Literature DB >> 29605397

Venous Thromboembolism in Children with Sickle Cell Disease: A Retrospective Cohort Study.

Gary M Woods1, Ruchika Sharma2, Susan Creary3, Sarah O'Brien3, Joseph Stanek4, Kan Hor5, Jennifer Young6, Amy L Dunn3, Riten Kumar7.   

Abstract

OBJECTIVES: To describe the cumulative incidence of venous thromboembolism (VTE) in children with sickle cell disease (SCD) followed at a single institution and report on the risk factors associated with VTE development. STUDY
DESIGN: Charts for all patients with SCD, aged 0-21 years, followed at Nationwide Children's Hospital over a 6-year period (January 1, 2009, to January 31, 2015) were reviewed. Data on VTE diagnosis, sex, body mass index/weight-for-length, SCD genotype, SCD clinical complications, central venous catheter (CVC) placement, and thrombophilia testing were collected.
RESULTS: Cumulative incidence of VTE in children with SCD followed at a single tertiary care institution was found to be 2.9% (12/414). Nine of the 12 VTE were CVC-associated. On univariate analysis, hemoglobin SS genotype (OR 10.7, 95% CI 1.4-83.5), CVC presence (OR 34.4, 95% CI 8.9-134.6), central nervous system vasculopathy (OR 19.4, 95% CI 5.6-63.4), chronic transfusion therapy (OR 30.6, 95% CI 8.9-122.2), and older age (P = .03) were associated with VTE. However, presence of CVC was the only independent risk factor identified on multivariable logistic regression analysis (OR 33.8, 95% CI 8.7-130.9).
CONCLUSION: In our institution, nearly 3% of children with SCD had a history of VTE. CVC is an independent predictor of VTE in children with SCD.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  sickle cell disease; venous thromboembolism

Mesh:

Year:  2018        PMID: 29605397     DOI: 10.1016/j.jpeds.2018.01.073

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  6 in total

1.  Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease.

Authors:  Andrew Srisuwananukorn; Rasha Raslan; Xu Zhang; Binal N Shah; Jin Han; Michel Gowhari; Robert E Molokie; Victor R Gordeuk; Santosh L Saraf
Journal:  Blood Adv       Date:  2020-05-12

2.  Treatment-Related Outcomes in Paget-Schroetter Syndrome-A Cross-Sectional Investigation.

Authors:  Riten Kumar; Katherine Harsh; Surbhi Saini; Sarah H O'Brien; Joseph Stanek; Patrick Warren; Jean Giver; Michael R Go; Bryce A Kerlin
Journal:  J Pediatr       Date:  2018-12-07       Impact factor: 4.406

3.  American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease.

Authors:  Robert I Liem; Sophie Lanzkron; Thomas D Coates; Laura DeCastro; Ankit A Desai; Kenneth I Ataga; Robyn T Cohen; Johnson Haynes; Ifeyinwa Osunkwo; Jeffrey D Lebensburger; James P Lash; Theodore Wun; Madeleine Verhovsek; Elodie Ontala; Rae Blaylark; Fares Alahdab; Abdulrahman Katabi; Reem A Mustafa
Journal:  Blood Adv       Date:  2019-12-10

4.  Vascular Instability and Neurological Morbidity in Sickle Cell Disease: An Integrative Framework.

Authors:  Hanne Stotesbury; Jamie M Kawadler; Patrick W Hales; Dawn E Saunders; Christopher A Clark; Fenella J Kirkham
Journal:  Front Neurol       Date:  2019-08-13       Impact factor: 4.003

5.  Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia - lessons learned for prophylaxis.

Authors:  Salam Alkindi; Anwaar R Al-Ghadani; Samah R Al-Zeheimi; Said Y Alkindi; Naglaa Fawaz; Samir K Ballas; Anil V Pathare
Journal:  J Int Med Res       Date:  2021-12       Impact factor: 1.671

6.  Evaluation of point-of-care International Normalized Ratio in sickle cell disease.

Authors:  Syeda Rahman; Andrew Srisuwananukorn; Robert E Molokie; Michel Gowhari; Franklin Njoku; Faiz Ahmed Hussain; James Lee; Edith A Nutescu; Victor R Gordeuk; Santosh L Saraf; Jin Han
Journal:  Res Pract Thromb Haemost       Date:  2021-05-27
  6 in total

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