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1.
Rev. Soc. Bras. Med. Trop ; 54: e0878-2020, 2021. tab, graf
Article in English | LILACS | ID: biblio-1155561

ABSTRACT

Abstract INTRODUCTION: Understanding the mortality-associated risk factors of coronavirus disease 2019 will impact clinical decisions. METHODS: This retrospective longitudinal study included patients hospitalized for coronavirus disease in Rio de Janeiro, Brazil. The Kaplan-Meier method and multivariate Cox regression analysis were used. RESULTS: Sequential Organ Failure Assessment score of ≥2 (hazard ratio 4.614; 95% confidence interval =2.210-9.634; p<0.001) and neutrophil/lymphocyte ratio of >5 (hazard ratio=2.616; 95% confidence interval=1.303-5.252; p=0.007) were independently associated with mortality. CONCLUSIONS: Sequential Organ Failure Assessment score and neutrophil/lymphocyte ratio on admission can identify coronavirus disease patients at increased risk of death and guide subsequent clinical decisions.


Subject(s)
Humans , Coronavirus Infections , Brazil/epidemiology , Retrospective Studies , Risk Factors , Longitudinal Studies , Betacoronavirus
2.
Cogitare enferm ; 3(1): 113-7, jan.-jun. 1998.
Article in Portuguese | LILACS, BDENF | ID: lil-253015

ABSTRACT

O artigo apresenta sugestöes e noçöes para a redaçäo de um trabalho. Trazem idéias gerais que possam facilitar a trajetória de acadêmicos nos caminhos da escrita, sem esgotar a temática, ao contrário, é um estimulo à produçäo literária porque o poder criativo e inovador é nato, basta colocar em prática as idéias.


Subject(s)
Humans , Writing
3.
Arq. bras. med. nav ; 52(2): 105-15, maio-ago. 1990. ilus, tab
Article in Portuguese | LILACS | ID: lil-126065

ABSTRACT

Relatamos o caso de um recém-nascido (RN) do sexo feminino com translocaçäo cromossômica desbalanceada (trissmia parcial 3p) associada com doença cardíaca congênita (completo de Fallot). O estudo citogenético da criança e do pai mostrou que o desfeito cromossômico era resultante de uma translocaçäo paterna desbalanceada da porçäo terminal do braço longo do cromossoma 2 e a porçäo média do braço curto do cromossomo 3 (46, XX,-2, + der 2 pat). Relatamos os achados clínicos e anatomopatológicos, além de revisäo bibliográfica


Subject(s)
Humans , Female , Infant, Newborn , Pregnancy , Chromosomes, Human, Pair 2 , Chromosomes, Human, Pair 3 , Tetralogy of Fallot/complications , Trisomy/complications , Karyotyping , Syndrome , Translocation, Genetic , Trisomy/diagnosis , Trisomy/pathology
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