RAPTOR C-19

SUMMARY   UPDATED - 10/08/2020

Point-of-care Tests (POCTs) can be used in community settings where there is no easy access to a specialist laboratory. They provide quick results that allow people to get immediate advice about self-isolation and treatment, potentially blocking further spread of infection in the community. Companies are quickly developing new rapid diagnostic tests, but we do not know how well they work. Some tests give a result like a pregnancy test by using a drop of blood from a finger prick. Others use saliva, or a swab to collect a sample from the nose or throat. GP practices have been testing for coronavirus since January 2020 with samples sent for laboratory tests. In this study, practices in the network will quickly compare new POCTs for coronavirus with laboratory tests so we can see how good the new tests are in a coordinated and efficient way.

Identification of Patients 

This study requires us to identify two groups of patients that are identified in two ways: first we have antibody testing for patients that have had COVID 19 (identified using database search and mail out/text) and second, we have antigen and antibody testing for patients suspected of currently having COVID 19 (identified using the app developed by UMed which will send texts to patients to remind them that if they currently suspect having COVID 19, they can be tested via their surgery). 

How do the searches work?

The searches are very simple for this study and identify only patients that have had COVID in the past using a variety of coding to include: patients identified based on lab evidence, patients clinically diagnosed with COVID and patients exposed to COVID (including suspected COVID cases). Age has not been included as this will be for all patients, including children. 

There are no VISION practices taking part in RAPTOR therefore this search will not be provided on here.

If you experience any problems downloading the information, please contact olga.zolle@oxfordhealth.nhs.uk  who is acting as lead facilitator for this study.  

Disclaimer:

Please note the resources provided are designed to assist with the identification of potentially suitable patients and to appropriately code these patient if required.

These resources have been developed based on the criteria provided by the relevant study team and whilst every effort has been made to make them universally implementable they rely on read codes and the data stored in the individual practice's clinical system. These resources are intended to assist with identification but should be used in conjunction with clinical oversight and a clear understanding of the study parameters.

While we endeavour to keep the information, tools and resources provided up to date and correct, we make no representations or warranties of any kind, express or implied, about the completeness, accuracy, reliability, suitability or availability with respect to the tools provided for any purpose. Any reliance you place on such information is therefore strictly at your own risk.

In no event will we be liable for any loss or damage including without limitation, indirect or consequential loss or damage, or any loss or damage whatsoever arising from loss of data or profits arising out of, or in connection with, the use of the tools provided.