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Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice

Fast‐acting insulin aspart (faster aspart) is a novel formulation of insulin aspart (IAsp) containing the additional excipients niacinamide and L‐arginine. The improved pharmacological profile and greater early glucose‐lowering action of faster aspart compared with IAsp suggests that faster aspart m...

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Autores principales: Evans, Mark, Ceriello, Antonio, Danne, Thomas, De Block, Christophe, DeVries, J. Hans, Lind, Marcus, Mathieu, Chantal, Nørgaard, Kirsten, Renard, Eric, Wilmot, Emma G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773364/
https://www.ncbi.nlm.nih.gov/pubmed/31144428
http://dx.doi.org/10.1111/dom.13798
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author Evans, Mark
Ceriello, Antonio
Danne, Thomas
De Block, Christophe
DeVries, J. Hans
Lind, Marcus
Mathieu, Chantal
Nørgaard, Kirsten
Renard, Eric
Wilmot, Emma G.
author_facet Evans, Mark
Ceriello, Antonio
Danne, Thomas
De Block, Christophe
DeVries, J. Hans
Lind, Marcus
Mathieu, Chantal
Nørgaard, Kirsten
Renard, Eric
Wilmot, Emma G.
author_sort Evans, Mark
collection PubMed
description Fast‐acting insulin aspart (faster aspart) is a novel formulation of insulin aspart (IAsp) containing the additional excipients niacinamide and L‐arginine. The improved pharmacological profile and greater early glucose‐lowering action of faster aspart compared with IAsp suggests that faster aspart may be advantageous for people with diabetes using continuous subcutaneous insulin infusion (CSII). The recent onset 5 trial was the first to evaluate the efficacy and safety of an ultra‐fast‐acting insulin in CSII therapy in a large number of participants with type 1 diabetes (T1D). Non‐inferiority of faster aspart to IAsp in terms of change from baseline in HbA1c was confirmed, with an estimated treatment difference (ETD) of 0.09% (95% CI, 0.01; 0.17; P < 0.001 for non‐inferiority [0.4% margin]). Faster aspart was superior to IAsp in terms of change from baseline in 1‐hour post‐prandial glucose (PPG) increment after a meal test (ETD [95% CI], −0.91 mmol/L [−1.43; −0.39]; P = 0.001), with statistically significant improvements also at 30 minutes and 2 hours. The overall rate of severe or blood glucose‐confirmed hypoglycaemia was not statistically significantly different between treatments, with an estimated rate ratio of 1.00 (95% CI, 0.85; 1.16). A numerical imbalance in severe hypoglycaemic episodes between faster aspart and IAsp was seen in the treatment (21 vs 7) and the 4‐week run‐in periods (4 vs 0). Experience from clinical practice indicates that all pump settings should be reviewed when initiating faster aspart with CSII, and that the use of continuous glucose monitoring or flash glucose monitoring, along with a good understanding of meal content and bolus type, may also facilitate optimal use. This review summarizes the available clinical evidence for faster aspart administered via CSII and highlights practical considerations based on clinical experience that may help healthcare providers and individuals with T1D successfully initiate and adjust faster aspart with CSII.
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spelling pubmed-67733642019-10-07 Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice Evans, Mark Ceriello, Antonio Danne, Thomas De Block, Christophe DeVries, J. Hans Lind, Marcus Mathieu, Chantal Nørgaard, Kirsten Renard, Eric Wilmot, Emma G. Diabetes Obes Metab Review Articles Fast‐acting insulin aspart (faster aspart) is a novel formulation of insulin aspart (IAsp) containing the additional excipients niacinamide and L‐arginine. The improved pharmacological profile and greater early glucose‐lowering action of faster aspart compared with IAsp suggests that faster aspart may be advantageous for people with diabetes using continuous subcutaneous insulin infusion (CSII). The recent onset 5 trial was the first to evaluate the efficacy and safety of an ultra‐fast‐acting insulin in CSII therapy in a large number of participants with type 1 diabetes (T1D). Non‐inferiority of faster aspart to IAsp in terms of change from baseline in HbA1c was confirmed, with an estimated treatment difference (ETD) of 0.09% (95% CI, 0.01; 0.17; P < 0.001 for non‐inferiority [0.4% margin]). Faster aspart was superior to IAsp in terms of change from baseline in 1‐hour post‐prandial glucose (PPG) increment after a meal test (ETD [95% CI], −0.91 mmol/L [−1.43; −0.39]; P = 0.001), with statistically significant improvements also at 30 minutes and 2 hours. The overall rate of severe or blood glucose‐confirmed hypoglycaemia was not statistically significantly different between treatments, with an estimated rate ratio of 1.00 (95% CI, 0.85; 1.16). A numerical imbalance in severe hypoglycaemic episodes between faster aspart and IAsp was seen in the treatment (21 vs 7) and the 4‐week run‐in periods (4 vs 0). Experience from clinical practice indicates that all pump settings should be reviewed when initiating faster aspart with CSII, and that the use of continuous glucose monitoring or flash glucose monitoring, along with a good understanding of meal content and bolus type, may also facilitate optimal use. This review summarizes the available clinical evidence for faster aspart administered via CSII and highlights practical considerations based on clinical experience that may help healthcare providers and individuals with T1D successfully initiate and adjust faster aspart with CSII. Blackwell Publishing Ltd 2019-06-19 2019-09 /pmc/articles/PMC6773364/ /pubmed/31144428 http://dx.doi.org/10.1111/dom.13798 Text en © 2019 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Evans, Mark
Ceriello, Antonio
Danne, Thomas
De Block, Christophe
DeVries, J. Hans
Lind, Marcus
Mathieu, Chantal
Nørgaard, Kirsten
Renard, Eric
Wilmot, Emma G.
Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
title Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
title_full Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
title_fullStr Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
title_full_unstemmed Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
title_short Use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
title_sort use of fast‐acting insulin aspart in insulin pump therapy in clinical practice
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773364/
https://www.ncbi.nlm.nih.gov/pubmed/31144428
http://dx.doi.org/10.1111/dom.13798
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