Volume 115, Issue 5 p. 456-465
Original Paper

A Japanese multi‐institutional collaborative study of antigen‐positive red blood cell (RBC) transfusions in patients with corresponding RBC antibodies

Chiaki Yamada

Transfusion and Cell Therapy, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Akihiro Takeshita

Corresponding Author

Transfusion and Cell Therapy, Hamamatsu University School of Medicine, Hamamatsu, Japan

Correspondence: Akihiro Takeshita, Transfusion and Cell Therapy, Hamamatsu University School of Medicine, 1‐20‐1 Handayama, Higashiku, Hamamatsu, Shizuoka, 431‐3192, Japan

E‐mail: akihirot@hama-med.ac.jp

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Hitoshi Ohto

Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan

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Ken Ishimaru

Blood Service Headquarters, Japanese Red Cross Society, Minato‐ku, Japan

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Kinuyo Kawabata

Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan

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Yuriko Nomaguchi

Division of Transfusion Medicine, Fukuoka University, Fukuoka, Japan

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Yasue Haraguchi

Department of Blood Transfusion Medicine and Cell Therapy, Kagoshima University, Kagoshima, Japan

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Misao Abe

Blood Transfusion & Cell Therapy, Kansai Medical University, Moriguchi, Japan

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Koki Sobue

Division of Blood Transfusion, Toho University, Ota‐ku, Japan

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Hiroyuki Takenouchi

Department of Transfusion and Cell Therapy, University of Miyazaki, Miyazaki, Japan

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Junko Takadate

Division of Central Clinical Laboratory, Iwate Medical University, Morioka, Japan

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Masami Kamimura

Division of Blood Transfusion, Niigata University, Niigata, Japan

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Akiko Katai

Department of Transfusion Medicine, Aichi Medical University, Aichi‐gun, Japan

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Daisuke Kasai

Department of Clinical Laboratory, Nagano Municipal Hospital, Nagano, Japan

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Yumiko Minami

Division of Transfusion Medicine, Osaka Medical College, Takatsuki, Japan

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Tatsuya Sugimoto

Division of Medical Technology and Department of Blood Transfusion Service, Tokai University, Isehara, Japan

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Junko Michino

Division of Clinical Laboratory, Transfusion Medicine and Cell Therapy, University of Toyama, Toyama, Japan

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Kazuhiro Nagai

Transfusion and Cell Therapy Unit, Nagasaki University, Nagasaki, Japan

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Mikako Kumagai

Division of Blood Transfusion, Akita University, Akita, Japan

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Yuichi Hasegawa

Department of Transfusion Medicine, University of Tsukuba, Tsukuba, Japan

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Keiko Ishizuka

Transfusion and Cell Therapy, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Naoki Ohtomo

Center for Transfusion Medicine and Cell Therapy, Tokyo Medical and Dental University, Bunkyo‐ku, Japan

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Naotomo Yamada

Department of Transfusion Medicine, Saga University, Saga, Japan

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Kazuo Muroi

Division of Cell Transplantation and Transfusion, Jichi Medical University, Shimotsuke, Japan

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Tadashi Matsushita

Department of Transfusion Medicine, Nagoya University, Nagoya, Japan

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Koki Takahashi

Blood Service Headquarters, Japanese Red Cross Society, Minato‐ku, Japan

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First published: 02 March 2020
Citations: 2

Abstract

Background and objectives

It is sometimes difficult to obtain antigen‐negative red blood cells (RBCs) for patients with antibodies against RBCs. However, the frequency and severity of the adverse reactions have not been well elucidated. Here, we conducted a multi‐institutional collaborative study to clarify the background, frequency and clinical significance of antigen‐positive RBC transfusions to patients with the respective antibodies.

Materials and methods

The survey included the background of patients, antigens on RBCs transfused, total amount of antigen‐positive RBCs transfused, results from antibody screen and direct antiglobulin tests, specificity of antibodies, adverse reactions and efficacies. All antibodies were surveyed regardless of their clinical significance.

Results

In all, 826 cases containing 878 antibodies were registered from 45 institutions. The main reasons for antigen‐positive RBC transfusions included ‘negative by indirect antiglobulin test’ (39%) and ‘detection of warm autoantibodies’ (25%). In 23 cases (3% of total), some adverse reactions were observed after antigen‐positive RBC transfusion, and 25 antibodies (9 of 119 clinically significant and 16 of 646 insignificant antibodies) were detected. Non‐specific warm autoantibodies were detected in 9 cases, anti‐E in 5 cases, 2 cases each of anti‐Lea, anti‐Jra or cold alloantibodies, and 1 case each of anti‐Dib, anti‐Leb or anti‐P1. Other antibodies were detected in 2 further cases. Five (22%) of these 23 cases, who had anti‐E (3 cases) or anti‐Jra (2 cases), experienced clinically apparent haemolysis.

Conclusions

Adverse reactions, especially haemolysis, were more frequently observed in cases with clinically significant antibodies than those with clinically insignificant antibodies (P < 0·001).

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