Coronary Artery Disease, Stable Angina
Conditions
Brief summary
The Prospective REgistry of Stable Angina manaGEment and Treatment (PRESAGE) is an observational study on an all-comer stable angina population hospitalised in a highly specialized cardiovascular centre with cardiac surgery facilities. The aim of the study is to assess the clinical characteristics, treatment modalities, early and long-term outcomes in this population.
Detailed description
The Prospective REgistry of Stable Angina manaGEment and Treatment (PRESAGE) is a single-center, observational study recruiting consecutive patients with stable angina, who were diagnosed and treated in the 3rd Chair and Department of Cardiology in the Silesian Centre for Heart Diseases in Zabrze, Poland. The Silesian Centre for Heart Diseases is a highly specialised cardiology centre with cardiac surgery facilities The main objective of the PRESAGE Registry is to clarify the overall clinical characteristics of patients with stable angina, their demographics and clinical profile, current management, early and long-term outcomes, with regard to the administered treatment. The diagnosis of stable angina was based on clinical characterization, coronary angiography, and the current guidelines of the European Society of Cardiology. Patients with vasospastic and/or microvascular angina were also included to the registry. Performance of coronary angiography is the criterion of the enrolment in the registry. Patients with acute coronary syndromes are excluded from the analysis. Data collection is patient-based (not event-based). 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 cardiac adverse events.
Interventions
None listed
Sponsors
Silesian Centre for Heart Diseases
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
* symptom based diagnosis of stable angina
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 5 year |
Secondary
| Measure | Time frame |
|---|---|
| Number of participants with reported myocardial infarction | From date of inclusion until the date of first event, assessed up to 5 year |
| Number of participants with reported cerebrovascular insult | From date of inclusion until the date of first event, assessed up to 5 year |
| Number of participants with reported acute coronary syndrome driven revascularisation | From date of inclusion until the date of first event, assessed up to 5 year |
Countries
Poland
Contacts
Primary ContactPiotr Desperak, MD
Outcome results
None listed