HHE Pathology 2019 | Page 12

considering the measurement of plasma glucose, one of the most common biomarker tests. There are many IVD methods for plasma glucose, but they all comply with the traceability chain so that the result obtained in the routine laboratory can be traced back to a primary reference material of pure glucose. As a result, there is excellent agreement between methods for plasma glucose, and results from elsewhere can be interpreted with confidence. For structurally simple molecules, like many of those measured routinely in clinical chemistry, pure substance is available, and it is possible to have a complete unbroken traceability chain. Even for some protein molecules it is possible to achieve full metrological traceability by using a unique, signature peptide as the primary reference material. Consequently, there are a growing number of important biomarkers where method standardisation has been achieved in a way comparable to plasma glucose. Regrettably, most of the biomarkers measured in laboratory medicine are not structurally simple molecules. For example, complex proteins, nucleic acids, viruses and bacteria are clinically important biomarkers that may not be available as pure substance and reference methods of measurement are unlikely to be available. In these circumstances full metrological traceability is not possible. The adoption of international conventional calibrators, with values assigned by experts, represents traceability part of the way up the chain and the use of such calibrators provides a reference against which methods can be harmonised to reduce between method variability. The Joint Committee for Traceability in Laboratory Medicine (JCTLM) The JCTLM was established in 2002 through a declaration between the International Bureau of Weights and Measures (BIPM), the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) and the International Laboratory Accreditation Cooperation (ILAC) in response to the implementation of the European Community Directive 98.79/EC on in vitro medical devices. JCTLM currently has >50 members from 20 countries and its membership is growing rapidly. The aim of the JCTLM is to support world-wide comparability, reliability and Laboratory medicine specialists equivalence of should choose methods that are measurement results traceable to global standards to aid in laboratory medicine, for improving health the interpretation of patient results care and facilitating national and international trade in IVD devices, by: • Promoting the concept of traceability of measurement results • Evaluating reference materials, reference measurement procedures and reference measurement services for laboratory medicine with respect to conformity with appropriate international standards; • Facilitating the identification and prioritisation of measurands requiring international traceability and comparability and thereby encouraging appropriate organisations to accept responsibility 12 HHE 2019 | hospitalhealthcare.com