Cargando…

Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies

BACKGROUND: Guidelines and clinical practice vary considerably with respect to thrombosis prophylaxis during plaster cast immobilization of the lower extremity. Identifying patients at high risk for the development of venous thromboembolism (VTE) would provide a basis for considering individual thro...

Descripción completa

Detalles Bibliográficos
Autores principales: Nemeth, Banne, van Adrichem, Raymond A., van Hylckama Vlieg, Astrid, Bucciarelli, Paolo, Martinelli, Ida, Baglin, Trevor, Rosendaal, Frits R., le Cessie, Saskia, Cannegieter, Suzanne C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640574/
https://www.ncbi.nlm.nih.gov/pubmed/26554832
http://dx.doi.org/10.1371/journal.pmed.1001899
_version_ 1782400095283576832
author Nemeth, Banne
van Adrichem, Raymond A.
van Hylckama Vlieg, Astrid
Bucciarelli, Paolo
Martinelli, Ida
Baglin, Trevor
Rosendaal, Frits R.
le Cessie, Saskia
Cannegieter, Suzanne C.
author_facet Nemeth, Banne
van Adrichem, Raymond A.
van Hylckama Vlieg, Astrid
Bucciarelli, Paolo
Martinelli, Ida
Baglin, Trevor
Rosendaal, Frits R.
le Cessie, Saskia
Cannegieter, Suzanne C.
author_sort Nemeth, Banne
collection PubMed
description BACKGROUND: Guidelines and clinical practice vary considerably with respect to thrombosis prophylaxis during plaster cast immobilization of the lower extremity. Identifying patients at high risk for the development of venous thromboembolism (VTE) would provide a basis for considering individual thromboprophylaxis use and planning treatment studies. The aims of this study were (1) to investigate the predictive value of genetic and environmental risk factors, levels of coagulation factors, and other biomarkers for the occurrence of VTE after cast immobilization of the lower extremity and (2) to develop a clinical prediction tool for the prediction of VTE in plaster cast patients. METHODS AND FINDINGS: We used data from a large population-based case–control study (MEGA study, 4,446 cases with VTE, 6,118 controls without) designed to identify risk factors for a first VTE. Cases were recruited from six anticoagulation clinics in the Netherlands between 1999 and 2004; controls were their partners or individuals identified via random digit dialing. Identification of predictor variables to be included in the model was based on reported associations in the literature or on a relative risk (odds ratio) > 1.2 and p ≤ 0.25 in the univariate analysis of all participants. Using multivariate logistic regression, a full prediction model was created. In addition to the full model (all variables), a restricted model (minimum number of predictors with a maximum predictive value) and a clinical model (environmental risk factors only, no blood draw or assays required) were created. To determine the discriminatory power in patients with cast immobilization (n = 230), the area under the curve (AUC) was calculated by means of a receiver operating characteristic. Validation was performed in two other case–control studies of the etiology of VTE: (1) the THE-VTE study, a two-center, population-based case–control study (conducted in Leiden, the Netherlands, and Cambridge, United Kingdom) with 784 cases and 523 controls included between March 2003 and December 2008 and (2) the Milan study, a population-based case–control study with 2,117 cases and 2,088 controls selected between December 1993 and December 2010 at the Thrombosis Center, Fondazione IRCCS Ca’ Granda–Ospedale Maggiore Policlinico, Milan, Italy. The full model consisted of 32 predictors, including three genetic factors and six biomarkers. For this model, an AUC of 0.85 (95% CI 0.77–0.92) was found in individuals with plaster cast immobilization of the lower extremity. The AUC for the restricted model (containing 11 predictors, including two genetic factors and one biomarker) was 0.84 (95% CI 0.77–0.92). The clinical model (consisting of 14 environmental predictors) resulted in an AUC of 0.77 (95% CI 0.66–0.87). The clinical model was converted into a risk score, the L-TRiP(cast) score (Leiden–Thrombosis Risk Prediction for patients with cast immobilization score), which showed an AUC of 0.76 (95% CI 0.66–0.86). Validation in the THE-VTE study data resulted in an AUC of 0.77 (95% CI 0.58–0.96) for the L-TRiP(cast) score. Validation in the Milan study resulted in an AUC of 0.93 (95% CI 0.86–1.00) for the full model, an AUC of 0.92 (95% CI 0.76–0.87) for the restricted model, and an AUC of 0.96 (95% CI 0.92–0.99) for the clinical model. The L-TRiP(cast) score resulted in an AUC of 0.95 (95% CI 0.91–0.99). Major limitations of this study were that information on thromboprophylaxis was not available for patients who had plaster cast immobilization of the lower extremity and that blood was drawn 3 mo after the thrombotic event. CONCLUSIONS: These results show that information on environmental risk factors, coagulation factors, and genetic determinants in patients with plaster casts leads to high accuracy in the prediction of VTE risk. In daily practice, the clinical model may be the preferred model as its factors are most easy to determine, while the model still has good predictive performance. These results may provide guidance for thromboprophylaxis and form the basis for a management study.
format Online
Article
Text
id pubmed-4640574
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-46405742015-11-13 Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies Nemeth, Banne van Adrichem, Raymond A. van Hylckama Vlieg, Astrid Bucciarelli, Paolo Martinelli, Ida Baglin, Trevor Rosendaal, Frits R. le Cessie, Saskia Cannegieter, Suzanne C. PLoS Med Research Article BACKGROUND: Guidelines and clinical practice vary considerably with respect to thrombosis prophylaxis during plaster cast immobilization of the lower extremity. Identifying patients at high risk for the development of venous thromboembolism (VTE) would provide a basis for considering individual thromboprophylaxis use and planning treatment studies. The aims of this study were (1) to investigate the predictive value of genetic and environmental risk factors, levels of coagulation factors, and other biomarkers for the occurrence of VTE after cast immobilization of the lower extremity and (2) to develop a clinical prediction tool for the prediction of VTE in plaster cast patients. METHODS AND FINDINGS: We used data from a large population-based case–control study (MEGA study, 4,446 cases with VTE, 6,118 controls without) designed to identify risk factors for a first VTE. Cases were recruited from six anticoagulation clinics in the Netherlands between 1999 and 2004; controls were their partners or individuals identified via random digit dialing. Identification of predictor variables to be included in the model was based on reported associations in the literature or on a relative risk (odds ratio) > 1.2 and p ≤ 0.25 in the univariate analysis of all participants. Using multivariate logistic regression, a full prediction model was created. In addition to the full model (all variables), a restricted model (minimum number of predictors with a maximum predictive value) and a clinical model (environmental risk factors only, no blood draw or assays required) were created. To determine the discriminatory power in patients with cast immobilization (n = 230), the area under the curve (AUC) was calculated by means of a receiver operating characteristic. Validation was performed in two other case–control studies of the etiology of VTE: (1) the THE-VTE study, a two-center, population-based case–control study (conducted in Leiden, the Netherlands, and Cambridge, United Kingdom) with 784 cases and 523 controls included between March 2003 and December 2008 and (2) the Milan study, a population-based case–control study with 2,117 cases and 2,088 controls selected between December 1993 and December 2010 at the Thrombosis Center, Fondazione IRCCS Ca’ Granda–Ospedale Maggiore Policlinico, Milan, Italy. The full model consisted of 32 predictors, including three genetic factors and six biomarkers. For this model, an AUC of 0.85 (95% CI 0.77–0.92) was found in individuals with plaster cast immobilization of the lower extremity. The AUC for the restricted model (containing 11 predictors, including two genetic factors and one biomarker) was 0.84 (95% CI 0.77–0.92). The clinical model (consisting of 14 environmental predictors) resulted in an AUC of 0.77 (95% CI 0.66–0.87). The clinical model was converted into a risk score, the L-TRiP(cast) score (Leiden–Thrombosis Risk Prediction for patients with cast immobilization score), which showed an AUC of 0.76 (95% CI 0.66–0.86). Validation in the THE-VTE study data resulted in an AUC of 0.77 (95% CI 0.58–0.96) for the L-TRiP(cast) score. Validation in the Milan study resulted in an AUC of 0.93 (95% CI 0.86–1.00) for the full model, an AUC of 0.92 (95% CI 0.76–0.87) for the restricted model, and an AUC of 0.96 (95% CI 0.92–0.99) for the clinical model. The L-TRiP(cast) score resulted in an AUC of 0.95 (95% CI 0.91–0.99). Major limitations of this study were that information on thromboprophylaxis was not available for patients who had plaster cast immobilization of the lower extremity and that blood was drawn 3 mo after the thrombotic event. CONCLUSIONS: These results show that information on environmental risk factors, coagulation factors, and genetic determinants in patients with plaster casts leads to high accuracy in the prediction of VTE risk. In daily practice, the clinical model may be the preferred model as its factors are most easy to determine, while the model still has good predictive performance. These results may provide guidance for thromboprophylaxis and form the basis for a management study. Public Library of Science 2015-11-10 /pmc/articles/PMC4640574/ /pubmed/26554832 http://dx.doi.org/10.1371/journal.pmed.1001899 Text en © 2015 Nemeth et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nemeth, Banne
van Adrichem, Raymond A.
van Hylckama Vlieg, Astrid
Bucciarelli, Paolo
Martinelli, Ida
Baglin, Trevor
Rosendaal, Frits R.
le Cessie, Saskia
Cannegieter, Suzanne C.
Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies
title Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies
title_full Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies
title_fullStr Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies
title_full_unstemmed Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies
title_short Venous Thrombosis Risk after Cast Immobilization of the Lower Extremity: Derivation and Validation of a Clinical Prediction Score, L-TRiP(cast), in Three Population-Based Case–Control Studies
title_sort venous thrombosis risk after cast immobilization of the lower extremity: derivation and validation of a clinical prediction score, l-trip(cast), in three population-based case–control studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640574/
https://www.ncbi.nlm.nih.gov/pubmed/26554832
http://dx.doi.org/10.1371/journal.pmed.1001899
work_keys_str_mv AT nemethbanne venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT vanadrichemraymonda venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT vanhylckamavliegastrid venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT bucciarellipaolo venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT martinelliida venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT baglintrevor venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT rosendaalfritsr venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT lecessiesaskia venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies
AT cannegietersuzannec venousthrombosisriskaftercastimmobilizationofthelowerextremityderivationandvalidationofaclinicalpredictionscoreltripcastinthreepopulationbasedcasecontrolstudies