About this trial
Studying the incremental role of frailty in predicting in-hospital, short-term (30 days), and mid-term (6 months) bleeding in ACS patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
- Patients must be suffering from acute coronary syndrome ( STEMI - NSTEMI ) at the time of recruitment
- Patients must be older than 65 years
Disqualifiers
- Patients younger than 65 years
- Refusal of participation
- In - hospital death unrelated to bleeding
Trial population
Patients presenting with acute coronary syndrome ( STEMI and NSTEMI) and are older than 65 years
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Bleeding Academic Research Consortium ( BARC ) type 3 to 5
Type 3: Major bleeding (with subtypes) 3a: Overt bleeding plus hemoglobin drop of 3-5 g/dL, or Transfusion with ≤2 units of blood. 3b: Hemoglobin drop ≥5 g/dL, Cardiac tamponade, Bleeding requiring surgical intervention, or Bleeding requiring intravenous vasoactive agents. 3c: Intracranial hemorrhage (excluding microbleeds), Intraocular bleeding compromising vision. Type 4: CABG-related bleeding Perioperative bleeding within 48 hours of coronary artery bypass grafting (CABG) and Reoperation for bleeding, ≥5 units of blood transfused, Chest tube output ≥2 L in 24 hours, or Cardiac tamponade. Type 5: Fatal bleeding 5a: Probable fatal bleeding (no autopsy or imaging confirmation). 5b: Definite fatal bleeding (confirmed by autopsy or imaging)
Secondary outcomes
Bleeding Academic Research Consortium ( BARC ) type 0, 1 or 2
Type 0 : no bleeding Type 1: Bleeding that is not actionable and does not require medical attention Type 2 : Any bleeding that requires medical attention, hospitalization, or evaluation by a health care professional. but does not meet criteria for type 3, 4 or 5.
Locations
Sponsors and contacts
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