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Intermediate Susceptibility Dose-Dependent Breakpoints For High-Dose Rifampin, Isoniazid, and Pyrazinamide Treatment in Multidrug-Resistant Tuberculosis Programs.耐多药结核病项目中高剂量利福平、异烟肼和吡嗪酰胺治疗的中敏剂量依赖性折点。
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A Faropenem, Linezolid, and Moxifloxacin Regimen for Both Drug-Susceptible and Multidrug-Resistant Tuberculosis in Children: FLAME Path on the Milky Way.用于儿童药敏性结核病和耐多药结核病的法罗培南、利奈唑胺和莫西沙星治疗方案:银河系上的FLAME路径
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基于吉非替尼药代动力学/药效学的肺部和脑膜耐多药结核的最佳剂量。

Gatifloxacin Pharmacokinetics/Pharmacodynamics-based Optimal Dosing for Pulmonary and Meningeal Multidrug-resistant Tuberculosis.

机构信息

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, Texas.

Institute for Clinical Pharmacodynamics, Schenectady, New York.

出版信息

Clin Infect Dis. 2018 Nov 28;67(suppl_3):S274-S283. doi: 10.1093/cid/ciy618.

DOI:10.1093/cid/ciy618
PMID:30496459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6904296/
Abstract

BACKGROUND

Gatifloxacin is used for the treatment of multidrug-resistant tuberculosis (MDR-TB). The optimal dose is unknown.

METHODS

We performed a 28-day gatifloxacin hollow-fiber system model of tuberculosis (HFS-TB) study in order to identify the target exposures associated with optimal kill rates and resistance suppression. Monte Carlo experiments (MCE) were used to identify the dose that would achieve the target exposure in 10000 adult patients with meningeal or pulmonary MDR-TB. The optimal doses identified were validated using probit analyses of clinical data from 2 prospective clinical trials of patients with pulmonary and meningeal tuberculosis. Classification and regression-tree (CART) analyses were used to identify the gatifloxacin minimum inhibitory concentration (MIC) below which patients failed or relapsed on combination therapy.

RESULTS

The target exposure associated with optimal microbial kill rates and resistance suppression in the HFS-TB was a 0-24 hour area under the concentration-time curve-to-MIC of 184. MCE identified an optimal gatifloxacin dose of 800 mg/day for pulmonary and 1200 mg/day for meningeal MDR-TB, and a clinical susceptibility breakpoint of MIC ≤ 0.5 mg/L. In clinical trials, CART identified that 79% patients failed therapy if MIC was >2 mg/L, but 98% were cured if MIC was ≤0.5 mg/L. Probit analysis of clinical data demonstrated a >90% probability of a cure in patients if treated with 800 mg/day for pulmonary tuberculosis and 1200 mg/day for meningeal tuberculosis. Doses ≤400 mg/day were suboptimal.

CONCLUSIONS

Gatifloxacin doses of 800 mg/day and 1200 mg/day are recommended for pulmonary and meningeal MDR-TB treatment, respectively. Gatifloxacin has a susceptible dose-dependent zone at MICs 0.5-2 mg/L.

摘要

背景

加替沙星用于治疗耐多药结核病(MDR-TB)。最佳剂量未知。

方法

我们进行了为期 28 天的加替沙星中空纤维系统结核模型(HFS-TB)研究,以确定与最佳杀伤率和耐药抑制相关的目标暴露量。蒙特卡罗实验(MCE)用于确定在 10000 例患有脑膜或肺 MDR-TB 的成年患者中实现目标暴露量所需的剂量。使用前瞻性肺和脑膜结核患者临床试验的临床数据进行概率分析,验证了确定的最佳剂量。分类和回归树(CART)分析用于确定加替沙星最低抑菌浓度(MIC)低于该值时,患者在联合治疗中失败或复发。

结果

HFS-TB 中与最佳微生物杀伤率和耐药抑制相关的目标暴露量是 0-24 小时浓度-时间曲线下面积与 MIC 的比值为 184。MCE 确定了肺 MDR-TB 的最佳加替沙星剂量为 800mg/天,脑膜 MDR-TB 的最佳剂量为 1200mg/天,临床药敏折点为 MIC≤0.5mg/L。临床试验中,CART 确定如果 MIC>2mg/L,79%的患者治疗失败,但如果 MIC≤0.5mg/L,98%的患者治愈。对临床数据的概率分析表明,如果用 800mg/天治疗肺结核和 1200mg/天治疗脑膜炎,患者的治愈率超过 90%。剂量≤400mg/天则效果不佳。

结论

建议分别使用 800mg/天和 1200mg/天的剂量治疗肺和脑膜 MDR-TB。加替沙星在 MIC 为 0.5-2mg/L 时有一个敏感剂量依赖性区域。