Acute Heart Failure (AHF), Acute Myocardial Infarction (AMI), Heart Failure
Conditions
Keywords
Vericiguat, Guideline-Directed Medical Therapy, Heart Failure, Acute myocardial infarction
Brief summary
Heart failure (HF) is a severe cardiovascular disease with extremely high morbidity and mortality rates worldwide, and ischemic cardiomyopathy is an important cause of heart failure. Vericiguat is a soluble guanylate cyclase stimulator which has been verified to improve the cardiovascular outcomes in heart failure patients. The VICTORIA trial excluded patients with acute coronary syndrome in 3 months prior to the study start, so it is still unclear about the efficacy and safety of vericiguat in heart failure after acute myocardial infarction. So we conducted this multi-center, prospective, cohort study to estimate the efficacy and safety of vericiguat in HF patients after acute myocardial infarction.
Detailed description
Heart failure (HF) is a severe cardiovascular disease with extremely high morbidity and mortality rates worldwide, and ischemic cardiomyopathy is an important cause of heart failure. According to different studies, acute heart failure occurs in-hospital in about 14-36% of patients after acute myocardial infarction (AMI)1 and the presence of HF on admission or the occurrence of HF during hospitalization in patients with AMI are strong risk factors for poor prognosis. The incidence of HF in AMI varies according to population differences. For example, in patients with STEMI, the incidence of acute heart failure is relatively high because of the greater extent of the infarction and the longer duration of coronary occlusion, whereas patients with NSTEMI, although at lower risk of developing heart failure in the acute phase, have an increased risk of developing chronic heart failure in the long term. Advanced age, previous history of heart failure, chronic kidney disease, multibranch vasculopathy, and delayed opening of the infarct-related artery are major risk factors. In addition, comorbidities such as diabetes and hypertension increase the risk of developing heart failure. The goals of treatment for HF after AMI are to improve cardiac function, reduce symptoms, and prevent further myocardial injury. Basic therapy consists of prompt opening of the infarct-related artery (e.g., percutaneous coronary intervention) and the administration of optimized pharmacological treatments such as antiplatelets, beta-blockers, ACEI/ARBs and aldosterone antagonists. In the acute phase, diuretics and positive inotropic agents may be used to relieve severe symptoms. Besides, other HF medication such as SGLT2i are effective in patients with heart failure whether or not it is caused by ischemia. Vericiguat is a soluble guanylate cyclase stimulator which has been verified to improve the cardiovascular outcomes in heart failure patients. The VICTORIA trial excluded patients with acute coronary syndrome in 3 months prior to the study start, so it is still unclear about the efficacy and safety of vericiguat in heart failure after acute myocardial infarction. The VIC-MI trial is a multi-center, prospective, open-label cohort study to estimate the efficacy and safety of vericiguat in HF patients after acute myocardial infarction.
Interventions
DRUGVericiguat
Patients enrolled in the experimental group will receive 26 weeks of oral vericiguat on top of the standard treatment, with vericiguat at a dose of 2.5 mg once a day, doubled every fortnight to a maximum dose of 10 mg once a day at the end of week 6 of the visit, which will be maintained for the duration of the treatment.
Sponsors
The Second Affiliated Hospital of Chongqing Medical University
The First Affiliated Hospital of Chongqing Medical Universty
Dongying Zhang
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
The sonographer who interpreted the report, statistician and the investigating physician who completed the 6-minute walk test could not be aware of the grouping of the patients
Intervention model description
This study is a multicenter, prospective, randomized controlled trial in which patients will be randomized into either the experimental or control group by uniform stratification from the main centre.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 18 years old * Undertaking revascularization for criminal coronary artery during hospitalization * Acute heart failure occurs within 14 days in hospital after STEMI or NSTEMI, meeting all of the following criteria: typical symptoms or signs of heart failure; Treatment with oral or intravenous diuretics is required; LVEF measured by echocardiography is ≤ 45%; Elevated levels of NT proBNP in patients with sinus rhythm ≥ 1000pg/ml and atrial fibrillation/flutter ≥ 1600pg/ml * eGFR ≥ 15 ml/min/1.73m2 * Informed consent has to be given in written form
Exclusion criteria
* Plan to undergo staged revascularization or if the criminal coronary artery has not been successfully opened * Severe and uncontrolled lung diseases, such as newly developed pulmonary embolism, primary pulmonary hypertension, acute exacerbation of COPD, etc * Severe liver and kidney dysfunction, Child Pugh grade C or eGFR \< 15ml/min/1.73m2 * Allergies to ACEI, ARB, ARNI, beta blockers, SGLT2i, MRA, Vericiguat, and other medications * Symptomatic hypotension or systolic blood pressure less than 90mmHg after discontinuing intravenous medication * Women in the perinatal period or those planning to conceive * Patients planning to undergo elective surgical treatment or tumor chemotherapy * Diagnosed as Takotsubo cardiomyopathy or nonobstructive acute myocardial infarction (MINOCA) * Previous diagnosis of cardiomyopathy, including but not limited to dilated cardiomyopathy, hypertrophic cardiomyopathy, etc. * Autoimmune disease or infectious diseases with typical cardiovascular damage, such as syphilis, systemic lupus erythematosus, etc. * Diagnosed with severe heart valve disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Serum NT-proBNP Level | Up to 24 weeks | The primary endpoint of the study is NT-proBNP at the baseline & at the completion of the 24 week intervention |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| NYHA functional class | Up to 24 weeks | NYHA functional class at the baseline & at the completion of the 24 week intervention |
| Worsening heart failure event | Up to 24 weeks | Time to first worsening heart failure event in 24 weeks after randomization |
| 6-minute walk distance | Up to 24 weeks | 6-minute walk distance at the baseline & at the completion of the 24 week intervention |
| Left ventricular end-diastolic diameter | Up to 24 weeks | LVEDD measured by echocardiography at the baseline & at the completion of the 24 week intervention |
| Left ventricular global longitudinal strain | Up to 24 weeks | GLS measured by echocardiography at the baseline & at the completion of the 24 week intervention |
| Left ventricular ejection fraction | Up to 24 weeks | LVEF measured by echocardiography at the baseline & at the completion of the 24 weeks intervention |
Countries
China
Contacts
Primary ContactDongying Zhang, Professor
Backup ContactJunlong Chen, M.D.
Outcome results
None listed