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. (C) 2019 The Authors. Published by Elsevier Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 1622-1630 |
| Number of pages | 9 |
| Journal | Clinical Therapeutics |
| Volume | 41 |
| Issue number | 8 |
| Early online date | 1 Jun 2019 |
| DOIs | |
| Publication status | Published - Aug 2019 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- dose selection
- DPP-4 inhibitors
- summary of product characteristics
- renal impairment
- Type 2 diabetes mellitus
- UK general practice
- TYPE-2 DIABETES-MELLITUS
- PEPTIDASE 4 INHIBITORS
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