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Interventions for Tuberculosis Control and Elimination 2002

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Thioacetazone replaced para-aminosalicylic acid very rapidly throughout<br />

English-speaking sub-Saharan Africa because of the better tolerance <strong>and</strong><br />

important cost savings.<br />

Isoniazid plus rifampicin<br />

With the introduction of rifampicin, a more rapid conversion was demonstrated<br />

when it replaced streptomycin (figure 48). 487 This was, however, not<br />

the main progress made with rifampicin-containing chemotherapy. In a trial<br />

in France, rifampicin-containing regimens were tested in three different dura-<br />

Per cent positive<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

RMP+INH+EMB<br />

0 4 8 12 16 20<br />

Month of treatment<br />

66<br />

SM+INH+EMB<br />

Figure 48. Effect of replacing streptomycin by rifampicin on culture conversion. 487<br />

tions of chemotherapy: six, nine, <strong>and</strong> 12 months. 502,503 It was demonstrated<br />

that nine months of isoniazid plus rifampicin, supplemented by either ethambutol<br />

or streptomycin during the first three months, was the optimum duration,<br />

502 <strong>and</strong> the relapse rate during a remarkable mean follow-up time of<br />

101 months with this regimen was only two out of 85 patients. 503<br />

The use of rifampicin provided curative treatment of less than one<br />

year’s duration, <strong>and</strong> the term “short-course chemotherapy” became the br<strong>and</strong><br />

name of this new successful strategy. 504<br />

Isoniazid plus rifampicin plus pyrazinamide (plus a fourth drug)<br />

Despite its remarkable efficacy in experimental models, 505,506 pyrazinamide<br />

was not retained in routine chemotherapy because of its hepatotoxicity.

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