New combination for patients with latent tuberculosis infection: A pilot study

Background: Latent tuberculosis infection (LTBI) is characterized by the presence of immune responses to Mycobacterium tuberculosis without clinical evidence of active TB. LTBI treatment among persons at risk for progression to active disease is an important strategy for TB control and elimination....

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Main Authors: Te-Yu Lin, Feng-Cheng Liu
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Journal of Medical Sciences
Subjects:
Online Access:http://www.jmedscindmc.com/article.asp?issn=1011-4564;year=2018;volume=38;issue=6;spage=252;epage=257;aulast=Lin
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spelling doaj-cf4bf55252ac42a3b73a5565c1482f182020-11-24T21:48:39ZengWolters Kluwer Medknow PublicationsJournal of Medical Sciences1011-45642018-01-0138625225710.4103/jmedsci.jmedsci_46_18New combination for patients with latent tuberculosis infection: A pilot studyTe-Yu LinFeng-Cheng LiuBackground: Latent tuberculosis infection (LTBI) is characterized by the presence of immune responses to Mycobacterium tuberculosis without clinical evidence of active TB. LTBI treatment among persons at risk for progression to active disease is an important strategy for TB control and elimination. This prospective observational study aimed to compare the incidences of hepatitis and side effects between a new 2-month combination regimen of isoniazid, rifampin and pyrazinamid (2HRZ) plus excipient and the standard 3-month regimen of isoniazid and rifapentine (3HP) for LTBI treatment in Taiwan. Materials and Methods: Between January 1, 2017, and December 31, 2017, all patients aged ≥20 years diagnosed LTBI were included in the study. Demographic and baseline laboratory assessment of the patients at diagnosis was collected. Eligible individuals were allocated to the 2-month regimen comprising HUEXC030, isoniazid, rifampin, and pyrazinamide (2HRZ) or 3-month regimen with isoniazid and rifapentine (HP). All symptoms and side effects during treatment were recorded. Results: Nineteen patients received the 2-month regimen with HRZ plus HUEXC030, while 23 received the 3-month regimen with HP. The treatment completion rates were 73.7% and 82.6% in the 2- and 3-month regimen groups, respectively. The most common side effects during treatment were fatigue/myalgia/weakness, loss of appetite, and rash. The aspartate aminotransferase, alanine aminotransferase, and total bilirubin levels were similar in both groups after 4 weeks of treatment. Conclusions: This study demonstrates that LTBI patients receiving the 2-month regimen with HRZ plus HUEXC030 experienced similar side effects including hepatitis as patients on the 3-month regimen with HP. This new combination treatment regimen may be an alternative for the treatment of LTBI.http://www.jmedscindmc.com/article.asp?issn=1011-4564;year=2018;volume=38;issue=6;spage=252;epage=257;aulast=LinLatent tuberculosis infectionisoniazidpyrazinamide and HUEXC030isoniazid and rifapentinerifampin
collection DOAJ
language English
format Article
sources DOAJ
author Te-Yu Lin
Feng-Cheng Liu
spellingShingle Te-Yu Lin
Feng-Cheng Liu
New combination for patients with latent tuberculosis infection: A pilot study
Journal of Medical Sciences
Latent tuberculosis infection
isoniazid
pyrazinamide and HUEXC030
isoniazid and rifapentine
rifampin
author_facet Te-Yu Lin
Feng-Cheng Liu
author_sort Te-Yu Lin
title New combination for patients with latent tuberculosis infection: A pilot study
title_short New combination for patients with latent tuberculosis infection: A pilot study
title_full New combination for patients with latent tuberculosis infection: A pilot study
title_fullStr New combination for patients with latent tuberculosis infection: A pilot study
title_full_unstemmed New combination for patients with latent tuberculosis infection: A pilot study
title_sort new combination for patients with latent tuberculosis infection: a pilot study
publisher Wolters Kluwer Medknow Publications
series Journal of Medical Sciences
issn 1011-4564
publishDate 2018-01-01
description Background: Latent tuberculosis infection (LTBI) is characterized by the presence of immune responses to Mycobacterium tuberculosis without clinical evidence of active TB. LTBI treatment among persons at risk for progression to active disease is an important strategy for TB control and elimination. This prospective observational study aimed to compare the incidences of hepatitis and side effects between a new 2-month combination regimen of isoniazid, rifampin and pyrazinamid (2HRZ) plus excipient and the standard 3-month regimen of isoniazid and rifapentine (3HP) for LTBI treatment in Taiwan. Materials and Methods: Between January 1, 2017, and December 31, 2017, all patients aged ≥20 years diagnosed LTBI were included in the study. Demographic and baseline laboratory assessment of the patients at diagnosis was collected. Eligible individuals were allocated to the 2-month regimen comprising HUEXC030, isoniazid, rifampin, and pyrazinamide (2HRZ) or 3-month regimen with isoniazid and rifapentine (HP). All symptoms and side effects during treatment were recorded. Results: Nineteen patients received the 2-month regimen with HRZ plus HUEXC030, while 23 received the 3-month regimen with HP. The treatment completion rates were 73.7% and 82.6% in the 2- and 3-month regimen groups, respectively. The most common side effects during treatment were fatigue/myalgia/weakness, loss of appetite, and rash. The aspartate aminotransferase, alanine aminotransferase, and total bilirubin levels were similar in both groups after 4 weeks of treatment. Conclusions: This study demonstrates that LTBI patients receiving the 2-month regimen with HRZ plus HUEXC030 experienced similar side effects including hepatitis as patients on the 3-month regimen with HP. This new combination treatment regimen may be an alternative for the treatment of LTBI.
topic Latent tuberculosis infection
isoniazid
pyrazinamide and HUEXC030
isoniazid and rifapentine
rifampin
url http://www.jmedscindmc.com/article.asp?issn=1011-4564;year=2018;volume=38;issue=6;spage=252;epage=257;aulast=Lin
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