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Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus

INTRODUCTION: To assess secondary metformin monotherapy (MM) failure in a real-world type 2 diabetes mellitus (T2DM) cohort. RESEARCH DESIGN AND METHODS: Using the IQVIA Electronic Medical Record (formerly GE Centricity) database, adults with T2DM who initiated MM between January 1, 2012 and June 30...

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Autores principales: Weiss, Tracey, Iglay, Kristy, Gulati, Tania, Rajpathak, Swapnil, Yang, Lingfeng, Blonde, Lawrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230991/
https://www.ncbi.nlm.nih.gov/pubmed/34167954
http://dx.doi.org/10.1136/bmjdrc-2021-002127
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author Weiss, Tracey
Iglay, Kristy
Gulati, Tania
Rajpathak, Swapnil
Yang, Lingfeng
Blonde, Lawrence
author_facet Weiss, Tracey
Iglay, Kristy
Gulati, Tania
Rajpathak, Swapnil
Yang, Lingfeng
Blonde, Lawrence
author_sort Weiss, Tracey
collection PubMed
description INTRODUCTION: To assess secondary metformin monotherapy (MM) failure in a real-world type 2 diabetes mellitus (T2DM) cohort. RESEARCH DESIGN AND METHODS: Using the IQVIA Electronic Medical Record (formerly GE Centricity) database, adults with T2DM who initiated MM between January 1, 2012 and June 30, 2016 and achieved glycemic control (hemoglobin A1c (HbA1c) <7% (53 mmol/mol); index date) were analyzed. Secondary MM failure was defined in two ways: loss of glycemic control (HbA1c ≥7% (53 mmol/mol)) and treatment change (addition or switch of antihyperglycemic agent). Multivariable logistic regression models assessed the association between secondary MM failure and sociodemographic and clinical factors. RESULTS: The analysis included 4775 patients initiating MM. 32.9% and 19.2% experienced secondary MM failure at 24 months measured as loss of glycemic control and treatment change, respectively. Multivariable logistic regression found that women (OR=1.3, 95% CI 1.1 to 1.5) compared with men, lower Charlson Comorbidity Index (CCI) (OR=0.89, 95% CI 0.86 to 0.93), and lower baseline HbA1c (OR=0.93, 95% CI 0.88 to 0.98) were associated with increased likelihood of loss of glycemic control. Lower CCI was associated with increased likelihood of treatment change (OR=0.78, 95% CI 0.75 to 0.82). CONCLUSIONS: The observed frequency of secondary MM failure underscores the importance of the American Diabetes Association’s recommendation for glycemic monitoring of at least every 6 months so that timely therapeutic adjustments can be made.
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spelling pubmed-82309912021-07-09 Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus Weiss, Tracey Iglay, Kristy Gulati, Tania Rajpathak, Swapnil Yang, Lingfeng Blonde, Lawrence BMJ Open Diabetes Res Care Emerging Technologies, Pharmacology and Therapeutics INTRODUCTION: To assess secondary metformin monotherapy (MM) failure in a real-world type 2 diabetes mellitus (T2DM) cohort. RESEARCH DESIGN AND METHODS: Using the IQVIA Electronic Medical Record (formerly GE Centricity) database, adults with T2DM who initiated MM between January 1, 2012 and June 30, 2016 and achieved glycemic control (hemoglobin A1c (HbA1c) <7% (53 mmol/mol); index date) were analyzed. Secondary MM failure was defined in two ways: loss of glycemic control (HbA1c ≥7% (53 mmol/mol)) and treatment change (addition or switch of antihyperglycemic agent). Multivariable logistic regression models assessed the association between secondary MM failure and sociodemographic and clinical factors. RESULTS: The analysis included 4775 patients initiating MM. 32.9% and 19.2% experienced secondary MM failure at 24 months measured as loss of glycemic control and treatment change, respectively. Multivariable logistic regression found that women (OR=1.3, 95% CI 1.1 to 1.5) compared with men, lower Charlson Comorbidity Index (CCI) (OR=0.89, 95% CI 0.86 to 0.93), and lower baseline HbA1c (OR=0.93, 95% CI 0.88 to 0.98) were associated with increased likelihood of loss of glycemic control. Lower CCI was associated with increased likelihood of treatment change (OR=0.78, 95% CI 0.75 to 0.82). CONCLUSIONS: The observed frequency of secondary MM failure underscores the importance of the American Diabetes Association’s recommendation for glycemic monitoring of at least every 6 months so that timely therapeutic adjustments can be made. BMJ Publishing Group 2021-06-24 /pmc/articles/PMC8230991/ /pubmed/34167954 http://dx.doi.org/10.1136/bmjdrc-2021-002127 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://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/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Emerging Technologies, Pharmacology and Therapeutics
Weiss, Tracey
Iglay, Kristy
Gulati, Tania
Rajpathak, Swapnil
Yang, Lingfeng
Blonde, Lawrence
Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
title Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
title_full Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
title_fullStr Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
title_full_unstemmed Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
title_short Secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
title_sort secondary metformin monotherapy failure in individuals with type 2 diabetes mellitus
topic Emerging Technologies, Pharmacology and Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230991/
https://www.ncbi.nlm.nih.gov/pubmed/34167954
http://dx.doi.org/10.1136/bmjdrc-2021-002127
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