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Am J Trop Med Hyg ; 73(5): 842-9, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16282291

RESUMO

We assessed the prophylactic efficacy of azithromycin (250 mg/day) against malaria in 276 adults in western Thailand in a randomized, double-blind, placebo-controlled trial. After antimalarial suppressive treatment, volunteers were randomized in a 2:1 ratio to either the azithromycin or placebo, respectively. Study medication was given for an average of 74 days. The azithromycin group (n = 179) had five endpoint parasitemias (1 Plasmodium vivax and 4 P. falciparum), and the placebo group (n = 97) had 28 endpoint parasitemias (21 P. vivax, 5 P. falciparum, and 2 mixed infections). Adverse events and compliance and withdrawal rates were similar in both groups. The protective efficacy (PE) of azithromycin was 98% for P. vivax (95% confidence interval [CI] = 88-100%). There were too few cases to reliably estimate the efficacy of azithromycin for P. falciparum (PE =71%, 95% C =-14-94%). We conclude that daily azithromycin was safe, well-tolerated, and had a high efficacy for the prevention of P. vivax malaria.


Assuntos
Antimaláricos/uso terapêutico , Azitromicina/uso terapêutico , Malária Vivax/prevenção & controle , Parasitemia/prevenção & controle , Adulto , Animais , Antimaláricos/administração & dosagem , Azitromicina/administração & dosagem , Quimioprevenção , Método Duplo-Cego , Feminino , Humanos , Malária Vivax/epidemiologia , Malária Vivax/parasitologia , Masculino , Parasitemia/epidemiologia , Parasitemia/parasitologia , Plasmodium vivax/efeitos dos fármacos , Tailândia/epidemiologia , Resultado do Tratamento
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