首页> 外文期刊>Canada communicable disease report =: Relev?des maladies transmissibles au Canada >A summary of the Transfusion Transmitted Injuries Surveillance System: 2006 – 2012
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A summary of the Transfusion Transmitted Injuries Surveillance System: 2006 – 2012

机译:2006 – 2012年输血传播伤害监测系统摘要

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Abstract Background: The Transfusion Transmitted Injuries Surveillance System (TTISS) is a pan-Canadian surveillance system established by the Public Health Agency of Canada (the Agency) in partnership with the provinces and territories to capture non-nominal data on adverse transfusion reactions in Canadian hospitals providing transfusion services with the overarching goal of improving patient safety. Objective: To summarize transfusion-related adverse reactions reported to the TTISS between 2006 and 2012. Methods: Hospitals from 10 provinces and two territories participated in the TTISS by collecting and submitting data on all transfusion-related reactions or injuries to the provincial / territorial blood coordinating offices. This data was sent to the Agency where it was consolidated, cleaned, validated and analyzed by type of reactions or outcome. Corresponding rates were also calculated using the total number of units of blood components transfused as a denominator. Results: From 2006 to 2012, a total of 3,957 adverse reactions were reported to the TTISS, excluding minor allergic reactions. Of these, 2,920 (73.8%) were related to transfusion of blood components and 1,036 (26.2%) were from the transfusion of blood products. Among reactions related to the transfusion of blood components, the most common were: transfusion-associated circulatory overload (n = 1,242, 42.5%), severe allergic / anaphylactic / anaphylactoid reactions (n=411; 14.1%) and hypotensive reactions (n=298; 10.2%). Among those related to transfusion of blood products, close to one-half were intravenous immunoglobulin (IVIG) headache (n=295; 28.5%) or delayed hemolytic reaction (n=175; 16.9%). Death definitely attributable to transfusion was extremely rare: only one case diagnosed with transfusion-related acute lung injury was identified between 2006 and 2012. Conclusion: The majority of reactions attributable to transfusion resulted in minor or no sequelae. Strengthening the TTISS will improve the monitoring of adverse transfusion reactions which is one of the key components of an overall patient safety strategy. Current initiatives to improve data quality include the development of transfusion-associated circulatory overload / transfusion-related acute lung injury recognition algorithm and the collection of appropriate denominators for the calculation of the rates of adverse reactions from the transfusion of blood products.
机译:摘要背景:输血传播伤害监测系统(TTISS)是由加拿大公共卫生局(CA)与各省和地区合作建立的泛加拿大监视系统,用于捕获有关加拿大不良输血反应的非标称数据提供输血服务的医院的首要目标是提高患者的安全性。目的:总结2006年至2012年间报告给TTISS的输血相关不良反应。方法:来自10个省和两个地区的医院参加了TTISS,收集并提交了所有与输血相关的反应或对省/地区血液的伤害的数据协调办公室。将该数据发送到原子能机构,在此根据反应或结果的类型对其进行合并,清理,确认和分析。还使用输血的血液成分单位总数作为分母来计算相应的比率。结果:从2006年到2012年,TTISS总共报告了3957例不良反应,不包括轻微的过敏反应。其中,有2,920名(73.8%)与输血有关,有1,036名(26.2%)与输血有关。在与输血相关的反应中,最常见的是:与输血相关的循环超负荷(n = 1,242,42.5%),严重的过敏/过敏/类过敏反应(n = 411; 14.1%)和降压反应(n = 298; 10.2%)。在与输血相关的那些中,近一半为静脉免疫球蛋白(IVIG)头痛(n = 295; 28.5%)或延迟溶血反应(n = 175; 16.9%)。绝对归因于输血的死亡极为罕见:2006年至2012年之间仅发现一例被诊断为与输血相关的急性肺损伤。结论:大部分归因于输血的反应未引起或仅引起后遗症。加强TTISS将改善对不良输血反应的监测,这是整体患者安全策略的关键组成部分之一。当前改善数据质量的措施包括开发与输血相关的循环超负荷/与输血相关的急性肺损伤识别算法,以及收集适当的分母来计算输血产品的不良反应率。

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