, Hong-Guo Peng, Jun Ni, Heyu Hou, Ming Jansen, A. J. Gerard Ann Hematol Original Article Infectious complications are common and sometimes life threatening in patients with immune thrombocytopenia (ITP), mainly due to the immune-suppressive therapy. Recent evidence suggests a potential role of platelets in the inflammation process. In this clinical study, we further investigated the role of thrombocytopenia on infections in patients with primary ITP. We retrospectively evaluated data from the recently published large randomized clinical trial of a cohort of 195 patients with primary ITP, who were randomized for prednisone or high-dose dexamethasone. From 158 patients (81%), data on platelet count and infections within the first month of treatment were collected. In this period, 24% of the ITP patients had an infection. Patients with infection had significant lower platelet counts during the first month of treatment leading to a significant lower therapy response at 1 month and a significant longer hospital stay (14.0 versus 9.8 days). Additionally, Cox regression analysis showed that an increase in platelet count of 20 × 10(9)/L led to a reduction of 52% in infections in the next week, showing low platelet count is a significant risk factor for infection. Platelet transfusion led to an increase in platelet count in ITP patients without infection, but not in patients with infection. In conclusion, infections are common in patients with primary ITP leading to significant worse response rates and a longer hospital stay. Interestingly, low platelet count was independently correlated with an increased risk of infection. Springer Berlin Heidelberg 2018-05-18 2018 /pmc/articles/PMC6097778/ /pubmed/29777278 http://dx.doi.org/10.1007/s00277-018-3367-9 Text en © The Author(s) 2018 Open Access This 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.
spellingShingle Original Article
Qu, Mingming
Liu, Qiang
Zhao, Hong-Guo
Peng, Jun
Ni, Heyu
Hou, Ming
Jansen, A. J. Gerard
Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
title Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
title_full Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
title_fullStr Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
title_full_unstemmed Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
title_short Low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
title_sort low platelet count as risk factor for infections in patients with primary immune thrombocytopenia: a retrospective evaluation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097778/
https://www.ncbi.nlm.nih.gov/pubmed/29777278
http://dx.doi.org/10.1007/s00277-018-3367-9
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