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Therapeutic rather than prophylactic platelet transfusion policy for severe thrombocytopenia during liver transplantation

机译:肝移植过程中严重血小板减少的治疗性而非预防性血小板输注策略

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Platelet transfusion (PTx) has been identified as an important risk factor for morbidity and mortality after liver transplantation (LTx). Our aim was to evaluate the safety of therapeutic rather than prophylactic PTx policy in severe thrombocytopenic patients undergoing LTx. Recipients of LTx were divided into two groups: group I (GI) (n = 76) platelet count (PC) >= 50 x 10(9)/l and group II (GII) PC <50 x 10(9)/l (n = 76). Platelets were transfused following a thromboelastometry protocol and clinical signs of diffuse bleeding. Both groups were compared regarding hemoglobin (Hb), international normalized ratio (INR), fibrinogen level, blood loss (BL), blood products required, percentage of bloodless surgery, duration of mechanical ventilation, ICU stay, and vascular complications. Each group was further subdivided according to PTx into (GI NPTx and GII NPTx) with no platelet transfusion (NPTx) and (GI PTx and GII PTx) received PTx. These subgroups were further compared for some variables. Base line Hb was significantly higher while INR was significantly lower in GI. 75% avoided PTx in GII. Comparisons of BL, packed red blood cells (PRBCs), and cryoprecipitate transfusion were insignificant. Fresh frozen plasma (FFP) transfusion was higher and the percentage of bloodless surgery was lower in GII. In GII, PC increased after start of surgery. Two cases of hepatic artery thrombosis in GI and one in GII were recorded. Recovery of platelets was quicker, and duration of mechanical ventilation and ICU stay was shorter in NPTx patients regardless the base line PC. Cut-off values of PC 30 >= 10(9)/l (with sensitivity 73.7% and specificity 78.8%, p<0.01), BL of 3750 ml in GI (sensitivity of 75% and specificity of 69%, p<0.01) and of 3250 ml in GII (sensitivity of 84.2% and specificity of 87.7% (p<0.01)) could indicate the need of PTx. With therapeutic approach, 75% of patients in GII could avoid unnecessary PTx with its hazards without excessive bleeding. PC in GII increased intraoperatively, PTx may lead to delayed recovery of platelets, increased duration of mechanical ventilation and ICU stay. The given cut-off values may help to guide PTx.
机译:血小板输注(PTx)已被确定为肝移植(LTx)发病率和死亡率的重要危险因素。我们的目标是评估在接受LTx的严重血小板减少症患者中治疗性PTx策略而非预防性PTx策略的安全性。 LTx的接收者分为两组:I组(GI)(n = 76)血小板计数(PC)> = 50 x 10(9)/ l和II组(GII)PC <50 x 10(9)/ l (n = 76)。遵循血栓弹力测定规程和弥散性出血的临床体征输注血小板。比较两组的血红蛋白(Hb),国际标准化比率(INR),纤维蛋白原水平,失血(BL),所需血液制品,无血手术百分比,机械通气时间,ICU停留时间和血管并发症。根据PTx将每组进一步细分为(GI NPTx和GII NPTx),不进行血小板输注(NPTx),(GI PTx和GII PTx)接受PTx。这些亚组进一步比较了一些变量。胃肠道基线Hb显着较高,而INR显着较低。 GII中75%避免使用PTx。 BL,充盈的红细胞(PRBCs)和冷沉淀输血的比较是微不足道的。在GII中,新鲜冷冻血浆(FFP)输血较高,无血手术的百分比较低。在GII中,手术开始后PC升高。记录了2例GI的肝动脉血栓形成和1例GII的肝动脉血栓形成。无论基线PC值是多少,NPTx患者的血小板恢复速度都更快,机械通气时间和ICU停留时间更短。 PC 30> = 10(9)/ l的临界值(灵敏度为73.7%,特异性为78.8%,p <0.01),GI中的BL为3750 ml(灵敏度为75%,特异性为69%,p <0.01) )和3250 ml的GII(灵敏度为84.2%,特异性为87.7%(p <0.01))可能表明需要PTx。通过治疗方法,GII中有75%的患者可以避免不必要的PTx,因为它的危害性而不会引起大量出血。术中GII中的PC升高,PTx可能导致血小板恢复延迟,机械通气时间延长和ICU停留。给定的截止值可能有助于指导PTx。

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