Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients

Overview

General objective: To compare the efficacy and safety of primary angioplasty(PA) with that of thrombolytic therapy (TT) for the treatment of AMI in patients \>=75 years old with ST-segment elevation or LBBB AMI \<6 hours of evolution without contraindications for TT. Hypothesis: The therapeutical strategy based on PA is superior to that based initially on TT in patients \>=75 years old with AMI. Participating Centers: 27 Spanish hospitals performing \>50 PA/year. Primary Endpoint (PE): Incidence of the aggregate of death of any cause, reinfarction or disabling stroke at 30 days. There are also 7 secondary endpoints (SE). Procedure: Diagnosis of inclusion/exclusion criteria --\> Centralized randomization --\> Treatment allocation to 1) TT with weight adjusted TNK + unfractionated heparin or 2) PA within 120 minutes. Estimated Sample size and recruitment time: 570 patients in 19 months. Follow-up: Blinded evaluation of events (PROBE regulations) specified in PE and SE at 30 days and 12 months. Quality control: 100% variable and follow-up review by external CRO. Safety Committee and Event Adjudication Committee formed by experts not participating in the study.

Hypothesis of the study. In patients of 75 or more years of age with AMI and ST-elevation or LBBB, the treatment strategy based on primary angioplasty is superior to the treatment strategy based on initial fibrinolytic therapy for reducing the incidence of death, re-infarction and disabling CVA at 30 days. This benefit is maintained at 12 months. Objectives General objective of the study. To compare the efficacy and safety of primary angioplasty and fibrinolytic treatment in \>=75 year-old patients with AMI eligible for fibrinolytic therapy in Spanish medical centers with an active program of primary angioplasty. Primary end point: Incidence of the combined end point of all-cause death, re-infartion or disabling stroke at 30 days Secondary end points: * All-cause death at 30 days * Incidence of the combined end point of all-cause death, disabling CVA or de novo heart failure at 30 days * Incidence of recurrent ischemia requiring emergency catheterization in the first 30 days * Cause of death at 30 days classified in three groups: 1. Shock or heart (pump) failure 2. Mechanical complications (ruptures) or electromechanical dissociation 3. Other causes (including bleeding) * Incidence of major bleeding during hospital admission * All-cause mortality at 12 months * Period of time elapsed until presentation of any of the composite of all-cause death, reinfarction or disabling CVA at 12 months * Period of time elapsed until the presentation of any composite of all-cause death, reinfarction, disabling CVA or non-elective hospital readmission for cardiac causes (unstable angina, heart failure, non-elective coronary revascularization at 12 months. TYPE AND DESIGN OF THE CLINICAL TRIAL Clinical trial status Phase IV trial Description of randomization process The treatment strategy will be determined by a centralized randomization process, using a telephone system. Eligible patients will be randomized to one of two (2) treatment arms: fibrinolytic treatment or primary angioplasty. Control and design This is a randomized multicenter, open blind clinical trial designed to compare the efficacy and safety of primary angioplasty vs. thrombolytic treatment in \>=75 year-old patients with AMI and ST-elevation or de novo LBBB, eligible for thrombolysis, admitted at Spanish medical centers that have an active primary angioplasty program, within the first 6 hours after symptom onset. Masking techniques Being an open trial there are not masking techniques, nor will there be an emergency opening procedure of emergency codes. Pre-inclusion / clearance period Not applicable SUBJECT SELECTION Inclusion / exclusion criteria Subjects must be \>=75 years of age with AMI and ST-elevation or de novo LBBB, eligible for thrombolytic therapy, admitted in any Spanish medical center in which there is an active primary angioplasty program within the first 6 hours after symptom onset. Each patient must fulfill all inclusion criteria and none of the exclusion criteria. Inclusion criteria: 1. Subjects of 75 or more years of age 2. Diagnosis of AMI: chest pain or any symptom of myocardial ischemia of, at least, 20 minutes of duration, not responding to nitrate therapy, an evolution period of less than 6 hours after symptom onset until randomization process, and, at least, one of the following alterations: 1. ST-elevation \>=2 mm in 2 or more precordial leads 2. ST-elevation \>=1 mm in 2 or more anterior leads 3. Complete de novo (or probably de novo) left bundle branch block (LBBB) 3. Subject should be able to give informed consent prior to randomization process and should agree to fulfill all procedures described in the protocol, including follow-up after hospital discharge. A written consent signed by a close relative with witness is also acceptable. Exclusion criteria: 1. Documented contraindication to the use of fibrinolytics. 1.1. Internal active bleeding or known history of hemorrhagic diathesis 1.2. History of previous CVA of any kind or at any time 1.3. Intracranial tumor, arteriovenous malformation, aneurysm or cerebral aneurysm repair 1.4. Major surgery, parenchymal biopsy, ocular surgery or severe traumatism in the 6 weeks prior to randomization 1.5. Unexplained puncture in a non-compressible vascular location in the last 24 hours prior to randomization 1.6. Confirmed arterial hypertension with a reliable measurement of systolic AP \>180 mmHg or diastolic AP \>110 mmHg 1.7. Known thrombocytopenia \< 100.000 platelets/mL 1.8. Prolonged (\>20 minutes) or traumatic cardiopulmonar resuscitation (CPR) in the 2 weeks prior to randomization 1.9. History or signs suggesting aortic dissection 2. Cardiogenic shock 3. Estimated door-to-needle time \>120 minutes 4. Administration of fibrinolysis in the 14 days prior to randomization 5. Administration of any glycoprotein IIa/IIIb inhibitor in the 24 hours prior to randomization 6. Administration of any Low Molecular Weight Heparin (LMWH) in the 8 hours prior to randomization 7. Actual oral anticoagulant treatment 8. Suspected AMI secondary to occlusion of one lesion treated previously with a percutaneous coronary intervention (within the previous 30 days for angioplasty or conventional stent and within the previous 12 months for coated stents) 9. Dementia or acute confusional state at the time of randomization 10. Subject incapacity or unwillingness to give informed consent -at least, verbally 11. Known renal failure (basal creatinine\> 2,5 mg/dl) 12. Reduced life expectancy (\<12 months) due to advanced or terminal concomitant condition 13. Subject participation in another clinical trial (assessing a drug or a device) in the 30 days prior to randomization Diagnostic criteria for the pathologies of the study Patients with a diagnosis of AMI presenting with: * Chest pain or any symptom of myocardial ischemia of, at least, 20 minutes of duration, not responding to nitrate therapy and an evolution period of less than 6 hours after symptom onset until randomization process, with, at least, one of the following alterations: * ST-elevation \>=2 mm in 2 or more precordial leads * ST-elevation \>=1 mm in 2 or more anterior leads * Complete de novo (or probably de novo) left bundle branch block (LBBB) Estimate of sample size For the following conditions: α = 0.05 (2 tailed), power: 80% (β = 0.20) and assuming a composite event incidence rate (death, reinfarction and disabling CVA) based on previous registries (21.7% in the fibrinolysis group and 12.8% in the PA group), a sample size of 282 patients per group is needed to demonstrate that difference (8.9% in absolute terms and 40% in relative terms). Assuming a loss to follow-up rate of 1%, the total number is 570 patients Estimated loss of patients prior to randomization During a period of 3 months all patients meeting inclusion criteria who, for any reason, are not enrolled in the study will be included in a registry with an abbreviated CRF recording inclusion/exclusion criteria, the reason for non-enrollment and follow-up at 30 days and 12 months.