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Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes
OBJECTIVE: To test the effect of an automated system providing real-time estimates of HbA(1c), glucose variability, and risk for hypoglycemia. RESEARCH DESIGN AND METHODS: For 1 year, 120 adults with type 1 diabetes (69 female/51 male, age = 39.1 [14.3] years, duration of diabetes 20.3 [12.9] years,...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024338/ https://www.ncbi.nlm.nih.gov/pubmed/21216860 http://dx.doi.org/10.2337/dc10-1366 |
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author | Kovatchev, Boris P. Mendosa, Pamela Anderson, Stacey Hawley, Jeffrey S. Ritterband, Lee M. Gonder-Frederick, Linda |
author_facet | Kovatchev, Boris P. Mendosa, Pamela Anderson, Stacey Hawley, Jeffrey S. Ritterband, Lee M. Gonder-Frederick, Linda |
author_sort | Kovatchev, Boris P. |
collection | PubMed |
description | OBJECTIVE: To test the effect of an automated system providing real-time estimates of HbA(1c), glucose variability, and risk for hypoglycemia. RESEARCH DESIGN AND METHODS: For 1 year, 120 adults with type 1 diabetes (69 female/51 male, age = 39.1 [14.3] years, duration of diabetes 20.3 [12.9] years, HbA(1c) = 8.0 [1.5]), performed self-monitoring of blood glucose (SMBG) and received feedback at three increasingly complex levels, each continuing for 3 months: level 1—routine SMBG; level 2—adding estimated HbA(1c), hypoglycemia risk, and glucose variability; and level 3—adding estimates of symptoms potentially related to hypoglycemia. The subjects were randomized to feedback sequences of either levels 1-2-3 or levels 2-3-1. HbA(1c), symptomatic hypoglycemia, and blood glucose awareness were evaluated at baseline and at the end of each level. RESULTS: For all subjects, HbA(1c) was reduced from 8.0 to 7.6 from baseline to the end of study (P = 0.001). This effect was confined to subjects with baseline HbA(1c) >8.0 (from 9.3 to 8.5, P < 0.001). Incidence of symptomatic moderate/severe hypoglycemia was reduced from 5.72 to 3.74 episodes/person/month (P = 0.019), more prominently for subjects with a history of severe hypoglycemia (from 7.20 to 4.00 episodes, P = 0.008) and for those who were hypoglycemia unaware (from 6.44 to 3.71 episodes, P = 0.045). The subjects’ ratings of the feedback were positive, with up to 89% approval of the provided features. CONCLUSIONS: Feedback of SMBG data and summary SMBG-based measures resulted in improvement in average glycemic control and reduction in moderate/severe hypoglycemia. These effects were most prominent in subjects who were at highest risk at the baseline. |
format | Text |
id | pubmed-3024338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-30243382012-02-01 Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes Kovatchev, Boris P. Mendosa, Pamela Anderson, Stacey Hawley, Jeffrey S. Ritterband, Lee M. Gonder-Frederick, Linda Diabetes Care Original Research OBJECTIVE: To test the effect of an automated system providing real-time estimates of HbA(1c), glucose variability, and risk for hypoglycemia. RESEARCH DESIGN AND METHODS: For 1 year, 120 adults with type 1 diabetes (69 female/51 male, age = 39.1 [14.3] years, duration of diabetes 20.3 [12.9] years, HbA(1c) = 8.0 [1.5]), performed self-monitoring of blood glucose (SMBG) and received feedback at three increasingly complex levels, each continuing for 3 months: level 1—routine SMBG; level 2—adding estimated HbA(1c), hypoglycemia risk, and glucose variability; and level 3—adding estimates of symptoms potentially related to hypoglycemia. The subjects were randomized to feedback sequences of either levels 1-2-3 or levels 2-3-1. HbA(1c), symptomatic hypoglycemia, and blood glucose awareness were evaluated at baseline and at the end of each level. RESULTS: For all subjects, HbA(1c) was reduced from 8.0 to 7.6 from baseline to the end of study (P = 0.001). This effect was confined to subjects with baseline HbA(1c) >8.0 (from 9.3 to 8.5, P < 0.001). Incidence of symptomatic moderate/severe hypoglycemia was reduced from 5.72 to 3.74 episodes/person/month (P = 0.019), more prominently for subjects with a history of severe hypoglycemia (from 7.20 to 4.00 episodes, P = 0.008) and for those who were hypoglycemia unaware (from 6.44 to 3.71 episodes, P = 0.045). The subjects’ ratings of the feedback were positive, with up to 89% approval of the provided features. CONCLUSIONS: Feedback of SMBG data and summary SMBG-based measures resulted in improvement in average glycemic control and reduction in moderate/severe hypoglycemia. These effects were most prominent in subjects who were at highest risk at the baseline. American Diabetes Association 2011-02 2011-01-20 /pmc/articles/PMC3024338/ /pubmed/21216860 http://dx.doi.org/10.2337/dc10-1366 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Original Research Kovatchev, Boris P. Mendosa, Pamela Anderson, Stacey Hawley, Jeffrey S. Ritterband, Lee M. Gonder-Frederick, Linda Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes |
title | Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes |
title_full | Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes |
title_fullStr | Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes |
title_full_unstemmed | Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes |
title_short | Effect of Automated Bio-Behavioral Feedback on the Control of Type 1 Diabetes |
title_sort | effect of automated bio-behavioral feedback on the control of type 1 diabetes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024338/ https://www.ncbi.nlm.nih.gov/pubmed/21216860 http://dx.doi.org/10.2337/dc10-1366 |
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