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Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes

INTRODUCTION: Glycemic targets and glucose-lowering regimens should be individualized based on multiple factors, including the presence of comorbidities. We examined contemporary patterns of glycemic control and use of medications known to cause hypoglycemia among adults with diabetes across age and...

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Autores principales: McCoy, Rozalina G, Lipska, Kasia J, Van Houten, Holly K, Shah, Nilay D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039576/
https://www.ncbi.nlm.nih.gov/pubmed/32075810
http://dx.doi.org/10.1136/bmjdrc-2019-001007
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author McCoy, Rozalina G
Lipska, Kasia J
Van Houten, Holly K
Shah, Nilay D
author_facet McCoy, Rozalina G
Lipska, Kasia J
Van Houten, Holly K
Shah, Nilay D
author_sort McCoy, Rozalina G
collection PubMed
description INTRODUCTION: Glycemic targets and glucose-lowering regimens should be individualized based on multiple factors, including the presence of comorbidities. We examined contemporary patterns of glycemic control and use of medications known to cause hypoglycemia among adults with diabetes across age and multimorbidity. RESEARCH DESIGN AND METHODS: We retrospectively examined glycosylated hemoglobin (HbA(1c)) levels and rates of insulin/sulfonylurea use as a function of age and multimorbidity using administrative claims and laboratory data for adults with type 2 diabetes included in OptumLabs Data Warehouse, 1 January 2014 to 31 December 2016. Comorbidity burden was assessed by counts of any of 16 comorbidities specified by guidelines as warranting relaxation of HbA(1c) targets, classified as being diabetes concordant (diabetes complications or risk factors), discordant (unrelated to diabetes), or advanced (life limiting). RESULTS: Among 194 157 patients with type 2 diabetes included in the study, 45.2% had only concordant comorbidities, 30.6% concordant and discordant, 2.7% only discordant, and 13.0% had ≥1 advanced comorbidity. Mean HbA(1c) was 7.7% among 18–44 year-olds versus 6.9% among ≥75 year-olds, and was higher among patients with comorbidities: 7.3% with concordant only, 7.1% with discordant only, 7.1% with concordant and discordant, and 7.0% with advanced comorbidities compared with 7.4% among patients without comorbidities. The odds of insulin use decreased with age (OR 0.51 (95% CI 0.48 to 0.54) for age ≥75 vs 18–44 years) but increased with accumulation of concordant (OR 5.50 (95% CI 5.22 to 5.79) for ≥3 vs none), discordant (OR 1.72 (95% CI 1.60 to 1.86) for ≥3 vs none), and advanced (OR 1.45 (95% CI 1.25 to 1.68) for ≥2 vs none) comorbidities. Conversely, sulfonylurea use increased with age (OR 1.36 (95% CI 1.29 to 1.44) for age ≥75 vs 18–44 years) but decreased with accumulation of concordant (OR 0.76 (95% CI 0.73 to 0.79) for ≥3 vs none), discordant (OR 0.70 (95% CI 0.64 to 0.76) for ≥3 vs none), but not advanced (OR 0.86 (95% CI 0.74 to 1.01) for ≥2 vs none) comorbidities. CONCLUSIONS: The proportion of patients achieving low HbA(1c) levels was highest among older and multimorbid patients. Older patients and patients with higher comorbidity burden were more likely to be treated with insulin to achieve these HbA(1c) levels despite potential for hypoglycemia and uncertain long-term benefit.
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spelling pubmed-70395762020-03-03 Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes McCoy, Rozalina G Lipska, Kasia J Van Houten, Holly K Shah, Nilay D BMJ Open Diabetes Res Care Epidemiology/Health Services Research INTRODUCTION: Glycemic targets and glucose-lowering regimens should be individualized based on multiple factors, including the presence of comorbidities. We examined contemporary patterns of glycemic control and use of medications known to cause hypoglycemia among adults with diabetes across age and multimorbidity. RESEARCH DESIGN AND METHODS: We retrospectively examined glycosylated hemoglobin (HbA(1c)) levels and rates of insulin/sulfonylurea use as a function of age and multimorbidity using administrative claims and laboratory data for adults with type 2 diabetes included in OptumLabs Data Warehouse, 1 January 2014 to 31 December 2016. Comorbidity burden was assessed by counts of any of 16 comorbidities specified by guidelines as warranting relaxation of HbA(1c) targets, classified as being diabetes concordant (diabetes complications or risk factors), discordant (unrelated to diabetes), or advanced (life limiting). RESULTS: Among 194 157 patients with type 2 diabetes included in the study, 45.2% had only concordant comorbidities, 30.6% concordant and discordant, 2.7% only discordant, and 13.0% had ≥1 advanced comorbidity. Mean HbA(1c) was 7.7% among 18–44 year-olds versus 6.9% among ≥75 year-olds, and was higher among patients with comorbidities: 7.3% with concordant only, 7.1% with discordant only, 7.1% with concordant and discordant, and 7.0% with advanced comorbidities compared with 7.4% among patients without comorbidities. The odds of insulin use decreased with age (OR 0.51 (95% CI 0.48 to 0.54) for age ≥75 vs 18–44 years) but increased with accumulation of concordant (OR 5.50 (95% CI 5.22 to 5.79) for ≥3 vs none), discordant (OR 1.72 (95% CI 1.60 to 1.86) for ≥3 vs none), and advanced (OR 1.45 (95% CI 1.25 to 1.68) for ≥2 vs none) comorbidities. Conversely, sulfonylurea use increased with age (OR 1.36 (95% CI 1.29 to 1.44) for age ≥75 vs 18–44 years) but decreased with accumulation of concordant (OR 0.76 (95% CI 0.73 to 0.79) for ≥3 vs none), discordant (OR 0.70 (95% CI 0.64 to 0.76) for ≥3 vs none), but not advanced (OR 0.86 (95% CI 0.74 to 1.01) for ≥2 vs none) comorbidities. CONCLUSIONS: The proportion of patients achieving low HbA(1c) levels was highest among older and multimorbid patients. Older patients and patients with higher comorbidity burden were more likely to be treated with insulin to achieve these HbA(1c) levels despite potential for hypoglycemia and uncertain long-term benefit. BMJ Publishing Group 2020-02-19 /pmc/articles/PMC7039576/ /pubmed/32075810 http://dx.doi.org/10.1136/bmjdrc-2019-001007 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Epidemiology/Health Services Research
McCoy, Rozalina G
Lipska, Kasia J
Van Houten, Holly K
Shah, Nilay D
Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
title Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
title_full Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
title_fullStr Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
title_full_unstemmed Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
title_short Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
title_sort paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes
topic Epidemiology/Health Services Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039576/
https://www.ncbi.nlm.nih.gov/pubmed/32075810
http://dx.doi.org/10.1136/bmjdrc-2019-001007
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