Frailty Syndrome in Daily Practice of Interventional Cardiology Ward

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The impact of frailty on immediate and long term outcomes of invasive treatment of coronary artery disease is not fully characterized. The assessment of frailty may help physicians in the selection of best treatment option and in the timing and modality of the follow-up. The FRAilty syndrome in daily Practice of Interventional CArdiology ward (FRAPICA) study is designed with the aim to validate the use of the Fried frailty scale and instrumental activities of daily living scale (IADL) as prognostic tools in patients admitted to hospital for symptomatic coronary artery disease, either stable, unstable, or acute coronary syndrome (ACS). The FRAPICA study is a single center prospective study enrolling patients aged ≥65 years. The aims are (1) to describe Fried frailty scale and IADL scale distribution before hospital discharge and (2) to investigate the prognostic role of Fried frailty and IADL scores. The outcomes are: (1) results of invasive treatment, (2) its complications (periinterventional MI, contrast-induced nephropathy, blood loss), (3) three-year all-cause mortality, cardiovascular mortality, stroke, myocardial infarction, reintervention, heart failure, hospital readmission for any cause, and a composite of the above mentioned. Ancillary analyses will be focused on different clinical presentations, different tools to assess frailty and risk stratification. The FRAPICA program will fill critical gaps in the understanding of the relation between frailty, cardiovascular disease, interventional procedures and outcome. It will enable more personalized risk assessment and identification of new targets for interventions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 65
Healthy Volunteers: f
View:

• aged ≥ 65

• symptomatic coronary artery disease A) stable B) unstable C) NSTEMI D) STEMI

• written, informed consent

Locations
Other Locations
Poland
II Dept. of Cardiology in Zabrze Medical University of Silesia
RECRUITING
Zabrze
Contact Information
Primary
Andrzej R Tomasik, M.D. Ph.D., FESC
tomasik@poczta.onet.pl
0048323732372
Backup
Ewa Nowalany-Kozielska, Prof.
kl2karz@sum.edu.pl
0048323732372
Time Frame
Start Date: 2017-05-17
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 1000
Treatments
Stable coronary artery disease
Patients with stable effort angina wil be enrolled. Based on coronary angiography, heart team will decide on medical, percutaneous angioplasty, or bypass grafting.
Unstable coronary artery disease
Patients with unstable angina wil be enrolled. Based on coronary angiography, heart team will decide on medical, percutaneous angioplasty, or bypass grafting.
Non-ST elevation myocardial infarction
Patients with non-ST elevation myocardial infarction wil be enrolled. Based on coronary angiography, heart team will decide on medical, percutaneous angioplasty, or bypass grafting.
ST-elevation myocardial infarction
Patients with ST elevation myocardial infarction wil be enrolled. In majority of patients primary percutaneous coronary intervention will be performed. Based on coronary angiography, heart team will decide on further medical treatment, percutaneous angioplasty, or bypass grafting.
Sponsors
Leads: Medical University of Silesia

This content was sourced from clinicaltrials.gov