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Erschienen in: Clinical Drug Investigation 4/2013

01.04.2013 | Original Research Article

A Multinational, Observational Study to Investigate the Efficacy, Safety and Tolerability of Acarbose as Add-On or Monotherapy in a Range of Patients: The GlucoVIP Study

verfasst von: Weiwei Zhang, DongJun Kim, Elizabeth Philip, Zahid Miyan, Irina Barykina, Birgit Schmidt, Herbert Stein

Erschienen in: Clinical Drug Investigation | Ausgabe 4/2013

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Abstract

Background and Objectives

The burden of type 2 diabetes mellitus is growing rapidly, particularly in the Asia-Pacific region. The aim of this international, large-scale, observational study was to investigate the efficacy and tolerability of the antidiabetic agent acarbose as add-on or monotherapy in a range of patients with type 2 diabetes, including those with cardiovascular morbidities. The majority of practices were included from high-burden regions (predominantly those in the Asia-Pacific region).

Methods

This was an observational study conducted in 15 countries/regions. Adults with pre-treated or untreated type 2 diabetes prescribed acarbose as add-on or monotherapy were eligible. Two-hour postprandial blood glucose (2-h PPG), glycosylated haemoglobin (HbA1c) and fasting blood glucose (FBG) were measured over a 3-month observation period.

Results

A total of 15,034 patients were valid for the efficacy analysis and 15,661 for the safety analysis (mean age was 57.6 years and 92.6 % of patients were Asian). Mean (SD) 2-h PPG decreased by −71.9 (62.3) mg/dL, to 170.2 (46.5) mg/dL at final visit (after 12.8 [4.1] weeks). Mean HbA1c decreased by −1.1 % (1.3) to 7.2 % (1.1) and mean FBG decreased by −33.0 (43.3) mg/dL to 124.8 (30.5) mg/dL. Acarbose was effective regardless of the presence of cardiovascular co-morbidities or diabetic complications. The efficacy of acarbose was rated ‘very good’ or ‘good’ in 85.5 % of patients, and tolerability as ‘very good’ or ‘good’ in 84.9 % of patients. Drug-related adverse events, mainly gastrointestinal, were reported in 490/15,661 patients (3.13 %).

Conclusion

The results of this observational study support the notion that acarbose is effective, safe and well tolerated in a large cohort of Asian patients with type 2 diabetes.
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Metadaten
Titel
A Multinational, Observational Study to Investigate the Efficacy, Safety and Tolerability of Acarbose as Add-On or Monotherapy in a Range of Patients: The GlucoVIP Study
verfasst von
Weiwei Zhang
DongJun Kim
Elizabeth Philip
Zahid Miyan
Irina Barykina
Birgit Schmidt
Herbert Stein
Publikationsdatum
01.04.2013
Verlag
Springer International Publishing AG
Erschienen in
Clinical Drug Investigation / Ausgabe 4/2013
Print ISSN: 1173-2563
Elektronische ISSN: 1179-1918
DOI
https://doi.org/10.1007/s40261-013-0063-3

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