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淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义
OBJECTIVE: To explore incidence, risk factors and prognosis of the first 6 months infectious events in adults with newly diagnosed primary immune thrombocytopenia (ITP), and evaluate the value of initial absolute lymphocyte count (ALC) in predicting infection. METHODS: The initial clinical records a...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Editorial office of Chinese Journal of Hematology
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343024/ https://www.ncbi.nlm.nih.gov/pubmed/25641143 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.01.008 |
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collection | PubMed |
description | OBJECTIVE: To explore incidence, risk factors and prognosis of the first 6 months infectious events in adults with newly diagnosed primary immune thrombocytopenia (ITP), and evaluate the value of initial absolute lymphocyte count (ALC) in predicting infection. METHODS: The initial clinical records and infectious events during 6 months of 217 adult with newly diagnosed ITP were retrospectively analyzed. Statistical methods were used to analyze risk factors of the 6 months infections in adults ITP, the prediction of ALC in risk of infection, and the association of ALC and prognosis. RESULTS: Infection rate of ITP patients accepting therapy within 6 months after the initial diagnosis was 13.8% (30/217), and infection rate of patients≥60 years of age 25% (14/56). Multivariate unconditioned Logistic analysis showed that gender and ALC were independent risk factors for the 6 months infection of ITP patients (P< 0.05, 95%CI 1.150–7.298, OR 2.722 and P<0.001, 95% CI 6.802–80.749, OR 23.436). Cutoff value of ALC was 1.225×10(9)/L, sensitivity and specificity of its value were 0.866 and 0.700 respectively. Infection rate of ALC>1.225×10(9)/L in adult ITP was lower than of ALC≤1.225×10(9)/L (5.3% vs 45.7%, χ(2)=49.151, P< 0.001). Furthermore, persistent recovery and the 1-year mortality rate after diagnosis had no difference among patients of different ALC (28.0% vs 26.0%, χ(2)=0.071, P>0.05, and 98.6% vs 97.8%, χ(2)=0.095, P> 0.05). There were no significant differences in persistent recovery in patients with and without infection (30.0% vs 27.3%, χ(2)=0.096,P>0.05). The 1-year mortality rate after diagnosis was significantly lower in those patients who developed an infection (93.3% vs 99.3%, χ(2)=4.607, P<0.05). CONCLUSION: Initial ALC was an independent risk factor of 6 months infection in adult ITP. It could be a predictive index of infection within 6 months of the initial diagnosis in ITP patients. Infection as an important factor affected the survival of ITP patients. |
format | Online Article Text |
id | pubmed-7343024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73430242020-07-16 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To explore incidence, risk factors and prognosis of the first 6 months infectious events in adults with newly diagnosed primary immune thrombocytopenia (ITP), and evaluate the value of initial absolute lymphocyte count (ALC) in predicting infection. METHODS: The initial clinical records and infectious events during 6 months of 217 adult with newly diagnosed ITP were retrospectively analyzed. Statistical methods were used to analyze risk factors of the 6 months infections in adults ITP, the prediction of ALC in risk of infection, and the association of ALC and prognosis. RESULTS: Infection rate of ITP patients accepting therapy within 6 months after the initial diagnosis was 13.8% (30/217), and infection rate of patients≥60 years of age 25% (14/56). Multivariate unconditioned Logistic analysis showed that gender and ALC were independent risk factors for the 6 months infection of ITP patients (P< 0.05, 95%CI 1.150–7.298, OR 2.722 and P<0.001, 95% CI 6.802–80.749, OR 23.436). Cutoff value of ALC was 1.225×10(9)/L, sensitivity and specificity of its value were 0.866 and 0.700 respectively. Infection rate of ALC>1.225×10(9)/L in adult ITP was lower than of ALC≤1.225×10(9)/L (5.3% vs 45.7%, χ(2)=49.151, P< 0.001). Furthermore, persistent recovery and the 1-year mortality rate after diagnosis had no difference among patients of different ALC (28.0% vs 26.0%, χ(2)=0.071, P>0.05, and 98.6% vs 97.8%, χ(2)=0.095, P> 0.05). There were no significant differences in persistent recovery in patients with and without infection (30.0% vs 27.3%, χ(2)=0.096,P>0.05). The 1-year mortality rate after diagnosis was significantly lower in those patients who developed an infection (93.3% vs 99.3%, χ(2)=4.607, P<0.05). CONCLUSION: Initial ALC was an independent risk factor of 6 months infection in adult ITP. It could be a predictive index of infection within 6 months of the initial diagnosis in ITP patients. Infection as an important factor affected the survival of ITP patients. Editorial office of Chinese Journal of Hematology 2015-01 /pmc/articles/PMC7343024/ /pubmed/25641143 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.01.008 Text en 2015年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal. |
spellingShingle | 论著 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
title | 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
title_full | 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
title_fullStr | 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
title_full_unstemmed | 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
title_short | 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
title_sort | 淋巴细胞绝对值对成人原发免疫性血小板减少症患者诊断后6个月内合并感染的预测意义 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343024/ https://www.ncbi.nlm.nih.gov/pubmed/25641143 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.01.008 |
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