Article
Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S.
Thrombosis and haemostasis - 1 Sept 1994
De Stefano V, Leone G, Mastrangelo S, Tripodi A, Rodeghiero F, Castaman G, Barbui T, Finazzi G, Bizzi B, Mannucci P M
Abstract excerpt
The clinical history of 238 patients with inherited thrombophilia (AT III = 94, PC = 103, PS = 41) was analyzed retrospectively at diagnosis and in the follow-up period after diagnosis. At diagnosis 129 patients (54%) had suffered from thrombosis, with a recurrence rate of 48%. The most frequent...
Topics
- Adult
- Age of Onset
- Antithrombin III Deficiency
- Disease Susceptibility
- Female
- Fibrinolytic Agents
- Follow-Up Studies
- Genetic Predisposition to Disease
- Humans
- Incidence
- Male
- Middle Aged
- Patient Compliance
- Postoperative Complications