Multidrug-resistant Tuberculosis
Multidrug-resistant tuberculosis: past, present and future Ivan Bastian and Franyoise Portaels Mycobacteriology Unit. Institute of Tropical Medicine. Antwerp. Belgium The Lord hath created medicines out of the earth and he that is wise will not abhor them. Ecclesiasticus 38:4, quoted by Selman Waksman when accepting the 1952 Nobel Prize for Medicine that was awarded for the discovery of the first effective antituberculosis drug. streptomycin. which was derived from the soil bacterium, Streptomyces grisells. 1. HISTORICAL PERSPECTIVE This book has been published at the close of the twentieth century when the medical profession and the general community are increasingly concerned about the threat of multidrug-resistant tuberculosis (MDRTB)[1. 2]. However, at this epoch, it is enlightening to move back from our immediate concerns about MDRTB 'hot spots' in Asia, South America, and the former Soviet Union [3], and to place our current predicament in an historical context. If the results of the global survey of antituberculosis drug resistance conducted by the World Health Organisation (WHO) and the International Union against Tuberculosis and Lung Disease (IUATLD) can be extrapolated, only 2. 2% of TB cases worldwide are due to multi drug­ resistant strains [3]. At the beginning of the 20th century, all TB cases were refractory to all available therapies. Great advances had been made during the 19th century in the understanding of the epidemiology and pathogenesis of TB, and in the diagnosis of the disease (reviewed in references 4-7).
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Multidrug-resistant Tuberculosis
Multidrug-resistant tuberculosis: past, present and future Ivan Bastian and Franyoise Portaels Mycobacteriology Unit. Institute of Tropical Medicine. Antwerp. Belgium The Lord hath created medicines out of the earth and he that is wise will not abhor them. Ecclesiasticus 38:4, quoted by Selman Waksman when accepting the 1952 Nobel Prize for Medicine that was awarded for the discovery of the first effective antituberculosis drug. streptomycin. which was derived from the soil bacterium, Streptomyces grisells. 1. HISTORICAL PERSPECTIVE This book has been published at the close of the twentieth century when the medical profession and the general community are increasingly concerned about the threat of multidrug-resistant tuberculosis (MDRTB)[1. 2]. However, at this epoch, it is enlightening to move back from our immediate concerns about MDRTB 'hot spots' in Asia, South America, and the former Soviet Union [3], and to place our current predicament in an historical context. If the results of the global survey of antituberculosis drug resistance conducted by the World Health Organisation (WHO) and the International Union against Tuberculosis and Lung Disease (IUATLD) can be extrapolated, only 2. 2% of TB cases worldwide are due to multi drug­ resistant strains [3]. At the beginning of the 20th century, all TB cases were refractory to all available therapies. Great advances had been made during the 19th century in the understanding of the epidemiology and pathogenesis of TB, and in the diagnosis of the disease (reviewed in references 4-7).
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Multidrug-resistant Tuberculosis

Multidrug-resistant Tuberculosis

Multidrug-resistant Tuberculosis

Multidrug-resistant Tuberculosis

Paperback(Softcover reprint of the original 1st ed. 2000)

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Overview

Multidrug-resistant tuberculosis: past, present and future Ivan Bastian and Franyoise Portaels Mycobacteriology Unit. Institute of Tropical Medicine. Antwerp. Belgium The Lord hath created medicines out of the earth and he that is wise will not abhor them. Ecclesiasticus 38:4, quoted by Selman Waksman when accepting the 1952 Nobel Prize for Medicine that was awarded for the discovery of the first effective antituberculosis drug. streptomycin. which was derived from the soil bacterium, Streptomyces grisells. 1. HISTORICAL PERSPECTIVE This book has been published at the close of the twentieth century when the medical profession and the general community are increasingly concerned about the threat of multidrug-resistant tuberculosis (MDRTB)[1. 2]. However, at this epoch, it is enlightening to move back from our immediate concerns about MDRTB 'hot spots' in Asia, South America, and the former Soviet Union [3], and to place our current predicament in an historical context. If the results of the global survey of antituberculosis drug resistance conducted by the World Health Organisation (WHO) and the International Union against Tuberculosis and Lung Disease (IUATLD) can be extrapolated, only 2. 2% of TB cases worldwide are due to multi drug­ resistant strains [3]. At the beginning of the 20th century, all TB cases were refractory to all available therapies. Great advances had been made during the 19th century in the understanding of the epidemiology and pathogenesis of TB, and in the diagnosis of the disease (reviewed in references 4-7).

Product Details

ISBN-13: 9789401057943
Publisher: Springer Netherlands
Publication date: 11/05/2012
Series: Resurgent and Emerging Infectious Diseases , #1
Edition description: Softcover reprint of the original 1st ed. 2000
Pages: 312
Product dimensions: 6.30(w) x 9.45(h) x 0.03(d)

Table of Contents

1 — Introduction.- 2 — The epidemiology of multidrug-resistant tuberculosis in the United States and other established market economies.- 3 — Epidemiology of multidrug-resistant tuberculosis in low- and middle-income countries.- 4 — The interaction of human immunodeficiency virus and multidrug-resistant Mycobacterium tuberculosis.- 5 — Clinical mismanagement and other factors producing antituberculosis drug resistance.- 6 — The molecular mechanisms of drug resistance in Mycobacterium tuberculosis.- 7 — DOTS and multidrug-resistant tuberculosis.- 8 — Conventional methods for antimicrobial susceptibility testing of Mycobacterium tuberculosis.- 9 — Novel rapid antimicrobial susceptibility tests for Mycobacterium tuberculosis.- 10 — Pharmacology of the second-line antituberculosis drugs.- 11 — Treatment of multidrug-resistant tuberculosis.- 12 — Treatment of multidrug-resistant tuberculosis in developing countries.- 13 — Treatment of outcome of multidrug-resistant tuberculosis.- 14 — Chemoprophylaxis and BCG in contacts of multidrug- resistant tuberculosis.- 15 — Multidrug-resistant tuberculosis and the health care worker.- 16 — The development of new chemotherapeutics for multidrug-resistant tuberculosis.- 17 — Population dynamics and control of multidrug-resistant tuberculosis.- 18 — Administrative, engineering, and personal protective measures for controlling Mycobacterium tuberculosis.- 19 — Making DOTS-Plus work.
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