Randomized, Controlled Trial of Daily Iron Supplementation and Intermittent Sulfadoxine‐Pyrimethamine for the Treatment of Mild Childhood Anemia in Western Kenya
Author(s) -
Meghna Desai,
Joanne V. Mei,
Simon Kariuki,
Kathleen Wannemuehler,
Penelope A. Phillips–Howard,
Bernard L. Nahlen,
Piet A. Kager,
John Vulule,
Feiko O. ter Kuile
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/367986
Subject(s) - placebo , medicine , anemia , sulfadoxine , malaria , parasitemia , randomized controlled trial , pyrimethamine , hemoglobin , gastroenterology , immunology , chloroquine , plasmodium falciparum , alternative medicine , pathology
A randomized, placebo-controlled treatment trial was conducted among 546 anemic (hemoglobin concentration, 7-11 g/dL) children aged 2-36 months in an area with intense malaria transmission in western Kenya. All children used bednets and received a single dose of sulfadoxine-pyrimethamine (SP) on enrollment, followed by either intermittent preventive treatment (IPT) with SP at 4 and 8 weeks and daily iron for 12 weeks, daily iron and IPT with SP placebo, IPT and daily iron placebo, or daily iron placebo and IPT with SP placebo (double placebo). The mean hemoglobin concentration at 12 weeks, compared with that for the double-placebo group, was 1.14 g/dL (95% confidence interval [CI], 0.82-1.47 g/dL) greater for the IPT+iron group, 0.79 g/dL (95% CI, 0.46-1.10 g/dL) greater for the iron group, and 0.17 g/dL (95% CI, -0.15-0.49 g/dL) greater for the IPT group. IPT reduced the incidence of malaria parasitemia and clinic visits, but iron did not. The combination of IPT and iron supplementation was most effective in the treatment of mild anemia. Although IPT prevented malaria, the hematological benefit it added to that of a single dose of SP and bednet use was modest.
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