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Journal of Chinese Pharmaceutical Sciences ›› 2025, Vol. 34 ›› Issue (11): 1024-1032.DOI: 10.5246/jcps.2025.11.076

• Original articles • Previous Articles     Next Articles

Efficacy and safety of empagliflozin in patients with type 2 diabetes mellitus and concurrent heart failure

Ying Wang*(), Huan Yu, Tingting Yan, Wenfei Pan   

  1. Department of Pharmacy, Fuwai Hospital, Chinese Academy of Medical Sciences, Beijing 100037, China
  • Received:2025-08-15 Revised:2025-09-20 Accepted:2025-10-08 Online:2025-12-02 Published:2025-12-02
  • Contact: Ying Wang
  • Supported by:
    Fund of the "Special Project on Diabetes Prevention, Treatment and Management Research" of the Beijing Chronic Disease Prevention and Health Education Research Association (Grant No. MBZX0042023004).

Abstract:

This study focused on a specific cohort of patients with type 2 diabetes mellitus (T2DM) complicated by heart failure (HF), aiming to evaluate the differences in treatment efficacy and safety between the original research formulation and the centralized procurement version of empagliflozin. Conducted as a retrospective study, 406 hospitalized patients with T2DM and HF admitted to our hospital between June 2022 and June 2023 were recruited and divided into two groups: a control group and an observation group, based on the type of empagliflozin administered. Through the application of rigorous statistical methodologies, comprehensive data collection, systematic organization, and detailed analysis were performed for both groups. The findings revealed that, following treatment with the two types of empagliflozin, a significant difference was observed in creatinine clearance rate between the groups. However, no statistically significant changes were detected in other critical efficacy indicators, including fasting blood glucose, glycated hemoglobin, N-terminal pro-B-type natriuretic peptide (NT-proBNP), left ventricular ejection fraction (LVEF), and glomerular filtration rate (GFR), before and after treatment. From an economic perspective, the observation group demonstrated a clear cost advantage, with both total drug expenditures and the specific cost of empagliflozin being significantly lower than those in the control group. In conclusion, for patients with T2DM and HF, the centralized procurement version of empagliflozin offered comparable efficacy and safety to the original research formulation, with the exception of differences in creatinine clearance rate. The significant cost advantage of the centralized procurement version highlighted its value in clinical drug selection and hospital pharmacy management. These findings underscored the importance of considering both clinical outcomes and economic factors in optimizing treatment strategies for real-world practice.

Key words: Type 2 diabetes mellitus, Heart failure, Empagliflozin, Efficacy, Safety

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