Study on Frailty and Outcomes in Older Adults Undergoing Treatment for Coronary Artery Disease
Led by Medical University of Silesia · Updated on 2023-04-12
1000
Participants Needed
1
Research Sites
156 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are investigating how frailty affects the immediate and long-term outcomes of invasive treatments for coronary artery disease in older adults aged 65 and above. The study aims to validate the Fried frailty scale and the instrumental activities of daily living IADL scale as tools to predict patient outcomes. This research focuses on patients admitted with stable, unstable, or acute coronary syndromes to better understand the role of frailty in their care.
Participants include those with stable angina, unstable angina, non-ST elevation myocardial infarction NSTEMI, and ST elevation myocardial infarction STEMI. Based on coronary angiography results, a heart team decides the best treatment approach, which may be medical management, percutaneous angioplasty, or bypass grafting. Most STEMI patients receive primary percutaneous coronary intervention. The study observes treatments during hospital admission and treatment decisions by the heart team.
During the hospital stay, frailty is assessed using the Fried phenotype and IADL scales before discharge, typically around day 4. Researchers track results of the invasive treatments and any complications such as heart attacks during procedures, kidney injury from contrast dye, and bleeding. Long-term outcomes including mortality, stroke, heart failure, reintervention, and hospital readmission are monitored for up to three years. This study aims to help personalize risk assessment and improve care for frail elderly patients with coronary artery disease.
CONDITIONS
Brief Title
Frailty Syndrome in Daily Practice of Interventional Cardiology Ward
Research Team
A
Andrzej R Tomasik, M.D. Ph.D., FESC
E
Ewa Nowalany-Kozielska, Prof.
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Symptomatic coronary artery disease including stable angina, unstable angina, NSTEMI, or STEMI
Able to provide written, informed consent
You will not qualify if you...
Lack of consent to participate in the study
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Diagnostic Evaluation
Duration - Up to hospital discharge, on average 4 days
Participants undergo coronary angiography to evaluate their coronary artery disease and determine appropriate treatment.
1 hospital stay with assessments
Long-term Monitoring
Duration - Up to 36 months
Participants are monitored for major cardiovascular events following their interventional treatment or medical management.
Periodic follow-up visits over 36 months
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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Published Research Related To This Trial
Frailty syndrome in daily practice of interventional cardiology ward-rationale and design of the FRAPICA trial: A STROBE-compliant prospective observational study.
Ewa Wołoszyn-Horák, Robert Salamon, Katarzyna Chojnacka...