DPP-4 Inhibitor Dose Selection According to Manufacturer Specifications: A Contemporary Experience From UK General Practice
- PMID: 31164243
- DOI: 10.1016/j.clinthera.2019.05.010
DPP-4 Inhibitor Dose Selection According to Manufacturer Specifications: A Contemporary Experience From UK General Practice
Erratum in
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Corrigendum to "DPP-4 Inhibitor Dose Selection According to Manufacturer Specifications: A Contemporary Experience From UK General Practice" [Clinical Therapeutics 41 (8) (2019) 1622-1630].Clin Ther. 2020 Apr;42(4):726-727. doi: 10.1016/j.clinthera.2020.02.001. Epub 2020 Feb 15. Clin Ther. 2020. PMID: 32067743 No abstract available.
Abstract
Recently, 2 dipeptidyl peptidase-4 (DPP-4) inhibitors, sitagliptin and saxagliptin, adjusted dosing specification from creatinine clearance to glomerular filtration rate, more typically reported in routine laboratory tests. This cross-sectional study examines all DPP-4 inhibitor initiations that require dose adjustment and the dose selection using data from UK general practice. Results indicate that 34% of patients taking a nonlinagliptin DPP-4 inhibitor were given a higher dose and 11% a lower dose than specified in the Summary of Product Characteristics. This reinforces the deviation from Summary of Product Characteristics prescription of DPP-4 inhibitors identified in earlier studies despite improvement in compatibility with routine reporting.
Keywords: DPP-4 inhibitors; Type 2 diabetes mellitus; UK general practice; dose selection; renal impairment; summary of product characteristics.
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.
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