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Artemisinin-based combination therapy for ... - The Cochrane Library

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Early vomiting<br />

Not reported.<br />

D I S C U S S I O N<br />

Summary of main results<br />

Efficacy (as measured by total failure)<br />

<strong>The</strong> WHO has set two standards <strong>for</strong> antimalarial drugs:<br />

1. that a total failure rate (adjusted <strong>for</strong> new infections) of ><br />

10% should trigger a change of first-line drug policy; and<br />

2. that a new drug being adopted as policy should have total<br />

failure rates (adjusted <strong>for</strong> new infections) of < 5%.<br />

This review has demonstrated that:<br />

• In head to head trials the newest ACT, dihydroartemisininpiperaquine,<br />

achieved the standard of < 5% total failure in 15 out<br />

of the 17 studies it was involved in. DHA-P appears to be at least<br />

as effective as AS+MQ in Asia (eight trials) providing a valuable<br />

alternative to current <strong>therapy</strong>. In clinical trials in Africa, DHA-P<br />

may be more effective than the current widely used options AL6<br />

(four trials) and AS+AQ (one trial), although these two drugs<br />

continue to per<strong>for</strong>m well in many areas (Figure 3; Figure 4).<br />

<strong>Artemisinin</strong>-<strong>based</strong> <strong>combination</strong> <strong>therapy</strong> <strong>for</strong> treating uncomplicated malaria (Review)<br />

Copyright © 2009 <strong>The</strong> <strong>Cochrane</strong> Collaboration. Published by John Wiley & Sons, Ltd.<br />

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