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العنوان
Impact of DApagliflozin on Cardiac Function following Anterior Myocardial Infarction in Non-Diabetic Patients – DACAMI/
الناشر
Ain Shams University.
المؤلف
Younis,Omar Hassan Ali .
هيئة الاعداد
باحث / عمر حسن على يونس
مشرف / محمد خيري عبد الدايم
مشرف / باسم الظريف
مشرف / أحمد عبد السلام
مشرف / سامح عطية
تاريخ النشر
2022
عدد الصفحات
138.p;
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
أمراض القلب والطب القلب والأوعية الدموية
تاريخ الإجازة
1/1/2022
مكان الإجازة
جامعة عين شمس - كلية الطب - Cardiovascular Medicine
الفهرس
Only 14 pages are availabe for public view

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Abstract

Background: This study aims at identifying if there is a role for Sodium glucose co-transporter 2 inhibitors (SGLT2i) in the event of acute myocardial infarction. Patients who presented with anterior ST- elevation myocardial infarction (STEMI) & had undergone successful primary percutaneous coronary intervention for the left anterior descending coronary were randomized into a study group & a control group. The study group received dapagliflozin 10 mg once daily. The primary endpoint was cardiac function assessed by both; a biomarker (i.e.: N-terminal pro-Brain Natriuretic Peptide – NT-proBNP) measured at baseline & at 12 weeks post the cardiac event & echocardiographic parameters (left ventricular ejection fraction, left ventricular diastolic dimension & left ventricular mass index) assessed at baseline, 4-weeks & 12-weeks post the cardiac event.
Results: from October 2021 to April 2022, a final 100 patients were randomized. The median DROP of NT- proBNP in the study group was significant compared to the control group (p-value 0.043). In addition, the decrease in the left ventricular mass index (LV mass index) was also significant in the study group compared to the control group.
Conclusions: Dapagliflozin seems to have a role in preventing left ventricular dysfunction & maintaining cardiac function following anterior ST-elevation myocardial infarction. More Large-scale trials need to be done to further confirm these findings.
This trial is registered retrospectively at the US National Institutes of Health (ClinicalTrial.gov) with identifier number: NCT05424315 – June 16th, 2022. (https://ClinicalTrials.gov/ct2/show/nct05424315)