Deriving Dosages for Levofloxacin Tuberculosis Preventive Treatment for Young People Exposed to Rifampicin-Resistant Tuberculosis.

IF 4.5 2区 医学 Q2 IMMUNOLOGY
Belén P Solans, Ryo Miyakawa, Maureen Shin, Anneke C Hesseling, Yasmine White, Tiziana Masini, Avinash Kanchar, Dennis Falzon, Radojka M Savic
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引用次数: 0

Abstract

Background: Tuberculosis (TB) is the leading single bacterial cause of death worldwide. In 2023, approximately 400 000 people developed multidrug- and rifampicin-resistant TB (MDR/RR-TB), which complicates treatment. TB preventive treatment (TPT) is a critical strategy to prevent the progression from TB infection to TB disease among those at risk. In February 2024, based on data from 2 randomized controlled trials, levofloxacin was strongly recommended by the World Health Organization (WHO) as a TPT option in people of all ages exposed to MDR/RR-TB. There are uncertainties about the optimal dosing of levofloxacin in children and adolescents when using dispersible and solid formulations. We used pharmacokinetic modeling and simulations to determine the best dosing strategy in people aged up to 19 years for both formulations of levofloxacin.

Methods: A previously developed population pharmacokinetic model of levofloxacin in children (0.2-16.8 years) was used and applied to new WHO harmonized weight bands. Simulations were conducted using demographic data from countries with the highest incidence of RR- or MDR-TB. Two currently available levofloxacin formulations (100 mg pediatric, dispersible tablets and 250 mg solid tablets) were considered.

Results: A dosing regimen by weight band was developed for levofloxacin when used as TPT in people aged 0-19 years exposed to MDR/RR-TB. Doses correspond to 8-33 mg/kg for the 100 mg dispersible tablets and 10-42 mg/kg for 250 mg solid tablets. These doses achieve adequate adult target exposure levels.

Conclusions: Pragmatic, weight-band dosing strategies help simplify the administration of MDR/RR-TB TPT and have been included in WHO guidance.

对暴露于利福平耐药结核病的年轻人进行左氧氟沙星结核病预防治疗的剂量确定。
背景:结核病(TB)是世界范围内导致死亡的主要单一细菌原因。2023年,约有40万人患上耐多药和利福平结核病(MDR/RR-TB),使治疗复杂化。结核病预防治疗(TPT)是预防高危人群从结核感染发展为结核病的一项关键战略。2024年2月,根据两项随机对照试验的数据,世界卫生组织(世卫组织)强烈推荐左氧氟沙星作为耐多药/耐药结核病暴露人群的TPT选择。在儿童和青少年中使用分散剂和固体制剂时,左氧氟沙星的最佳剂量存在不确定性。我们使用药代动力学建模和模拟来确定两种左氧氟沙星配方在19岁以下人群中的最佳给药策略。方法:采用先前建立的儿童(0.2 ~ 16.8岁)左氧氟沙星人群药代动力学模型,并将其应用于新的WHO统一体重带。利用来自耐药或耐多药结核病发病率最高的国家的人口统计数据进行了模拟。考虑了两种目前可用的左氧氟沙星配方(100毫克小儿分散片和250毫克固体片)。结果:在0-19岁MDR/RR-TB暴露人群中,左氧氟沙星作为TPT使用时,建立了体重带给药方案。100毫克分散片剂的剂量为8-33毫克/公斤,250毫克固体片剂的剂量为10-42毫克/公斤。这些剂量达到了适当的成人目标暴露水平。结论:实用的体重带给药策略有助于简化MDR/RR-TB TPT的管理,并已列入世卫组织指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Infectious Diseases
Journal of Infectious Diseases 医学-传染病学
CiteScore
13.50
自引率
3.10%
发文量
449
审稿时长
2-4 weeks
期刊介绍: Published continuously since 1904, The Journal of Infectious Diseases (JID) is the premier global journal for original research on infectious diseases. The editors welcome Major Articles and Brief Reports describing research results on microbiology, immunology, epidemiology, and related disciplines, on the pathogenesis, diagnosis, and treatment of infectious diseases; on the microbes that cause them; and on disorders of host immune responses. JID is an official publication of the Infectious Diseases Society of America.
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