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Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis
Aims: To compare rates and predictors of documented hypoglycaemia in type 2 diabetes patients treated with either basal insulin supported oral therapy (BOT), conventional therapy (CT) or supplementary insulin therapy (SIT) in primary care. Methods: Data from 10,842 anonymous patients (mean age ± SD:...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
German Medical Science GMS Publishing House
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311049/ https://www.ncbi.nlm.nih.gov/pubmed/25698911 http://dx.doi.org/10.3205/000205 |
_version_ | 1782354945445462016 |
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author | Kostev, Karel Dippel, Franz W. Rathmann, Wolfgang |
author_facet | Kostev, Karel Dippel, Franz W. Rathmann, Wolfgang |
author_sort | Kostev, Karel |
collection | PubMed |
description | Aims: To compare rates and predictors of documented hypoglycaemia in type 2 diabetes patients treated with either basal insulin supported oral therapy (BOT), conventional therapy (CT) or supplementary insulin therapy (SIT) in primary care. Methods: Data from 10,842 anonymous patients (mean age ± SD: 54 ± 8 yrs) on BOT, 2,407 subjects (56 ± 7 yrs) on CT, and 7,480 patients (52 ± 10 yrs) using SIT from 1,198 primary care practices were retrospectively analyzed (Disease Analyzer, Germany: 01/2005–07/2013). Stepwise logistic regression (≥1 documented hypoglycaemia: ICD code) was used to evaluate risk factors of hypoglycemia. Results: The unadjusted rates (95% CI) per 100 patient-years of documented hypoglycaemia were 1.01 (0.80–1.20) (BOT), 1.68 (1.10–2.30) (CT), and 1.61 (1.30–1.90) (SIT), respectively. The odds of having ≥1 hypoglycemia was increased for CT (OR; 95% CI: 1.71; 1.13–2.58) and SIT (1.55; 1.15–2.08) (reference: BOT). Previous hypoglycemia (OR: 11.24; 6.71–18.85), duration of insulin treatment (days) (1.06; 1.05–1.07), history of transient ischemic attack (TIA)/stroke (1.91; 1.04–3.50), and former salicylate prescriptions (1.44; 1.06–1.98) also showed an increased odds of having hypoglycemia. Higher age was associated with a slightly lower odds ratio (per year: 0.98; 0.97–0.99). Conclusions: Insulin naïve type 2 diabetes patients in primary care, initiated with CT and SIT have an increased risk of hypoglycaemia compared to BOT, which is in line with previous randomized controlled trials. As hypoglycaemic events are associated with an increased mortality risk, this real-world finding is of clinical relevance. |
format | Online Article Text |
id | pubmed-4311049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | German Medical Science GMS Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-43110492015-02-19 Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis Kostev, Karel Dippel, Franz W. Rathmann, Wolfgang Ger Med Sci Article Aims: To compare rates and predictors of documented hypoglycaemia in type 2 diabetes patients treated with either basal insulin supported oral therapy (BOT), conventional therapy (CT) or supplementary insulin therapy (SIT) in primary care. Methods: Data from 10,842 anonymous patients (mean age ± SD: 54 ± 8 yrs) on BOT, 2,407 subjects (56 ± 7 yrs) on CT, and 7,480 patients (52 ± 10 yrs) using SIT from 1,198 primary care practices were retrospectively analyzed (Disease Analyzer, Germany: 01/2005–07/2013). Stepwise logistic regression (≥1 documented hypoglycaemia: ICD code) was used to evaluate risk factors of hypoglycemia. Results: The unadjusted rates (95% CI) per 100 patient-years of documented hypoglycaemia were 1.01 (0.80–1.20) (BOT), 1.68 (1.10–2.30) (CT), and 1.61 (1.30–1.90) (SIT), respectively. The odds of having ≥1 hypoglycemia was increased for CT (OR; 95% CI: 1.71; 1.13–2.58) and SIT (1.55; 1.15–2.08) (reference: BOT). Previous hypoglycemia (OR: 11.24; 6.71–18.85), duration of insulin treatment (days) (1.06; 1.05–1.07), history of transient ischemic attack (TIA)/stroke (1.91; 1.04–3.50), and former salicylate prescriptions (1.44; 1.06–1.98) also showed an increased odds of having hypoglycemia. Higher age was associated with a slightly lower odds ratio (per year: 0.98; 0.97–0.99). Conclusions: Insulin naïve type 2 diabetes patients in primary care, initiated with CT and SIT have an increased risk of hypoglycaemia compared to BOT, which is in line with previous randomized controlled trials. As hypoglycaemic events are associated with an increased mortality risk, this real-world finding is of clinical relevance. German Medical Science GMS Publishing House 2015-01-12 /pmc/articles/PMC4311049/ /pubmed/25698911 http://dx.doi.org/10.3205/000205 Text en Copyright © 2015 Kostev et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. |
spellingShingle | Article Kostev, Karel Dippel, Franz W. Rathmann, Wolfgang Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
title | Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
title_full | Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
title_fullStr | Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
title_full_unstemmed | Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
title_short | Risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
title_sort | risk of hypoglycaemia in type 2 diabetes patients under different insulin regimens: a primary care database analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311049/ https://www.ncbi.nlm.nih.gov/pubmed/25698911 http://dx.doi.org/10.3205/000205 |
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