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2.
J Hosp Infect ; 111: 132-139, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33582200

RESUMO

BACKGROUND: Vancomycin-resistant enterococci (VRE) may cause nosocomial outbreaks. This article describes all VRE carriers that were identified in 2018 at Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands. AIM: To investigate the genetic relatedness of VRE isolates and the possibility of a common environmental reservoir using environmental sampling and whole-genome sequencing (WGS). METHODS: Infection control measures consisted of contact isolation, contact surveys, point prevalence screening, environmental sampling, cleaning and disinfection. VRE isolates were sequenced using a MiSeq sequencer (Illumina, San Diego, CA, USA), and assembled using SPAdes v.3.10.1. A minimal spanning tree and a neighbour joining tree based on allelic diversity of core-genome multi-locus sequence typing and accessory genes were created using Ridom SeqSphere+ software (Ridom GmbH, Münster, Germany). FINDINGS: Over a 1-year period, 19 VRE carriers were identified; of these, 17 were part of two outbreaks. Before environmental cleaning and disinfection, 55 (14%) environmental samples were VRE-positive. Fifty-one isolates (23 patient samples and 28 environmental samples) were available for WGS analysis. Forty-four isolates were assigned to ST117-vanB, five were assigned to ST17-vanB, and two were assigned to ST80-vanB. Isolates from Outbreak 1 (N=22) and Outbreak 2 (N=22) belonged to ST117-vanB; however, WGS showed a different cluster type with 257 allelic differences. CONCLUSION: WGS of two outbreak strains provided discriminatory information regarding genetic relatedness, and rejected the hypothesis of a common environmental reservoir. A high degree of environmental contamination was associated with higher VRE transmission. Quantification of environmental contamination may reflect the potential for VRE transmission and could therefore support the infection control measures.


Assuntos
Infecção Hospitalar , Enterococcus faecium , Infecções por Bactérias Gram-Positivas , Enterococos Resistentes à Vancomicina , Infecção Hospitalar/epidemiologia , Surtos de Doenças , Enterococcus faecium/genética , Infecções por Bactérias Gram-Positivas/epidemiologia , Hospitais de Ensino , Humanos , Tipagem de Sequências Multilocus , Países Baixos , Vancomicina , Enterococos Resistentes à Vancomicina/genética
3.
J Genet Couns ; 27(4): 920-926, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-29372364

RESUMO

For couples at high risk of transmitting a cancer predisposition to offspring, reproductive decision-making can be challenging. As the choice between available reproductive options is preference-sensitive, the use of a decision aid can support these couples in their decisional process. The present study aims to investigate preferences and needs of involved stakeholders regarding the development and implementation of a patient decision aid. Semi-structured interviews assessing the needs and preferences regarding the content and functionalities of a decision support program were conducted among seven couples at risk for hereditary cancer and among eight clinical geneticists involved in oncogenetic counseling. Many similarities were found between the expressed preferences and needs of both stakeholder groups concerning the content, barriers and facilitating factors regarding the use of the decision aid, and its implementation. Emphasis was placed on the use of simple non-medical language, an extensive explanation of the procedures and techniques used in prenatal diagnosis (PND) and preimplantation genetic diagnosis (PGD), and the role of health care providers to refer couples to the decision aid. Both stakeholder groups were in favor of incorporating narrative stories in the decision aid. Integrating the present findings with knowledge on reproductive decisional motives and considerations is essential in guiding the development of a decision aid that corresponds to the preferences and needs of end-users. TRIAL REGISTRATION: NTR5467.


Assuntos
Aconselhamento Genético/psicologia , Predisposição Genética para Doença/psicologia , Síndromes Neoplásicas Hereditárias/psicologia , Pais/psicologia , Diagnóstico Pré-Implantação/psicologia , Tomada de Decisões , Feminino , Humanos , Masculino , Síndromes Neoplásicas Hereditárias/genética , Preferência do Paciente , Gravidez , Diagnóstico Pré-Natal
4.
Ann Clin Biochem ; 28 ( Pt 1): 55-9, 1991 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-2024936

RESUMO

A new membrane-based device is described for the quantitative separation of plasma from blood cells using neither centrifugation nor pipetting. The concentration of cholesterol in the isolated plasma was determined using a newly developed instrument, the Primetest. The results were in good agreement with those obtained in the hospital laboratory.


Assuntos
Coleta de Amostras Sanguíneas , Membranas Artificiais , Plasma , Coleta de Amostras Sanguíneas/instrumentação , Centrifugação , Humanos , Laboratórios Hospitalares , Kit de Reagentes para Diagnóstico
6.
J Clin Chem Clin Biochem ; 16(3): 187-9, 1978 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-650158

RESUMO

A simple and specific detection method for multiple forms of cystine aminopeptidase (oxytocinase-isoenzymes) in pregnancy serum is described using S-benzyl-L-nitroanilide as substrate. The relative distribution of both cystine aminopeptidase isoenzymes at different stages of pregnancy is given.


Assuntos
Aminopeptidases/sangue , Cistinil Aminopeptidase/sangue , Isoenzimas/sangue , Eletroforese em Gel de Poliacrilamida , Feminino , Humanos , Métodos , Gravidez
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