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1.
Am J Clin Nutr ; 63(6): 884-90, 1996 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8644682

RESUMO

The effect of daily rather than weekly iron supplementation was compared in women who were 8-24 wk pregnant. One group (n = 68) received 60 mg Fe/d, the second group (n = 71) received 120 mg Fe/wk, given at once. Supplementation lasted 11.3 wk on average, depending on gestational date at entry, and was not supervised. Hemoglobin increased in both groups (P < 0.001); serum ferritin did not change significantly. There was no significant difference between groups for changes in hemoglobin and serum ferritin. In a subgroup of women with a hemoglobin concentration < 110 g/L at baseline (n = 45 daily; n = 54 weekly) no significant within-group changes occurred in serum ferritin, but the change in the daily group was 4.1 micrograms/L higher than in the weekly group (P = 0.049). Compliance, as indicated by two positive stool tests, was approximately equal to 54.3% in the daily group and 62.2% in the weekly group. We conclude that for the complete sample of subjects, the treatment effect of daily compared with weekly supplementation was similar under conditions resembling a normal antenatal care program.


Assuntos
Ferro/administração & dosagem , Gravidez/sangue , Adulto , Análise de Variância , Anemia Ferropriva/sangue , Anemia Ferropriva/epidemiologia , Anemia Ferropriva/prevenção & controle , Relação Dose-Resposta a Droga , Fezes/química , Feminino , Ferritinas/sangue , Alimentos Fortificados , Hemoglobinas/análise , Humanos , Indonésia/epidemiologia , Enteropatias Parasitárias/sangue , Enteropatias Parasitárias/complicações , Enteropatias Parasitárias/epidemiologia , Ferro/análise , Ferro/sangue , Análise Multivariada , Cooperação do Paciente , Complicações Hematológicas na Gravidez/sangue , Complicações Hematológicas na Gravidez/epidemiologia , Complicações Hematológicas na Gravidez/prevenção & controle , Complicações Parasitárias na Gravidez/sangue , Complicações Parasitárias na Gravidez/epidemiologia , Prevalência
2.
J Nutr ; 122(1): 101-7, 1992 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-1729457

RESUMO

A randomized, double-masked, placebo-controlled clinical trial was conducted with 236 preschool children, age 3-6 y, in Indonesia to assess immune status in mild vitamin A deficiency. The immune response to tetanus immunization was used as a measure of immune competence. Clinically normal children (n = 118) and children with mild xerophthalmia (n = 118) were randomly assigned to receive oral vitamin A (60,000 micrograms retinol equivalent) or placebo treatment for a total of four study groups. Two weeks after treatment, children were immunized with diphtheria-pertussis-tetanus vaccine. The immunoglobulin G (IgG) responses to tetanus at baseline and 3 wk following immunization were measured by ELISA. After adjusting for previous tetanus immunization, clinically normal and xerophthalmic children receiving vitamin A had a significantly greater IgG response to tetanus than clinically normal and xerophthalmic children receiving placebo (P less than 0.05). These results suggest that children with mild vitamin A deficiency have a relative immune depression compared with children who have been supplemented to normal vitamin A levels.


Assuntos
Toxoide Tetânico/imunologia , Deficiência de Vitamina A/imunologia , Formação de Anticorpos , Criança , Pré-Escolar , Método Duplo-Cego , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Masculino , Vitamina A/sangue , Vitamina A/uso terapêutico , Xeroftalmia/dietoterapia
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