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toman's tuberculosis case detection, treatment and monitoring

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25. What are the current recommendations<br />

for st<strong>and</strong>ard regimens?<br />

A. Harries 1<br />

The aims of <strong>treatment</strong> regimens are to: cure the patient, prevent death from active<br />

disease or its late effects, prevent the emergence <strong>and</strong> spread of drug-resistant organisms,<br />

minimize relapse, <strong>and</strong> protect the community from continued transmission of<br />

infection.<br />

All <strong>treatment</strong> regimens have two phases – an initial intensive phase <strong>and</strong> a continuation<br />

phase (1, 2).<br />

Initial intensive phase<br />

The initial intensive phase of <strong>treatment</strong> is designed to kill actively growing <strong>and</strong> semidormant<br />

bacilli. This means a shorter duration of infectiousness, usually with rapid<br />

smear conversion (80–90%) after 2–3 months of <strong>treatment</strong>. The initial phase of<br />

rifampicin-containing regimens should always be directly observed in order to ensure<br />

adherence. That phase usually involves between three <strong>and</strong> five drugs. If initial<br />

resistance rates are high, use of a three-drug regimen carries the risk of selecting<br />

drug-resistant mutants, especially in patients with high bacillary loads, i.e. with smearpositive<br />

pulmonary <strong>tuberculosis</strong>. Use of a four-drug regimen reduces the risk both of<br />

drug resistance developing <strong>and</strong> of failures <strong>and</strong> relapses. If a patient defaults on <strong>treatment</strong><br />

after the initial intensive phase, relapse is less likely.<br />

Continuation phase<br />

The continuation phase eliminates most residual bacilli <strong>and</strong> reduces failures <strong>and</strong><br />

relapses. At the start of the continuation phase, numbers of bacilli are low <strong>and</strong> there<br />

is less chance of selecting drug-resistant mutants: fewer drugs are therefore needed.<br />

St<strong>and</strong>ard <strong>tuberculosis</strong> <strong>treatment</strong> regimens<br />

Treatment regimens recommended by WHO (1) are shown in Table 27. St<strong>and</strong>ard<br />

codes are used for <strong>tuberculosis</strong> <strong>treatment</strong> regimens: each <strong>tuberculosis</strong> drug is represented<br />

by a st<strong>and</strong>ard abbreviation <strong>and</strong> each regimen has two phases. The number<br />

1 Technical Adviser, Malawi National Tuberculosis Control Programme, Lilongwe, Malawi.<br />

124

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