Rifapentine for the treatment of latent tuberculosis

被引:2
作者
Egelund, Eric F. [1 ,2 ]
Peloquin, Charles A. [1 ,2 ,3 ]
机构
[1] Univ Florida, Coll Pharm, Dept Pharmacotherapy & Translat Res, Gainesville, FL USA
[2] Univ Florida, Infect Dis Pharmacokinet Lab, Gainesville, FL USA
[3] Univ Florida, Emerging Pathogens Inst, Gainesville, FL USA
关键词
Latent tuberculosis; mycobacterium tuberculosis; rifamycins; rifapentine; ANTITUBERCULOSIS DRUG RIFAPENTINE; MYCOBACTERIUM-TUBERCULOSIS; PULMONARY TUBERCULOSIS; POPULATION PHARMACOKINETICS; PROTEIN-BINDING; DOSE RIFAPENTINE; 12-DOSE REGIMEN; RIFAMPIN; MOXIFLOXACIN; INFECTION;
D O I
10.1080/17512433.2016.1222270
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The goal of this article is to review the use of rifapentine in the treatment of latent tuberculosis infection (LTBI). Controlling LTBI is an important part of the global strategy to end the spread of tuberculosis. Rifapentine's potent sterilizing effect against Mycobacterium tuberculosis combined with its long half-life make it an attractive LTBI treatment option. Areas covered: A systematic literature search of Pubmed using the terms rifapentine' and tuberculosis' was performed. Articles identified were cross-referenced for other relevant publications. The mechanisms of action and resistance, pharmacokinetic and pharmacodynamics, potential drug interactions and side effects are discussed. Expert commentary: Rifapentine in combination with isoniazid for twelve weeks is the best available option for treating latent TB in the majority of patients in the United States due to its favorable safety profile and the increased likelihood of completing therapy. Currently, rifapentine is not registered or available in other countries.
引用
收藏
页码:1253 / 1261
页数:9
相关论文
共 75 条
[1]   Pregnancy-induced changes in pharmacokinetics - A mechanistic-based approach [J].
Anderson, GD .
CLINICAL PHARMACOKINETICS, 2005, 44 (10) :989-1008
[2]  
[Anonymous], 2009, 1 GLOB C SICKL CELL
[3]   Rifampin markedly decreases and gemfibrozil increases the plasma concentrations of atorvastatin and its metabolites [J].
Backman, JT ;
Lulurila, H ;
Neuvonen, M ;
Neuvonen, PJ .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 78 (02) :154-167
[4]   The spectrum of latent tuberculosis: rethinking the biology and intervention strategies [J].
Barry, Clifton E., III ;
Boshoff, Helena I. ;
Dartois, Veronique ;
Dick, Thomas ;
Ehrt, Sabine ;
Flynn, JoAnne ;
Schnappinger, Dirk ;
Wilkinson, Robert J. ;
Young, Douglas .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (12) :845-855
[5]   Rifampicin seems to act as both an inducer and an inhibitor of the metabolism of repaglinide [J].
Bidstrup, TB ;
Stilling, N ;
Damkier, P ;
Scharling, B ;
Thomsen, MS ;
Brosen, K .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 60 (02) :109-114
[6]   Three months of weekly rifapentine plus isoniazid is less hepatotoxic than nine months of daily isoniazid for LTBI [J].
Bliven-Sizemore, E. E. ;
Sterling, T. R. ;
Shang, N. ;
Benator, D. ;
Schwartzman, K. ;
Reves, R. ;
Drobeniuc, J. ;
Bock, N. ;
Villarino, M. E. .
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2015, 19 (09) :1039-1044
[7]  
Bliven-Sizemore EKA, 2011, 4 INT WORKSH CLIN PH
[8]   Comparative pharmacokinetics and pharmacodynamics of the rifamycin antibacterials [J].
Burman, WJ ;
Gallicano, K ;
Peloquin, C .
CLINICAL PHARMACOKINETICS, 2001, 40 (05) :327-341
[9]  
CDC, 2011, Reported Tuberculosis in the United States 2010
[10]   An update on the use of rifapentine for tuberculosis therapy [J].
Chan, John Gar Yan ;
Bai, Xiaoxue ;
Traini, Daniela .
EXPERT OPINION ON DRUG DELIVERY, 2014, 11 (03) :421-431