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报告的与溶剂/去污剂血浆相关的输血相关急性肺损伤-病例系列。

Reported transfusion-related acute lung injury associated with solvent/detergent plasma - A case series.

机构信息

Department of Intensive Care, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Laboratory of Experimental Intensive Care and Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Transfusion. 2022 Mar;62(3):594-599. doi: 10.1111/trf.16822. Epub 2022 Feb 17.

Abstract

BACKGROUND

Antibody-mediated transfusion-related acute lung injury (TRALI) is caused by donor HLA or HNA antibodies in plasma-containing products. In the Netherlands 55,000 units of solvent/detergent plasma (SDP), a pooled plasma product, are transfused yearly. It's produced by combining plasma from hundreds of donors, diluting harmful antibodies. Due to a lack of reported cases following implementation, some have labeled SDP as "TRALI safe".

STUDY DESIGN AND METHODS

Pulmonary transfusion reactions involving SDP reported to the Dutch national hemovigilance network in 2016-2019 were reviewed. Reporting hospitals were contacted for additional information, cases with TRALI and imputability definite, probable, or possible were included and informed consent was sought.

RESULTS

A total of three TRALI and nine TACO cases were reported involving SDP. The imputability of one TRALI case was revised from possible to unlikely and excluded; in one case no informed consent was obtained. We present a case description of TRALI following SDP transfusion in a 69-year-old male, 3 days following endovascular aortic aneurysm repair. The patient received one unit of SDP to correct a heparin-induced coagulopathy, prior to removal of a spinal catheter post-operatively. Within five hours he developed hypoxemic respiratory failure requiring intubation, hypotension, bilateral chest infiltrates, and leucopenia. The patient made a full recovery.

CONCLUSION

This case of TRALI, following transfusion of a single unit of SDP to a patient without ARDS risk factors, demonstrates that TRALI can occur with this product. Clinicians should remain vigilant and continue to report suspected cases, to help further understanding of SDP-associated TRALI.

摘要

背景

抗体介导的输血相关性急性肺损伤(TRALI)是由血浆制品中的供体 HLA 或 HNA 抗体引起的。在荷兰,每年输注 55000 单位溶剂/去污剂血浆(SDP),这是一种混合血浆产品,通过合并来自数百名供体的血浆来稀释有害抗体。由于实施后缺乏报告病例,有人将 SDP 标记为“TRALI 安全”。

研究设计和方法

对 2016 年至 2019 年向荷兰全国血液监测网络报告的涉及 SDP 的肺部输血反应进行了回顾。与报告医院联系以获取更多信息,包括 TRALI 和可归因性明确、可能或可能的病例,并征求了知情同意。

结果

共报告了三例 SDP 相关的 TRALI 和九例 TACO 病例。一例 TRALI 病例的可归因性从可能改为不太可能,并被排除;在一例病例中,未获得知情同意。我们报告了一例 69 岁男性在血管内主动脉瘤修复后 3 天接受 SDP 输血后发生 TRALI 的病例。该患者在手术后移除脊髓导管前因肝素诱导的凝血障碍接受了 1 单位 SDP。五小时内,他出现低氧性呼吸衰竭,需要插管,低血压,双侧胸部浸润和白细胞减少。患者完全康复。

结论

本例 TRALI 是在没有 ARDS 危险因素的患者输注 1 单位 SDP 后发生的,表明该产品可发生 TRALI。临床医生应保持警惕,并继续报告疑似病例,以帮助进一步了解 SDP 相关的 TRALI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3258/9306621/c838b01b89b8/TRF-62-594-g001.jpg

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