Chen Chao, Guo Dai-Hong, Cao Xiutang, Cai Yun, Xu Yuanjie, Zhu Man, Ma Liang
Department of Pharmacy, Chinese PLA General Hospital, Beijing, China.
Department of Medical Statistics, Chinese PLA General Hospital, Beijing, China.
Curr Ther Res Clin Exp. 2012 Dec;73(6):195-206. doi: 10.1016/j.curtheres.2012.07.002.
Linezolid (LZD), an oxazolidinone antibiotic agent, has excellent activity and bioavailability against most methicillin-sensitive and methicillin-resistant gram-positive bacteria. Although LZD is generally well tolerated, several studies have found adverse hematologic effects, of which thrombocytopenia is of most concern.
To investigate the risk factors for thrombocytopenia in patients who received oral or parenteral LZD therapy between February 1 and November 30, 2010.
Data were extracted retrospectively from the electronic medical records in our hospital information system. Thrombocytopenia was defined as either a final platelet count of <100 × 10(9)/L (criterion 1) or a 25% reduction from the baseline platelet count (criterion 2). Risk factors were determined using logistic regression analysis, and clinical features were predicted using receiver operating characteristic curves.
The study included 254 patients, with mean (SD) age of 59 (17.66) years. The duration of LZD therapy was 9.43 (5.63) days. Thrombocytopenia developed in 69 patients (27.2%), as defined by criterion 1, and in 127 patients (50%), as defined by criterion 2. At univariate analysis, age, weight, creatinine clearance, serum albumin concentration, baseline platelet count, daily dosage, and concomitant use of caspofungin, levofloxacin, and meropenem were significant risk factors for thrombocytopenia. At multivariate analysis and using ROC curves, daily dose ≥18.75 mg/kg, baseline platelet count ≤181 × 10(9)/L, duration of LZD therapy ≥10 days, and concomitant use of caspofungin and levofloxacin were independent risk factors for thrombocytopenia as defined by criterion 1, whereas creatinine clearance ≤88.39 mL/min/1.73 m(2), serum albumin concentration ≤33.5 g/L, daily dose ≥18.46 mg/kg, and caspofungin were independent risk factors for thrombocytopenia as defined by criterion 2.
The incidence of LZD-related thrombocytopenia in the Chinese population is much higher than that suggested by the drug instructions. Low pretreatment platelet count, low body weight, low serum albumin concentration, long-term drug administration, advanced age, renal insufficiency, and concomitant use of caspofungin, levofloxacin, and meropenem have been identified as risk factors. Although predictors have been proposed for use in clinical practice to screen for patients at high risk who require intensified monitoring, further research on the dosage-based pharmacokinetics and pharmacodynamics of LZD are urgently needed.
利奈唑胺(LZD)是一种恶唑烷酮类抗生素,对大多数甲氧西林敏感和耐药的革兰氏阳性菌具有优异的活性和生物利用度。尽管LZD一般耐受性良好,但多项研究发现了不良血液学影响,其中血小板减少最为令人担忧。
调查2010年2月1日至11月30日期间接受口服或胃肠外LZD治疗患者发生血小板减少的危险因素。
回顾性提取我院信息系统电子病历中的数据。血小板减少定义为最终血小板计数<100×10⁹/L(标准1)或血小板计数较基线水平降低25%(标准2)。采用逻辑回归分析确定危险因素,并使用受试者工作特征曲线预测临床特征。
该研究纳入254例患者,平均(标准差)年龄为59(17.66)岁。LZD治疗持续时间为9.43(5.63)天。按照标准1,69例患者(27.2%)发生血小板减少;按照标准2,127例患者(50%)发生血小板减少。单因素分析时,年龄、体重、肌酐清除率、血清白蛋白浓度、基线血小板计数、每日剂量以及同时使用卡泊芬净、左氧氟沙星和美罗培南是血小板减少的显著危险因素。多因素分析并使用ROC曲线时,每日剂量≥18.75mg/kg、基线血小板计数≤181×10⁹/L、LZD治疗持续时间≥10天以及同时使用卡泊芬净和左氧氟沙星是按照标准1定义的血小板减少的独立危险因素,而肌酐清除率≤88.39mL/min/1.73m²、血清白蛋白浓度≤33.5g/L、每日剂量≥18.46mg/kg以及卡泊芬净是按照标准2定义的血小板减少的独立危险因素。
中国人群中LZD相关血小板减少的发生率远高于药品说明书提示的发生率。已确定治疗前血小板计数低、体重低、血清白蛋白浓度低、长期用药、高龄、肾功能不全以及同时使用卡泊芬净、左氧氟沙星和美罗培南为危险因素。尽管已提出预测指标用于临床实践中筛查需要加强监测的高危患者,但迫切需要对LZD基于剂量的药代动力学和药效学进行进一步研究。