ADA Standards of Care 2023 — Key Updates
A clear overview of the most relevant ADA recommendations for HbA1c use in diagnosis and long‑term diabetes management, including thresholds, testing frequency, and clinical decision points.
A clear overview of the most relevant ADA recommendations for HbA1c use in diagnosis and long‑term diabetes management, including thresholds, testing frequency, and clinical decision points.
How HbA1c supports both initial diagnosis and ongoing monitoring, and why it remains a cornerstone marker despite biological and analytical limitations.
A comparison of major analytical technologies (HPLC, immunoassay, enzymatic methods, capillary electrophoresis), highlighting their principles, strengths, and potential sources of bias.
Guidance on recognizing and managing interferences such as hemoglobin variants, anemia, altered red cell turnover, and other factors that may distort HbA1c values.
Key criteria for evaluating or transitioning to a new testing system, including accuracy, workflow efficiency, standardization, and alignment with NGSP/IFCC requirements.
Real‑world examples illustrating how analytical challenges are addressed in practice, and how optimized workflows can improve reliability and clinical impact.
“Understanding the strengths and limitations of HbA1c methodologies is essential for accurate diabetes diagnosis and monitoring.”
Hemoglobin A1c (HbA1c) remains a cornerstone in the diagnosis and monitoring of diabetes, and its proper use is central to implementing the 2023 American Diabetes Association (ADA) guidelines. While HbA1c testing is widely adopted, interpreting results requires a solid understanding of the underlying methodologies, their strengths and limitations, and the clinical scenarios in which HbA1c may be misleading.
This session will review the role of HbA1c in diabetes management, summarize key recommendations from the current ADA guidelines, and provide an overview of commonly used testing methodologies. Attention will be given to analytical principles, comparative advantages and disadvantages of different methods, and the practical factors laboratories must consider when selecting or transitioning HbA1c platforms. Special situations, including cases where unusual result patterns point to analytical interferences or clinical confounders such as hemoglobin variants, will be discussed to illustrate problem-solving approaches in the laboratory setting.
Drawing from Emory University Hospital’s experience, Dr. Janetta Bryksin will highlight both the theoretical and practical aspects of HbA1c testing, emphasizing how laboratories can optimize accuracy, efficiency, and clinical value in diabetes care.
Dr. Bryksin is the System Medical Director for Core Laboratories at Emory Healthcare in Atlanta.
She is a board‑certified clinical chemist with extensive experience in method evaluation, laboratory standardization, and the implementation of advanced testing technologies.
Her work focuses on improving analytical quality, managing interferences, and ensuring reliable HbA1c testing aligned with ADA and NGSP/IFCC standards.

Educational Webinar with Dr.Matthew C. Wagner

Educational Webinar with David G. Grenache, PhD, D(ABCC) Chief Scientific Officer, TriCore Reference Laboratories
Information intended for healthcare professionals.
This section contains information intended for wide distribution and may therefore contain product details or information that is not available or valid in your country. Carefully read the instructions in the reagent package inserts and instrument manuals. Please contact your local Sebia representative.
System Medical Director for Core Laboratories, Emory Healthcare (EHC), Atlanta, GA
