ORIGINAL ARTICLE |
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Year : 2013 | Volume
: 17
| Issue : 8 | Page : 530-533 |
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Clinical experience with insulin detemir, biphasic insulin aspart and insulin aspart in people with type 2 diabetes: Results from the Delhi cohort of the A 1 chieve study
Sudhir Tripathi1, Neeru Gera2, Anil Motta3, Rajiva Gupta4
1 Sri Ganga Ram Hospital, New Delhi, India 2 Max Hospitals, New Delhi, India 3 Max Super Speciality Hospital, New Delhi, India 4 Upchaar Speciality Centre, New Delhi, India
Correspondence Address:
Sudhir Tripathi Sri Ganga Ram Hospital New Delhi India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2230-8210.122118
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Background: The A 1 chieve, a multicentric (28 countries), 24-week, non-interventional study evaluated the safety and effectiveness of insulin detemir, biphasic insulin aspart and insulin aspart in people with T2DM (n = 66,726) in routine clinical care across four continents. Materials and Methods: Data was collected at baseline, at 12 weeks and at 24 weeks. This short communication presents the results for patients enrolled from Delhi, India. Results: A total of 2242 patients were enrolled in the study. Four different insulin analogue regimens were used in the study. Patients had started on or were switched to biphasic insulin aspart (n = 1515), insulin detemir (n = 521), insulin aspart (n = 176), basal insulin plus insulin aspart (n = 11) and other insulin combinations (n = 19). At baseline glycaemic control was poor for both insulin naïve (mean HbA 1 c: 10.0%) and insulin user (mean HbA 1 c: 11.0%) groups. After 24 weeks of treatment both the groups showed improvement in HbA 1 c (insulin naïve: −3.1%, insulin users: −3.6%). SADRs including major hypoglycaemic events or episodes did not occur in any of the study patients. Conclusion: Starting or switching to insulin analogues was associated with improvement in glycaemic control with a low rate of hypoglycaemia. |
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