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FROM THE EDITOR


Diabetes testing guidelines deserve support from the lab community


D


By Linda Wilson Senior Editor


iabetes is one of the most common chronic diseases in the United States. In 2018, 34.2 million Americans, or 1 in 10,


had diabetes and 88 million American adults, or 1 in 3, had prediabetes, according to the Centers for Disease Control and Prevention (CDC). In addition, 7.3 million adults aged 18 years or older who met laboratory criteria for diabetes were not even aware that they had the disease. Diabetes also is a major contributor to the


nation’s annual healthcare tab. In a 2018 report, the American Diabetes Association (ADA) said the total estimated 2017 direct medical costs from diagnosed cases of diabetes was $237 billion. On an individual level, each person diagnosed with diabetes incurs average medical expen-


ditures of $16,752 per year, of which about $9,601 is directly attributable to diabetes, the ADA said, adding that this per-person cost is about 2.3 times higher than it is for people without a diabetes diagnosis. None of this is news to clinical laboratorians. Testing to diagnose new cases of diabetes and prediabetes or to monitor blood sugar control in existing cases of diabetes is an important part of the daily workflow at many clinical labs. What may be news to laboratorians, however, is an ongoing effort on the part of the ADA and the American Association for Clinical Chemistry (AACC) to update diabetes testing guidelines. The guidelines were first crafted in 2002 and revised in 2011. The nine-member expert committee has been working on reviewing new medical evidence and writing revisions for several years. The committee members released a preliminary draft of the guidelines at the AACC’s annual meeting in September. Medical Laboratory Observer describes some of those recommendations and the overall guideline-review process in an article in this issue. As you know, standardization of diagnostic methods and measures ensures that a patient will get the same result no matter what lab performs the testing. In fact, the idea of standardization that is based on medical evidence is a central tenant of the healthcare industry’s efforts to improve the quality of patient care. Committee members have put in many volunteer hours so far: about a month of 40-hour work weeks, according to the estimate of one committee member. It is important work, and I am glad that this group has agreed to undertake this endeavor. Committee Chairperson David Sacks MB, ChB, FRCPath, Adjunct Professor


of Medicine, Georgetown University; Clinical Professor of Pathology, George Washington University, told me he cannot predict when the preliminary guidelines will be in final form. The COVID-19 pandemic has slowed forward momentum in this project — just as it has for so many others. I urge all of you to learn about the preliminary guidelines. You will have an opportunity to submit comments at some point in the process. And once the recommendations become final, you should evaluate them and consider what, if any, procedures you should update in your lab’s daily work to align with the recommendations. I welcome your comments, questions, and opinions – please send them to me at lwilson@mlo-online.com.


4 DECEMBER 2021 MLO-ONLINE.COM MEDICAL LABORATORY OBSERVER Vol.53, No.12


Group Publisher/Executive Editor Kristine Russell


krussell@mlo-online.com


Senior Editor Linda Wilson


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MLO EDITORIAL ADVISORY BOARD


John Brunstein, PhD, Biochemistry (Molecular Virology) President & CSO PathoID, Inc., British Columbia, Canada


John A. Gerlach, PhD, D(ABHI) Laboratory Director Michigan State University, East Lansing, MI


Barbara Strain, MA, SM(ASCP), CVAHP Principal, Barbara Strain Consulting LLC Formerly Director, Value Management University of Virginia Health System, Charlottesville, VA


Jeffrey D. Klausner, MD, MPH Professor of Preventive Medicine in the Division of Dis- ease Prevention, Policy and Global Health, Department of Preventive Medicine at University of Southern California Keck School of Medicine.


Susan McQuiston, JD, MT(ASCP), SCy(ASCP) Instructor, Biomedical Laboratory Diagnostics Program Michigan State University, East Lansing, MI


Donna Beasley, DLM(ASCP) Director


Huron Healthcare, Chicago, IL


Anthony Kurec, MS, H(ASCP)DLM Clinical Associate Professor, Emeritus SUNY Upstate Medical University, Syracuse, NY


Suzanne Butch, MLS(ASCP)CM , SBBCM Freelance Consultant, Ann Arbor, MI


Paul R. Eden, Jr., MT(ASCP), PhD Lt. Col., USAF (ret.) (formerly) Chief, Laboratory Services 88th Diagnostics/Therapeutics Squadron Wright-Patterson AFB, OH Daniel J. Scungio, MT (ASCP), SLS, CQA (ASQ) Consultant at Dan the Lab Safety Man and Safety Officer at Sentara Healthcare, Norfolk, VA


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(ISSN: 0580-7247). Published monthly, with an additional issue in NOVEMBER, by Endeavor Business Media, LLC., 2477 Stickney Point Rd, Suite 221B, Sarasota, FL 34231 (941) 388-7050. Subscription rates: $127.60/ year in the U.S.; $154.88 Canada/Mexico; Intl. subscriptions are $221.43/year. All issues of MLO are available on microfilm from University Microfilms International, Box 78, 300 N. Zeeb Rd., Ann Arbor, MI 48106. Current single copies (if available) $15.00 each (U.S); and $20.00 each (Intl.). Back issues (if available) $17.60 each (U.S.); $22.00 each (Intl.). Payment must be made in U.S. funds on a U.S. bank/ branch within the continental U.S. and accompany request. Subscription inquiries: subscriptions@endeavorb2b.com. MLO is indexed in the Cumulative Index for Nursing and Allied Health Literature and Lexis-Nexis. MLO Cover/CE, Clinical Issues, and Lab Management features are peer reviewed. Title®


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