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1.
Transfus Clin Biol ; 26(1): 60-68, 2019 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-30145110

RESUMO

The populations infected with malaria have developed genetic defense mechanisms in order to protect themselves against the most serious complications of this disease. Those mechanisms have been associated from the perspective of co-adaptive process with some genetic diseases widely present in humans as sickle-cell disease, sickle cell trait and glucose-6-phosphate dehydrogenase deficiency (G6PD). Biochemically, polymorphic mutations at the erythrocyte level have been widely studied, however there is no clear statement of the mechanisms used for resistance against the causative agent of malaria. The purpose of this review is to introduce the molecular and biochemical basis of defense mechanisms associated with two of those adaptations: sickle-cell trait and Glucose-6-phosphate Dehydrogenase Deficiency (G6PD). The first one is a hemoglobinopathy while the second one is the most frequent enzymopathy present in humans.


Assuntos
Eritrócitos/parasitologia , Deficiência de Glucosefosfato Desidrogenase/genética , Malária/epidemiologia , Traço Falciforme/genética , Adaptação Fisiológica/genética , Colômbia/epidemiologia , Humanos , Malária/genética , Mutação , Polimorfismo Genético , Prevalência
2.
Trop Med Int Health ; 22(1): 21-31, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27770602

RESUMO

OBJECTIVE: The aim of this study was to estimate the incremental budget impact (IBI) of a rapid diagnostic test to detect G6PDd in male patients infected with Plasmodium vivax in the Brazilian Amazon, as compared with the routine protocol recommended in Brazil which does not include G6PDd testing. METHODS: The budget impact analysis was performed from the perspective of the Brazilian health system, in the Brazilian Amazon for the years 2013, 2014 and 2015. The analysis used a decision model to compare two scenarios: the first consisting of the routine recommended in Brazil which does not include prior diagnosis of dG6PD, and the second based on the use of RDT CareStart™ G6PD (CS-G6PD) in all male subjects diagnosed with vivax malaria. The expected implementation of the diagnostic test was 30% in the first year, 70% the second year and 100% in the third year. RESULTS: The analysis identified negative IBIs which were progressively smaller in the 3 years evaluated. The sensitivity analysis showed that the uncertainties associated with the analytical model did not significantly affect the results. CONCLUSION: A strategy based on the use of CS-G6PD would result in better use of public resources in the Brazilian Amazon.


Assuntos
Técnicas e Procedimentos Diagnósticos/economia , Deficiência de Glucosefosfato Desidrogenase/diagnóstico , Deficiência de Glucosefosfato Desidrogenase/epidemiologia , Malária Vivax/epidemiologia , Programas de Rastreamento/economia , Antimaláricos/uso terapêutico , Brasil/epidemiologia , Orçamentos , Técnicas de Apoio para a Decisão , Humanos , Malária Vivax/tratamento farmacológico , Masculino , Modelos Econométricos , Primaquina/uso terapêutico , Fatores de Tempo
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