Introduction of 7-day amotosalen/ultraviolet A light pathogen-reduced platelets in Honduras: Impact on platelet availability in a lower middle-income country.

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-10-07 DOI:10.1111/vox.13740
Marcelo Pedraza, Julio Mejia, John P Pitman, Glenda Arriaga
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Abstract

Background and objectives: Honduras became the first lower middle-income country (LMIC) to adopt amotosalen/UVA pathogen-reduced (PR) platelet concentrates (PCs) as a national platelet safety measure in 2018. The Honduran Red Cross (HRC) produces ~70% of the national platelet supply using the platelet-rich plasma (PRP) method. Between 2015 and 2018, PCs were screened with bacterial culture and issued as individual, non-pooled PRP units with weight-based dosing and 5-day shelf-life. PR PCs were produced in six-PRP pools with a standardized dose (≥3.0 × 1011), no bacterial screening and 7-day shelf-life. Gamma irradiation and leukoreduction were not used.

Materials and methods: PC production and distribution data were retrospectively analysed in two periods. Period 1 (P1) included 3 years of PRP PCs and a transition year (2015-18). Period 2 (P2) included 5 years of PR PCs (2019-23). PC doses were standardized to an equivalent adult dose for both periods. Descriptive statistics were calculated.

Results: HRC produced 10% more PC doses per year on average in P2 compared to P1. Mean annual waste at HRC declined from 23.9% in P1 to 1.1% in P2. Two urban regions consumed 96% of PC doses in P1 and 88.3% in P2. PC distributions increased in 14/18 regions.

Conclusion: Standardized dosage, PR and 7-day shelf-life increased PC availability, reduced waste, eliminated bacterial screening and avoided additional costs for arboviral testing, leukoreduction and irradiation. Access to PC transfusion remains limited in Honduras; however, the conversion to pooled PR PCs illustrates the potential to sustainably expand PC distribution in an LMIC.

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在洪都拉斯引入 7 天阿莫吐林/紫外线 A 光病原体减少血小板:对中低收入国家血小板供应的影响。
背景和目标:洪都拉斯于 2018 年成为第一个采用阿莫他林/UVA 病原体还原(PR)血小板浓缩物(PCs)作为国家血小板安全措施的中低收入国家(LMIC)。洪都拉斯红十字会(HRC)使用富血小板血浆(PRP)方法生产全国约 70% 的血小板供应。2015 年至 2018 年期间,PC 经细菌培养筛选后作为单独的非集合 PRP 单位发放,按体重计量,保质期为 5 天。PR PCs 以六个 PRP 池的形式生产,剂量标准化(≥3.0 × 1011),不进行细菌筛选,保质期为 7 天。未使用伽马辐照和白细胞还原法:对两个时期的 PC 生产和销售数据进行了回顾性分析。第一阶段(P1)包括 3 年的 PRP PC 和一个过渡年(2015-18 年)。第二阶段(P2)包括 5 年的 PR PC(2019-23 年)。两个时期的 PC 剂量均标准化为等效成人剂量。计算了描述性统计结果:与 P1 相比,HRC 在 P2 期间平均每年多生产 10%的 PC 剂量。HRC的年平均废物量从P1的23.9%下降到P2的1.1%。两个城市地区在 P1 和 P2 分别消耗了 96% 和 88.3% 的 PC 剂量。14/18 个地区的 PC 分布有所增加:结论:标准化剂量、PR 和 7 天保质期提高了 PC 的可用性,减少了浪费,消除了细菌筛查,并避免了虫媒病毒检测、减白和辐照的额外成本。洪都拉斯获得 PC 输血的机会仍然有限;但是,转用集中 PR PC 表明,在低收入国家和地区可持续扩大 PC 的分发范围。
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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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