Heart Failure
Conditions
Keywords
heart failure, prognosis, clinical characteristics
Brief summary
The Contemporary Modalities In Treatment of Heart Failure Registry (COMMIT-HF) is an observational study on an all-comer systolic heart failure population hospitalized in a highly specialized cardiovascular center. The aim of the study is to assess the clinical characteristics, treatment modalities and prognosis in this population.
Detailed description
The Contemporary Modalities In Treatment of Heart Failure Registry (COMMIT-HF) is a single-center observational study that is underway in the 3rd Chair and Department of Cardiology of Silesian Center for Heart Diseases in Zabrze, Poland. Data collection is patient-based (not event-based). The main objective of the COMMIT-HF Registry is to clarify the overall clinical characteristics of systolic heart failure patients, their demographics and clinical profile, current management, in-hospital outcomes and long-term follow-up, with regard to the administered treatment. The study population is formed by all-comer patients hospitalized in cardiology wards and intensive cardiac care units with a diagnosis of systolic heart failure. For the purpose of this study heart failure is defined as a set of symptoms resulting from myocardial systolic function impairment, confirmed in resting transthoracic echocardiography with left ventricular ejection fraction (LVEF) ≤35%. Patients with acute coronary syndromes are excluded from the analysis. Complete patient demographics; medical history, complete hospitalization data (diagnostic and therapeutic) and in-hospital results are collected in an electronic form by the attending physician. The patients are under constant follow-up for all cause mortality and major adverse events.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* symptom based diagnosis of heart failure * echocardiographically confirmed impaired left ventricular ejection fraction ≤35%.
Exclusion criteria
* acute coronary syndrome on admission * ≥ 18 years old
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of participants with reported deaths from any cause | From date of inclusion until the date of death from any cause, assessed up to 1 year |
Secondary
| Measure | Time frame |
|---|---|
| Number of participants with reported cerebrovascular insult | From date of inclusion until the date of first event, assessed up to 1 year |
| Number of participants to undergo mechanical circulatory support implantation | From date of inclusion until the date implantation, assessed up to 1 year |
| Number of participants with reported heart-failure related rehospitalization | From date of inclusion until the date of first event, assessed up to 1 year |
| Number of participants with reported myocardial infarction | From date of inclusion until the date of first event, assessed up to 1 year |
| Number of participants to undergo orthotopic heart transplantation | From date of inclusion until the date transplantation, assessed up to 1 year |
Countries
Poland