This study is to provide the effectiveness and safety evidence in patients with heart failure of reduced ejection fraction (HFrEF) initiating Jardiance in real clinical practice in a larger Chinese population. The primary objective is to compare the risk of the composite outcome of cardiovascular (CV) death or hospitalisation for heart failure (HHF) in heart failure with reduced ejection fraction (HFrEF) patients initiating Jardiance with propensity score (PS) matched HFrEF patients initiating guideline-recommended non-sodium-glucose cotransporter-2 inhibitors (SGLT2i) medications (angiotensin-converting-enzyme inhibitors (ACEi)/angiotensin II receptor blocker (ARB)/angiotensin receptor-neprilysin inhibitor (ARNI), betablockers, and mineralocorticoid receptor antagonist (MRA)) in China, measured by the hazard ratio of the two groups.
Study Type
OBSERVATIONAL
Enrollment
5,000
Jardiance
non-SGLT2 inhibitors
Fuwai Hospital; National Center for Cardiovascular Diseases
Beijing, China
Time from the index date to the first hospitalisation for heart failure (HHF) or cardiovascular (CV) death
Time frame: From the index date to the end date of each individual's follow-up, up to 3 years
Time from the index date to cardiovascular (CV) death
Time frame: From the index date to the end date of each individual's follow-up, up to 3 years
Time from the index date to the first hospitalisation for heart failure (HHF)
Time frame: From the index date to the end date of each individual's follow-up, up to 3 years
Total number of HHFs at 30 days after the index date
Time frame: At 30 days after the index date
Total number of HHFs at 90 days after the index date
Time frame: At 90 days after the index date
Total number of HHFs at 1 year after the index date
Time frame: At 1 year after the index date
Time from the index date to all-cause death
Time frame: From the index date to the end date of each individual's follow-up, up to 3 years
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