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The Vienna Prediction Model for identifying patients at low risk of recurrent venous thromboembolism: a prospective cohort study.
Kyrle, Paul A; Eischer, Lisbeth; Sinkovec, Hana; Gressenberger, Paul; Gary, Thomas; Brodmann, Marianne; Heinze, Georg; Eichinger, Sabine.
Afiliación
  • Kyrle PA; Division of Hematology and Hemostasis, Department of Medicine I, Medical University of Vienna, Vienna A-1090, Austria.
  • Eischer L; Karl Landsteiner Institute of Thrombosis Research, Vienna A-1020, Austria.
  • Sinkovec H; Division of Hematology and Hemostasis, Department of Medicine I, Medical University of Vienna, Vienna A-1090, Austria.
  • Gressenberger P; Center for Medical Statistics, Informatics and Intelligent Systems, Institute of Clinical Biometrics, Medical University of Vienna, Vienna A-1090, Austria.
  • Gary T; Division of Angiology, Department of Medicine, Medical University of Graz, Graz A-8010, Austria.
  • Brodmann M; Division of Angiology, Department of Medicine, Medical University of Graz, Graz A-8010, Austria.
  • Heinze G; Division of Angiology, Department of Medicine, Medical University of Graz, Graz A-8010, Austria.
  • Eichinger S; Center for Medical Statistics, Informatics and Intelligent Systems, Institute of Clinical Biometrics, Medical University of Vienna, Vienna A-1090, Austria.
Eur Heart J ; 45(1): 45-53, 2024 Jan 01.
Article en En | MEDLINE | ID: mdl-37769352
BACKGROUND AND AIMS: Patients with unprovoked venous thromboembolism (VTE) have a high recurrence risk, and guidelines suggest extended-phase anticoagulation. Many patients never experience recurrence but are exposed to bleeding. The aim of this study was to assess the performance of the Vienna Prediction Model (VPM) and to evaluate if the VPM accurately identifies these patients. METHODS: In patients with unprovoked VTE, the VPM was performed 3 weeks after anticoagulation withdrawal. Those with a predicted 1-year recurrence risk of ≤5.5% were prospectively followed. Study endpoint was recurrent VTE over 2 years. RESULTS: A total of 818 patients received anticoagulation for a median of 3.9 months. 520 patients (65%) had a predicted annual recurrence risk of ≤5.5%. During a median time of 23.9 months, 52 patients had non-fatal recurrence. The recurrence risk was 5.2% [95% confidence interval (CI) 3.2-7.2] at 1 year and 11.2% (95% CI 8.3-14) at 2 years. Model calibration was adequate after 1 year. The VPM underestimated the recurrence risk of patients with a 2-year recurrence rate of >5%. In a post-hoc analysis, the VPM's baseline hazard was recalibrated. Bootstrap validation confirmed an ideal ratio of observed and expected recurrence events. The recurrence risk was highest in men with proximal deep-vein thrombosis or pulmonary embolism and lower in women regardless of the site of incident VTE. CONCLUSIONS: In this prospective evaluation of the performance of the VPM, the 1-year rate of recurrence in patients with unprovoked VTE was 5.2%. Recalibration improved identification of patients at low recurrence risk and stratification into distinct low-risk categories.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Embolia Pulmonar / Tromboembolia Venosa Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Eur Heart J Año: 2024 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Embolia Pulmonar / Tromboembolia Venosa Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Eur Heart J Año: 2024 Tipo del documento: Article País de afiliación: Austria