Events in 2023

Delegates will understand:

The pathophysiological aspects of Vitamin B12.
The role of the laboratory in the diagnosis of Vitamin B12 deficiency.

Join some of our panel members for our lunchtime session where we will be hosting an antibody workshop. Looking at different types of antibodies and how to positively identify or eliminate any suspected clincially significant antibodies, whilst testing your knowledge and skills.

The aim is to make the session fun and interactive, focusing on some top tips for solving those antibody mysteries.

Specialist portfolios: Updated, flexible and achievable

Trichophyton indotinaea is a newly described species of dermatophyte that has emerged with the last 10 years in India, and some Middle Eastern countries. It causes tinea corporis and tinea cruris mainly (ringworm infection of the torso and groin) and can spread to the arms, legs and face. T. indotineae is also characterised by a reduced susceptibility or outright resistance to one of the commonly used and otherwise highly effective antifungals, terbinafine. While high levels of cases are seen in Indida, countries outside of India and the Middle East are now seeing imported cases and the UK is not alone. Working with colleagues in London we have identified signficant numbers of cases and are now understanding how difficult these infections are to treat, even with antifungals that the organism should be sensitive to. Lesions are only superficial, but are itchy and disfiguring, and often relapse after initial antifungal therapy. We are continuing to learn about the epidemiology, transmission, diagnosis and treatment of this emerging infection.

A case study into iron deficiency polycythaemia diagnosis, looking at the pathology and how this relates to the results we see and investigations to confirm diagnosis.

Generation X,Y,Z: Ageism in the workplace and its impact on service delivery

What is ISO 22367 and how can it help the laboratory comply with the risk requirements of ISO15189

Help, nothing compatible

A myositis-related autoantibody can now be identified in the majority of patients with myositis. They identify homogeneous patient subgroups and are key tools in developing a personalised approach to disease management. There is substantial clinical interest in exploiting myositis autoantibodies as biomarkers, and consequently, a large number of commercial assays have been developed for their detection. Several different commercial assays have now been developed to detect myositis relevant autoantibodies. Many have been developed with the practicalities of clinical practice in mind, offering rapid, affordable, and often multiplex testing. Despite this progress, the perfect system has yet to be realised.

Commercial testing systems do not detect all known myositis relevant autoantibodies and concerns have been raised about the sensitivity and specificity of some assays, including to their ability detect some autoantibodies strongly associated with malignancy and ILD; important causes of mortality and morbidity.

The advantages and disadvantages of different myositis autoantibody testing systems will be discussed. Evidence for the reliability of different types of assays in comparison to immunoprecipitation, as the reference standard, will be reviewed along with testing strategies that make the most of existing technology.

This presentation will give delegates attending an:

Overview of the pre-analytical processing pathway and potential risks associated with each stage.
Historical/current/prospective optimisation of the pre-analytical pathway.
Understanding of the near-future perspectives for standardisation-will technologies such image analysis and spatial profiling affect the practice of pathology laboratories.