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Venous Thromboembolism after Allogeneic Pediatric Hematopoietic Stem Cell Transplantation: A Single-Center Study
Insights
Venous thromboembolism (VTE) is uncommon in pediatric hematopoietic stem cell transplant (HSCT) recipients. Inherited risk factors did not significantly correlate with VTE events in this study.
Area of Science:
- Hematology
- Pediatric Oncology
- Transplantation Medicine
Background:
- Venous thromboembolism (VTE) presents significant morbidity in pediatric patients undergoing hematopoietic stem cell transplantation (HSCT).
- Assessing pretransplant prothrombotic risk factors is crucial for understanding thrombosis in this vulnerable population.
Purpose of the Study:
- To determine the incidence of VTE in pediatric allogeneic HSCT recipients.
- To evaluate the contribution of inherited and acquired prothrombotic risk factors to the development of VTE post-HSCT.
Main Methods:
- Retrospective analysis of 92 pediatric patients undergoing allogeneic HSCT.
- Screening for inherited thrombophilia (Factor V Leiden, Prothrombin G20210A, MTHFR mutations) and acquired risk factors prior to HSCT.
- Monitoring for VTE events within 100 days post-HSCT.
Main Results:
- The incidence of VTE was 5.4% (5 out of 92 patients).
- A prothrombotic risk factor was identified in 3 VTE cases, and central venous catheters were present in 4 cases.
- No significant association was found between VTE and inherited prothrombotic risk factors.
Conclusions:
- VTE appears to be a low-frequency complication following pediatric HSCT.
- Low-molecular-weight heparin prophylaxis may contribute to the low VTE rate.
- Further prospective studies are needed to fully elucidate the role of inherited prothrombotic risk factors.
Introduction:
Venous thromboembolism (VTE) in children who undergo hematopoietic stem cell transplantation (HSCT) has high morbidity. The aim of this study is to assess the incidence of VTE in allogeneic pediatric HSCT recipients and the contribution of pretransplant prothrombotic risk factors to thrombosis.
Methods:
We retrospectively evaluated 92 patients between April 2010 and November 2012 undergoing allogeneic HSCT who had completed 100 days post-HSCT. Before HSCT, coagulation profiles; acquired and inherited prothrombotic risk factors including factor V Leiden, prothrombin G20210A, methylenetetrahydrofolate reductase (MTHFR) C677T, and MTHFR A1298C mutations; and serum homocysteine and lipoprotein(a), plasma antithrombin III, protein C, and protein S levels were obtained from all patients.
Results:
In the screening of thrombophilia, 8 patients (9%) were heterozygous for factor V Leiden, 5 (6%) were homozygous for MTHFR 677TT, 12 (14%) were homozygous for MTHFR 1298CC, and 2 (2%) were heterozygous for prothrombin G20210A mutation. We observed VTE in 5 patients (5.4%); a prothrombotic risk factor was found in 3 out of these 5 patients, while 4 out of 5 patients had central venous catheters. It was determined there was no significant relationship between VTE and inherited prothrombotic risk factors.
Discussion And Conclusion:
VTE after HSCT seems to be a low-frequency event that may be due to low-dose, low-molecular-weight heparin prophylaxis, and the role of inherited prothrombotic risk factors cannot be entirely excluded without a prospective study.
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