Serum immunofixation (IF) is routinely used in clinical laboratories to confirm the presence of an M-protein and determine its isotype. For laboratories looking for more of an automated method for the detection of M-proteins, immunotyping (IT) by capillary electrophoresis is also FDA-approved to confirm the presence of M-proteins and determine its isotype.
In this webinar, Dr. Katie Thoren will discuss a recent study comparing the performance of immunotyping to immunofixation for the detection of M-proteins. She will show that reviewer training and experience are critical to the correct interpretation of IT results and that the analytical and clinical sensitivity is similar to IF for the detection of M-proteins. Dr. Thoren will present the data, review the limitations of each test and discuss potential strategies for mitigating these limitations.
Describe how an immunotyping training program can improve the sensitivity of IT interpretation.
Identify the advantages of immunotyping over immunofixation in detecting M-proteins.
Explain the clinical sensitivity observed with immunofixation and immunotyping when each test is used in combination with serum-free light-chain results.
Summarize the limitations of immunofixation and immunotyping in detecting M-proteins and potential strategies to mitigate these limitations.
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Katie Thoren, PhD, DABCC
Assistant Attending Clinical Chemist, Department of Laboratory Medicine Memorial Sloan Kettering Cancer Center
HbA1c is routinely used in the clinical laboratory to diagnose and monitor diabetes mellitus. Many methods have been standardized to provide precise and accurate results for normal patients. For the other common Hb variants, most of the methods are now relatively free of analytical interference.