TOMÉ, M. R.; http://lattes.cnpq.br/5386146647519122; TOMÉ, Milena Ramos
Resumo:
The World Health Organization (WHO) recommends the use of
sulfamethoxazole-trimethoprim as intermittent prophylaxis for HIV-positive pregnant women;
however, its efficacy remains uncertain, necessitating the exploration of viable alternatives.
The initial search consisted of a systematic review conducted in the PubMed, Embase, and
Cochrane Library databases, which identified a set of relevant studies, of which three
randomized clinical trials, involving a total of 1,770 HIV-positive pregnant women, met the
inclusion criteria. The aim was to compare the monthly use of dihydroartemisinin-piperaquine
combined with daily sulfamethoxazole-trimethoprim versus the use of
sulfamethoxazole-trimethoprim alone. The intervention group exhibited a significant
reduction in the incidence of clinical malaria during pregnancy (RR 0.27; 95% CI 0.09-0.75;
p=0.01; I²=0%) as well as in the risk of malaria infection diagnosed by any method (RR 0.46;
95% CI 0.33-0.64; p<0.01; I²=0%). However, no significant changes were observed in the rate
of placental infection detected by histology (RR 0.47; 95% CI 0.23-0.96; p=0.04; I²=0%) or in
adverse gestational or neonatal outcomes. Thus, the combination of
dihydroartemisinin-piperaquine with sulfamethoxazole-trimethoprim proved effective in
reducing the cases of clinical malaria and the risk of malaria infection diagnosed by any
method, yet it did not demonstrate advantages regarding adverse gestational and neonatal
outcomes.