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Published on: September 22, 2013
GI complications in pediatric patients post-BMT
C C Barker1, R A Anderson, R S Sauve
1Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada. cbarker@cw.bc.ca
Insights
Pediatric bone marrow transplant (BMT) recipients frequently experience hepatic and gastrointestinal complications. Graft-versus-host disease (GVHD) and veno-occlusive disease (VOD) significantly impact liver function, while mucositis and diarrhea are common GI issues.
Area of Science:
- Pediatric Hematology/Oncology
- Gastroenterology
- Transplant Medicine
Background:
- Bone marrow transplantation (BMT) is a critical treatment for pediatric hematologic malignancies and other diseases.
- Post-transplant complications, particularly hepatic and gastrointestinal (GI), significantly affect patient outcomes.
- Understanding the incidence and etiology of these complications is crucial for improving pediatric BMT care.
Purpose of the Study:
- To comprehensively examine the spectrum and frequency of hepatic and gastrointestinal complications following pediatric BMT.
- To identify risk factors and potential differentiating markers for specific complications like graft-versus-host disease (GVHD) and veno-occlusive disease (VOD).
- To assess the impact of these complications on patient morbidity and mortality.
Main Methods:
- Retrospective study analyzing data from 132 pediatric patients who underwent 142 BMTs.
- Detailed review of medical records to identify and quantify hepatic and gastrointestinal complications.
- Statistical analysis to determine the incidence of various complications and their associations.
Main Results:
- High incidence of hyperbilirubinemia (28%) and clinically evident jaundice (16%).
- Acute GVHD occurred in 46% of patients, with significant liver (39%) and intestinal (60%) involvement.
- Veno-occlusive disease (VOD) affected 18% of patients; elevated transaminases were higher in GVHD/VOD.
- Biliary sludging (20%), mucositis (90%), vomiting (85%), and diarrhea (67%) were common GI issues.
- Diarrhea etiologies included GVHD (27%), viral infections (6%), C. difficile (8%), and unknown causes (28%).
- Gastrointestinal bleeding occurred in 8% and was disproportionately linked to ICU admission and 100-day mortality.
Conclusions:
- Hepatic and gastrointestinal complications are major contributors to morbidity and mortality in pediatric BMT recipients.
- Serum bilirubin levels may aid in differentiating between VOD and hepatic GVHD.
- Close monitoring and management of GI and hepatic complications are essential for improving survival rates post-pediatric BMT.
Abstract:
This retrospective study comprehensively examined hepatic and gastrointestinal complications post-bone marrow transplant (BMT) in a heterogeneous group of 132 pediatric patients that underwent 142 transplants. Hyperbilirubinemia occurred in 28% of this population with clinically evident jaundice in 16%. Acute graft-versus-host disease (GVHD) occurred in 46% of the population, with liver involvement in 39% and intestinal involvement in 60% of those with acute GVHD. Veno-occlusive disease (VOD) occurred in 18% of the population. A greater increase in hepatic transaminases was noted in GVHD and VOD than nonspecific liver injury. Serum bilirubin may help to differentiate between VOD and hepatic GVHD. Biliary sludging occurred in 20% of patients and was associated with increased morbidity. Common post transplant gastrointestinal complications included mucositis in 90%, vomiting in 85% and abdominal pain in 71%. TPN support post transplant was required in 91%. Diarrhea occurred in 67% with the most common identified etiologies reported as GVHD (27%), viral (6%), Clostridium difficile (8%) infections and unknown (28%). Typhilitis developed in 3.5%. Melena or hematochezia occurred in 11 patients (8%). However, gastrointestinal bleeding was disproportionately represented in intensive care unit admissions (5/27) and 100 day mortality (5/21). Gastrointestinal and hepatic complications represent a major cause of morbidity and mortality in pediatric BMT recipients.
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