Lumlertgul Nuttha, Srisawat Nattachai
Division of Nephrology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Excellence Center for Critical Care Nephrology, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand.
Int J Artif Organs. 2021 Jan;44(1):17-24. doi: 10.1177/0391398820917150. Epub 2020 May 11.
Excessive pro-inflammatory and anti-inflammatory cytokines are mediators for haemodynamic alterations, metabolic acidosis, and multi-organ failure in sepsis. Recently, oXiris haemofilter (Baxter, IL, USA) has been introduced as a novel haemofilter to mitigate inflammatory response during sepsis-associated acute kidney injury requiring renal replacement therapy. In the present case series, the researchers retrospectively reviewed critically ill patients with septic shock with the use of at least one oXiris haemofilter during continuous renal replacement therapy between June 2015 and December 2017. The timing for oXiris initiation was at the nephrologists' discretion. The impact of oXiris haemofilter was evaluated on mean arterial pressure, vasopressor dosage, Sequential Organ Failure Assessment score, lactate and base excess during 72 h after treatment. Thirty-five patients were enrolled in the study. An improvement of haemodynamic status was found, shown by increased mean arterial pressure by 6.1% ( = 0.35), decreased norepinephrine dose by 45.9% ( = 0.02), inotropic score by 26.4% ( = 0.02) and vasopressor dependency index by 40.5% ( = 0.01). Cardiovascular Sequential Organ Failure Assessment scores significantly decreased over 72 h ( = 0.02). Blood lactate levels and base excess also showed statistically significant improvements. The median filter lifetime was 23 (interquartile range = 14-36) hours. The intensive care unit mortality was 82.9%. Treatment with oXiris was safe and well-tolerated with no device-related adverse events. In conclusion, continuous renal replacement therapy with oXiris haemofilter is safe and may improve haemodynamic parameters in septic patients with severe renal dysfunction. Nonetheless, these findings were drawn from a retrospective analysis without a control group, and therefore cannot be generalised. Randomised controlled trials are warranted to confirm these findings.
促炎和抗炎细胞因子过度是脓毒症中血流动力学改变、代谢性酸中毒和多器官功能衰竭的介质。最近,oXiris血液滤过器(美国伊利诺伊州百特公司)作为一种新型血液滤过器被引入,用于在脓毒症相关急性肾损伤需要肾脏替代治疗期间减轻炎症反应。在本病例系列中,研究人员回顾性分析了2015年6月至2017年12月期间在持续肾脏替代治疗期间至少使用过一次oXiris血液滤过器的感染性休克重症患者。开始使用oXiris的时机由肾病科医生决定。评估了oXiris血液滤过器对治疗后72小时内平均动脉压、血管升压药剂量、序贯器官衰竭评估评分、乳酸和碱剩余的影响。35名患者纳入研究。发现血流动力学状态有所改善,表现为平均动脉压升高6.1%(=0.35)、去甲肾上腺素剂量降低45.9%(=0.02)、肌力评分降低26.4%(=0.02)和血管升压药依赖指数降低40.5%(=0.01)。心血管序贯器官衰竭评估评分在72小时内显著降低(=0.02)。血乳酸水平和碱剩余也有统计学上的显著改善。滤器中位使用寿命为23(四分位间距=14 - 36)小时。重症监护病房死亡率为82.9%。使用oXiris治疗安全且耐受性良好,未发生与设备相关的不良事件。总之,使用oXiris血液滤过器进行持续肾脏替代治疗是安全的,可能改善严重肾功能不全脓毒症患者的血流动力学参数。尽管如此,这些发现来自无对照组的回顾性分析,因此不能推广。有必要进行随机对照试验来证实这些发现。