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作 者:戈梦佳 陈恳[1,2] 马青变[3] 易湛苗[1] 翟所迪[1]
机构地区:[1]北京大学第三医院药剂科,100191 [2]北京大学药学院药事管理与临床药学系,100191 [3]北京大学第三医院急诊科,北京100191
出 处:《药物不良反应杂志》2016年第6期405-411,共7页Adverse Drug Reactions Journal
摘 要:目的综合评价利奈唑胺相关血小板减少的危险因素。方法检索有关数据库,收集建库至2016年6月收录的有关利奈唑胺相关血小板减少危险因素的病例对照研究,依据渥太华-纽卡斯尔质量评估量表(NOS)对纳入文献进行质量评价,采用 RevMan 5.3软件进行 Meta 分析,结果用 OR 及其95% CI 表示。结果纳入分析的文献为25篇,NOS 评分均≥7分。涉及4279例患者,其中血小板减少组1335例,无血小板减少组2944例。Meta 分析结果显示,利奈唑胺相关血小板减少的危险因素为基础 PLT <200×10^9∕ L(OR =3.64,95% CI:1.60~8.30,P =0.002),体重<50 kg (OR =2.44,95% CI:1.79~3.34,P <0.001),肌酐清除率<30 ml∕ min(OR =1.85,95% CI:1.29~2.67,P <0.001,用药疗程>14 d(OR =1.76,95% CI:1.17~2.65,P =0.006),以及年龄≥65岁(OR =1.54,95% CI:1.03~2.31,P =0.04)。结论肾功能重度损伤、基础 PLT 低、低体重、用药疗程长和高龄为利奈唑胺相关血小板减少的危险因素。Objective To evaluate the risk factors for thrombocytoenia related to linezolid(LZD) comprehensively. Methods The related databases were electronically searched for the case-control studies about risk factors for LZD-associated thrombocytoPenia from the incePtion to June 2016. The quality of the literature which was enrolled into the Meta-analysis evaluated by Newcastle-Ottawa Quality Assessment Scale (NOS),and then Meta-analysis was conducted using RevMan 5. 3 software. The results are Presented as odds risk( OR)and 95% confidence interval( CI). Results A total of 25 studies involving 4 279 Patients were entered, including 1 335 in the thrombocytoPenia grouP and 2 944 in the none thrombocytoPenia grouP. The NOS scores of all literature were greater than or equal to 7. The result of Meta-analysis showed that,the baseline Platelet count 〈 200 × 109 ∕ L(OR = 3. 64,95% CI:1. 60-8. 30,P =0. 002),body weight 〈 50 kg(OR = 2. 44,95% CI:1. 79-3. 34,P 〈 0. 001),creatinine clearance 〈 30 ml∕ min(OR = 1. 85,95% CI:1. 29-2. 67,P 〈 0. 001),duration of LZD theraPy 〉 14 days(OR = 1. 76, 95% CI:1. 17-2. 65,P = 0. 006)and age≥65 years(OR = 1. 54,95% CI:1. 03-2. 31,P = 0. 04)were identified as significant risk factors for LZD-associated thrombocytopenia. Conclusion Current evidence shows that the severe damage to renal function,low baseline Platelet count,low body weight,long-term LZD administration and advanced age are risk factors of LZD-related thrombocytopenia.
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