<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 3 Issue 2</issue_number>
<issue_period>2012 (April - June)</issue_period>
<title>Extensively Drug Resistant Tuberculosis: An Upcoming Challenge To Face And Treat. </title>
<abstract>Extensively drug resistant tuberculosis ( XDR- TB) has been reported by 45 countries worldwide , to World Health Organisation ( WHO ) . XDR-TB is a uniformly lethal disease that has emerged in countries with limited resources and high prevalence of tuberculosis , mainly as a result of previous inadequate or improper treatment and poor adherence by the patient to the treatment . It has been defined by WHO Global Task Force as –  lessThan i greaterThan Mycobacterial tuberculosis  lessThan /i greaterThan  infection that is resistant to isoniazid , rifampicin , any fluoroquinolone and at least one of the three injectable drugs i.e. amikacin , kanamycin and capreomycin . Patients co-infected with HIV were found to be at more risk to XDR- TB. An aggressive drug treatment regimens, as a part of comprehensive therapeutic approach including infection control measures, along with DOTS – plus implemented by WHO are required that can cure many patients with XDR – TB , who are not infected with HIV. Along with rapid recognition of cases and prompt contact recognition , drug therapy includes as first line agents , ethambutol and pyrazinamide for the entire duration of therapy . An injectable agent like kanamycin in streptomycin resistant cases , amikacin in kanamycin and streptomycin resistant cases , capreomycin and vyomycin in cases of kanamycin or streptomycin resistant cases should be included , along with monitoring for ototoxicity and nephrotoxicity .</abstract>
<authors>Dr. Sangeeta Bhanwra</authors>
<keywords>XDR-TB , DOTS-PLUS, injectable agents</keywords>
<pages>124-127</pages>
</article>
</Journal>
