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中国防痨杂志 ›› 2023, Vol. 45 ›› Issue (2): 165-171.doi: 10.19982/j.issn.1000-6621.20220301

• 论著 • 上一篇    下一篇

耐药结核病患者利奈唑胺血药浓度对血液系统毒性发生的影响

王红红, 郭少晨, 周文强, 刘忠泉, 朱慧, 陆宇()   

  1. 首都医科大学附属北京胸科医院/北京市结核病胸部肿瘤研究所药物研究室,北京 101149
  • 收稿日期:2022-08-09 出版日期:2023-02-10 发布日期:2023-02-01
  • 通信作者: 陆宇 E-mail:luyu4876@hotmail.com
  • 基金资助:
    北京市医院管理中心重点专科建设(ZYLX202123);北京市医院管理中心“登峰”人才培养计划(DFL20221402)

Influence of linezolid blood concentration on hematological toxicity in drug-resistant tuberculosis patients

Wang Honghong, Guo Shaochen, Zhou Wenqiang, Liu Zhongquan, Zhu Hui, Lu Yu()   

  1. Drug Research Office, Beijing Chest Hospital, Capital Medical University/Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing 101149, China
  • Received:2022-08-09 Online:2023-02-10 Published:2023-02-01
  • Contact: Lu Yu E-mail:luyu4876@hotmail.com
  • Supported by:
    Beijing Hospitals Authority Clinical Medicine Development of Special Funding Support(ZYLX202123);Beijing Municipal Administration of Hospitals’ Ascent Plan(DFL20221402)

摘要:

目的: 分析应用利奈唑胺的耐药结核病患者的血药浓度对发生血液系统毒性的影响,并探索血液系统毒性发生的其他危险因素。方法: 采用前瞻性队列研究方法,连续纳入首都医科大学附属北京胸科医院2019年1月至2021年2月应用含利奈唑胺化疗方案治疗的耐药结核病患者作为研究对象,共219例。收集研究对象的临床资料及服药后2h的血液标本。应用高效相色谱-质谱法测定利奈唑胺的血药浓度。通过绘制受试者工作特征曲线(receiver operating characteristic curve,ROC曲线)确定血药浓度(峰浓度)对血液系统毒性的诊断价值,并确定最佳诊断临界值;采用多因素logistic回归分析研究对象发生血液系统毒性的影响因素。结果: 219例研究对象中有92例(42.0%)发生了血液系统毒性反应,包括白细胞计数减少[15.5%(34/219)]、贫血[21.5%(47/219)]、血小板减少症[27.4%(60/219)]等,127例(58.0%)未发生任何相关毒性反应。发生血液系统毒性者利奈唑胺血药峰浓度为17.1(11.8,22.8)μg/ml,明显高于未发生者[14.7(10.4,18.0)μg/ml],差异有统计学意义(Z=-3.206,P=0.001)。未发生血液系统毒性者中的血清白蛋白<40g/L者的比例为29.1%(37/127),明显低于血清白蛋白≥40g/L者的比例[70.9%(90/127)],差异有统计学意义(χ2=7.998,P=0.005)。ROC曲线分析显示,利奈唑胺血药峰浓度对血液系统毒性有预测价值(曲线下面积为0.627),血药峰浓度为20.7μg/ml时是最佳诊断点。多因素logistic回归分析显示,血清白蛋白<40g/L者血液系统毒性发生的风险是血清白蛋白≥40g/L者的2.622倍(OR=2.622,95%CI:1.344~5.117);利奈唑胺血药峰浓度>20.7μg/ml者血液系统毒性发生的风险是血药峰浓度≤20.7μg/ml者的6.419倍(OR=6.419,95%CI:2.874~14.337)。结论: 利奈唑胺引起的血液系统毒性发生比例高,尤其对于血清白蛋白<40g/L和利奈唑胺血药峰浓度>20.7μg/ml的患者在应用利奈唑胺治疗时,应警惕血液系统毒性的发生。

关键词: 结核,肺, 抗药性, 抗结核药, 药物毒性, 评价研究

Abstract:

Objective: To analyze the influence of linezolid blood concentration on hematological toxicity in drug-resistant tuberculosis patients, as well as to explore other risk factors for hematopoietic toxicity. Methods: A prospective cohort study was conducted in 219 drug-resistant tuberculosis patients, all of them were continuously included and received chemotherapy treatment containing linezolid from January 2019 to February 2021 in Beijing Chest Hospital affiliated to Capital Medical University. Clinical data and blood samples 2 hours after administration were collected. A high performance liquid chromatography-mass spectrometry was used to measure the plasma concentrations of linezolid. The diagnostic value of blood drug concentration (peak concentration) on blood system toxicity was determined by drawing receiver operating characteristic curve (ROC curve), and the optimal diagnostic threshold was also determined. Multivariate logistic regression was used to analyze the influencing factors of blood system toxicity. Results: Among 219 subjects, 92 cases (42.0%) had hematological toxicity, including leukopenia (15.5%, 34/219), anemia (21.5%, 47/219), and thrombocytopenia (27.4%, 60/219), and the other 127 (58.0%) cases did not have any toxic reactions associated with linezolid. The peak plasma concentration of linezolid in patients with hematotoxicity was 17.1 (11.8, 22.8) μg/ml, significantly higher than that of non-occurrence (14.7 (10.4, 18.0) μg/ml)(Z=-3.206, P=0.001). Of patients without hematological toxicity, 29.1% (37/127) had serum albumin of <40 g/L, which was significantly lower than that of those with serum albumin ≥40 g/L (70.9%, 90/127)(χ2=7.998, P=0.005). Based on the ROC curve analysis, the linezolid’s peak concentration had predictive value on blood system toxicity (the area under the curve was 0.627), and 20.7 μg/ml of the linezolid’s peak concentration was the best diagnostic point. The multivariate logistic regression analysis showed that, the risk of hematotoxicity in patients with serum albumin <40 g/L was 2.622 times higher than that in patients with serum albumin ≥40 g/L (OR=2.622, 95%CI:1.344-5.117); the risk of blood system toxicity in patients with the peak plasma concentration of linezolid >20.7 μg/ml was 6.419 times higher than that in patients with the peak blood concentration≤20.7 μg/ml (OR=6.419, 95%CI:2.874-14.337). Conclusion: The proportion of hematological toxicity caused by linezolid is high. It is important to be aware of the possibility of blood system toxicity when administering linezolid to patients with serum albumin <40 g/L and linezolid peak plasma concentration >20.7 μg/ml.

Key words: Tuberculosis, pulmonary, Drug resistance, Antitubercular agents, Drug toxicity, Evaluation studies

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