Obstructive lung disease in children after allogeneic bone marrow transplantation
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Updated: Oct 24, 2026

Development of Obliterative Bronchiolitis in a Murine Model of Orthotopic Lung Transplantation
Published on: July 10, 2012
K R Schultz1, G J Green, D Wensley
1Department of Pediatrics, University of British Columbia, Vancouver, Canada.
Insights
Pediatric allogeneic bone marrow transplantation (BMT) carries a higher risk of obstructive lung disease (OLD) than previously thought. Chronic graft-versus-host disease (GVHD) and liver involvement are key risk factors in children post-BMT.
Area of Science:
- Pediatric Hematology/Oncology
- Pulmonology
- Transplantation Immunology
Background:
- Obstructive lung disease (OLD) is a known complication following allogeneic bone marrow transplantation (BMT).
- While adult OLD incidence is low (~3%), pediatric data is scarce.
- This study investigates OLD prevalence and risk factors in pediatric BMT recipients.
Purpose of the Study:
- To determine the incidence of obstructive lung disease (OLD) in pediatric patients after allogeneic bone marrow transplantation (BMT).
- To identify risk factors associated with the development of OLD in this population.
Main Methods:
- Retrospective analysis of 89 pediatric allogeneic BMTs performed between 1980-1992.
- Diagnosis of OLD based on clinical symptoms, pulmonary function tests, lung biopsy, and CT scans.
- Evaluation of 67 children surviving >90 days post-BMT for OLD development.
Main Results:
- 19.4% (13/67) of at-risk children developed OLD, with 3 cases being transient.
- High-risk factors for OLD included chronic graft-versus-host disease (GVHD) (37.1%), increased donor age, acute GVHD, and mismatched/unrelated donor transplants.
- No correlation found with methotrexate, total body irradiation, or CMV reactivity.
- In children with chronic GVHD, prior liver involvement (57.9%) was a significant predictor of OLD.
Conclusions:
- The prevalence of OLD in children post-allogeneic BMT is higher than in adults.
- Chronic GVHD, particularly with liver involvement, is a significant risk factor for pediatric OLD post-BMT.
- Further research is needed to confirm age as a risk factor for developing OLD after BMT.
Abstract:
Obstructive lung disease (OLD) has been described as a significant complication after allogeneic bone marrow transplantation (BMT). The incidence of OLD in adults appears to be low (approximately 3%), but there is little data for children. We analyzed 89 consecutive pediatric allogeneic BMTs, > or = 1.5 years post-BMT, performed at British Columbia's Children's Hospital from 1980 to 1992 for evidence of OLD. Diagnosis of OLD was based on clinical findings (nonproductive cough, wheezing, and dyspnea with no evidence of infection), pulmonary function tests (FEV1 < 80% and FEF25-75% < 60% predicted), lung biopsy, and computed tomography scan. Sixty-seven of the 89 children evaluated survived > or = 90 days and were classified as at risk for OLD. Thirteen of 67 (19.4%), developed OLD, 3 of which were transient. The development of OLD was strongly associated with the following high-risk groups: chronic graft-versus-host disease (GVHD) (37.1% OLD), increased donor age, acute GVHD, and either mismatched related or matched unrelated donor transplants. No correlation was found with methotrexate prophylaxis for GVHD, total body irradiation, or cytomegalovirus reactivity in either donor or recipient and the development of OLD. Further analysis of only children with chronic GVHD showed that liver involvement by GVHD before the onset of OLD (57.9%) was the only other significant predictive factor. We observed an overall increased prevalence of OLD in children compared with that previously reported in adults. Further studies are required to confirm whether age is a risk factor for development of OLD after allogeneic BMT.
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