Efficient granulocyte collection method using high concentrations of medium molecular weight hydroxyethyl starch.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
07 2023
Historique:
revised: 13 04 2023
received: 28 08 2022
accepted: 22 04 2023
medline: 14 7 2023
pubmed: 9 6 2023
entrez: 9 6 2023
Statut: ppublish

Résumé

Granulocyte transfusion therapy is a rational therapeutic option for patients with prolonged, severe neutropenia. Although high molecular weight hydroxyethyl starch (hHES) facilitates the separation of red blood cells during granulocyte collection, renal dysfunction has been noted as a potential side effect. HES130/0.4 (Voluven®) is a medium molecular weight HES (mHES) with superior safety profiles compared to hHES. Although HES130/0.4 is reportedly effective in the collection of granulocytes, we lack studies comparing the efficiency of granulocyte collection using HES130/0.4 and hHES. We retrospectively collected the data from 60 consecutive apheresis procedures performed on 40 healthy donors at the Okayama University Hospital between July 2013 and December 2021. All procedures were performed using the Spectra Optia system. Based on the HES130/0.4 concentration in the separation chamber, granulocyte collection methods using HES130/0.4 were classified into m0.46, m0.44, m0.37, and m0.8 groups. We used HES130/0.4 and hHES groups to compare the various sample collection methods. The median granulocyte collection efficiency (CE) was approximately 24.0% and 28.1% in the m0.8 and hHES groups, respectively, which were significantly higher than those in the m0.46, m0.44, and m0.37 groups. One month following granulocyte collection with HES130/0.4, no significant changes were observed in serum creatinine levels compared to those before the donation. Therefore, we propose a granulocyte collection approach employing HES130/0.4, which is comparable to the use of hHES in terms of the granulocyte CE. A high concentration of HES130/0.4 in the separation chamber was considered crucial for granulocyte collection.

Sections du résumé

BACKGROUND
Granulocyte transfusion therapy is a rational therapeutic option for patients with prolonged, severe neutropenia. Although high molecular weight hydroxyethyl starch (hHES) facilitates the separation of red blood cells during granulocyte collection, renal dysfunction has been noted as a potential side effect. HES130/0.4 (Voluven®) is a medium molecular weight HES (mHES) with superior safety profiles compared to hHES. Although HES130/0.4 is reportedly effective in the collection of granulocytes, we lack studies comparing the efficiency of granulocyte collection using HES130/0.4 and hHES.
STUDY DESIGN AND METHODS
We retrospectively collected the data from 60 consecutive apheresis procedures performed on 40 healthy donors at the Okayama University Hospital between July 2013 and December 2021. All procedures were performed using the Spectra Optia system. Based on the HES130/0.4 concentration in the separation chamber, granulocyte collection methods using HES130/0.4 were classified into m0.46, m0.44, m0.37, and m0.8 groups. We used HES130/0.4 and hHES groups to compare the various sample collection methods.
RESULTS
The median granulocyte collection efficiency (CE) was approximately 24.0% and 28.1% in the m0.8 and hHES groups, respectively, which were significantly higher than those in the m0.46, m0.44, and m0.37 groups. One month following granulocyte collection with HES130/0.4, no significant changes were observed in serum creatinine levels compared to those before the donation.
CONCLUSION
Therefore, we propose a granulocyte collection approach employing HES130/0.4, which is comparable to the use of hHES in terms of the granulocyte CE. A high concentration of HES130/0.4 in the separation chamber was considered crucial for granulocyte collection.

Identifiants

pubmed: 37293978
doi: 10.1111/trf.17450
doi:

Substances chimiques

Hydroxyethyl Starch Derivatives 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1344-1353

Informations de copyright

© 2023 AABB.

Références

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Auteurs

Takumi Kondo (T)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Keiko Fujii (K)

Division of Clinical Laboratory, Okayama University Hospital, Okayama, Japan.

Nobuharu Fujii (N)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Yuichi Sumii (Y)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Tomohiro Urata (T)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Maiko Kimura (M)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Masayuki Matsuda (M)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Shuntaro Ikegawa (S)

Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Kana Washio (K)

Department of Pediatrics/Pediatric Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Hideaki Fujiwara (H)

Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Noboru Asada (N)

Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Daisuke Ennishi (D)

Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Center for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan.

Hisakazu Nishimori (H)

Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Ken-Ichi Matsuoka (KI)

Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Fumio Otsuka (F)

Division of Clinical Laboratory, Okayama University Hospital, Okayama, Japan.
Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Yoshinobu Maeda (Y)

Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

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