Colavecchia A Carmine, Cohen David A, Harris Jesse E, Thomas Jeena M, Lindberg Scott, Leveque Christopher, Salazar Eric
Department of Pharmacy, Houston Methodist Hospital.
Department of Pathology and Genomic Medicine, Houston Methodist Hospital.
Transfusion. 2017 Dec;57(12):3026-3034. doi: 10.1111/trf.14328. Epub 2017 Sep 28.
Major bleeding in orthotopic liver transplantation is associated with significant morbidity and mortality. Limited literature exists regarding comparative effectiveness of prothrombin complex concentrate and fibrinogen concentrate during orthotopic liver transplantation on blood product utilization.
This retrospective, single-institution study evaluated the impact of prothrombin complex concentrate and fibrinogen concentrate on blood product utilization during orthotopic liver transplantation from December 2013 to April 2016. This study included patients age 18 years or older and excluded patients who received simultaneous heart or lung transplantation or did not meet documentation criteria. A propensity score matching technique was used to match patients who were exposed to prothrombin complex concentrate with unexposed patients, at a 2 to 1 ratio, to control for selection bias.
During this study, 212 patients received orthotopic liver transplantation with 39 prothrombin complex concentrate exposures. The matched study population included 39 patients who were exposed to prothrombin complex concentrate and 78 unexposed patients. Overall, 84.6% of patients who were exposed to prothrombin complex concentrate also received concomitant fibrinogen concentrate, whereas only 2% of patients in the control group received fibrinogen concentrate. After propensity score matching, no other factors that were included in the model differed significantly or had a standardized mean difference of 0.11 or greater. There was no statistical difference in the utilization of red blood cells or fresh frozen plasma for the exposed group versus the unexposed group after matching (mean ± standard deviation: red blood cell units, 12.4 ± 8.0 units vs. 9.7 ± 5.6 units [p = 0.058]; fresh-frozen plasma units, 10.0 ± 6.3 vs. 12.7 ± 9.7 units [p = 0.119], respectively).
The intraoperative use of prothrombin complex concentrate and fibrinogen concentrate during orthotopic liver transplantation did not reduce intraoperative blood product requirements at a single institution.
原位肝移植中的大出血与显著的发病率和死亡率相关。关于原位肝移植期间凝血酶原复合物浓缩物和纤维蛋白原浓缩物在血液制品使用方面的比较有效性,现有文献有限。
这项回顾性单机构研究评估了2013年12月至2016年4月期间凝血酶原复合物浓缩物和纤维蛋白原浓缩物对原位肝移植期间血液制品使用的影响。本研究纳入了18岁及以上的患者,排除了接受同期心脏或肺移植或不符合记录标准的患者。采用倾向评分匹配技术,以2:1的比例将接受凝血酶原复合物浓缩物治疗的患者与未接受治疗的患者进行匹配,以控制选择偏倚。
在本研究期间,212例患者接受了原位肝移植,其中39例接受了凝血酶原复合物浓缩物治疗。匹配后的研究人群包括39例接受凝血酶原复合物浓缩物治疗的患者和78例未接受治疗的患者。总体而言,接受凝血酶原复合物浓缩物治疗的患者中有84.6%也接受了纤维蛋白原浓缩物,而对照组中只有2%的患者接受了纤维蛋白原浓缩物。倾向评分匹配后,模型中纳入的其他因素无显著差异,标准化均差为0.11或更大。匹配后,暴露组与未暴露组在红细胞或新鲜冰冻血浆的使用上无统计学差异(平均值±标准差:红细胞单位,12.4±8.0单位对9.7±5.6单位[p = 0.058];新鲜冰冻血浆单位,10.0±6.3对12.7±9.7单位[p = 0.119])。
在单机构中,原位肝移植术中使用凝血酶原复合物浓缩物和纤维蛋白原浓缩物并未减少术中血液制品的需求量。