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Drug-Resistant Malaria - libdoc.who.int - World Health Organization

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OPENING ADDRESS / 11<br />

is also here and ready to continue their assistance in the field<br />

of malaria chemotherapy. This, in itself, is indicative of the<br />

importance and gravity of the problems being encountered in so<br />

many countries in this field. It is true that drug resistance 1S<br />

not exclusively linked to malaria and that other diseases, mainly<br />

communicable, have problems connnected with resistance of the<br />

causative agents to drugs. <strong>Drug</strong> resistance is not only a problem<br />

to present-day malariologists, since it had already been observed<br />

in the past that infections, particularly those with Plasmodium<br />

falciparum, did not respond to the same drug in the same manner,<br />

in different geographical areas. Marchiafava was the first, with<br />

Bignami, to note the difference in the clinical symptoms caused by<br />

P. f alciparum in East Africa and in Italy. This was confirmed by<br />

Robert Koch in the early part of this century. It was again<br />

observed by workers at the <strong>Malaria</strong> Therapy Station in Horton, UK,<br />

in 1920. More detailed studies carried out in the United States<br />

during the Second <strong>World</strong> War confirmed previous observations and<br />

also indicated that this problem could be resolved by adjusting<br />

the doses and regimens of drugs existing at that time.<br />

Since the initiation of malaria eradication programmes in<br />

most countries affected by malaria, with the exception of Africa<br />

south of the Sahara, the use of antimalarial drugs in malaria<br />

control/eradication was advocated mainly for the depletion of the<br />

parasite reservoir. Looking back at the late 1950s and 1960s, it<br />

is difficult to escape the impression that the resistance of<br />

P. f ale iparum to 4-aminoquino lines detec ted in South-East Asia and<br />

South America was considered more as a problem of academic<br />

<strong>int</strong>erest rather than as an obstacle to the eradication of the<br />

disease. However, the resurgence of the disease in the early<br />

1970s, particularly in South-East Asia and parts of Central and<br />

South America, coupled with the ever-increasing spread of<br />

P.falciparum resistance to 4-aminoquinolinos and more recently, to<br />

a combination of sulfadoxine/pyrimethamine, has become such an<br />

important problem that many health administrators are wondering<br />

how to continue with malaria control in areas where this problem<br />

occurs.<br />

Research on the development of antimalarial drugs has been<br />

pursued for many years and, in the last 10 to 15 years, more than<br />

250 000 compounds have been screened and tested but only a few<br />

could be considered as suitable candidates. But, even though the<br />

future does not seem very promising in this respect, there is no<br />

place for pessimism. We must continue with our efforts and with<br />

activities such as this meeting which has been organized to review<br />

every possibility available in the utilization of the existing<br />

antimalarial drugs and their combinations.<br />

It 1S<br />

scientists<br />

resistance.<br />

carried out<br />

a pleasure to see the enthusiasm with which so many<br />

have accepted to undertake the monitoring of drug<br />

In this respect the number of susceptibi lity tests<br />

in the last two years speaks for itself. However, the

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