Safety and Effectiveness of Switching from a Basal-only to Biphasic Insulin Aspart 30 Insulin Regimen
Purpose This sub-analysis of the A 1 chieve study evaluated the safety and effectiveness of changing from a basal-only insulin regimen to biphasic insulin aspart 30. Methods A 1 chieve was an international, multicenter, prospective, open-label, non-interventional, 24-week study in people with type 2...
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Published in | Diabetes therapy Vol. 4; no. 2; pp. 309 - 319 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Springer Healthcare
01.12.2013
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Purpose
This sub-analysis of the A
1
chieve study evaluated the safety and effectiveness of changing from a basal-only insulin regimen to biphasic insulin aspart 30.
Methods
A
1
chieve was an international, multicenter, prospective, open-label, non-interventional, 24-week study in people with type 2 diabetes mellitus starting/switching to therapy with biphasic insulin aspart 30, insulin detemir, or insulin aspart (alone/in combination) in routine clinical practice. This sub-analysis evaluated the safety and effectiveness of switching from basal insulin with either insulin glargine (GLA group) or insulin neutral protamine Hagedorn (NEU group) to biphasic insulin aspart 30.
Results
A total of 2,818 participants received biphasic insulin aspart 30 (1,395 in the GLA group and 1,423 in the NEU group). After 24 weeks of treatment, there were significant reductions in the proportion of patients with at least one hypoglycemia event: total [baseline vs. 24 weeks: 15.5% vs. 9.7% (
p
< 0.001) and 12.3% vs. 9.9% (
p
< 0.05), in NEU and GLA groups, respectively], major [2.5% vs. 0.08% (
p
< 0.001) and 1.2% vs. 0.08% (
p
< 0.001), in NEU and GLA groups, respectively] and nocturnal hypoglycemia [7.2% vs. 3.5% (
p
< 0.001) and 5.4% vs. 3.9% (
p
< 0.05), in NEU and GLA groups, respectively]. After 24 weeks of biphasic insulin aspart 30 there were statistically significant improvements from baseline in glycated hemoglobin, fasting plasma glucose, and post-prandial plasma glucose levels (
p
< 0.001) and in health-related quality of life (
p
< 0.001) in both groups.
Conclusions
Biphasic insulin aspart 30 may benefit patients with poor glycemic control on basal insulin regimens who are seeking to change treatment. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1869-6953 1869-6961 |
DOI: | 10.1007/s13300-013-0032-0 |