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HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study

Study question What is the extent and effect of excessive testing for glycated hemoglobin (HbA(1c)) among adults with controlled type 2 diabetes? Methods A retrospective analysis of data from a national administrative claims database included commercially insured individuals in the USA, 2001-13. Stu...

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Autores principales: McCoy, Rozalina G, Van Houten, Holly K, Ross, Joseph S, Montori, Victor M, Shah, Nilay D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673101/
https://www.ncbi.nlm.nih.gov/pubmed/26646052
http://dx.doi.org/10.1136/bmj.h6138
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author McCoy, Rozalina G
Van Houten, Holly K
Ross, Joseph S
Montori, Victor M
Shah, Nilay D
author_facet McCoy, Rozalina G
Van Houten, Holly K
Ross, Joseph S
Montori, Victor M
Shah, Nilay D
author_sort McCoy, Rozalina G
collection PubMed
description Study question What is the extent and effect of excessive testing for glycated hemoglobin (HbA(1c)) among adults with controlled type 2 diabetes? Methods A retrospective analysis of data from a national administrative claims database included commercially insured individuals in the USA, 2001-13. Study patients were aged 18 years or older, had type 2 diabetes with stable glycemic control (two consecutive tests showing HbA(1c)<7.0% within 24 months), did not use insulin, had no history of severe hypoglycemia or hyperglycemia, and were not pregnant. HbA(1c) testing frequency was measured within 24 months after the second (index) HbA(1c) test, and classified as guideline recommended (≤2 times/year), frequent (3-4 times/year), and excessive (≥5 times/year). Changes in treatment regimen were ascertained within three months of the index test. Study answer and limitations Of 31 545 patients in the study cohort (mean age 58 years; mean index HbA(1c) 6.2%), HbA(1c) testing frequency was excessive in 6% and frequent in 55%. Despite good glycemic control at baseline, treatment was further intensified by addition of glucose lowering drugs or insulin in 8.4% of patients (comprising 13%, 9%, and 7% of those tested excessively, frequently, and per guidelines, respectively; P<0.001). Compared with guideline recommended testing, excessive testing was associated with treatment intensification (odds ratio 1.35 (95% confidence interval 1.22 to 1.50)). Excessive testing rates remained unchanged in 2001-08, but fell significantly after 2009. The odds of excessive testing was 46% lower in 2011 than in 2001-02. The study population is not representative of all US patients with type 2 diabetes because it was restricted to commercially insured adults with stable and controlled diabetes not receiving insulin treatment. The study design did not capture the underuse of HbA(1c) testing. What this study adds In this US cohort of adults with stable and controlled type 2 diabetes, more than 60% received too many HbA(1c) tests, a practice associated with potential overtreatment with hypoglycemic drugs. Excessive testing contributes to the growing problem of waste in healthcare and increased patient burden in diabetes management. Funding, competing interests, data sharing NDS and RGM are funded partly by the Agency for Healthcare Research and Quality (R18HS18339) and AcademyHealth Delivery System Science Fellowship (2013), respectively. No competing interests declared. Additional data are available from mccoy.rozalina@mayo.edu.
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spelling pubmed-46731012015-12-18 HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study McCoy, Rozalina G Van Houten, Holly K Ross, Joseph S Montori, Victor M Shah, Nilay D BMJ Research Study question What is the extent and effect of excessive testing for glycated hemoglobin (HbA(1c)) among adults with controlled type 2 diabetes? Methods A retrospective analysis of data from a national administrative claims database included commercially insured individuals in the USA, 2001-13. Study patients were aged 18 years or older, had type 2 diabetes with stable glycemic control (two consecutive tests showing HbA(1c)<7.0% within 24 months), did not use insulin, had no history of severe hypoglycemia or hyperglycemia, and were not pregnant. HbA(1c) testing frequency was measured within 24 months after the second (index) HbA(1c) test, and classified as guideline recommended (≤2 times/year), frequent (3-4 times/year), and excessive (≥5 times/year). Changes in treatment regimen were ascertained within three months of the index test. Study answer and limitations Of 31 545 patients in the study cohort (mean age 58 years; mean index HbA(1c) 6.2%), HbA(1c) testing frequency was excessive in 6% and frequent in 55%. Despite good glycemic control at baseline, treatment was further intensified by addition of glucose lowering drugs or insulin in 8.4% of patients (comprising 13%, 9%, and 7% of those tested excessively, frequently, and per guidelines, respectively; P<0.001). Compared with guideline recommended testing, excessive testing was associated with treatment intensification (odds ratio 1.35 (95% confidence interval 1.22 to 1.50)). Excessive testing rates remained unchanged in 2001-08, but fell significantly after 2009. The odds of excessive testing was 46% lower in 2011 than in 2001-02. The study population is not representative of all US patients with type 2 diabetes because it was restricted to commercially insured adults with stable and controlled diabetes not receiving insulin treatment. The study design did not capture the underuse of HbA(1c) testing. What this study adds In this US cohort of adults with stable and controlled type 2 diabetes, more than 60% received too many HbA(1c) tests, a practice associated with potential overtreatment with hypoglycemic drugs. Excessive testing contributes to the growing problem of waste in healthcare and increased patient burden in diabetes management. Funding, competing interests, data sharing NDS and RGM are funded partly by the Agency for Healthcare Research and Quality (R18HS18339) and AcademyHealth Delivery System Science Fellowship (2013), respectively. No competing interests declared. Additional data are available from mccoy.rozalina@mayo.edu. BMJ Publishing Group Ltd. 2015-12-08 /pmc/articles/PMC4673101/ /pubmed/26646052 http://dx.doi.org/10.1136/bmj.h6138 Text en © McCoy et al 2015 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
McCoy, Rozalina G
Van Houten, Holly K
Ross, Joseph S
Montori, Victor M
Shah, Nilay D
HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study
title HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study
title_full HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study
title_fullStr HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study
title_full_unstemmed HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study
title_short HbA(1c) overtesting and overtreatment among US adults with controlled type 2 diabetes, 2001-13: observational population based study
title_sort hba(1c) overtesting and overtreatment among us adults with controlled type 2 diabetes, 2001-13: observational population based study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673101/
https://www.ncbi.nlm.nih.gov/pubmed/26646052
http://dx.doi.org/10.1136/bmj.h6138
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