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2.
Public Health ; 182: 170-172, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-32334183

RESUMEN

OBJECTIVE: With the current SARS-CoV2 outbreak, countless tests need to be performed on potential symptomatic individuals, contacts and travellers. The gold standard is a quantitative polymerase chain reaction (qPCR)-based system taking several hours to confirm positivity. For effective public health containment measures, this time span is too long. We therefore evaluated a rapid test in a high-prevalence community setting. STUDY DESIGN: Thirty-nine randomly selected individuals at a COVID-19 screening centre were simultaneously tested via qPCR and a rapid test. Ten previously diagnosed individuals with known SARS-CoV-2 infection were also analysed. METHODS: The evaluated rapid test is an IgG/IgM-based test for SARS-CoV-2 with a time to result of 20 min. Two drops of blood are needed for the test performance. RESULTS: Of 49 individuals, 22 tested positive by repeated qPCR. In contrast, the rapid test detected only eight of those positive correctly (sensitivity: 36.4%). Of the 27 qPCR-negative individuals, 24 were detected correctly (specificity: 88.9%). CONCLUSION: Given the low sensitivity, we recommend not to rely on an antibody-based rapid test for public health measures such as community screenings.


Asunto(s)
Betacoronavirus/aislamiento & purificación , Técnicas de Laboratorio Clínico/normas , Servicios de Salud Comunitaria , Infecciones por Coronavirus/diagnóstico , Brotes de Enfermedades , Tamizaje Masivo/normas , Neumonía Viral/diagnóstico , Pruebas en el Punto de Atención , Adulto , Anciano , COVID-19 , Prueba de COVID-19 , Infecciones por Coronavirus/epidemiología , Femenino , Humanos , Masculino , Tamizaje Masivo/métodos , Persona de Mediana Edad , Pandemias , Neumonía Viral/epidemiología , Reacción en Cadena de la Polimerasa , SARS-CoV-2 , Sensibilidad y Especificidad , Factores de Tiempo
3.
Int J Hyg Environ Health ; 224: 113449, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-31978723

RESUMEN

Between August 2018 and June 2019, a river system in Germany that supplies a drinking water reservoir and is subject to the discharge from two sewage treatment plants was monitored for antibiotic residues via liquid chromatography-tandem mass spectrometry, antibiotic resistance genes (including blaNDM, blaVIM, blaOXA-48, blaKPC, blaGIM, blaSME, blaIMI, blaIMP, blaSPM, blaSIM, blaOXA-23, blaOXA-24, blaOXA-51, blaOXA-58, mcr) via qualitative real-time PCR and antibiotic-resistant bacteria [belonging to the ESKAPE-group (Enterococcus faecium, Staphyhlococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacter ssp.; with resistance against Carbapenemases, Cephalosporines and Colistin) and Escherichia coli] based on cultivation methods followed by a characterization via MALDI-TOF MS and susceptibility testing applying microdilution. Residues of macrolide antibiotics such as clarithromycin (up to 0.60 µg/L) and residues of sulfamethoxazole (up to 0.40 µg/L) and trimethoprim (up to 0.39 µg/L) were detected downstream of the sewage treatment plants. In addition, no antibiotic residues were detected upstream the respective sewage treatment plants, except for anhydroerythromycin (n = 1,

Asunto(s)
Agua Potable/microbiología , Farmacorresistencia Bacteriana Múltiple/genética , Contaminación del Agua/estadística & datos numéricos , Monitoreo del Ambiente , Alemania , Pruebas de Sensibilidad Microbiana , Contaminación del Agua/análisis
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