TY - JOUR
T1 - Hematopoietic cell infusion-related adverse events in pediatric/small recipients in a prospective/multicenter study
AU - Ikeda, Kazuhiko
AU - Ohto, Hitoshi
AU - Yamada-Fujiwara, Minami
AU - Okuyama, Yoshiki
AU - Fujiwara, Shin ichiro
AU - Muroi, Kazuo
AU - Mori, Takehiko
AU - Kasama, Kinuyo
AU - Kanamori, Heiwa
AU - Iseki, Tohru
AU - Nagamura-Inoue, Tokiko
AU - Kameda, Kazuaki
AU - Kanda, Junya
AU - Nagai, Kazuhiro
AU - Fujii, Nobuharu
AU - Ashida, Takashi
AU - Hirose, Asao
AU - Takahashi, Tsutomu
AU - Minakawa, Keiji
AU - Tanosaki, Ryuji
N1 - Funding Information:
We thank Dr. S. Otsuki (Japan Institute of Statistical Technology) for statistical analysis; Dr. M. Takanashi (Cell Therapy Committee, JSTMCT) for the valuable advice in carrying out the study; and N. Kurokawa and T. Kodama (JSTMCT) for their assistance.
Publisher Copyright:
© 2020 AABB
PY - 2020/5/1
Y1 - 2020/5/1
N2 - BACKGROUND: Hematopoietic cell infusion-related adverse events (HCI-AEs) in hematopoietic stem cell transplantations (HSCTs) have been largely attributed to toxicity of dimethyl sulfoxide (DMSO) for cryopreservation, but HSC products also contain various cells and plasma components. Our recent prospective study of 1125 HSCT recipients revealed the highest overall HCI-AE rate in bone marrow transplantation (BMT) using fresh/noncryopreserved products, although products of peripheral blood stem cell transplantation and cord blood transplantation (CBT) are generally cryopreserved with DMSO containing smaller plasma volumes. We aimed to clarify if product volume and component effects are more substantial in small recipients including children. STUDY DESIGN AND METHODS: We performed subgroup analysis on 219 recipients of 45 kg or less body weight (whole small recipients), including 90 children (pediatric recipients), from the original cohort (general recipients). RESULTS: Whereas overall HCI-AE rates did not differ among hematopoietic stem cell sources in the general recipients, bradycardia most often occurred after CBT in whole small recipients. Conversely, whole small and general recipients shared the same trend of having the highest rate of hypertension in BMT. The overall HCI-AE rate was higher in allogeneic HSCT compared with autologous HSCT. Notably, pediatric recipients showed a 10-fold higher incidence of nausea and vomiting in allogeneic HSCT compared with autologous HSCT, suggesting a possible role of allogeneic antigens. Multivariate analysis identified a relatively large infusion volume per body weight as a significant factor correlating with HCI-AE in whole small recipients. CONCLUSIONS: We should be aware of product volume and specific HCI-AEs such as nausea and vomiting in small patients including children.
AB - BACKGROUND: Hematopoietic cell infusion-related adverse events (HCI-AEs) in hematopoietic stem cell transplantations (HSCTs) have been largely attributed to toxicity of dimethyl sulfoxide (DMSO) for cryopreservation, but HSC products also contain various cells and plasma components. Our recent prospective study of 1125 HSCT recipients revealed the highest overall HCI-AE rate in bone marrow transplantation (BMT) using fresh/noncryopreserved products, although products of peripheral blood stem cell transplantation and cord blood transplantation (CBT) are generally cryopreserved with DMSO containing smaller plasma volumes. We aimed to clarify if product volume and component effects are more substantial in small recipients including children. STUDY DESIGN AND METHODS: We performed subgroup analysis on 219 recipients of 45 kg or less body weight (whole small recipients), including 90 children (pediatric recipients), from the original cohort (general recipients). RESULTS: Whereas overall HCI-AE rates did not differ among hematopoietic stem cell sources in the general recipients, bradycardia most often occurred after CBT in whole small recipients. Conversely, whole small and general recipients shared the same trend of having the highest rate of hypertension in BMT. The overall HCI-AE rate was higher in allogeneic HSCT compared with autologous HSCT. Notably, pediatric recipients showed a 10-fold higher incidence of nausea and vomiting in allogeneic HSCT compared with autologous HSCT, suggesting a possible role of allogeneic antigens. Multivariate analysis identified a relatively large infusion volume per body weight as a significant factor correlating with HCI-AE in whole small recipients. CONCLUSIONS: We should be aware of product volume and specific HCI-AEs such as nausea and vomiting in small patients including children.
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U2 - 10.1111/trf.15786
DO - 10.1111/trf.15786
M3 - Article
C2 - 32306410
AN - SCOPUS:85083490435
SN - 0041-1132
VL - 60
SP - 1015
EP - 1023
JO - Transfusion
JF - Transfusion
IS - 5
ER -