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IDegLira for the Real-World Treatment of Type 2 Diabetes in Italy: Protocol and Interim Results from the REX Observational Study.

Authors :
Fadini, Gian Paolo
Buzzetti, Raffaella
Fittipaldi, Maria Rosa
D'Incau, Ferruccio
Da Porto, Andrea
Girelli, Angela
Simoni, Lucia
Lastoria, Giusi
Consoli, Agostino
REX study group
Iazzetta, Nicolangelo
Di Giovanni, Giuseppe
Carbonara, Ornella
Aragiusto, Concetta
Carleo, Diego
Da Rosa, Nicoletta
Martedì, Emilia
Landolfi, Luigi
Marracino, Marta
Tortora, Anna
Source :
Diabetes Therapy; Aug2022, Vol. 13 Issue 8, p1483-1497, 15p
Publication Year :
2022

Abstract

Introduction: IDegLira was shown to maintain glycemic control while reducing risk of hypoglycemia and body weight gain. The REX study was designed to generate real-world evidence on the use of IDegLira in Italian clinical practice in two different subgroups of patients, those switching to IDegLira from a basal insulin-supported oral therapy (BOT group) and those from a basal plus bolus insulin regimen (BB group). Methods: Adult patients with T2D diagnosed for at least 12 months and having started IDegLira 2–3 months prior to enrolment, coming from a BOT or BB regimen, were enrolled in this multicenter observational prospective cohort study conducted in 28 Italian centers. This paper presents the methodological framework of the REX study and provides the interim analysis results describing the patients' baseline characteristics and the clinical reasons for IDegLira treatment initiation. Results: Of the 360 patients enrolled in the REX study, 331 were considered eligible for this interim analysis, 76.4% in the BOT and 23.6% in the BB group. Mean (SD) HbA1c was 8.5% (1.4) in the BOT and 8.2% (1.7) in the BB group. The most common T2D complications were diabetic macroangiopathy and diabetic nephropathy in both groups. The median (interquartile range) insulin daily dose before IDegLira was 15.0 (10.0–20.0) units in the BOT group and 42 (30.0–52.0) in the BB group. Oral antidiabetics were taken by 98% and 51.3% of patients, respectively. The main reason for switching to IDegLira was the inadequate glycemic control in the BOT group (86% of patients), and the intent to simplify the treatment in the BB group (66.7%). Conclusions: IdegLira is initiated after BOT in inadequately controlled patients to improve glycemic control, whereas in BB patients it is used to simplify the therapeutic regimen. Final results of the REX study will shed light on patients' outcomes after IdegLira treatment under routine clinical care. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18696953
Volume :
13
Issue :
8
Database :
Complementary Index
Journal :
Diabetes Therapy
Publication Type :
Academic Journal
Accession number :
158137069
Full Text :
https://doi.org/10.1007/s13300-022-01287-z