Repeated apheresis donations cause important iron deficiency in male Japanese donors.

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-08-12 DOI:10.1111/vox.13720
Takeshi Odajima, Nelson H Tsuno, Junko Iwasaki, Koji Matsuzaki, Fumihiko Ishimaru, Rie Okubo, Junko Murakami, Kaori Kitsukawa, Katsuya Ikuta, Kazuo Muroi, Masahiro Satake, Shuichi Kino
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Abstract

Background and objectives: In Japan, apheresis donation of plasma is allowed to a maximum of 24 times a year, and plateletpheresis are counted as two plasmapheresis donations. Diversion of the initial blood flow is conducted for all donations, and additionally, blood remaining in apheresis machine circuit is lost. Here, we aimed to investigate on the health impact of frequent apheresis donations, as measured by the serum ferritin (sFer).

Materials and methods: A total of 538 male apheresis donors and 538 age-matched whole blood (WB) donors, who gave informed consent to join the study, were enrolled. sFer were compared, according to age. Another group of 19 apheresis donors were followed during four consecutive donations.

Results: About half (48%) of repeat male apheresis donors had iron deficiency (sFer < 26 ng/mL), compared with lower rates (13.9%) among male WB donors. It was evident in all age groups, except for teenagers, possibly because of the lower number of donations. Follow-up of the 19 donors for 4 months revealed a progressive decrease in sFer.

Conclusion: Blood remaining in the apheresis machine circuit and diversion of the initial blood flow have been implicated in iron deficiency for many years. Taking the present results, the manufacturer of apheresis equipment was requested to improve it to allow rinseback of the remaining blood, which was achieved only for plateletpheresis. Until further improvement, plasmapheresis frequency was reduced to 12 times a year. Additional measures, such as oral supplementation of iron, need to be considered.

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重复无细胞捐献会导致日本男性捐献者严重缺铁。
背景和目的:在日本,血浆分离捐献每年最多允许 24 次,血小板分离捐献算作两次血浆分离捐献。所有捐献都要对初始血流进行分流,此外,无采血机回路中的剩余血液也会流失。在此,我们旨在通过血清铁蛋白(sFer)的测量,研究频繁捐献血液对健康的影响:共招募了 538 名男性血液净化捐献者和 538 名年龄匹配的全血(WB)捐献者,他们都在知情同意的情况下参加了研究。对另一组 19 名无偿献血者进行了连续四次献血的跟踪调查:结果:约有一半(48%)的重复男性血液净化捐献者患有缺铁症(sFer 结论:在血液净化机中残留的血液可能会导致缺铁症:多年来,血液滞留在血液净化机回路中和初始血流分流一直被认为与缺铁有关。根据目前的结果,我们要求无细胞疗法设备的制造商对设备进行改进,以便能够冲洗剩余的血液,但只有血小板无细胞疗法能够做到这一点。在进一步改进之前,血浆置换的次数减少到每年 12 次。还需要考虑其他措施,如口服铁补充剂。
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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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