Table 4.
Author-Year | N | Study design and follow-up (months) | Location and incidence of embolic events (%/person-year) | Stipulated therapy | Conclusion (embolic events) |
---|---|---|---|---|---|
Gonzalez-Lavin et al33 1984 | 528 | Retrospective; 30.5 | Group 1: WAR < 6 weeks 206 pts; Group 2: > 8 weeks 322 pts | Bovine pericardial bioprosthesis; low risk. | |
Group 1 = 4.6 Group 2 = 0.36 | |||||
Turpie et al34 1988 | 210 | Randomized; 3 | Group 1: INR 2.5-4.0 108 pts; Group 2: INR 2.0-2.25 102 pts | Less intensive regimen was similar for embolic events and had fewer bleeding episodes. | |
MBP | |||||
Orszulak et al10 1995 | 285 | Retrospective; | MBP 2.5 | Not informed | High risk of CVA (40%/ person-year) in the first month; |
Goldsmith et al35 1998 | 145 | Retrospective; | ABP 0.3 | ASA | In the first three months there was no increased risk of thromboembolism; |
Moinuddeen et al36 1998 | 185 | Retrospective; 3 | ABP 2.8 x 2.6 | WAR 109 x NAT 76 pts | Early OA was not effective in reducing embolic events |
Brueck et al37 2007 | 288 | Retrospective; Observational; 12 | ABP | ASA 132 x NAT 156 pts | No benefit of ASA versus nothing; |
Duraes et al11 | 184 | Prospective. Observational | MBP and ABP | ASA 59 x NAT 125 pts | Low incidence. No benefit of ASA versus nothing. |
N: sample size; AF: atrial fibrillation; ABP: aortic bioprosthesis; MBP: mitral bioprosthesis; NAT: No antithrombotic therapy; EF: ejection fraction; OA: oral anticoagulation; CVA: cerebrovascular accident; pts: Patients; ASA: aspirin.