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1.
J Clin Virol ; 129: 104537, 2020 08.
Article in English | MEDLINE | ID: covidwho-633879

ABSTRACT

BACKGROUND: Broad and decentralised testing of SARS-CoV-2 RNA genomes is a WHO-recommended strategy to contain the SARS-CoV-2 pandemic by identifying infected cases in order to minimize onward transmission. With the need to increase the test capacities in Austria, nation-wide numerous laboratories rapidly implemented assays for molecular detection of SARS-CoV-2 based on real-time RT-PCR assays. The objective of this study was to monitor reliability of the laboratory results for SARS-CoV-2 RNA detection through an external quality assessment (EQA) scheme. METHODS: For this, the Center for Virology, Medical University of Vienna was tasked by the Federal Ministry of Social Affairs, Health, Care and Consumer Protection to perform the first Austrian EQA on SARS-CoV-2 which was organised in cooperation with the Austrian Association for Quality Assurance and Standardization of Medical and Diagnostic Tests (ÖQUASTA). Data were analysed on the basis of qualitative outcome of testing in relation to the nucleic acid (NA) extraction and detection methods used. RESULTS AND CONCLUSION: A total of 52 laboratories participated, contributing results from 67 test panels comprising 42 distinct combinations of NA extraction and PCR reagents. By testing 3 positive (CT values: S1, 28.4; S2, 33.6; S3, 38.5) and 1 negative sample, no false-positive results were obtained by any of the laboratories. Otherwise, 40/67 tests (60 %) detected all positive samples correctly as positive, but 25/67 tests (37 %) did not detect the weakest positive sample (S3), and 3 % reported S2 and S3 as false-negative. Improvement in test sensitivity by focusing on NA extraction and/or PCR-based detection is recommended.


Subject(s)
Betacoronavirus/isolation & purification , Clinical Laboratory Techniques/methods , Clinical Laboratory Techniques/standards , Coronavirus Infections/diagnosis , Laboratory Proficiency Testing/organization & administration , Molecular Diagnostic Techniques/methods , Molecular Diagnostic Techniques/standards , Pneumonia, Viral/diagnosis , Austria , COVID-19 , COVID-19 Testing , COVID-19 Vaccines , Diagnostic Errors/statistics & numerical data , Humans , Pandemics , Real-Time Polymerase Chain Reaction/methods , Real-Time Polymerase Chain Reaction/standards , SARS-CoV-2 , Sensitivity and Specificity
2.
Infection ; 48(4): 647-651, 2020 Aug.
Article in English | MEDLINE | ID: covidwho-597398

ABSTRACT

We report the successful management of a patient with severe respiratory failure due to COVID-19 admitted to an intensive care unit complicated by secondary catheter-related infection of Candida glabrata. We are discussing some of the clinical challenges and the pitfalls in molecular diagnosis of SARS-CoV-2, including the fact that a positive PCR result may not always reflect infectiousness.


Subject(s)
Candidemia/drug therapy , Coronavirus Infections/therapy , Disease Management , Pneumonia, Viral/therapy , Respiratory Distress Syndrome/virology , Aged , Antifungal Agents/therapeutic use , Austria , Betacoronavirus , COVID-19 , Candidemia/virology , Coinfection/microbiology , Coinfection/virology , Coronavirus Infections/complications , Coronavirus Infections/diagnostic imaging , Humans , Hypertension/complications , Intensive Care Units , Male , Pandemics , Pneumonia, Viral/complications , Pneumonia, Viral/diagnostic imaging , SARS-CoV-2 , Tomography, X-Ray Computed , Treatment Outcome
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