Re-evaluating treatment thresholds in patient blood management: Female patients experience more perioperative anaemia and higher transfusion rates in major elective surgery.

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-10-01 Epub Date: 2024-07-24 DOI:10.1111/vox.13717
Sumedha Arya, Alanna Howell, Lee Vernich, Yulia Lin, Katerina Pavenski, John Freedman
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Abstract

Background and objectives: By optimizing erythropoiesis, patient blood management (PBM) programmes can reduce transfusions, lower mortality and provide cost-effective care. While definitions of anaemia have historically varied by sex, for the purposes of PBM, anaemia is defined as a haemoglobin <130 g/L. Our objective was to describe whether perioperative anaemia and transfusion rates in the PBM setting vary by sex.

Materials and methods: We conducted a retrospective study of the Ontario Nurse Transfusion Coordinators Program (ONTraC) database from 2018 to 2022. ONTraC collects data from 25 Ontario hospitals which together account for >70% of Ontario's provincial blood use (~400,000 units per year). We collected data on patients undergoing elective isolated coronary artery bypass graft surgery (CABG), open heart valve replacement, CABG plus valve replacement, single-knee arthroplasty and single-hip arthroplasty.

Results: From 2018 to 2022, 17,700 patients were included in the ONTraC program; 47% were females (N = 8376). Across almost all years and procedures, females were found to have a significantly lower pre-operative, nadir and discharge haemoglobin as compared with males, irrespective of PBM interventions. Transfusion rates were significantly higher for females; this was most pronounced in cardiac surgery.

Conclusion: Females experienced more perioperative anaemia and higher transfusion rates. Historic sex-specific definitions of anaemia may contribute to a greater tolerance of anaemia in females. Prioritizing females for multimodal PBM and consistently achieving a pre-operative haemoglobin >130 g/L may reduce the amount of red blood cell (RBC) transfusions that female patients receive.

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重新评估患者血液管理的治疗阈值:女性患者在择期大手术中围术期贫血更严重,输血率更高。
背景和目的:通过优化红细胞生成,患者血液管理 (PBM) 计划可以减少输血、降低死亡率并提供具有成本效益的护理。虽然贫血的定义历来因性别而异,但就患者血液管理计划而言,贫血被定义为血红蛋白 资料和方法:我们对安大略省护士血液管理计划进行了回顾性研究:我们对 2018 年至 2022 年安大略省护士输血协调员计划(ONTraC)数据库进行了一项回顾性研究。ONTraC 收集了安大略省 25 家医院的数据,这些医院的用血量占安大略省全省用血量的 70% 以上(每年约 40 万单位)。我们收集了接受择期孤立冠状动脉旁路移植手术(CABG)、开放式心脏瓣膜置换术、CABG 加瓣膜置换术、单膝关节置换术和单髋关节置换术患者的数据:从2018年到2022年,共有17700名患者被纳入ONTraC计划;其中47%为女性(N = 8376)。在几乎所有年份和手术中,无论采取何种 PBM 干预措施,女性的术前、最低点和出院血红蛋白均显著低于男性。女性的输血率明显更高;这在心脏手术中最为明显:结论:女性围术期贫血程度更严重,输血率更高。结论:女性围术期贫血的情况更多,输血率更高。历史上对贫血的性别定义可能导致女性对贫血的容忍度更高。优先考虑女性患者进行多模式 PBM 治疗,并持续实现术前血红蛋白大于 130 g/L,可减少女性患者的红细胞(RBC)输注量。
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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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