Obstructive lung disease in children after allogeneic bone marrow transplantation

K R Schultz1, G J Green, D Wensley

  • 1Department of Pediatrics, University of British Columbia, Vancouver, Canada.

Blood
|November 1, 1994
PubMed

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.