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Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance
BACKGROUND: Glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs) are an established treatment for patients with type 2 diabetes (T2D). Differences between GLP‐1RAs in pharmacokinetics, dosing regimens and clinical effects, including cardiovascular (CV) outcomes, mean there may be benefits to switchi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900946/ https://www.ncbi.nlm.nih.gov/pubmed/32975890 http://dx.doi.org/10.1111/ijcp.13731 |
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author | Jain, Akshay B. Ali, Amar Gorgojo Martínez, Juan J. Hramiak, Irene Kavia, Ketan Madsbad, Sten Potier, Louis Prohaska, Ben D. Strong, Jodi L. Vilsbøll, Tina |
author_facet | Jain, Akshay B. Ali, Amar Gorgojo Martínez, Juan J. Hramiak, Irene Kavia, Ketan Madsbad, Sten Potier, Louis Prohaska, Ben D. Strong, Jodi L. Vilsbøll, Tina |
author_sort | Jain, Akshay B. |
collection | PubMed |
description | BACKGROUND: Glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs) are an established treatment for patients with type 2 diabetes (T2D). Differences between GLP‐1RAs in pharmacokinetics, dosing regimens and clinical effects, including cardiovascular (CV) outcomes, mean there may be benefits to switching from one to another. However, clinical guidance on switching is lacking and data from clinical trials are limited. This article provides a clinical perspective and consensus on the benefits of switching between GLP‐1RAs, the triggers for switching and how best to manage this in clinical practice. Once weekly (OW) semaglutide is used as an example to illustrate how the authors might switch to a different GLP‐1RA in clinical practice. METHODS: Literature was searched and perspectives from 10 healthcare professionals with experience in switching patients with T2D to OW semaglutide from another GLP‐1RA were collated. RESULTS: Medical triggers for switching to another GLP‐1RA included HbA(1c) targets not being met, a desire for additional weight loss, poor adherence, patients moving to increased CV risk status and adverse effects with the current GLP‐1RA. Non‐medical triggers for switching included patient preference, cost, formulary changes and insurance mandates. Once the decision to switch is made, an individualised approach is recommended, based on considerations that include reimbursement requirements, treatment duration with (and dose of) previous GLP‐1RA, the patient's experience initiating the prior GLP‐1RA, any concomitant treatment and clinical characteristics. When switching, it is important to emphasise that treatment burden will not increase and that if gastrointestinal adverse effects occur, they are typically transient. Any transient gastrointestinal adverse effects that may occur (or recur) when switching to another GLP‐1RA can be reduced by slow up‐titration and advising patients to reduce food portion sizes and fat intake. CONCLUSION: Switching from one GLP‐1RA to another, such as OW semaglutide, can provide clinical benefits and may delay the need for treatment intensification. |
format | Online Article Text |
id | pubmed-7900946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79009462021-03-03 Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance Jain, Akshay B. Ali, Amar Gorgojo Martínez, Juan J. Hramiak, Irene Kavia, Ketan Madsbad, Sten Potier, Louis Prohaska, Ben D. Strong, Jodi L. Vilsbøll, Tina Int J Clin Pract Systematic Review BACKGROUND: Glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs) are an established treatment for patients with type 2 diabetes (T2D). Differences between GLP‐1RAs in pharmacokinetics, dosing regimens and clinical effects, including cardiovascular (CV) outcomes, mean there may be benefits to switching from one to another. However, clinical guidance on switching is lacking and data from clinical trials are limited. This article provides a clinical perspective and consensus on the benefits of switching between GLP‐1RAs, the triggers for switching and how best to manage this in clinical practice. Once weekly (OW) semaglutide is used as an example to illustrate how the authors might switch to a different GLP‐1RA in clinical practice. METHODS: Literature was searched and perspectives from 10 healthcare professionals with experience in switching patients with T2D to OW semaglutide from another GLP‐1RA were collated. RESULTS: Medical triggers for switching to another GLP‐1RA included HbA(1c) targets not being met, a desire for additional weight loss, poor adherence, patients moving to increased CV risk status and adverse effects with the current GLP‐1RA. Non‐medical triggers for switching included patient preference, cost, formulary changes and insurance mandates. Once the decision to switch is made, an individualised approach is recommended, based on considerations that include reimbursement requirements, treatment duration with (and dose of) previous GLP‐1RA, the patient's experience initiating the prior GLP‐1RA, any concomitant treatment and clinical characteristics. When switching, it is important to emphasise that treatment burden will not increase and that if gastrointestinal adverse effects occur, they are typically transient. Any transient gastrointestinal adverse effects that may occur (or recur) when switching to another GLP‐1RA can be reduced by slow up‐titration and advising patients to reduce food portion sizes and fat intake. CONCLUSION: Switching from one GLP‐1RA to another, such as OW semaglutide, can provide clinical benefits and may delay the need for treatment intensification. John Wiley and Sons Inc. 2020-11-03 2021-02 /pmc/articles/PMC7900946/ /pubmed/32975890 http://dx.doi.org/10.1111/ijcp.13731 Text en © 2020 The Authors. International Journal of Clinical Practice published by John Wiley & Sons Ltd This is an open access article under the terms of the http://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 | Systematic Review Jain, Akshay B. Ali, Amar Gorgojo Martínez, Juan J. Hramiak, Irene Kavia, Ketan Madsbad, Sten Potier, Louis Prohaska, Ben D. Strong, Jodi L. Vilsbøll, Tina Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance |
title | Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance |
title_full | Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance |
title_fullStr | Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance |
title_full_unstemmed | Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance |
title_short | Switching between GLP‐1 receptor agonists in clinical practice: Expert consensus and practical guidance |
title_sort | switching between glp‐1 receptor agonists in clinical practice: expert consensus and practical guidance |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900946/ https://www.ncbi.nlm.nih.gov/pubmed/32975890 http://dx.doi.org/10.1111/ijcp.13731 |
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