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Updated: Sep 15, 2025

Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017
Bronchodilator Response: Utility and implications in patients undergoing hematopoietic stem cell transplantation
Reid H Eggleston1, Mehrdad Hefazi Torghabeh2, Alexander S Niven1
1Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, USA.
Background:
Bronchodilator response (BDR) assessment is routinely included in pulmonary evaluation before hematopoietic cell transplantation (HCT), but its prognostic significance remains uncertain. Recent European Respiratory Society/American Thoracic Society (ERS/ATS) criteria changes complicate interpretation.
Research Question:
To examine associations between BDR and clinical outcomes in HCT recipients and compare prognostic utility of traditional versus revised BDR criteria.
Study Design And Methods:
In this single-center study of 1,255 adult allogeneic HCT recipients (2005-2021), we assessed BDR using both 2005 criteria (≥12 % and ≥200 mL increase in FEV1/FVC) and 2022 criteria (>10 % of predicted increase). Primary outcomes included bronchiolitis obliterans syndrome (BOS) development, 120-day ICU admission, and survival.
Results:
Among patients (58 % male, mean age 51.3 ± 13.6 years), positive BDR frequency was low (11.5 % by 2005 criteria, 14.2 % by 2022 criteria), with high concordance (>94 %). BDR did not predict BOS development, with similar pre-transplant FEV1 responses between patients who later developed BOS and those who did not (5.0 % vs. 4.9 %, p = 0.841). Unadjusted analyses showed pre-transplant BDR positivity using 2005 criteria was associated with increased mortality (HR = 1.45, p = 0.006) and ICU admission (HR = 1.65, p = 0.005), but these associations did not persist after adjusting for baseline FEV1 (aHR = 1.17, p = 0.275; aHR = 1.09, p = 0.648).
Interpretation:
BDR testing provides minimal additional prognostic information beyond baseline lung function assessment in HCT recipients and does not predict BOS development. Our findings support that BOS represents a fibroproliferative process distinct from disorders characterized by airway hyperresponsiveness, suggesting bronchodilator testing could be eliminated from standard HCT protocols without compromising risk assessment.
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