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Journal ArticleDOI

A comparative evaluation of sulfalene-trimethoprim and sulphormethoxine-pyrimethamine against falciparum malaria in thailand

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TLDR
The efficacies of combinations of sulfalene.trimethoprim (SF-T) and sulphormethoxine-pyrimethamine (S-P) against falciparum malaria in Thailand were assessed and no significant toxic side reactions were observed in subjects administered either one of the combination treatments.
Abstract
The efficacies of combinations of sulfalene.trimethoprim (SF-T) and sulphormethoxine-pyrimethamine (S-P) against falciparum malaria in Thailand were assessed. ThirtY'one patients were given a single dose of SF-T (1 g SF and 0.5 g T) and 34 patients were given Sop (1 g Sand 0.05 g P). Radical cures were observed in 84% of the patients given SF-T and in 91 % of those given S-P Clearances of fever and asexual parasitemias were similar. Factors of previous malaria infections as indicated by both the patients' medical history and by the presence of malaria fluore3cent antibodies and prior antimalarial ihtake showed no apparent influence on treatment outcome. No significant toxic side reactions were observed in subjects administered either one of the combination treatments. A plan for the field use of the long-acting sulfonamide combinations is proposed. Chloroquine-resistant falciparum malaria was ii:::,t reported from Thailand in 1962.' Since that time. investigations performed in Thailand by D:--. Tranakchit Harinasuta,2 SEATO 1vledical Resea:ch LaboratorylS and Thailand Malaria Operationai Research Unit" have shown rates ranging iron 50% to 100%. Because of this problem of chloroquine resis~ (znce and in view of the fact that administration 01 quinine to large numbers of patients in the field is operationally impractical, the need in TnaiIand for a simple and effective regimen against falcipal.:"um malaria is most urgent. Presently, two sulfonamide combinations have the potentlal for meeting this need. These are: 1) sulfalene-trimethoprim (SF-T), and 2) sulphor. Accepted 28 September 1972 ... This study was supported by the Agency f01 International Development, U. S. Department of State, and the U. S Almy, Department of Defense. This is contribution No. 1047 from the Army Malaria Research Progum. t Formerly Chief, TMORU. Plcsent address' American Embassy (Central America .Malatia. Research Station), APO New YOlk 09889. ~Forrncrly EpidemIOlogist, TMORU. § U. S. Army Medical Component, SEATO II Trad Pro{rincial Hospital, Thailand. methoxine (Fanasil,1il Roche)-pyrimethamine (S·P). The purpose of this study ''las to assess these two combinations agains t falciparum malaria in adult Thai males, with respect to rapidity of action, cure rate, the effect of pree."'{isting malaria antibodies on cure rate, and possible side effects, especially side effects in individuals whose erythrOlytes are deficient in glucose-6-ph05phate dehy· drogenase (G-6-PD) activity. MATERIALS ANn :urETHODS The site selected for study was Trad Province, located in Southeast Thailand approximately 400 km from Bangkok (see Fig. 1). Previous investigations have shown that the majority of Plasmodimn jalciparum, strains from this area are chloroquine resistant In 1968, investigations of the chloroquine sensitivity of P jaidparum were conducted in an area 50 km north of Trad Hospital.' Treatment failures following administration of chloroquine were obsen'cd in 8 (80%) of 10 subjects who receIved a total dosage of 25 mg (base)/kg and in 19 (100%) of 19 additional subjects who received a single. dose at 10 mg (base)/kg. Just prior to the present study, Colwell and co-workers reported, from the same hospital, a chloroquine-resistance rate of 93% in

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Antimalarial activity of mefloquine and qinghaosu

TL;DR: In a chloroquine-resistant Plasmodium falciparum endemic area of Hainan Island, China, 1·0 g oral mefloquine produced a radical cure in 47 of 48 semi-immune patients and showed a more rapid clearance of parasitaemia with qinghaosu and a greater inhibition of in-vivo trophozoite development.
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Resistance of Plasmodium falciparum malaria to sulfadoxine-pyrimethamine ('Fansidar') in a refugee camp in Thailand.

TL;DR: The results of this study suggest that fansidar resistance is prevalent at this camp and should prompt more exhaustive studies of the epidemiology of fansidars resistance in the area.
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Selection strength and hitchhiking around two anti-malarial resistance genes

TL;DR: Comparing microsatellite variation around two drug resistance genes in malaria parasite populations exposed to strong or weak selection by anti-malarial drugs demonstrates that different realizations of the same selective sweeps may vary considerably in size and shape, in a manner broadly consistent with selection history.
Journal ArticleDOI

Tracking Origins and Spread of Sulfadoxine-Resistant Plasmodium falciparum dhps Alleles in Thailand

TL;DR: The origins and spread of sulfadoxine-resistance-conferring dihydropteroate synthase (dhps) alleles in Thailand are described to suggest multiple and independent origins of resistant dhps alleles.
Journal ArticleDOI

Treatment of vivax malaria with sulfadoxine-pyrimethamine and with pyrimethamine alone.

TL;DR: Chloroquine remains the drug of choice for the termination of the acute attack of vivax malaria and subsequent primaquine is necessary for the prevention of relapse.
References
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Journal ArticleDOI

The evaluation of sulfonamides, alone or in combination with pyrimethamine, in the treatment of multi-resistant falciparum malaria.

TL;DR: The results indicate that combination of a sulfonamide with pyrimethamine enhanced the curative effect of either one alone or both alone and when combined with p Skyrimethamines, Midicel and Fanzil were superior to sulfadiazine.
Journal ArticleDOI

Sulphormethoxine in chloroquine-resistant falciparum malaria in Thailand.

TL;DR: Although these drugs have proved effective in chloroquine-resistant falciparum malaria, the risk of extending drug resistance should prompt caution in adopting such combinations for mass control therapy.
Journal ArticleDOI

Potentiation of pyrimethamine by sulphadiazine in human malaria

TL;DR: Pyrimethamine and sulphadiazine have been shown to potentiate each other in Gambian indigenes infected with P. falciparum, P. malariae, and P. ovale, and given together are as effective against asexual parasites as the M.E.D. of either drug given alone.
Journal ArticleDOI

Tetracycline treatment of chloroquine-resistant falciparum malaria in Thailand.

TL;DR: Tetracycline hydrochloride was evaluated in asymptomatic and acutely ill subjects naturally infected with chloroquine resistant strains of Plasmodium falciparum and a presumptive radical cure was demonstrated in 29 of 30 treated with the quinine-tetracyCline regimen, and in 15 of 36 treated in the qu inine-chloroquine regimen.
Journal ArticleDOI

Treatment of falciparum malaria with sulfalene and trimethoprim.

TL;DR: Patients whose infections had broken through prophylaxis by the sulfone di-formyl-DDS were unlikely to be cured by sulfalene and trimethoprim, but their parasites when transferred to other people proved sensitive to these drugs.
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