TY - JOUR
T1 - Diagnosis of Post-Hematopoietic Stem Cell Transplantation Bronchiolitis Obliterans Syndrome in Children
T2 - Time for a Rethink?
AU - Shanthikumar, Shivanthan
AU - Gower, William A.
AU - Cooke, Kenneth R.
AU - Bergeron, Anne
AU - Schultz, Kirk R.
AU - Barochia, Amisha
AU - Tamae-Kakazu, Maximiliano
AU - Charbek, Edward
AU - Reardon, Erin E.
AU - Calvo, Charlotte
AU - Casey, Alicia
AU - Cheng, Pi Chun
AU - Cole, Theresa S.
AU - Davies, Stella M.
AU - Das, Shailendra
AU - De, Alive
AU - Deterding, Robin R.
AU - Liptzin, Deborah R.
AU - Mechinaud, Francoise
AU - Rayment, Jonathan H.
AU - Robinson, Paul D.
AU - Siddaiah, Roopa
AU - Stone, Anne
AU - Srinivasin, Saumini
AU - Towe, Christopher T.
AU - Yanik, Gregory A.
AU - Iyer, Narayan P.
AU - Goldfarb, Samuel B.
N1 - Publisher Copyright:
© 2024 The American Society for Transplantation and Cellular Therapy
PY - 2024/8
Y1 - 2024/8
N2 - Hematopoietic stem cell transplantation (HSCT) is undertaken in children with the aim of curing a range of malignant and nonmalignant conditions. Unfortunately, pulmonary complications, especially bronchiolitis obliterans syndrome (BOS), are significant sources of morbidity and mortality post-HSCT. Currently, criteria developed by a National Institutes of Health (NIH) working group are used to diagnose BOS in children post-HSCT. Unfortunately, during the development of a recent American Thoracic Society (ATS) Clinical Practice Guideline on this topic, it became apparent that the NIH criteria have significant limitations in the pediatric population, leading to late diagnosis of BOS. Specific limitations include use of an outdated pulmonary function testing reference equation, a reliance on spirometry, use of a fixed forced expiratory volume in 1 second (FEV1) threshold, focus on obstructive defects defined by FEV1/vital capacity, and failure to acknowledge that BOS and infection can coexist. In this review, we summarize the evidence regarding the limitations of the current criteria. We also suggest potential evidence-based ideas for improving these criteria. Finally, we highlight a new proposed criteria for post-HSCT BOS in children that were developed by the authors of the recently published ATS clinical practice guideline, along with a pathway forward for improving timely diagnosis of BOS in children post-HSCT.
AB - Hematopoietic stem cell transplantation (HSCT) is undertaken in children with the aim of curing a range of malignant and nonmalignant conditions. Unfortunately, pulmonary complications, especially bronchiolitis obliterans syndrome (BOS), are significant sources of morbidity and mortality post-HSCT. Currently, criteria developed by a National Institutes of Health (NIH) working group are used to diagnose BOS in children post-HSCT. Unfortunately, during the development of a recent American Thoracic Society (ATS) Clinical Practice Guideline on this topic, it became apparent that the NIH criteria have significant limitations in the pediatric population, leading to late diagnosis of BOS. Specific limitations include use of an outdated pulmonary function testing reference equation, a reliance on spirometry, use of a fixed forced expiratory volume in 1 second (FEV1) threshold, focus on obstructive defects defined by FEV1/vital capacity, and failure to acknowledge that BOS and infection can coexist. In this review, we summarize the evidence regarding the limitations of the current criteria. We also suggest potential evidence-based ideas for improving these criteria. Finally, we highlight a new proposed criteria for post-HSCT BOS in children that were developed by the authors of the recently published ATS clinical practice guideline, along with a pathway forward for improving timely diagnosis of BOS in children post-HSCT.
KW - bronchiolitis obliterans
KW - bronchiolitis obliterans syndrome
KW - pediatrics
KW - stem cell transplantation
UR - http://www.scopus.com/inward/record.url?scp=85198163965&partnerID=8YFLogxK
U2 - 10.1016/j.jtct.2024.05.012
DO - 10.1016/j.jtct.2024.05.012
M3 - Review article
C2 - 38897861
AN - SCOPUS:85198163965
SN - 2666-6367
VL - 30
SP - 760
EP - 769
JO - Transplantation and Cellular Therapy
JF - Transplantation and Cellular Therapy
IS - 8
ER -