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Drug-induced QT interval shortening: potential harbinger of proarrhythmia and regulatory perspectives.药物引起的 QT 间期缩短:潜在的致心律失常先兆和监管视角。
Br J Pharmacol. 2010 Jan;159(1):58-69. doi: 10.1111/j.1476-5381.2009.00191.x. Epub 2009 Jun 25.
2
Short QT syndrome.短QT综合征
Ann Noninvasive Electrocardiol. 2005 Oct;10(4):436-40. doi: 10.1111/j.1542-474X.2005.00064.x.
3
International Conference on Harmonisation; guidance on E14 Clinical Evaluation of QT/QTc Interval Prolongation and Proarrhythmic Potential for Non-Antiarrhythmic Drugs; availability. Notice.国际协调会议;关于非抗心律失常药物QT/QTc间期延长和致心律失常潜力的E14临床评价指南;可用性。通知。
Fed Regist. 2005 Oct 20;70(202):61134-5.
4
Pharmacokinetic and pharmacodynamic profile of linezolid in healthy volunteers and patients with Gram-positive infections.利奈唑胺在健康志愿者和革兰氏阳性菌感染患者中的药代动力学和药效学特征。
J Antimicrob Chemother. 2003 May;51 Suppl 2:ii17-25. doi: 10.1093/jac/dkg248.
5
Pharmacokinetics and tolerance of single- and multiple-dose oral or intravenous linezolid, an oxazolidinone antibiotic, in healthy volunteers.恶唑烷酮类抗生素利奈唑胺在健康志愿者中的单剂量和多剂量口服及静脉给药的药代动力学和耐受性
J Antimicrob Chemother. 2003 May;51(5):1239-46. doi: 10.1093/jac/dkg180. Epub 2003 Mar 28.
6
Linezolid: its role in the treatment of gram-positive, drug-resistant bacterial infections.利奈唑胺:其在革兰氏阳性耐药细菌感染治疗中的作用。
Am Fam Physician. 2002 Feb 15;65(4):663-70.
7
Quinolone-induced QT interval prolongation: a not-so-unexpected class effect.喹诺酮类药物引起的QT间期延长:一种并非完全意外的类效应。
J Antimicrob Chemother. 2000 May;45(5):557-9. doi: 10.1093/jac/45.5.557.
8
Mechanism of action of oxazolidinones: effects of linezolid and eperezolid on translation reactions.恶唑烷酮类药物的作用机制:利奈唑胺和依哌唑胺对翻译反应的影响。
Antimicrob Agents Chemother. 1997 Oct;41(10):2132-6. doi: 10.1128/AAC.41.10.2132.

利奈唑胺标准治疗剂量和超治疗剂量对 QTc 间期延长无影响。

Lack of an effect of standard and supratherapeutic doses of linezolid on QTc interval prolongation.

机构信息

Pfizer, Inc., 235 East 42nd St., New York, NY 10017, USA.

出版信息

Antimicrob Agents Chemother. 2011 Sep;55(9):4302-7. doi: 10.1128/AAC.01723-10. Epub 2011 Jun 27.

DOI:10.1128/AAC.01723-10
PMID:21709083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3165302/
Abstract

A double-blind, placebo-controlled, four-way crossover study was conducted in 40 subjects to assess the effect of linezolid on corrected QT (QTc) interval prolongation. Time-matched, placebo-corrected QT intervals were determined predose and at 0.5, 1 (end of infusion), 2, 4, 8, 12, and 24 h after intravenous dosing of linezolid 600 and 1,200 mg. Oral moxifloxacin at 400 mg was used as an active control. The pharmacokinetic profile of linezolid was also evaluated. At each time point, the upper bound of the 90% confidence interval (CI) for placebo-corrected QTcF values (i.e., QTc values adjusted for ventricular rate using the correction methods of Fridericia) for linezolid 600 and 1,200-mg doses were <10 ms, which indicates an absence of clinically significant QTc prolongation. At 2 and 4 h after the moxifloxacin dose, corresponding to the population T(max), the lower bound of the two-sided 90% CI for QTcF when comparing moxifloxacin to placebo was >5 ms, indicating that the study was adequately sensitive to assess QTc prolongation. The pharmacokinetic profile of linezolid at 600 mg was consistent with previous observations. Systemic exposure to linezolid increased in a slightly more than dose-proportional manner at supratherapeutic doses, but the degree of nonlinearity was small. At a supratherapeutic single dose of 1,200 mg of linezolid, no treatment-related increase in adverse events was seen compared to 600 mg of linezolid, and no clinically meaningful effects on vital signs and safety laboratory evaluations were noted.

摘要

一项在 40 例受试者中进行的双盲、安慰剂对照、四交叉研究评估了利奈唑胺对校正 QT(QTc)间期延长的影响。在静脉给予利奈唑胺 600mg 和 1200mg 后,分别在给药前、0.5、1(输注结束时)、2、4、8、12 和 24 小时测定时间匹配的、安慰剂校正的 QT 间期。口服莫西沙星 400mg 作为活性对照。还评估了利奈唑胺的药代动力学特征。在每个时间点,利奈唑胺 600mg 和 1200mg 剂量的安慰剂校正 QTcF 值(即使用 Fridericia 校正方法校正心室率的 QTc 值)的 90%置信区间(CI)上限均<10ms,表明没有临床意义的 QTc 延长。在莫西沙星剂量后 2 和 4 小时,相当于群体 T(max),比较莫西沙星和安慰剂时 QTcF 的双侧 90%CI 的下限>5ms,表明该研究足以评估 QTc 延长。利奈唑胺的药代动力学特征与之前的观察结果一致。在治疗剂量下,利奈唑胺的系统暴露量以略高于剂量比例的方式增加,呈轻度非线性,但非线性程度较小。在利奈唑胺 1200mg 的超治疗剂量单剂量下,与 600mg 的利奈唑胺相比,未见与治疗相关的不良事件增加,且对生命体征和安全实验室评估无临床意义的影响。