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Pan Afr Med J ; 39: 244, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34659617

RESUMEN

Numerous genetic tests for the detection of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, including those based on the ever-popular real-time polymerase chain reaction (RT-qPCR) technique, have been reported. These diagnostic tests give false negatives particularly during the early and late stages of COVID-19 clearly indicating inadequate test sensitivity. The entire COVID-19 diagnostic workflow is often overlooked and given very little attention. Herein, we propose that volumetric modifications to COVID-19 workflows would significantly improve detection limits. We would therefore encourage researchers to adopt a holistic approach, in which all the steps of a COVID-19 diagnostic workflow, are carefully scrutinised, particularly those upstream factors at the viral sampling and pre-analytical stages.


Asunto(s)
Prueba de COVID-19/métodos , COVID-19/diagnóstico , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos , Prueba de COVID-19/normas , Reacciones Falso Negativas , Humanos , Límite de Detección , Reacción en Cadena en Tiempo Real de la Polimerasa/normas , Sensibilidad y Especificidad , Manejo de Especímenes
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