Reduced Testing Frequency for Glycated Hemoglobin, HbA1c, Is Associated With Deteriorating Diabetes Control

Author:

Driskell Owen J.12,Holland David3,Waldron Jenna L.4,Ford Clare4,Scargill Jonathan J.5,Heald Adrian56,Tran Martin1,Hanna Fahmy W.17,Jones Peter W.28,Pemberton R. John9,Fryer Anthony A.12

Affiliation:

1. Department of Clinical Biochemistry, University Hospital of North Staffordshire National Health Service Trust, Stoke-on-Trent, Staffordshire, U.K.

2. Institute of Science and Technology in Medicine, University of Keele, Stoke-on-Trent, Staffordshire, U.K.

3. National Pathology Benchmarking Service, Department of Medicines Management, Keele University, Staffordshire, U.K.

4. Department of Clinical Biochemistry, Royal Wolverhampton National Health Service Trust, Wolverhampton, U.K.

5. Department of Clinical Biochemistry, Salford Royal Hospital National Health Service Foundation Trust, U.K.

6. School of Medicine and Manchester Academic Health Sciences Centre, University of Manchester, Manchester, U.K.

7. Department of Diabetes and Endocrinology, University Hospital of North Staffordshire National Health Service Trust, Stoke-on-Trent, Staffordshire, U.K.

8. School of Computing and Mathematics, Keele University, Keele, Staffordshire, U.K.

9. Diabetes UK, North Staffordshire Branch, Newcastle-under-Lyme, Staffordshire, U.K.

Abstract

OBJECTIVE We previously showed that in patients with diabetes mellitus, glycated hemoglobin (HbA1c) monitoring outside international guidance on testing frequency is widespread. Here we examined the relationship between testing frequency and diabetes control to test the hypothesis that retest interval is linked to change in HbA1c level. RESEARCH DESIGN AND METHODS We examined repeat HbA1c tests (400,497 tests in 79,409 patients, 2008–2011) processed by three U.K. clinical laboratories. We examined the relationship between retest interval and 1) percentage change in HbA1c and 2) proportion of cases showing a significant HbA1c rise. The effect of demographics factors on these findings was also explored. RESULTS Our data showed that the optimal testing frequency required to maximize the downward trajectory in HbA1c was four times per year, particularly in those with an initial HbA1c of ≥7% (≥53 mmol/mol), supporting international guidance. Testing 3-monthly was associated with a 3.8% reduction in HbA1c compared with a 1.5% increase observed with annual testing; testing more frequently provided no additional benefit. Compared with annual monitoring, 3-monthly testing was associated with a halving of the proportion showing a significant rise in HbA1c (7–10 vs. 15–20%). CONCLUSIONS These findings provide, in a large, multicenter data set, objective evidence that testing outside guidance on HbA1c monitoring frequency is associated with a significant detrimental effect on diabetes control. To achieve the optimum downward trajectory in HbA1c, monitoring frequency should be quarterly, particularly in cases with suboptimal HbA1c. While this impact appears small, optimizing monitoring frequency across the diabetes population may have major implications for diabetes control and comorbidity risk.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference20 articles.

1. Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study;Stratton;BMJ,2000

2. National Institute for Health and Clinical Excellence. Type 1 diabetes (CG15) [article online], 2004. Available from http://guidance.nice.org.uk/CG15. Accessed 3 January 2014

3. National Institute for Health and Clinical Excellence. Type 2 diabetes (CG66) [article online], 2008. Available from http://guidance.nice.org.uk/CG66. Accessed 3 January 2014

4. Standards of medical care in diabetes—2011;American Diabetes Association;Diabetes Care,2011

5. Inappropriate requesting of glycated hemoglobin (Hb A1c) is widespread: assessment of prevalence, impact of national guidance, and practice-to-practice variability;Driskell;Clin Chem,2012

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