Relative Risk Reduction in Nonfatal MI with Prasugrel vs Clopidogrel
Patients treated with prasugrel were 23% less likely to experience a nonfatal MI than patients treated with clopidogrel.
Understanding the Data
The TRITON-TIMI 38 trial compared prasugrel to clopidogrel in patients with acute coronary syndrome undergoing percutaneous coronary intervention. Looking at the data presented:
- Nonfatal MI occurred in 7.3% of patients in the prasugrel group versus 9.5% in the clopidogrel group
- The hazard ratio (HR) was 0.77 (95% CI: 0.67-0.85)
Calculating Relative Risk Reduction
The relative risk reduction (RRR) is calculated using the formula: RRR = (1 - Hazard Ratio) × 100%
In this case: RRR = (1 - 0.77) × 100% = 23%
This means prasugrel reduced the relative risk of nonfatal MI by 23% compared to clopidogrel 1.
Clinical Context of the Finding
This 23% relative risk reduction in nonfatal MI was a key component of the overall benefit seen with prasugrel:
- The primary composite endpoint (cardiovascular death, nonfatal MI, or nonfatal stroke) was reduced by 19% (HR 0.81; 95% CI: 0.73-0.90) 1
- The benefit was primarily driven by the reduction in nonfatal MI 1
- The reduction in MI was evident both early (within first 3 days) and later (beyond 3 days) 2
Important Clinical Considerations
While prasugrel showed superior efficacy in reducing nonfatal MI, this benefit must be balanced against increased bleeding risk:
- Major bleeding was significantly higher with prasugrel (2.4% vs 1.8%; HR 1.32; 95% CI: 1.03-1.68) 1
- Fatal bleeding was also higher with prasugrel (0.4% vs 0.1%; p=0.002) 1
Special Populations with Unfavorable Risk-Benefit Profile
Three subgroups did not have favorable outcomes with prasugrel 1:
- Patients with prior stroke/TIA (contraindicated)
- Patients ≥75 years of age (no net benefit)
- Patients with body weight <60 kg (no net benefit)
Conclusion on Relative Risk Reduction
The correct interpretation of the data is that prasugrel treatment resulted in a 23% relative risk reduction in nonfatal MI compared to clopidogrel. This represents a clinically significant reduction in a key component of the primary endpoint, but must be considered alongside the increased bleeding risk when making treatment decisions.