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Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs

OBJECTIVE: Hyperglycemia is an independent risk factor in hospitalized patients for adverse outcomes, even if patients are not diabetic. We used continuous glucose monitoring to evaluate whether glycemic control (hyperglycemia) in the first 72 h after an intensive care admission was associated with...

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Autores principales: Pappada, Scott M., Woodling, Karina, Owais, Mohammad Hamza, Zink, Evan M., Dahbour, Layth, Tripathi, Ravi S., Khuder, Sadik A., Papadimos, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069852/
https://www.ncbi.nlm.nih.gov/pubmed/30064524
http://dx.doi.org/10.1186/s13104-018-3656-3
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author Pappada, Scott M.
Woodling, Karina
Owais, Mohammad Hamza
Zink, Evan M.
Dahbour, Layth
Tripathi, Ravi S.
Khuder, Sadik A.
Papadimos, Thomas J.
author_facet Pappada, Scott M.
Woodling, Karina
Owais, Mohammad Hamza
Zink, Evan M.
Dahbour, Layth
Tripathi, Ravi S.
Khuder, Sadik A.
Papadimos, Thomas J.
author_sort Pappada, Scott M.
collection PubMed
description OBJECTIVE: Hyperglycemia is an independent risk factor in hospitalized patients for adverse outcomes, even if patients are not diabetic. We used continuous glucose monitoring to evaluate whether glycemic control (hyperglycemia) in the first 72 h after an intensive care admission was associated with the need for admission to a post discharge long-term medical facility. RESULTS: We enrolled 59 coronary artery bypass grafting patients. Poor glycemic control was defined as greater than 33% of continuous glucose monitoring values < 70 and > 180 mg/dL (group 1); and then these patients were reevaluated with a less strict definition of poor glycemic control with greater than 25% of continuous glucose values < 70 and > 180 mg/dL (group 2). In group 1 4/10 (40.0%) whose glucose was not well controlled went to an extended care post discharge facility as opposed to 6/49 (12.2%) that were well controlled. In reevaluation as group 2, 5/14 (35.7%) whose glucose was not well controlled went to an extended care post discharge facility as opposed to 5/45 (11.1%) who were well controlled. Admission to a post discharge facility was increased in patients with poor glycemic control p = 0.045 and p = 0.042 for group 1 and group 2, and with odds ratios of 4.8 (95% CI 1.0–22.5) and 4.4 (95% CI 1.0–19.4), respectively.
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spelling pubmed-60698522018-08-06 Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs Pappada, Scott M. Woodling, Karina Owais, Mohammad Hamza Zink, Evan M. Dahbour, Layth Tripathi, Ravi S. Khuder, Sadik A. Papadimos, Thomas J. BMC Res Notes Research Note OBJECTIVE: Hyperglycemia is an independent risk factor in hospitalized patients for adverse outcomes, even if patients are not diabetic. We used continuous glucose monitoring to evaluate whether glycemic control (hyperglycemia) in the first 72 h after an intensive care admission was associated with the need for admission to a post discharge long-term medical facility. RESULTS: We enrolled 59 coronary artery bypass grafting patients. Poor glycemic control was defined as greater than 33% of continuous glucose monitoring values < 70 and > 180 mg/dL (group 1); and then these patients were reevaluated with a less strict definition of poor glycemic control with greater than 25% of continuous glucose values < 70 and > 180 mg/dL (group 2). In group 1 4/10 (40.0%) whose glucose was not well controlled went to an extended care post discharge facility as opposed to 6/49 (12.2%) that were well controlled. In reevaluation as group 2, 5/14 (35.7%) whose glucose was not well controlled went to an extended care post discharge facility as opposed to 5/45 (11.1%) who were well controlled. Admission to a post discharge facility was increased in patients with poor glycemic control p = 0.045 and p = 0.042 for group 1 and group 2, and with odds ratios of 4.8 (95% CI 1.0–22.5) and 4.4 (95% CI 1.0–19.4), respectively. BioMed Central 2018-07-31 /pmc/articles/PMC6069852/ /pubmed/30064524 http://dx.doi.org/10.1186/s13104-018-3656-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Note
Pappada, Scott M.
Woodling, Karina
Owais, Mohammad Hamza
Zink, Evan M.
Dahbour, Layth
Tripathi, Ravi S.
Khuder, Sadik A.
Papadimos, Thomas J.
Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
title Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
title_full Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
title_fullStr Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
title_full_unstemmed Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
title_short Continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
title_sort continuous glucose monitoring identifies relationship between optimized glycemic control and post-discharge acute care facility needs
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069852/
https://www.ncbi.nlm.nih.gov/pubmed/30064524
http://dx.doi.org/10.1186/s13104-018-3656-3
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