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Preventing Multidrug-Resistant Tuberculosis
Alan B. Bloch, MD, MPH;
Patricia M. Simone, MD;
Eugene McCray, MD;
Kenneth G. Castro, MD
JAMA. 1996;275(6):487-489.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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In the 5 years since the first major outbreaks of multidrug-resistant tuberculosis (MDR TB) in the United States were reported, the epidemiology of MDR TB has become clearer.1,2 Clinically, the course of illness can be devastating for both human immunodeficiency virus (HIV)—infected and noninfected persons, especially when diagnosis and adequate therapy are delayed.1,3 However, prompt diagnosis and appropriate therapy can improve the likelihood of a successful outcome.4-6 Directly observed therapy (DOT) has increasingly become the standard of care7 and has been accompanied by dramatic reductions in morbidity and drug resistance, including MDR TB.8,9 Evidence supports DOT as the adherence-promoting strategy of choice par excellence.
Reflecting an improvement in control efforts is the increase in the proportion of patients completing therapy. In 1993,82% of patients in the United States completed therapy within 12 months, compared with 77% in 1992 (Centers for Disease Control and Prevention [CDC],
. . . [Full Text PDF of this Article]
Author Affiliations
From the Division of Tuberculosis Elimination, National Center for HIV, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Ga.
Footnotes
This article is one of a series addressing emerging and reemerging global microbial threats.
Reprint requests to Division of Tuberculosis Elimination, Centers for Disease Control and Prevention, 1600 Clifton Rd, MS E-10, Atlanta, GA 30333 (Dr Bloch).
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