Risk of recurrence after a first unprovoked venous thromboembolism: external validation of the Vienna Prediction Model with pooled individual patient data

被引:52
作者
Marcucci, M. [1 ,2 ,3 ]
Iorio, A. [3 ]
Douketis, J. D. [4 ]
Eichinger, S. [5 ]
Tosetto, A. [6 ]
Baglin, T. [7 ]
Cushman, M. [8 ]
Palareti, G. [9 ]
Poli, D. [10 ]
Tait, R. C. [11 ]
Kyrle, P. A. [5 ]
机构
[1] Univ Milan, Geriatr, Fdn IRCCS Ca Granda, Osped Maggiore Policlin, Milan, Italy
[2] Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy
[3] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
[4] McMaster Univ, Dept Med, St Josephs Hosp, Hamilton, ON, Canada
[5] Med Univ Vienna, Dept Med 1, A-1090 Vienna, Austria
[6] S Bortolo Hosp, Dept Hematol, Vicenza, Italy
[7] Addenbrookes Hosp, Dept Haematol, Cambridge CB2 2QQ, England
[8] Univ Vermont, Dept Med, Colchester, VT USA
[9] Univ Bologna, Dept Med, Bologna, Italy
[10] Azienda Osped Univ Careggi, Ctr Riferimento Reg Trombosi, Florence, Italy
[11] Royal Infirm, Dept Haematol, Glasgow G31 2ER, Lanark, Scotland
关键词
decision support technique; pulmonary embolism; recurrence; venous thromboembolism; venous thrombosis; D-DIMER; PROGNOSTIC MODELS; THROMBOSIS;
D O I
10.1111/jth.12871
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundIn order to stratify patients with a first unprovoked venous thromboembolism (VTE) according to their recurrence risk and to identify those who would actually benefit from indefinite anticoagulation, three prediction models have been developed so far; none of them has been yet externally validated. ObjectiveTo externally validate the Vienna Prediction Model (VPM), a prediction guide for estimating the recurrence risk after a first unprovoked VTE developed through Cox modeling and including sex, D-dimer and index VTE site as predictors. Patients/MethodsNine hundred and four patients pooled from five prospective studies evaluating the prognostic value of D-dimer for VTE recurrence served as the validation cohort. The validity of the VPM in stratifying patients according to their relative recurrence risk (discrimination) and in predicting the absolute recurrence risk (calibration) was tested with survival analysis methods. ResultsThe ability of the VPM to distinguish patients' risk for recurrent VTE in the validation cohort was at least as good as in the original cohort, with a calibration slope of 1.17 (95% confidence interval 0.71-1.64; P=0.456 for the hypothesis of a significant difference from 1), and a c-statistic of 0.626 (vs. 0.651 in the original derivation cohort). The VPM absolute predictions in terms of cumulative rates tended to underestimate the observed recurrence rates at 12months. ConclusionsBy using a pooled individual patient database as a validation cohort, we confirmed the ability of the VPM to stratify patients with a first unprovoked VTE according to their risk of recurrence.
引用
收藏
页码:775 / 781
页数:7
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