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Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study

BACKGROUND: The relative importance of previous diagnosis and hereditary prothrombotic risk factors for cerebral venous thrombosis (CVT) in children in determining risk of a second cerebral or systemic venous thrombosis (VT), compared with other clinical, neuroimaging, and treatment variables, is un...

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Autores principales: Kenet, Gili, Kirkham, Fenella, Niederstadt, Thomas, Heinecke, Achim, Saunders, Dawn, Stoll, Monika, Brenner, Benjamin, Bidlingmaier, Christoph, Heller, Christine, Knöfler, Ralf, Schobess, Rosemarie, Zieger, Barbara, Sébire, Guillaume, Nowak-Göttl, Ulrike
Formato: Texto
Lenguaje:English
Publicado: Lancet Pub. Group 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1906729/
https://www.ncbi.nlm.nih.gov/pubmed/17560171
http://dx.doi.org/10.1016/S1474-4422(07)70131-X
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author Kenet, Gili
Kirkham, Fenella
Niederstadt, Thomas
Heinecke, Achim
Saunders, Dawn
Stoll, Monika
Brenner, Benjamin
Bidlingmaier, Christoph
Heller, Christine
Knöfler, Ralf
Schobess, Rosemarie
Zieger, Barbara
Sébire, Guillaume
Nowak-Göttl, Ulrike
author_facet Kenet, Gili
Kirkham, Fenella
Niederstadt, Thomas
Heinecke, Achim
Saunders, Dawn
Stoll, Monika
Brenner, Benjamin
Bidlingmaier, Christoph
Heller, Christine
Knöfler, Ralf
Schobess, Rosemarie
Zieger, Barbara
Sébire, Guillaume
Nowak-Göttl, Ulrike
author_sort Kenet, Gili
collection PubMed
description BACKGROUND: The relative importance of previous diagnosis and hereditary prothrombotic risk factors for cerebral venous thrombosis (CVT) in children in determining risk of a second cerebral or systemic venous thrombosis (VT), compared with other clinical, neuroimaging, and treatment variables, is unknown. METHODS: We followed up the survivors of 396 consecutively enrolled patients with CVT, aged newborn to 18 years (median 5·2 years) for a median of 36 months (maximum 85 months). In accordance with international treatment guidelines, 250 children (65%) received acute anticoagulation with unfractionated heparin or low-molecular weight heparin, followed by secondary anticoagulation prophylaxis with low-molecular weight heparin or warfarin in 165 (43%). RESULTS: Of 396 children enrolled, 12 died immediately and 22 (6%) had recurrent VT (13 cerebral; 3%) at a median of 6 months (range 0·1–85). Repeat venous imaging was available in 266 children. Recurrent VT only occurred in children whose first CVT was diagnosed after age 2 years; the underlying medical condition had no effect. In Cox regression analyses, non-administration of anticoagulant before relapse (hazard ratio [HR] 11·2 95% CI 3·4–37·0; p<0·0001), persistent occlusion on repeat venous imaging (4·1, 1·1–14·8; p=0·032), and heterozygosity for the G20210A mutation in factor II (4·3, 1·1–16·2; p=0·034) were independently associated with recurrent VT. Among patients who had recurrent VT, 70% (15) occurred within the 6 months after onset. CONCLUSION: Age at CVT onset, non-administration of anticoagulation, persistent venous occlusion, and presence of G20210A mutation in factor II predict recurrent VT in children. Secondary prophylactic anticoagulation should be given on a patient-to-patient basis in children with newly identified CVT and at high risk of recurrent VT. Factors that affect recanalisation need further research.
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spelling pubmed-19067292007-08-28 Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study Kenet, Gili Kirkham, Fenella Niederstadt, Thomas Heinecke, Achim Saunders, Dawn Stoll, Monika Brenner, Benjamin Bidlingmaier, Christoph Heller, Christine Knöfler, Ralf Schobess, Rosemarie Zieger, Barbara Sébire, Guillaume Nowak-Göttl, Ulrike Lancet Neurol Fast track — Articles BACKGROUND: The relative importance of previous diagnosis and hereditary prothrombotic risk factors for cerebral venous thrombosis (CVT) in children in determining risk of a second cerebral or systemic venous thrombosis (VT), compared with other clinical, neuroimaging, and treatment variables, is unknown. METHODS: We followed up the survivors of 396 consecutively enrolled patients with CVT, aged newborn to 18 years (median 5·2 years) for a median of 36 months (maximum 85 months). In accordance with international treatment guidelines, 250 children (65%) received acute anticoagulation with unfractionated heparin or low-molecular weight heparin, followed by secondary anticoagulation prophylaxis with low-molecular weight heparin or warfarin in 165 (43%). RESULTS: Of 396 children enrolled, 12 died immediately and 22 (6%) had recurrent VT (13 cerebral; 3%) at a median of 6 months (range 0·1–85). Repeat venous imaging was available in 266 children. Recurrent VT only occurred in children whose first CVT was diagnosed after age 2 years; the underlying medical condition had no effect. In Cox regression analyses, non-administration of anticoagulant before relapse (hazard ratio [HR] 11·2 95% CI 3·4–37·0; p<0·0001), persistent occlusion on repeat venous imaging (4·1, 1·1–14·8; p=0·032), and heterozygosity for the G20210A mutation in factor II (4·3, 1·1–16·2; p=0·034) were independently associated with recurrent VT. Among patients who had recurrent VT, 70% (15) occurred within the 6 months after onset. CONCLUSION: Age at CVT onset, non-administration of anticoagulation, persistent venous occlusion, and presence of G20210A mutation in factor II predict recurrent VT in children. Secondary prophylactic anticoagulation should be given on a patient-to-patient basis in children with newly identified CVT and at high risk of recurrent VT. Factors that affect recanalisation need further research. Lancet Pub. Group 2007-07 /pmc/articles/PMC1906729/ /pubmed/17560171 http://dx.doi.org/10.1016/S1474-4422(07)70131-X Text en . https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Fast track — Articles
Kenet, Gili
Kirkham, Fenella
Niederstadt, Thomas
Heinecke, Achim
Saunders, Dawn
Stoll, Monika
Brenner, Benjamin
Bidlingmaier, Christoph
Heller, Christine
Knöfler, Ralf
Schobess, Rosemarie
Zieger, Barbara
Sébire, Guillaume
Nowak-Göttl, Ulrike
Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
title Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
title_full Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
title_fullStr Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
title_full_unstemmed Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
title_short Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
title_sort risk factors for recurrent venous thromboembolism in the european collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study
topic Fast track — Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1906729/
https://www.ncbi.nlm.nih.gov/pubmed/17560171
http://dx.doi.org/10.1016/S1474-4422(07)70131-X
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