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Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant
We share our experience of using continuous subcutaneous insulin infusion (CSII) therapy and diabetes technology in six people (5 men) with type 1 diabetes (mean duration 36 years), who developed hyperglycemia post‐simultaneous kidney/pancreas (n = 5) or pancreas only (n = 1) transplant. All were on...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286788/ https://www.ncbi.nlm.nih.gov/pubmed/37191402 http://dx.doi.org/10.1111/jdi.14019 |
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author | Stathi, Dimitra Johnston, Thomas Hyslop, Rebecca Brackenridge, Anna Karalliedde, Janaka |
author_facet | Stathi, Dimitra Johnston, Thomas Hyslop, Rebecca Brackenridge, Anna Karalliedde, Janaka |
author_sort | Stathi, Dimitra |
collection | PubMed |
description | We share our experience of using continuous subcutaneous insulin infusion (CSII) therapy and diabetes technology in six people (5 men) with type 1 diabetes (mean duration 36 years), who developed hyperglycemia post‐simultaneous kidney/pancreas (n = 5) or pancreas only (n = 1) transplant. All were on immunosuppression and multiple daily injections of insulin prior to CSII. Four people were started on automated insulin delivery, and two people on CSII and intermittently scanned continuous glucose monitoring. With diabetes technology, the median time in range glucose improved from 37% (24–49%) to 56.6% (48–62%), and similarly, glycated hemoglobin fell from 72.7 mmol/mol (72–79 mmol/mol) to 64 mmol/mol (42–67 mmol/mol; P < 0.05 for both) with no concomitant increase in hypoglycemia. Use of diabetes technology improved glycemic parameters in people with type 1 diabetes with failing pancreatic graft function. Early use of such technology should be considered to improve diabetes control in this complex cohort. |
format | Online Article Text |
id | pubmed-10286788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102867882023-06-23 Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant Stathi, Dimitra Johnston, Thomas Hyslop, Rebecca Brackenridge, Anna Karalliedde, Janaka J Diabetes Investig Articles We share our experience of using continuous subcutaneous insulin infusion (CSII) therapy and diabetes technology in six people (5 men) with type 1 diabetes (mean duration 36 years), who developed hyperglycemia post‐simultaneous kidney/pancreas (n = 5) or pancreas only (n = 1) transplant. All were on immunosuppression and multiple daily injections of insulin prior to CSII. Four people were started on automated insulin delivery, and two people on CSII and intermittently scanned continuous glucose monitoring. With diabetes technology, the median time in range glucose improved from 37% (24–49%) to 56.6% (48–62%), and similarly, glycated hemoglobin fell from 72.7 mmol/mol (72–79 mmol/mol) to 64 mmol/mol (42–67 mmol/mol; P < 0.05 for both) with no concomitant increase in hypoglycemia. Use of diabetes technology improved glycemic parameters in people with type 1 diabetes with failing pancreatic graft function. Early use of such technology should be considered to improve diabetes control in this complex cohort. John Wiley and Sons Inc. 2023-05-16 /pmc/articles/PMC10286788/ /pubmed/37191402 http://dx.doi.org/10.1111/jdi.14019 Text en © 2023 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Articles Stathi, Dimitra Johnston, Thomas Hyslop, Rebecca Brackenridge, Anna Karalliedde, Janaka Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
title | Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
title_full | Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
title_fullStr | Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
title_full_unstemmed | Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
title_short | Diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: Case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
title_sort | diabetes technology including automated insulin delivery systems to manage hyperglycemia in a failing pancreatic graft: case series of people with type 1 diabetes and a pancreas kidney or pancreas‐only transplant |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286788/ https://www.ncbi.nlm.nih.gov/pubmed/37191402 http://dx.doi.org/10.1111/jdi.14019 |
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