再生障碍性贫血患者感染风险预测模型的开发:复发事件的生存分析

IF 2.8 Q2 INFECTIOUS DISEASES
Pirun Saelue, Thitichaya Penthinapong
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引用次数: 0

摘要

背景:在再生障碍性贫血(AA)患者中,感染相关并发症是导致死亡的主要原因。然而,人们对这些患者感染的预测因素了解有限。因此,本研究旨在评估感染的风险因素,并建立一个AA患者发生感染的风险预测模型:2004年1月至2020年12月期间,206名年龄≥15岁的AA患者被纳入本研究。采用复发事件方法进行生存分析,以确定与感染相关的预测因素,包括安德森和吉尔模型、普伦蒂斯、威廉姆斯和彼得森(PWP)总时间模型、PWP间隙时间模型、边际模型和虚弱模型。使用后向逐步回归法确定最佳模型,并使用500次重复取样的Bootstrapping法进行内部验证:中位随访时间为 2.95 年,AA 患者的感染发生率为每 100 人年 32.8 例。PWP总时间模型显示,肝硬化合并症、淋巴细胞≥80%和既往感染增加了感染风险,而骨髓细胞率≥20%则提供了保护。骨髓细胞率、淋巴细胞百分比、既往感染、肝硬化和血细胞比容(BLICH)模型用于预测感染风险。内部验证显示该模型校准良好:肝硬化、淋巴细胞≥80%、既往感染和骨髓细胞率
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Prediction Model for the Risk of Infection in Patients with Aplastic Anemia: Survival Analysis in Recurrent Events.

Background: In patients with aplastic anemia (AA), infection-related complications are the leading cause of mortality. However, limited knowledge about the predictive factors for infection in these patients exists. Thus, this study aimed to evaluate risk factors for infection and develop a risk prediction model for the occurrence of infection in patients with AA.

Materials and methods: Between January 2004 and December 2020, 206 patients with AA ≥15 years of age were included in this study. Survival analysis using recurrent event methodologies was conducted to identify predictive factors associated with infection, including the Anderson and Gill model; Prentice, Williams, and Peterson (PWP) Total Time model; PWP Gap Time model; marginal model; and frailty models. The best model was determined using backward stepwise regression, and internal validation was performed using the Bootstrapping method with 500 re-samplings.

Results: With a median follow-up of 2.95 years, the incidence rate of infection among patients with AA was 32.8 events per 100 person-years. The PWP Total Time model revealed that cirrhosis comorbidity, lymphocytes ≥80%, and previous infection increased the risk of infection, while bone marrow cellularity ≥20% offered protection. The bone marrow cellularity, lymphocyte percentage, previous Infection, cirrhosis, and hematocrit (BLICH) model was generated to predict the risk of infection. The internal validation showed a good calibration of this model.

Conclusion: Cirrhosis, lymphocytes ≥80%, previous infection, and bone marrow cellularity <20% are risk factors for infection in patients with AA. The BLICH model can predict the risk of infection in these patients.

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来源期刊
Infection and Chemotherapy
Infection and Chemotherapy INFECTIOUS DISEASES-
CiteScore
6.60
自引率
11.90%
发文量
71
审稿时长
22 weeks
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