Quantitative and Qualitative Hemostatic Response Assessed by ROTEM After Fibrinogen Concentrate and Platelet Administration During Liver Transplantation: A Case Report.

IF 0.8
Se Hoon Kim, Uzung Yoon
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Abstract

Patients undergoing liver transplantation experience dynamic alterations in hemostasis, as impaired fibrinogen synthesis, dysfibrinogenemia, hemodilution, and ongoing surgical bleeding collectively impair clot formation and strength. Fibrinogen abnormalities involve both quantitative deficiency and qualitative dysfunction. We report the case of a 70-year-old male with a Model for End-Stage Liver Disease (MELD) score of 36 who underwent orthotopic liver transplantation for acute liver failure following a cholecystectomy. During the reperfusion phase, diffuse oozing was noted with a plasma fibrinogen of 100 mg/dL and ROTEM-FIBTEM maximum clot firmness (MCF) of 6 mm. An initial 2 g dose of fibrinogen concentrate raised plasma fibrinogen to 150 mg/dL but resulted in only a minimal increase in FIBTEM MCF to 7 mm. A subsequent 2 g dose increased plasma fibrinogen to 175 mg/dL and restored FIBTEM MCF to 13 mm, within the normal range. EXTEM MCF approached the reference range only after one bag of platelet transfusion, suggesting concurrent qualitative platelet impairment. After these interventions, bleeding clinically ceased, and there were no hemorrhagic complications postoperatively. These findings underscore the importance of combined serial quantitative and qualitative hemostatic assessment to guide transfusion management during liver transplantation.

肝移植中纤维蛋白原浓缩物和血小板应用后定量和定性止血反应的ROTEM评价:1例报告。
接受肝移植的患者会经历止血的动态改变,如纤维蛋白原合成受损、纤维蛋白原异常血症、血液稀释和持续的手术出血共同损害凝块的形成和强度。纤维蛋白原异常包括定量缺陷和定性功能障碍。我们报告一例70岁男性,终末期肝病模型(MELD)评分为36分,因胆囊切除术后急性肝衰竭接受原位肝移植。在再灌注阶段,弥漫性渗出,血浆纤维蛋白原为100 mg/dL, rotem - fitem最大凝块硬度(MCF)为6 mm。最初2 g剂量的纤维蛋白原浓缩物使血浆纤维蛋白原升高至150 mg/dL,但只导致fitem MCF轻微增加至7 mm。随后的2g剂量使血浆纤维蛋白原增加到175 mg/dL,并使FIBTEM MCF恢复到13 mm,在正常范围内。仅输一袋血小板后,EXTEM MCF才接近参考范围,提示同时存在定性血小板损伤。经这些干预后,临床出血停止,术后无出血性并发症。这些发现强调了联合系列定量和定性止血评估对指导肝移植期间输血管理的重要性。
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