Abstract |
The aim of the study was to examine the extent to which patients with type 2 diabetes mellitus (T2DM) initiating a dipeptidyl peptidase 4 (DPP-4) inhibitor, who had no recorded objective evidence to justify dose adjustment, were initiated on the manufacturer-specified dose. Adopting a cross-sectional study design and using data from the UK General Practice, this study showed that at least 10% of patients with T2DM and a creatinine clearance level >50 mL/min initiating treatment with a DPP-4 inhibitor were prescribed a dose lower than specified in the Summary of Product Characteristics. This study provides further insights regarding DPP-4 inhibitor dose selection with respect to manufacturer specification in relation to renal function.
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Authors | Dionysis Spanopoulos, Brendan Barrett, Michael Busse, Toni Roman, Chris Poole |
Journal | Clinical therapeutics
(Clin Ther)
Vol. 40
Issue 8
Pg. 1424-1428.e4
(08 2018)
ISSN: 1879-114X [Electronic] United States |
PMID | 30049504
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2018 Elsevier Inc. All rights reserved. |
Chemical References |
- Dipeptidyl-Peptidase IV Inhibitors
- Hypoglycemic Agents
- Creatinine
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Topics |
- Creatinine
(blood)
- Cross-Sectional Studies
- Diabetes Mellitus, Type 2
(complications, drug therapy)
- Dipeptidyl-Peptidase IV Inhibitors
(administration & dosage)
- Humans
- Hypoglycemic Agents
(administration & dosage)
- Primary Health Care
(statistics & numerical data)
- Renal Insufficiency, Chronic
(complications, physiopathology)
- United Kingdom
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