Oxford, UK, 24 March 2011
The National Institute for Health and Clinical Excellence (NICE) released new clinical guidelines for the use of innovative TB blood tests called interferon-gamma release assays (IGRAs) for diagnosing latent tuberculosis infection (LTBI) on 24th March 2011.
Previous guidelines for diagnosis of LTBI released by NICE in 2006 recommended the use of a two step approach, starting with the Mantoux skin test and then only using IGRAs to confirm positive results.
In recognition of the mounting clinical evidence in favour of IGRA technology, the new guidelines recommend going straight to an IGRA test in a number of specified indications including:
In addition, the new guidelines recommend that an IGRA test be considered for initial use in individuals for whom Mantoux testing may be less reliable, such as those who have been BCG vaccinated, and for use in individuals whose Mantoux test result is positive.
These interventions are designed to identify subjects with LTBI so that they can be treated before they convert to active disease. This proactive approach will help to reduce the rates of active TB disease in the UK which have been rising over the past decade.
Until recently, the only test available to identify LTBI has been the Mantoux skin test which has been used for over 100 years and suffers from a variety of problems such as a high false negative rate amongst the immunocompromised and a high false positive rate amongst those who have been BCG vaccinated. The new IGRA tests recommended in these guidelines have been designed to overcome the deficiencies of the Mantoux test.
Oxford Immunotec Chief Executive, Peter Wrighton-Smith commented:
“I very much welcome the new guidelines from NICE which recognise the superior accuracy and convenience of IGRA testing in many populations. I am optimistic that the adoption of these guidelines will help to reverse the steadily increasing rates of TB seen in the UK over the past decade.”
For more information, please visithttp://www.igraguidelines.com/