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利福平浓度低于治疗水平与结核病治疗不良结局相关。

Subtherapeutic Rifampicin Concentration Is Associated With Unfavorable Tuberculosis Treatment Outcomes.

作者信息

Ramachandran Geetha, Chandrasekaran Padmapriyadarshini, Gaikwad Sanjay, Agibothu Kupparam Hemanth Kumar, Thiruvengadam Kannan, Gupte Nikhil, Paradkar Mandar, Dhanasekaran Kavitha, Sivaramakrishnan Gomathi Narayan, Kagal Anju, Thomas Beena, Pradhan Neeta, Kadam Dileep, Hanna Luke Elizabeth, Balasubramanian Usha, Kulkarni Vandana, Murali Lakshmi, Golub Jonathan, Gupte Akshay, Shivakumar Shri Vijay Bala Yogendra, Swaminathan Soumya, Dooley Kelly E, Gupta Amita, Mave Vidya

机构信息

National Institute for Research in Tuberculosis, Chennai.

Byramjee Jeejeebhoy Government Medical College, Pune, India.

出版信息

Clin Infect Dis. 2020 Mar 17;70(7):1463-1470. doi: 10.1093/cid/ciz380.

Abstract

BACKGROUND

The relationships between first-line drug concentrations and clinically important outcomes among patients with tuberculosis (TB) remain poorly understood.

METHODS

We enrolled a prospective cohort of patients with new pulmonary TB receiving thrice-weekly treatment in India. The maximum plasma concentration of each drug was determined at months 1 and 5 using blood samples drawn 2 hours postdose. Subtherapeutic cutoffs were: rifampicin <8 µg/mL, isoniazid <3 µg/mL, and pyrazinamide <20 µg/mL. Factors associated with lower log-transformed drug concentrations, unfavorable outcomes (composite of treatment failure, all-cause mortality, and recurrence), and individual outcomes were examined using Poisson regression models.

RESULTS

Among 404 participants, rifampicin, isoniazid, and pyrazinamide concentrations were subtherapeutic in 85%, 29%, and 13%, respectively, at month 1 (with similar results for rifampicin and isoniazid at month 5). Rifampicin concentrations were lower with human immunodeficiency virus coinfection (median, 1.6 vs 4.6 µg/mL; P = .015). Unfavorable outcome was observed in 19%; a 1-μg/mL decrease in rifampicin concentration was independently associated with unfavorable outcome (adjusted incidence rate ratio [aIRR], 1.21 [95% confidence interval {CI}, 1.01-1.47]) and treatment failure (aIRR, 1.16 [95% CI, 1.05-1.28]). A 1-μg/mL decrease in pyrazinamide concentration was associated with recurrence (aIRR, 1.05 [95% CI, 1.01-1.11]).

CONCLUSIONS

Rifampicin concentrations were subtherapeutic in most Indian patients taking a thrice-weekly TB regimen, and low rifampicin and pyrazinamide concentrations were associated with poor outcomes. Higher or more frequent dosing is needed to improve TB treatment outcomes in India.

摘要

背景

结核病(TB)患者一线药物浓度与临床重要结局之间的关系仍未得到充分了解。

方法

我们纳入了印度一组接受每周三次治疗的新发肺结核患者的前瞻性队列。在第1个月和第5个月,使用给药后2小时采集的血样测定每种药物的最大血浆浓度。亚治疗阈值为:利福平<8μg/mL、异烟肼<3μg/mL和吡嗪酰胺<20μg/mL。使用泊松回归模型检查与较低对数转换药物浓度、不良结局(治疗失败、全因死亡率和复发的综合)以及个体结局相关的因素。

结果

在404名参与者中,第1个月时利福平、异烟肼和吡嗪酰胺浓度低于治疗水平的分别为85%、29%和13%(第5个月时利福平和异烟肼的结果相似)。合并人类免疫缺陷病毒感染时利福平浓度较低(中位数,1.6 vs 4.6μg/mL;P = 0.015)。观察到19%的患者出现不良结局;利福平浓度每降低1μg/mL与不良结局独立相关(调整发病率比[aIRR],1.21[95%置信区间{CI},1.01 - 1.47])和治疗失败(aIRR,1.16[95%CI,1.05 - 1.28])。吡嗪酰胺浓度每降低1μg/mL与复发相关(aIRR,1.05[95%C,1.01 - 1.11])。

结论

在大多数接受每周三次结核病治疗方案的印度患者中,利福平浓度低于治疗水平,低利福平和吡嗪酰胺浓度与不良结局相关。在印度需要更高剂量或更频繁给药以改善结核病治疗结局。

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