# \[e-drug\] Lancet: Antimalarial combinations

**URL:** <https://talk.edrugplus.org/t/e-drug-lancet-antimalarial-combinations/20152>\
**Category:** e-drug\
**Created:** [July 20, 2004, 6:40am UTC](https://talk.edrugplus.org/t/e-drug-lancet-antimalarial-combinations/20152 "2004-07-20T06:40:25Z")\
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**Post date:** [July 20, 2004, 6:40am UTC](https://talk.edrugplus.org/t/e-drug-lancet-antimalarial-combinations/20152/1 "2004-07-20T06:40:25Z")

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E-drug: Lancet: Antimalarial combinations  
---------------------------------------------

Antimalarial combinations  
Peter Gottfried Kremsner, Sanjeev Krishna Lancet 2004; 364: 285-94

[http://www.thelancet.com/journal/vol364/iss9430/full/llan.364.9430.review\_and\_opinion.30244.1](http://www.thelancet.com/journal/vol364/iss9430/full/llan.364.9430.review_and_opinion.30244.1)  
[Repair long URL]  
Multidrug resistance has rendered monotherapy for malaria useless in  
most parts of the world, and has also compromised the usefulness of  
many of the available combination chemotherapies. New antimalarial  
regimens are, therefore, urgently needed. We review the various  
antimalarial combinations that can be used to treat otherwise drug  
resistant disease, and discuss what defines an ideal antimalarial  
combination regimen.

This long article discuss the rationale for combinations of  
antimalarials, their roles and their comparative efficacy.

Combinations discussed in detail are

Artemisinin-containing regimens

Sulfadoxine-pyrimethamine

Sulfadoxine-pyrimethamine+chloroquine

Sulfadoxine-pyrimethamine+amodiaquine

Sulfadoxine-pyrimethamine+quinine

Sulfadoxine-pyrimethamine-mefloquine

Atovaquone-proguanil

Chlorproguanil-dapsone

Quinine+tetracycline

Quinine+clindamycin

Artesunate+amodiaquine

Artesunate+sulfadoxine-pyrimethamine

Artemether-lumefantrine

Artesunate+mefloquine

The authors conclude  
The future  
Multidrug resistance in parasites has forced the use of combination  
antimalarial regimens. The need for effective treatments has thrown  
together antimalarial combinations that have often worked better than  
monotherapies, though sometimes only temporarily. However, we are  
still far from discovery of an ideal regimen. The best options  
available now include: mefloquine+ artesunate, which works well in  
Thailand, although little is known about how this combination  
translates to high transmission areas; and clindamycin+quinine, which  
is effective in non-immune individuals, suggesting that  
clindamycin+artesunate should also be studied.  
Dihydroartemisinin-piperaquine and fosmidomycin-clindamycin are  
promising treatment candidates. Until better regimens become  
available there are enormous demands on policy makers to choose  
between existing combinations, many of which have not been  
sufficiently studied for informed judgments to be made.

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