Development and validation of a nomogram to predict linezolid-induced thrombocytopenia in hospitalized adults.

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Ya Yang, Xiaogang Hu, Ya Ran, Hongqian Wang, Peishu Fu, Pengpeng Wan, Zhongqing Deng, Xiaoqin Lang, Ning Wang, Fengjun Sun, Yahan Fan, Yuntao Jia
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引用次数: 0

Abstract

Background: Linezolid (LZD) is used to treat infectious diseases caused by Gram-positive bacteria, but thrombocytopenia is one of the main adverse reactions to LZD administration. Early prediction of linezolid-induced thrombocytopenia (LI-TP) is of great importance to improve the clinical outcomes and prognoses. The aim of this study was to develop and validate a prediction model for LI-TP.

Methods: A retrospective cohort of hospitalized adults receiving LZD therapy (January 2014-June 2022) was analyzed. Independent risk factors for LI-TP were identified via logistic regression in the training set (n = 757). A nomogram model for LI-TP were developed based on independent risk factors, and verified in validation set (n = 123).

Results: The incidence of LI-TP was 13.5% (102/757). A logistic regression model was developed based on the seven independent risk factors, including age (≥ 60 y), duration of LZD therapy (> 11 d), bPLT (< 308 × 109/L), ALT (> 100 IU/L), Ccr (< 67.5 mL/min), and concomitant use with VPA or Tac (p < 0.01) and transformed into a quantifiable nomogram. The nomogram demonstrated strong discrimination with AUCs of 0.760 in training (95% CI: 0.709-0.812, P < 0.001) and 0.767 in validation (95% CI: 0.635-0.899, P < 0.001). The calibration curves and Hosmer-Lemeshow tests confirmed good reliability and specificity of the nomogram model.

Conclusion: This nomogram provides a practical tool for stratifying LI-TP risk, which provide an important reference for enabling timely clinical interventions to enhance LZD safety.

用于预测住院成人利奈唑胺诱发的血小板减少症的nomogram预测图的开发和验证。
背景:利奈唑胺(LZD)用于治疗革兰氏阳性菌引起的感染性疾病,但血小板减少是使用利奈唑胺的主要不良反应之一。早期预测利奈唑胺所致的血小板减少症(li - topia, LI-TP)对改善临床结局和预后具有重要意义。本研究的目的是建立并验证LI-TP的预测模型。方法:回顾性分析2014年1月至2022年6月期间接受LZD治疗的住院成人患者。通过逻辑回归在训练集中确定LI-TP的独立危险因素(n = 757)。基于独立危险因素建立LI-TP的nomogram模型,并在验证集(n = 123)中进行验证。结果:LI-TP的发生率为13.5%(102/757)。基于年龄(≥60岁)、LZD治疗持续时间(10 ~ 11 d)、bPLT (9/L)、ALT (10 ~ 100 IU/L)、Ccr等7个独立危险因素建立logistic回归模型。结论:该nomogram可为LI-TP风险分层提供实用工具,为及时采取临床干预措施提高LZD安全性提供重要参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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