afstoting na beenmergtransplantatie chronic lung rejection bronchiolitis obliterans lung rejection after hematopoietic stemcell transplantation
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
2 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patients whom are selected for hematopoietic stem cell transplantation
Exclusion criteria
Exclusion criteria: no informed consent all patients after hematopoietic stem cell transplantation will be included except patients that do not want to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identifying biomarkers in the peripheral blood that predict BOS by a sgnificant elevation before a lungfunction decline occurs (i.e. a drop in FEV1 of 20%) after allogeneic hemtopoietic stem cell transplantation. . | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the incidence and outcome of allo-reactive lung syndromes (i.e. BOS and other ARLS) in patients that underwent allogeneic haematopoietic stem cell transplantation. | — |
Countries
Netherlands
Outcome results
None listed