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Updates: Goodman & Gilman's The Pharmacological Basis of Therapeutics
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Updates
9/29/2008: New Advances in the Chemotherapy of Tuberculosis—Part 1 of 3: Recent Advances in New Drug Development
Tawanda Gumbo
Division of Infectious Diseases, University of Texas Southwestern Medical Center, Dallas
Topics Discussed:
adenosine triphosphate; antitubercular agents; chemotherapy regimen; dna gyrase; drug resistance; drug resistance, multiple; extrapulmonary tuberculosis; fluoroquinolones; gatifloxacin; isoniazid; moxifloxacin; mycolic acids; pharmacodynamics; pharmacokinetic; pharmacokinetics; pharmacotherapy; pyrazinamide; rifampin; streptomycin; tuberculosis.
Related to
Table 47-1
;
Excerpt:
"Tuberculosis (TB) has long been, and remains, the most important infectious killer of human beings. Worldwide, the current disease burden is 15 million active cases per year. Standard treatment consists of isoniazid, rifampin, and pyrazinamide for 2 months, followed by intermittent rifampin and isoniazid for 4 months. In case of resistance to isoniazid, initial therapy also includes ethambutol, which is continued until isoniazid susceptibility is documented. To ensure compliance, therapy is ideally administered as directly observed therapy. However, analysis of a series of 11 clinical trials has raised important questions about the effectiveness of directly observed therapy.
1
Moreover, the extended duration of the standard “short course” chemotherapy complicates treatment, especially in resource-poor countries, and may result in poor compliance that can lead to the development of drug resistance. Despite completion of therapy, morbidity is still considerable and recurrence occurs commonly.
2,3
Outcomes are especially poor in extra-pulmonary TB. ..."
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