LONDON (Reuters) - A British COVID-19 test known as DnaNudge that gives results in just over an hour and which requires no laboratory was accurate in almost all cases, an academic review in the Lancet has found.
Faster testing could allow more people to return to work or permit testing on entry to hospital, thus slowing a second spike in coronavirus infections.
The new test, based on the design of a DNA test developed by a professor at Imperial College London, received approval for clinical use by the Medicines and Healthcare Products Regulatory Agency (MHRA) at the end of April after successful trials.
In a study in The Lancet Microbe, the test was found to have an average sensitivity – the ability to correctly identify those with COVID-19 – of 94.4% and a specificity – correctly identifying those without the disease – of 100%.
“These results suggest that the CovidNudge test, which can be performed at a patient’s bedside without the need to handle any sample material, has comparable accuracy to standard laboratory testing,” Professor Graham Cooke, lead author of the study from the Department of Infectious Disease at Imperial College London, said.
The Lancet paper described the test, which requires one nostril swab, as “a sensitive, specific, and rapid point of care test for the presence of SARS-CoV-2 without laboratory handling or sample pre-processing”.
Health Secretary Matt Hancock told LBC radio that Britain was rolling out the tests across hospitals.
Hancock said the machines could also be deployed at other locations such as schools.
Each box can run one test at a time so could process about 16 tests per day, said a spokeswoman for the company that produces the tests.
For the text of the Lancet paper: here
Reporting by Guy Faulconbridge; editing by Kate Holton and Gareth Jones
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