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冷沉淀 ABO 配型的实践模式与 ABO 相容和不相容冷沉淀输注后患者结局的关系。

Practice patterns of ABO-matching for cryoprecipitate and patient outcomes after ABO-compatible versus incompatible cryoprecipitate.

机构信息

Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

Department of Anesthesiology and Pain Medicine, University of Toronto, Toronto, Ontario, Canada.

出版信息

Vox Sang. 2022 Sep;117(9):1105-1111. doi: 10.1111/vox.13330. Epub 2022 Jul 6.

Abstract

BACKGROUND AND OBJECTIVES

This sub-study of the FIBRES trial sought to examine the patterns of ABO-compatible cryoprecipitate administration and to identify adverse consequences of ABO-incompatible cryoprecipitate.

MATERIALS AND METHODS

This was a post hoc analysis of data collected from the FIBRES randomized clinical trial comparing fibrinogen concentrate with cryoprecipitate in the treatment of bleeding related to hypofibrinogenemia after cardiac surgery. The primary outcome was the percentage of administered cryoprecipitate that was ABO-compatible. Secondary outcomes were adverse events at 28 days. A follow-up survey was distributed to the FIBRES participating sites to examine the rationale behind the identified cryoprecipitate ABO-matching practice patterns.

RESULTS

A total of 363 patients were included: 53 (15%) received ABO-incompatible cryoprecipitate and 310 (85%) received ABO-compatible cryoprecipitate. There was an increased incidence of post-operative anaemia in the ABO-incompatible group (15; 28.3%) in comparison to the ABO-compatible (44; 14.2%) group (p = 0.01) at 28 days, which was unrelated to haemolysis, without a significant difference in transfusion requirement. In the multivariable logistic regression models accounting for clustering by site, there was no observed statistically significant association between the administration of ABO-incompatible cryoprecipitate and any other adverse outcomes. Nine out of 11 sites did not have a policy requiring ABO-matched cryoprecipitate.

CONCLUSION

This sub-study demonstrated that most cryoprecipitate administered in practice is ABO-compatible, despite the absence of guidelines or blood bank policies to support this practice. A signal towards increased risk of post-operative anaemia may be explained by higher rates of urgent surgery (vs. elective) in the ABO-incompatible group. Future studies should prospectively examine the impact of ABO-compatible versus incompatible cryoprecipitate to conclusively establish if there is a meaningful clinical impact associated with the administration of ABO-incompatible cryoprecipitate.

摘要

背景与目的

本项 FIBRES 试验的子研究旨在检查 ABO 相容冷沉淀的输注模式,并确定 ABO 不相容冷沉淀的不良后果。

材料与方法

这是一项对 FIBRES 随机临床试验数据的事后分析,该试验比较了纤维蛋白原浓缩物与心脏手术后低纤维蛋白原血症相关出血时冷沉淀的治疗效果。主要结局是输注的冷沉淀中 ABO 相容的比例。次要结局是 28 天的不良事件。一项随访调查分发给 FIBRES 参与的站点,以检查确定的冷沉淀 ABO 匹配实践模式背后的原理。

结果

共纳入 363 例患者:53 例(15%)接受 ABO 不相容冷沉淀,310 例(85%)接受 ABO 相容冷沉淀。在 28 天的时间内,ABO 不相容组的术后贫血发生率更高(15 例;28.3%),而 ABO 相容组(44 例;14.2%)(p=0.01),这与溶血无关,输血需求无显著差异。在考虑站点聚类的多变量逻辑回归模型中,输注 ABO 不相容冷沉淀与任何其他不良结局之间没有观察到统计学上的显著关联。11 个站点中有 9 个没有要求 ABO 匹配冷沉淀的政策。

结论

本子研究表明,尽管缺乏指南或血库政策来支持这种做法,但在实践中输注的大多数冷沉淀是 ABO 相容的。术后贫血风险增加的信号可能是由于 ABO 不相容组中紧急手术(与择期手术相比)的比例较高。未来的研究应前瞻性地检查 ABO 相容与不相容冷沉淀的影响,以明确确定输注 ABO 不相容冷沉淀是否与临床意义相关。

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