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Metabolic control in type 2 diabetic patients treated with empagliflozin: A case series
Wilfredo Navarrete1, Pilar Durruty2, Eileen Andrade1
1Consultorio Adosado de Especialidades, Hospital Peñaflor, Peñaflor, Chile.
Background:
Type 2 diabetes mellitus is a highly prevalent disease and is associated with increased morbidity and mortality. Due to the low percentage of adequate glycemic control, new strategies for the treatment of type 2 diabetes mellitus have been sought, including sodium-glucose cotransporter type 2 inhibitorss.
Objective:
To describe the evolution of patients with type 2 diabetes mellitus with insulin requirements treated with empagliflozin at the Peñaflor Hospital. The primary objective was to evaluate the efficacy of the medication regarding glycosylated hemoglobin A1c (HbA1c). The secondary objectives were: 1) achievement of HbA1c equal to or less than 7.5% according to survival analysis. 2) Change in glomerular filtration rate and urinary albumin excretion post treatment.
Methods:
Review of clinical records of all patients treated with empagliflozin from November 2019 to June 2023. Average follow-up of 19 (16.3 to 40) months. To compare HbA1c values according to follow-up ranges, the paired T test or Wilcoxon test was used.
Results:
We included 58 patients, 15 men and 43 women (74.1%), with an average age of 58.5 ± 9.2 years, ranging from 35 to 75 years. Baseline HbA1c of 10.3 ± 1.6% and 8.98% ± 2.2 in a follow-up of 18 to 24 months post-treatment, resulted in a decrease of 1.27% (p = 0.002; confidence interval 95%: 0.5 to 2.03). The most common adverse effect was urinary tract infection.
Conclusions:
Patients with type 2 diabetes mellitus with insulin requirements treated with empagliflozin at the Peñaflor Hospital achieved better glycemic control with few adverse effects.
Insights
Empagliflozin effectively improved glycemic control in type 2 diabetes mellitus patients requiring insulin. This sodium-glucose cotransporter type 2 inhibitor showed significant HbA1c reduction with a manageable safety profile.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Pharmacology
Background:
- Type 2 diabetes mellitus (T2DM) is a widespread condition linked to significant morbidity and mortality.
- Inadequate glycemic control remains a challenge in T2DM management.
- Sodium-glucose cotransporter type 2 inhibitors (SGLT2is) represent a novel therapeutic strategy for T2DM.
Purpose of the Study:
- To evaluate the efficacy of empagliflozin in T2DM patients with insulin requirements at Peñaflor Hospital.
- Primary objective: assess the impact of empagliflozin on glycosylated hemoglobin A1c (HbA1c).
- Secondary objectives: analyze HbA1c achievement below 7.5%, changes in glomerular filtration rate, and urinary albumin excretion.
Main Methods:
- Retrospective review of clinical records for patients treated with empagliflozin from November 2019 to June 2023.
- Average patient follow-up duration of 19 months (range: 16.3-40 months).
- Statistical analysis included paired t-tests or Wilcoxon tests to compare HbA1c values across follow-up periods.
Main Results:
- The study included 58 patients (15 men, 43 women) with an average age of 58.5 years.
- Baseline HbA1c of 10.3% decreased to 8.98% at 18-24 months follow-up, a significant reduction of 1.27% (p=0.002).
- Urinary tract infection was the most frequently reported adverse effect.
Conclusions:
- Empagliflozin demonstrated effectiveness in improving glycemic control for T2DM patients on insulin therapy.
- The treatment was associated with a notable reduction in HbA1c levels.
- Empagliflozin exhibited a favorable safety profile with minimal adverse events.
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