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Interventions for Tuberculosis Control and Elimination 2002

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tionally considered to belong to groups at risk of tuberculous infection.<br />

Only nine cases of tuberculosis occurred in the entire cohort of more than<br />

500 patients during a follow-up period of 30 months following cessation<br />

of treatment with six months of either placebo or isoniazid: three in the<br />

isoniazid group <strong>and</strong> six in the placebo group. This corresponds to an overall<br />

protection of 52%, yet with 95% cent confidence intervals including<br />

zero.<br />

In Nairobi, Kenya, HIV-positive patients were r<strong>and</strong>omly assigned to<br />

receive either daily isoniazid <strong>for</strong> six months or placebo (irrespective of the<br />

tuberculin skin test result). 888 Outcome measures were incidence of tuberculosis<br />

<strong>and</strong> death. The follow-up period from enrolment onwards was a<br />

median of 1.8 years. The protection among persons with positive tuberculin<br />

skin test reactions (not further defined) was 40%, yet with confidence<br />

intervals overlapping zero. There was a slight, statistically significant reduction<br />

in risk of death among tuberculin-positive isoniazid recipients compared<br />

to the controls.<br />

Spontaneously healed tuberculosis with fibrotic residuals<br />

Patients with tuberculosis that has healed spontaneously with fibrotic lesions<br />

are frequently found, <strong>and</strong> remain an important source of reactivation tuberculosis,<br />

particularly in countries where the tuberculosis risk has been rapidly<br />

declining <strong>and</strong> most cases are the result of endogenous reactivation. Three<br />

such studies are shown here (figure 81).<br />

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Figure 81. Protection from isoniazid preventive therapy against tuberculosis among<br />

patients with fibrotic lesions, hemodialysis, or silicosis. 123,641,891-893<br />

134

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