Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia.
Transfusion Research Unit, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia.
Br J Haematol. 2017 Oct;179(1):131-141. doi: 10.1111/bjh.14804. Epub 2017 Jun 27.
We aimed to compare hypofibrinogenaemia prevalence in major bleeding patients across all clinical contexts, fibrinogen supplementation practice, and explore the relationship between fibrinogen concentrations and mortality. This cohort study included all adult patients from 20 hospitals across Australia and New Zealand who received massive transfusion between April 2011 and October 2015. Of 3566 patients, 2829 (79%) had fibrinogen concentration recorded, with a median first and lowest concentration of 2·0 g/l (interquartile range [IQR] 1·5-2·7) and 1·8 g/l (IQR 1·3-2·4), respectively. Liver transplant (1·7 g/l, IQR 1·2-2·1), trauma (1·8, IQR 1·3-2·5) and vascular surgery (1·9 g/l, IQR 1·4-2·5) had lower concentrations. Total median fibrinogen dose administered from all products was 7·3 g (IQR 3·3-13·0). Overall, 1732 (61%) received cryoprecipitate and 9 (<1%) fibrinogen concentrate. Time to cryoprecipitate issue in those with initial fibrinogen concentration <1 g/l was 2·5 h (IQR 1·2-4·3 h). After adjustment, initial fibrinogen concentration had a U-shaped association with in-hospital mortality [adjusted odds ratios: fibrinogen <1 g/l, 2·31 (95% confidence interval (CI) 1·48-3·60); 1-1·9 g/l, 1·29 (95% CI 0·99-1·67) and >4 g/l, 2·03 (95% CI 1·35-3·04), 2-4 g/l reference category]. The findings indicate areas for practice improvement including timely administration of cryoprecipitate, which is the most common source of concentrated fibrinogen in Australia and New Zealand.
我们旨在比较不同临床背景下大出血患者的低纤维蛋白原血症发生率、纤维蛋白原补充的实践情况,并探讨纤维蛋白原浓度与死亡率之间的关系。这项队列研究纳入了 2011 年 4 月至 2015 年 10 月期间澳大利亚和新西兰 20 家医院接受大量输血的所有成年患者。在 3566 名患者中,有 2829 名(79%)记录了纤维蛋白原浓度,中位数首次和最低浓度分别为 2.0 g/l(四分位间距[IQR]1.5-2.7)和 1.8 g/l(IQR 1.3-2.4)。肝移植(1.7 g/l,IQR 1.2-2.1)、创伤(1.8,IQR 1.3-2.5)和血管外科(1.9 g/l,IQR 1.4-2.5)的浓度较低。所有产品输注的总纤维蛋白原中位数剂量为 7.3 g(IQR 3.3-13.0)。总体而言,1732 名(61%)患者接受了冷沉淀,9 名(<1%)患者接受了纤维蛋白原浓缩物。初始纤维蛋白原浓度<1 g/l 的患者输注冷沉淀的时间为 2.5 小时(IQR 1.2-4.3 小时)。调整后,初始纤维蛋白原浓度与院内死亡率呈 U 型关联[校正优势比:纤维蛋白原<1 g/l,2.31(95%置信区间[CI]1.48-3.60);1-1.9 g/l,1.29(95%CI 0.99-1.67)和>4 g/l,2.03(95%CI 1.35-3.04),2-4 g/l 参考类别]。研究结果表明,在实践中需要改进包括及时输注冷沉淀,这是澳大利亚和新西兰最常用的浓缩纤维蛋白原来源。