Cappabianca Giangiuseppe, Mariscalco Giovanni, Biancari Fausto, Maselli Daniele, Papesso Francesca, Cottini Marzia, Crosta Sandro, Banescu Simona, Ahmed Aamer B, Beghi Cesare
Department of Surgical and Morphological Sciences, Cardiac Surgery Unit, Varese University Hospital, University of Insubria, Varese, Italy.
Department of Cardiovascular Sciences, Clinical Sciences Wing, Glenfield Hospital, University of Leicester, Groby Road, Leicester, LE39QP, UK.
Crit Care. 2016 Jan 6;20:5. doi: 10.1186/s13054-015-1172-6.
Bleeding after cardiac surgery requiring surgical reexploration and blood component transfusion is associated with increased morbidity and mortality. Although prothrombin complex concentrate (PCC) has been used satisfactorily in bleeding disorders, studies on its efficacy and safety after cardiopulmonary bypass are limited.
Between January 2005 and December 2013, 3454 consecutive cardiac surgery patients were included in an observational study aimed at investigating the efficacy and safety of PCC as first-line coagulopathy treatment as a replacement for fresh frozen plasma (FFP). Starting in January 2012, PCC was introduced as solely first-line treatment for bleeding following cardiac surgery.
After one-to-one propensity score-matched analysis, 225 pairs of patients receiving PCC (median dose 1500 IU) and FFP (median dose 2 U) were included. The use of PCC was associated with significantly decreased 24-h post-operative blood loss (836 ± 1226 vs. 935 ± 583 ml, p < 0.0001). Propensity score-adjusted multivariate analysis showed that PCC was associated with significantly lower risk of red blood cell (RBC) transfusions (odds ratio [OR] 0.50; 95% confidence interval [CI] 0.31-0.80), decreased amount of RBC units (β unstandardised coefficient -1.42, 95% CI -2.06 to -0.77) and decreased risk of transfusion of more than 2 RBC units (OR 0.53, 95% CI 0.38-0.73). Patients receiving PCC had an increased risk of post-operative acute kidney injury (AKI) (OR 1.44, 95% CI 1.02-2.05) and renal replacement therapy (OR 3.35, 95% CI 1.13-9.90). Hospital mortality was unaffected by PCC (OR 1.51, 95% CI 0.84-2.72).
In the cardiac surgery setting, the use of PCC compared with FFP was associated with decreased post-operative blood loss and RBC transfusion requirements. However, PCC administration may be associated with a higher risk of post-operative AKI.
心脏手术后需要再次手术探查及输血的出血与发病率和死亡率增加相关。尽管凝血酶原复合物浓缩剂(PCC)已成功用于出血性疾病,但关于其在体外循环后疗效和安全性的研究有限。
2005年1月至2013年12月期间,3454例连续心脏手术患者纳入一项观察性研究,旨在调查PCC作为一线凝血病治疗替代新鲜冰冻血浆(FFP)的疗效和安全性。从2012年1月起,PCC被引入作为心脏手术后出血的唯一一线治疗。
经过一对一倾向评分匹配分析,纳入了225对接受PCC(中位剂量1500 IU)和FFP(中位剂量2 U)的患者。使用PCC与术后24小时失血量显著减少相关(836±1226 vs. 935±583 ml,p<0.0001)。倾向评分调整后的多变量分析显示,PCC与红细胞(RBC)输血风险显著降低相关(比值比[OR]0.50;95%置信区间[CI]0.31 - 0.80),RBC单位数量减少(β非标准化系数 -1.42,95% CI -2.06至 -0.77)以及输注超过2个RBC单位的风险降低(OR 0.53,95% CI 0.38 - 0.73)。接受PCC的患者术后急性肾损伤(AKI)风险增加(OR 1.44,95% CI 1.02 - 2.05)和肾脏替代治疗风险增加(OR 3.35,95% CI 1.13 - 9.90)。住院死亡率不受PCC影响(OR 1.51,95% CI 0.84 - 2.72)。
在心脏手术中,与FFP相比,使用PCC与术后失血量减少和RBC输血需求降低相关。然而,给予PCC可能与术后AKI风险较高相关。