Literature DB >> 26048878

Prevalence of cerebral and pulmonary thrombosis in patients with cyanotic congenital heart disease.

A S Jensen1, L Idorn1, C Thomsen2, P von der Recke3, J Mortensen4, K E Sørensen5, U Thilén6, E Nagy7, K F Kofoed1, S R Ostrowski8, L Søndergaard1.   

Abstract

BACKGROUND: Patients with cyanotic congenital heart disease (CCHD) have a high prevalence of thrombosis, the most frequently described locations being the cerebral and pulmonary vessels. The reported prevalence of both cerebral infarction and pulmonary thrombosis has been highly variable. The aim of this study was to examine the prevalence of both cerebral and pulmonary thrombosis in CCHD according to medical history and imaging. In addition, the role of known erythrocytosis and haemostatic abnormalities as risk factors was evaluated. METHODS AND
RESULTS: A cross-sectional descriptive study examining 98 stable adult patients with CCHD with a medical questionnaire, blood samples, MRI of the cerebrum (n=72), multidetector CT imaging (MDCT) of the thorax (n=76) and pulmonary scintigraphy (ventilation/perfusion/single-photon emission computerised tomography/CT) (n=66). The prevalence of cerebral infarction and pulmonary thrombosis according to imaging were 47% and 31%, respectively. Comparing the findings with previous medical history revealed a large under-reporting of thrombosis with only 22% of the patients having a clinical history of stroke and 25% of pulmonary thrombosis. There was no association between the degree of erythrocytosis or haemostatic abnormalities and the prevalence of thrombosis.
CONCLUSIONS: Patients with CCHD have a prevalence of both cerebral and pulmonary thrombosis of around 30%-40%, which is much higher than that reported previously. Furthermore, there is a large discrepancy between clinical history and imaging findings, suggesting a high prevalence of silent thrombotic events. Neither erythrocytosis nor haemostatic abnormalities were associated with the prevalence of thrombosis in patients with CCHD. TRIAL REGISTRATION NUMBER: http://www.cvk.sum.dk/CVK/Home/English.aspx (H-KF-2006-4068). Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

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Year:  2015        PMID: 26048878     DOI: 10.1136/heartjnl-2015-307657

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


  13 in total

1.  A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle.

Authors:  Cai-Xia Lu; Wei Wang; Qian Wang; Xing-Yuan Liu; Yi-Qing Yang
Journal:  Pediatr Cardiol       Date:  2018-02-21       Impact factor: 1.655

Review 2.  Thromboembolic complications in adult congenital heart disease: the knowns and the unknowns.

Authors:  Magalie Ladouceur; Clément Karsenty; Victor Waldmann; Barbara Mulder; Sébastien Hascoet
Journal:  Clin Res Cardiol       Date:  2020-10-09       Impact factor: 5.460

3.  Arterial Ischemic Stroke Secondary to Cardiac Disease in Neonates and Children.

Authors:  Melissa G Chung; Kristin P Guilliams; Jenny L Wilson; Lauren A Beslow; Michael M Dowling; Neil R Friedman; Sahar M A Hassanein; Rebecca Ichord; Lori C Jordan; Mark T Mackay; Mubeen F Rafay; Michael Rivkin; Marcela Torres; Dimitrios Zafeiriou; Gabrielle deVeber; Christine K Fox
Journal:  Pediatr Neurol       Date:  2019-06-27       Impact factor: 3.372

Review 4.  Brain in Congenital Heart Disease Across the Lifespan: The Cumulative Burden of Injury.

Authors:  Ariane Marelli; Steven P Miller; Bradley Scott Marino; Angela L Jefferson; Jane W Newburger
Journal:  Circulation       Date:  2016-05-17       Impact factor: 29.690

5.  TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.

Authors:  Ri-Tai Huang; Juan Wang; Song Xue; Xing-Biao Qiu; Hong-Yu Shi; Ruo-Gu Li; Xin-Kai Qu; Xiao-Xiao Yang; Hua Liu; Ning Li; Yan-Jie Li; Ying-Jia Xu; Yi-Qing Yang
Journal:  Int J Med Sci       Date:  2017-03-11       Impact factor: 3.738

6.  Does Tetralogy of Fallot affect brain aging? A proof-of-concept study.

Authors:  Marina Codari; Giacomo Davide Edoardo Papini; Luca Melazzini; Francesca Romana Pluchinotta; Francesco Secchi; Mario Carminati; Alessandro Frigiola; Massimo Chessa; Francesco Sardanelli
Journal:  PLoS One       Date:  2018-08-21       Impact factor: 3.240

7.  Brain vascular changes in adults with congenital heart disease: A systematic review.

Authors:  Luca Melazzini; Marina Codari; Paolo Vitali; Francesco Sardanelli
Journal:  Neuroimage Clin       Date:  2019-05-27       Impact factor: 4.881

8.  Ischemic Stroke in Adults With Congenital Heart Disease: A Population-Based Cohort Study.

Authors:  Mette Glavind Bülow Pedersen; Morten S Olsen; Morten Schmidt; Søren P Johnsen; Christopher Learn; Henning B Laursen; Nicolas L Madsen
Journal:  J Am Heart Assoc       Date:  2019-07-18       Impact factor: 5.501

Review 9.  Risk Factors, Prophylaxis, and Treatment of Venous Thromboembolism in Congenital Heart Disease Patients.

Authors:  Michael Silvey; Leonardo R Brandão
Journal:  Front Pediatr       Date:  2017-06-19       Impact factor: 3.418

10.  MEF2C loss-of-function mutation contributes to congenital heart defects.

Authors:  Xiao-Hui Qiao; Fei Wang; Xian-Ling Zhang; Ri-Tai Huang; Song Xue; Juan Wang; Xing-Biao Qiu; Xing-Yuan Liu; Yi-Qing Yang
Journal:  Int J Med Sci       Date:  2017-09-08       Impact factor: 3.738

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