Transfusion Reactions in Patients, Dutch National Hemovigilance Office, The Hague, the Netherlands.
Transfusion. 2011 Jun;51(6):1278-83. doi: 10.1111/j.1537-2995.2010.02969.x. Epub 2010 Dec 6.
Transfusion-related acute lung injury (TRALI) is one of the most serious complications of blood transfusion. It can be caused by incompatible white blood cell antibodies in transfused plasma. The objective of this study was to quantify the reduction of TRALI after introduction of male-only plasma for transfusion as a preventive measure, which took effect in 2007.
In the Netherlands all cases of TRALI are reported to the national hemovigilance office. All reported cases of TRALI from 2002 to November 2009 were considered for inclusion. Those meeting the Canadian consensus clinical definition were included and subdivided according to whether or not the patient had received quarantine fresh-frozen plasma (Q-FFP) in the 6-hour period before the reaction. The numbers of TRALI cases involving plasma donated before the measure and of those involving plasma donated after the measure were compared to TRALI cases that did not involve Q-FFP to adjust for reporting bias.
A total of 110 cases were included in the analysis. Of 68 cases before the measure, 36 involved Q-FFP. Thirty-one cases occurred after the measure of which eight involved Q-FFP. Eleven occurred in the transitional period, of which four involved Q-FFP. The population-attributable risk of premeasure plasma among TRALI cases occurring before the measure was 0.33 (95% confidence interval, 0.09-0.51).
In the Netherlands the male-only Q-FFP measure was associated with a 33% reduction of TRALI cases.
输血相关性急性肺损伤(TRALI)是输血最严重的并发症之一。它可能是由于输注血浆中的不相容白细胞抗体引起的。本研究的目的是量化 2007 年引入男性专用血浆作为预防措施后 TRALI 的减少。
在荷兰,所有 TRALI 病例都报告给国家血液监测办公室。考虑纳入 2002 年至 2009 年 11 月期间报告的所有 TRALI 病例。符合加拿大共识临床定义的病例被纳入,并根据患者在反应前 6 小时内是否接受过隔离新鲜冷冻血浆(Q-FFP)进行细分。比较措施前血浆涉及的 TRALI 病例数和措施后血浆涉及的 TRALI 病例数与不涉及 Q-FFP 的 TRALI 病例数,以调整报告偏倚。
共有 110 例病例纳入分析。在措施之前的 68 例中,有 36 例涉及 Q-FFP。措施后发生了 31 例,其中 8 例涉及 Q-FFP。11 例发生在过渡期,其中 4 例涉及 Q-FFP。在措施之前发生的 TRALI 病例中,前测血浆的人群归因风险为 0.33(95%置信区间,0.09-0.51)。
在荷兰,男性专用 Q-FFP 措施与 TRALI 病例减少 33%相关。