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Hematopoietic cell infusion-related adverse events in pediatric/small recipients in a prospective/multicenter study.
Ikeda, Kazuhiko; Ohto, Hitoshi; Yamada-Fujiwara, Minami; Okuyama, Yoshiki; Fujiwara, Shin-Ichiro; Muroi, Kazuo; Mori, Takehiko; Kasama, Kinuyo; Kanamori, Heiwa; Iseki, Tohru; Nagamura-Inoue, Tokiko; Kameda, Kazuaki; Kanda, Junya; Nagai, Kazuhiro; Fujii, Nobuharu; Ashida, Takashi; Hirose, Asao; Takahashi, Tsutomu; Minakawa, Keiji; Tanosaki, Ryuji.
Afiliação
  • Ikeda K; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Ohto H; Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan.
  • Yamada-Fujiwara M; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Okuyama Y; Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan.
  • Fujiwara SI; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Muroi K; Division of Blood Transfusion and Cell Therapy, Tohoku University Hospital, Sendai, Japan.
  • Mori T; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Kasama K; Division of Transfusion and Cell Therapy, Tokyo Metropolitan Komagome Hospital, Tokyo, Japan.
  • Kanamori H; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Iseki T; Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke, Japan.
  • Nagamura-Inoue T; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Kameda K; Cell Transplantation and Transfusion, Jichi Medical University, Tochigi, Japan.
  • Kanda J; Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
  • Nagai K; Department of Transfusion Medicine, Tokyo Jikei University Hospital, Tokyo, Japan.
  • Fujii N; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Ashida T; Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan.
  • Hirose A; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Takahashi T; Department of Transfusion Medicine and Cell Therapy, Chiba University Hospital, Chiba, Japan.
  • Minakawa K; Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
  • Tanosaki R; Institution of Medical Science, University of Tokyo, Tokyo, Japan.
Transfusion ; 60(5): 1015-1023, 2020 05.
Article em En | MEDLINE | ID: mdl-32306410
ABSTRACT

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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peso Corporal / Transplante de Células-Tronco Hematopoéticas / Reação Transfusional Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Transfusion Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peso Corporal / Transplante de Células-Tronco Hematopoéticas / Reação Transfusional Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Transfusion Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão