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The potential role of incretin therapy in the hospital setting

Hyperglycemia has been associated with increased morbidity and mortality in hospitalized patients. Insulin has traditionally been the drug of choice for managing hyperglycemia in this setting, but carries a significant risk of hypoglycemia. Incretin-based therapies, including glucagon-like peptide-1...

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Autores principales: Macdonald, Jennifer J., Neupane, Shristi, Gianchandani, Roma Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469200/
https://www.ncbi.nlm.nih.gov/pubmed/28702223
http://dx.doi.org/10.1186/s40842-015-0005-5
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author Macdonald, Jennifer J.
Neupane, Shristi
Gianchandani, Roma Y.
author_facet Macdonald, Jennifer J.
Neupane, Shristi
Gianchandani, Roma Y.
author_sort Macdonald, Jennifer J.
collection PubMed
description Hyperglycemia has been associated with increased morbidity and mortality in hospitalized patients. Insulin has traditionally been the drug of choice for managing hyperglycemia in this setting, but carries a significant risk of hypoglycemia. Incretin-based therapies, including glucagon-like peptide-1, glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors, have potential use in the hospital. These agents have a relatively low risk of hypoglycemia, favorable short-term side effect profile, and can be used alone or in combination with insulin. Several small studies have supported the safety and efficacy of incretin therapies in the inpatient setting with the majority of data coming from the intensive care setting. Large-scale clinical studies are needed to further evaluate the potential role of incretins in the management of inpatient hyperglycemia.
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spelling pubmed-54692002017-07-12 The potential role of incretin therapy in the hospital setting Macdonald, Jennifer J. Neupane, Shristi Gianchandani, Roma Y. Clin Diabetes Endocrinol Review Article Hyperglycemia has been associated with increased morbidity and mortality in hospitalized patients. Insulin has traditionally been the drug of choice for managing hyperglycemia in this setting, but carries a significant risk of hypoglycemia. Incretin-based therapies, including glucagon-like peptide-1, glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors, have potential use in the hospital. These agents have a relatively low risk of hypoglycemia, favorable short-term side effect profile, and can be used alone or in combination with insulin. Several small studies have supported the safety and efficacy of incretin therapies in the inpatient setting with the majority of data coming from the intensive care setting. Large-scale clinical studies are needed to further evaluate the potential role of incretins in the management of inpatient hyperglycemia. BioMed Central 2015-07-01 /pmc/articles/PMC5469200/ /pubmed/28702223 http://dx.doi.org/10.1186/s40842-015-0005-5 Text en © MacDonald et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Review Article
Macdonald, Jennifer J.
Neupane, Shristi
Gianchandani, Roma Y.
The potential role of incretin therapy in the hospital setting
title The potential role of incretin therapy in the hospital setting
title_full The potential role of incretin therapy in the hospital setting
title_fullStr The potential role of incretin therapy in the hospital setting
title_full_unstemmed The potential role of incretin therapy in the hospital setting
title_short The potential role of incretin therapy in the hospital setting
title_sort potential role of incretin therapy in the hospital setting
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469200/
https://www.ncbi.nlm.nih.gov/pubmed/28702223
http://dx.doi.org/10.1186/s40842-015-0005-5
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