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Published on: June 11, 2012
Comparative effectiveness of oral diabetes drug combinations in reducing glycosylated hemoglobin
James H Flory1, Dylan S Small, Patricia A Cassano
1Weill Cornell Medical College, 525 East 68th Street, Baker Pavilion 20th Floor, NY 10021, USA.
Aims:
To provide evidence on the comparative effectiveness of oral diabetes drug combinations.
Methods:
We performed a retrospective, observational cohort study of glycosylated hemoglobin change in outpatients newly exposed to dual- or triple-drug oral diabetes treatment.
Results:
Adjusted response to a second drug added to metformin ranged from 0.85 to 1.21% glycosylated hemoglobin decline. Response to a third drug was smaller (0.53-0.91%). Higher baseline glycosylated hemoglobin was associated with larger response; sulfonylurea effectiveness declined over time; and thiazolidinediones were more effective in obese patients and women.
Conclusion:
Observational data provide results qualitatively consistent with the limited available randomized data on diabetes drug effectiveness, and extend these findings into common clinical scenarios where randomized data are unavailable. Sex and BMI influence the comparative effectiveness of diabetes drug combinations.
Insights
Adding a second or third oral diabetes medication to metformin can lower glycosylated hemoglobin. Effectiveness varies by drug combination, baseline levels, and patient factors like sex and BMI.
Area of Science:
- Endocrinology
- Pharmacology
- Clinical Medicine
Background:
- Type 2 diabetes management often involves combination oral pharmacotherapy.
- Evidence on the comparative effectiveness of these combinations is crucial for optimizing treatment strategies.
Purpose of the Study:
- To evaluate the comparative effectiveness of dual- and triple-drug oral diabetes treatment regimens.
- To assess factors influencing treatment response in a real-world clinical setting.
Main Methods:
- Retrospective observational cohort study design.
- Analysis of glycosylated hemoglobin (HbA1c) change in outpatients.
- Inclusion of patients initiating dual- or triple-drug oral diabetes therapy.
Main Results:
- Adding a second drug to metformin resulted in an adjusted HbA1c decline of 0.85% to 1.21%.
- Adding a third drug yielded a smaller HbA1c decline of 0.53% to 0.91%.
- Higher baseline HbA1c, sulfonylurea effectiveness over time, and differential effectiveness of thiazolidinediones in specific patient subgroups (obese, women) were observed.
Conclusions:
- Observational data align with existing randomized trial findings on oral diabetes drug effectiveness.
- These findings extend evidence to clinical scenarios lacking randomized data.
- Patient sex and body mass index (BMI) significantly impact the comparative effectiveness of oral diabetes drug combinations.
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