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Journal of Clinical Pathology 2004;57:344-345; doi:10.1136/jcp.2003.010918
Copyright © 2004 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.
Journal of Clinical Pathology 2004;57:344-345
© 2004 BMJ Publishing Group Ltd & Association of Clinical Pathologists

EDITORIAL

HbA1c measurement

HbA1c measurement

E S Kilpatrick

Correspondence to:
Correspondence to:
Dr E S Kilpatrick
Department of Clinical Biochemistry, Hull Royal Infirmary, Anlaby Road, Hull HU3 2JZ, UK; eric_kilpatrick@hotmail.com


As methods improve, inherent limitations become more apparent

Keywords: International Federation of Clinical Chemistry; glycated haemoglobin

Abbreviations: DCCT, Diabetes Control and Complications Trial; IFCC, International Federation of Clinical Chemistry; HbA1c, glycated haemoglobin; UKPDS, United Kingdom Prospective Diabetes Study

The first 150 words of the full text of this article appear below.

It is difficult to overestimate the contribution made by glycated haemoglobin measurement (usually in the form of HbA1c) to the management of patients with diabetes mellitus and the reliance now placed on the test by clinicians. Before its introduction as a routine test in the late 1970s and early 1980s, objectively assessing glycaemic control relied on measures such as 24 hour urine glucose excretions1 and daily blood glucose profiles.2 By comparison, measurement of HbA1c gave a much more reliable measure of glucose control over the prolonged period of the previous six to eight weeks.3 The clinical usefulness of the test was cemented by major trials, such as the Diabetes Control and Complications Trial (DCCT) in type 1 diabetes4 and the United Kingdom Prospective Diabetes Study (UKPDS) in type 2 diabetes.5 Both showed that improved glycaemic control, as assessed by HbA1c, could lead to substantial reductions in . . . [Full text of this article]


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