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Published in: Diabetes Therapy 1/2013

Open Access 01-06-2013 | Original Research

Safety and Effectiveness of Bolus Insulin Aspart in People with Type 2 Diabetes: A1chieve Sub-Analysis

Authors: Hoosen Randeree, Andreas Liebl, Issam Hajjaji, Mohammad Khamseh, Lenita Zajdenverg, Jian-Wen Chen, Jihad Haddad

Published in: Diabetes Therapy | Issue 1/2013

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Abstract

Introduction

This sub-analysis evaluated clinical safety and effectiveness of bolus insulin aspart [with/without oral glucose-lowering drugs (OGLDs)] as the only insulin therapy.

Methods

A1chieve was an international, multicenter, prospective, open-label, non-interventional, observational, 24-week study in people with type 2 diabetes mellitus starting/switching to biphasic insulin aspart 30, insulin detemir or insulin aspart treatment (alone/in combination) in routine clinical practice. This sub-analysis evaluated clinical safety and effectiveness of bolus insulin aspart (±OGLDs) as the only insulin therapy. Data were analyzed for all patients, insulin-experienced and insulin-naive sub-groups, and sub-groups defined by the number of OGLDs prescribed at baseline (no OGLDs, one OGLD or ≥two OGLDs). Safety and effectiveness endpoints were assessed at baseline and following 24 weeks’ therapy.

Results

In total, 2,026 patients were included (insulin-experienced, n = 561; insulin-naive, n = 1,465) in this sub-analysis. Significant improvements from baseline after 24 weeks’ treatment with insulin aspart ± OGLDs were observed across all sub-groups for: glycated hemoglobin (range of means across sub-groups −1.6 to −2.4%; p < 0.001 for all comparisons), fasting plasma glucose (−2.5 to −3.8 mmol/l; p < 0.001 for all comparisons), post-breakfast post-prandial glucose (−3.4 to −5.8 mmol/l; p < 0.001 for all comparisons), and health-related quality of life (HRQoL; p < 0.001 for all comparisons). The proportion of patients reporting hypoglycemia events was significantly reduced from baseline after 24 weeks (insulin-naive cohort: 7.9–2.8%; p < 0.001; insulin-experienced cohort: 23.2–7.8%; p < 0.001). There were no reports of major hypoglycemia events at 24 weeks; risk of nocturnal hypoglycemia was <0.6 events/person-year. No serious adverse drug reactions were reported.

Conclusion

Insulin aspart ± OGLDs is associated with significant improvements in glycemic control and HRQoL, without increased risk of hypoglycemia, in people with type 2 diabetes and sub-optimal glucose control.
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Metadata
Title
Safety and Effectiveness of Bolus Insulin Aspart in People with Type 2 Diabetes: A1chieve Sub-Analysis
Authors
Hoosen Randeree
Andreas Liebl
Issam Hajjaji
Mohammad Khamseh
Lenita Zajdenverg
Jian-Wen Chen
Jihad Haddad
Publication date
01-06-2013
Publisher
Springer Healthcare
Published in
Diabetes Therapy / Issue 1/2013
Print ISSN: 1869-6953
Electronic ISSN: 1869-6961
DOI
https://doi.org/10.1007/s13300-013-0026-y

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