Efficacy and safety of add-on dapagliflozin therapy in patients with type 2 diabetes
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Abstract
Objective: To evaluate the efficacy and safety of add-on dapagliflozin 10mg in type 2 diabetes. Subject and method: A cross-sectional study, follow-up for 12 weeks, comparing before and after treatment on 124 patients with type 2 diabetes, outpatient treatment at 108 Military Central Hospital from 12/2021 to 4/2022, with HbA1c level 7%-10%, on at least 1 OAD previous, supplemented with dapagliflozin 10mg. All patients were clinically examined and tested at the time of drug supplementation and after 12 weeks. Result: After 12 weeks of additional treatment: HbA1c by -0.54% (95% confidence interval [CI]: -0.64, -0.44, p<0.001), FPG was -1.12mmol/l (CI 95%: -0.77, -1.44; p<0.001) body weight was -1.0kg (CI 95%: -1.35, -0.69, p<0.001)), and systolic/diastolic blood pressure by -3.6/-1.4mmHg. The proportion of patients achieving HbA1c < 7% target was 13.7%, the proportion of patients who were poorly controlled (HbA1c > 8%) decreased from 62.1% at baseline to 33.1% at 3 months, 62.3% of patients showed simultaneous reductions in HbA1c and body weight. Adverse events: 6.5% patients had mild symptoms of hypoglycemia, mainly in patients taking > 3 hypoglycemic drugs, 6.5% had genital tract infection, twice as many women as men, 8.1% had urinary tract infections. Diabetic ketoacidosis, hyperosmolarity, or amputation did not occur during the treatment period. Conclusion: Add-on therapy with dapagliflozin 10mg significantly improves glycemic control, body weight and blood pressure in patients with type 2 diabetes.
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References
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