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Switching between GLP-1 receptor agonists in clinical practice: expert consensus and practical guidance

Publikation: Bidrag til tidsskriftReviewpeer review

DOI

  1. Oral Treatment of Glucocorticoid-Induced Diabetes Mellitus: A Systematic Review

    Publikation: Bidrag til tidsskriftLetterpeer review

  2. Clinical use of the co-formulation of insulin degludec and insulin aspart

    Publikation: Bidrag til tidsskriftReviewpeer review

  • Akshay B Jain
  • Amar Ali
  • Juan J Gorgojo Martínez
  • Irene Hramiak
  • Ketan Kavia
  • Sten Madsbad
  • Louis Potier
  • Ben D Prohaska
  • Jodi L Strong
  • Tina Vilsbøll
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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 HbA1c 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.

OriginalsprogEngelsk
Artikelnummere13731
TidsskriftInternational Journal of Clinical Practice
Vol/bind75
Udgave nummer2
Sider (fra-til)e13731
ISSN1368-5031
DOI
StatusUdgivet - feb. 2021

ID: 60934536