Pharmacological treatment during AMI and in secondary prevention: the scientific evidence
| STUDIES | DRUG | No. PATIENTS | FOLLOW-UP | VAR. | P |
|---|---|---|---|---|---|
| During infarction | |||||
| ISIS-2 (1988) [45] | ASPIRIN 160 mg | 17,187 | 15 MONTHS | - 19% | < 0.001 |
| APRICOT (1991) [61] | ASPIRIN 325 mg | 300 | 3 MONTHS | -- | NS |
| After infarction | |||||
| AMIS (1980) [6] | ASPIRIN 1000 mg | 4,524 | 3 YEARS | + 11% | 0.02 |
| PARIS I (1980) [72] | ASA 325mg /ASA + DIPYRIDAMOLE | 2,026 | 3 YEARS | - 12% | NS |
| PARIS II (1986) [53] | ASPIRIN 325mg + DIPYRIDAMOLE | 3,128 | 23 MONTHS | - 2% | NS |
| CAPRIE (1996) [28] | CLOPIDOGREL 75 mg vs ASA 325 mg | 6,302 | 1.91 YEARS | +3.7% | NS |
| META-ANALYSES | No. STUDIES | No. PATIENTS | VAR. | P |
|---|---|---|---|---|
| During infarction | ||||
| YUSUF (1988) [100] | 2 | 17,600 | -21% | <0.0001 |
| BASINSKI (1991) [8] | 13 | NR | -23% | 0.02 |
| ROUX (1992) [82] | 32 | 3,698 | -20% | 0.001 |
| ANTIPLATELET TRIALISTS COLL. (1994) [4] | 9 | 18,773 | -29%* | <0.00001 |
| After infarction | ||||
| YUSUF (1988) [100] | 10 | 18,500 | -11% | <0.01 |
| ANTIPLATELET TRIALISTS COLL. (1994) [4] | 11 | 19,791 | - 25%* | <0.0001 |
NR = not reported
* myocardial infarction, stroke and vascular death
ACC/AHA GUIDELINES
|
ANMCO-SIC CLINICAL GUIDELINESASA, 160 mg/die, should be given to all patients after AMI without contraindications (active peptic ulcer, haemorrhagic diathesis, allergy) |
| STUDY | DRUGS | No.PATIENTS | FOLLOW-UP | VAR | P |
|---|---|---|---|---|---|
| PRISM-PLUS (1998) [74] | Tirofiban vs Heparin vs Tirofiban + Heparin | 1,915 | 6 MONTHS | -1.4% | NS |
| PRISM (1998) [73] | Tirofiban vs Heparin | 3,232 | 30 DAYS | -36% | 0.02 |
| PARAGON (1998) [69] | Lamifiban (low-high dose) vs Heparin | 2,282 | 1 YEAR | -17% | NS |
| PURSUIT (1998) [75] | Eptifibatide vs Placebo | 10,948 | 30 DAYS | -5% | NS |
ACC/AHA GUIDELINES
|
ANMCO-SIC CLINICAL GUIDELINESNo indications |