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1.
J Pediatr ; 139(1): 141-7, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11445809

RESUMO

The case of an infant with multiple, rapidly progressive, soft-tissue infections is presented. Despite features suggesting a neutrophil disorder, results of screening tests of phagocyte function were normal. A novel, multifaceted leukocyte disorder-distinguished by defects in shape change, chemotaxis, ingestion, degranulation, superoxide anion production, and bactericidal activity-was established secondary to a defect in Rac2.


Assuntos
Neutrófilos/fisiologia , Infecções dos Tecidos Moles/genética , Proteínas rac de Ligação ao GTP/genética , Atividade Bactericida do Sangue , Quimiotaxia de Leucócito , Humanos , Recém-Nascido , Masculino , Fagocitose , Transdução de Sinais , Infecções dos Tecidos Moles/imunologia , Superóxidos/metabolismo , Proteína RAC2 de Ligação ao GTP
2.
J Pediatr ; 136(2): 201-8, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10657826

RESUMO

OBJECTIVE: To compare the health outcomes, costs, and incremental cost-effectiveness of universal neonatal screening for sickle cell disease (SCD) with screening targeted to African Americans. STUDY DESIGN: A cost-effectiveness analysis was done by using a Markov simulation model that considered the costs and outcomes associated with the prevention and treatment of sepsis in those with sickle cell anemia and sickle beta(0)-thalassemia. Three strategies were compared: (1) no screening, (2) targeted screening of African Americans, and (3) universal screening for SCD. RESULTS: In the base case analysis, targeted screening of African Americans compared with no screening cost $6709 per additional year of life saved, and universal screening compared with targeted screening cost $30,760 per additional year of life saved. In a sensitivity analysis, the cost per additional year of life saved with universal screening compared with targeted screening was positively correlated with the delivery rate of targeted screening and was inversely related to the proportion of African Americans in the population. CONCLUSIONS: Targeted screening of African American newborns for SCD compared with no screening is always cost-effective. Universal screening compared with targeted screening always identifies more infants with disease, prevents more deaths, and is cost-effective given certain delivery rates for targeted screening and proportions of African Americans in the population.


Assuntos
Anemia Falciforme/prevenção & controle , Triagem Neonatal , Anemia Falciforme/diagnóstico , Anemia Falciforme/etnologia , População Negra , Análise Custo-Benefício , Técnicas de Apoio para a Decisão , Humanos , Recém-Nascido , Cadeias de Markov , Triagem Neonatal/economia , Triagem Neonatal/métodos , Avaliação de Resultados em Cuidados de Saúde , Sensibilidade e Especificidade , Estados Unidos/epidemiologia
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