Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Med Mycol ; 62(9)2024 Sep 06.
Artigo em Inglês | MEDLINE | ID: mdl-39237463

RESUMO

Several false positive low serum cryptococcal antigen (SCrAg) reports by lateral flow assay (LFA) were identified in late 2016 at our tertiary care hospital. After the recall and correction of the problem in the reagent, we studied the significance of SCrAg LFA ≤ 1:10 from January 2017 to October 2023. Of 20 patients with 31 samples of SCrAg LFA ≤ 1:10, 14 patients (70%) were classified as true positives, four (20%) were indeterminate, and only two (10%) patients were false positives. If a new SCrAg LFA ≤ 1:10 is detected, it should be repeated, and additional workup should be pursued.


We studied the significance of low serum cryptococcal antigen (SCrAg) titer lateral flow assay (LFA) ≤ 1:10 from January 2017 to October 2023. Of 20 patients with SCrAg LFA ≤ 1:10, only two patients (10%) were false positives. If a new SCrAg ≤ 1:10 is detected, it should be repeated, and additional workup should be done.


Assuntos
Antígenos de Fungos , Criptococose , Cryptococcus , Centros de Atenção Terciária , Humanos , Antígenos de Fungos/sangue , Antígenos de Fungos/imunologia , Criptococose/diagnóstico , Criptococose/sangue , Masculino , Feminino , Cryptococcus/imunologia , Pessoa de Meia-Idade , Reações Falso-Positivas , Adulto , Idoso , Estudos Retrospectivos
2.
BMC Genet ; 4 Suppl 1: S70, 2003 Dec 31.
Artigo em Inglês | MEDLINE | ID: mdl-14975138

RESUMO

The goal of this study is to evaluate, compare, and contrast several standard and new linkage analysis methods. First, we compare a recently proposed confidence set approach with MAPMAKER/SIBS. Then, we evaluate a new Bayesian approach that accounts for heterogeneity. Finally, the newly developed software SIMPLE is compared with GENEHUNTER. We apply these methods to several replicates of the Genetic Analysis Workshop 13 simulated data to assess their ability to detect the high blood pressure genes on chromosome 21, whose positions were known to us prior to the analyses. In contrast to the standard methods, most of the new approaches are able to identify at least one of the disease genes in all the replicates considered.


Assuntos
Simulação por Computador/estatística & dados numéricos , Ligação Genética/genética , Teorema de Bayes , Cromossomos Humanos Par 20/genética , Cromossomos Humanos Par 21/genética , Intervalos de Confiança , Feminino , Heterogeneidade Genética , Humanos , Hipertensão/genética , Masculino , Modelos Genéticos , Locos de Características Quantitativas/genética , Software/estatística & dados numéricos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA