Literature DB >> 28803492

Rifampin vs. rifapentine: what is the preferred rifamycin for tuberculosis?

Omamah Alfarisi1, Wael A Alghamdi2,3, Mohammad H Al-Shaer2,3, Kelly E Dooley1, Charles A Peloquin2,3.   

Abstract

INTRODUCTION: One-third of the world's population is infected with Mycobacterium tuberculosis (M.tb.). Latent tuberculosis infection (LTBI) can progress to tuberculosis disease, the leading cause of death by infection. Rifamycin antibiotics, like rifampin and rifapentine, have unique sterilizing activity against M.tb. What are the advantages of each for LTBI or tuberculosis treatment? Areas covered: We review studies assessing the pharmacokinetics (PK), pharmacodynamics (PD), drug interaction risk, safety, and efficacy of rifampin and rifapentine and provide basis for comparing them. Expert commentary: Rifampin has shorter half-life, higher MIC against M.tb, lower protein binding, and better distribution into cavitary contents than rifapentine. Drug interactions for the two drugs maybe similar in magnitude. For LTBI, rifapentine is effective as convenient, once-weekly, 12-week course of treatment. Rifampin is also effective for LTBI, but must be given daily for four months, therefore, drug interactions are more problematic. For drug-sensitive tuberculosis disease, rifampin remains the standard of care. Safety profile of rifampin is better-described; adverse events differ somewhat for the two drugs. The registered once-weekly rifapentine regimen is inadequate, but higher doses of either drugs may shorten the treatment duration required for effective management of TB. Results of clinical trials evaluating high-dose rifamycin regimens are eagerly awaited.

Entities:  

Keywords:  Tuberculosis; pharmacodynamics; pharmacokinetics; rifampin; rifamycin; rifapentine

Mesh:

Substances:

Year:  2017        PMID: 28803492     DOI: 10.1080/17512433.2017.1366311

Source DB:  PubMed          Journal:  Expert Rev Clin Pharmacol        ISSN: 1751-2433            Impact factor:   5.045


  12 in total

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Review 2.  Novel Approaches for the Treatment of Pulmonary Tuberculosis.

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3.  The potential use of rifabutin for treatment of patients diagnosed with rifampicin-resistant tuberculosis.

Authors:  Michael G Whitfield; Robin M Warren; Vanessa Mathys; Lesley Scott; Elise De Vos; Wendy Stevens; Elizabeth M Streicher; Guido Groenen; Frederick A Sirgel; Annelies Van Rie
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Review 4.  A Pharmacology Perspective of Simultaneous Tuberculosis and Hepatitis C Treatment.

Authors:  Russell R Kempker; Wael A Alghamdi; Mohammad H Al-Shaer; Gena Burch; Charles A Peloquin
Journal:  Antimicrob Agents Chemother       Date:  2019-10-07       Impact factor: 5.191

5.  Rifapentine Polylactic Acid Sustained-Release Microsphere Complex for Spinal Tuberculosis Therapy: Preparation, in vitro and in vivo Studies.

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6.  Comparative Efficacy of Rifapentine Alone and in Combination with Isoniazid for Latent Tuberculosis Infection: a Translational Pharmacokinetic-Pharmacodynamic Modeling Study.

Authors:  Kendra K Radtke; Jacqueline P Ernest; Nan Zhang; Nicole C Ammerman; Eric Nuermberger; Robert Belknap; Rosanna Boyd; Timothy R Sterling; Rada M Savic
Journal:  Antimicrob Agents Chemother       Date:  2021-10-04       Impact factor: 5.191

7.  Rifampin-resistant/multidrug-resistant Tuberculosis in Alberta, Canada: Epidemiology and treatment outcomes in a low-incidence setting.

Authors:  Brett D Edwards; Jenny Edwards; Ryan Cooper; Dennis Kunimoto; Ranjani Somayaji; Dina Fisher
Journal:  PLoS One       Date:  2021-02-16       Impact factor: 3.240

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Journal:  Infect Drug Resist       Date:  2021-09-14       Impact factor: 4.003

9.  Systematic measurement of combination-drug landscapes to predict in vivo treatment outcomes for tuberculosis.

Authors:  Jonah Larkins-Ford; Talia Greenstein; Nhi Van; Yonatan N Degefu; Michaela C Olson; Artem Sokolov; Bree B Aldridge
Journal:  Cell Syst       Date:  2021-08-31       Impact factor: 10.304

10.  Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds.

Authors:  Karen Y Velasco-Alzate; Anelize Bauermeister; Marcelo M P Tangerina; Tito M C Lotufo; Marcelo J P Ferreira; Paula C Jimenez; Gabriel Padilla; Norberto P Lopes; Letícia V Costa-Lotufo
Journal:  Mar Drugs       Date:  2019-11-28       Impact factor: 5.118

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