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Thrombotic events after pediatric liver transplantation
Chee Yee Ooi1, Leonardo R Brandão, Lauren Zolpys
1SickKids Transplant Centre, Toronto, ON, Canada.
Insights
Early thrombosis (TE) affects 16% of pediatric liver transplant (LT) recipients. Deep vein thrombosis (DVT) occurred in 8%, highlighting the need for further research into prevention strategies.
Area of Science:
- Pediatric Hepatology
- Transplant Surgery
- Vascular Medicine
Background:
- Thrombotic events (TE) pose a significant risk for morbidity and mortality in pediatric liver transplant (LT) recipients.
- Understanding the incidence and characteristics of early TE is crucial for improving patient outcomes.
Purpose of the Study:
- To determine the incidence of early TE within the first month post-pediatric LT.
- To compare the characteristics of pediatric LT recipients with and without TE.
Main Methods:
- Retrospective review of 88 pediatric LT cases from January 2002 to October 2007.
- Doppler confirmation of deep vein thrombosis (DVT) and arterial thromboembolism (ATE) within the first month post-transplant.
Main Results:
- Overall incidence of early TE was 16% (14/88 patients).
- DVT occurred in 8% (7/88) and ATE in 8% (7/88) of patients.
- Six patients (6.8%) developed symptomatic central venous line-related DVT.
Conclusions:
- The incidence of early TE post-pediatric LT is substantial (16%), with DVT accounting for half of these events.
- No significant differences in baseline characteristics were found between patients with and without TE.
- Prospective studies are needed to investigate prophylactic anticoagulation and modifiable risk factors.
Abstract:
TE may contribute to morbidity and mortality after LT. The objectives were to determine the incidence of early TE post-pediatric LT and compare differences between children with and without TE. A retrospective review of 88 transplanted children (January 2002-October 2007) was performed to determine the incidence of Doppler-confirmed DVT and ATE in the first month post-LT. Fourteen (16%) patients developed TE: DVT in seven (8%) and ATE in seven (8%) patients. Six of 88 (6.8%) developed symptomatic CVL-related DVT. Median (range) time post-LT to DVT and ATE were 7 (4-18) and 8 (1-31) days, respectively. There was no significant difference in age/body weight at LT between patients with or without DVT and ATE. There was no significant difference between patients with or without HAT in age and weight at LT, cold ischemic time, duration of surgery, hematocrit levels, whole-organ graft type, intraoperative FFP, high-risk CMV status, or early acute cellular rejection. In conclusion, the incidence of early TE post-pediatric LT was 16%, including DVT in 8%. Prospective studies are necessary to evaluate the role of prophylactic anticoagulation and potential modifiable risk factors post-pediatric LT.
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