Service d'Anesthésie-Réanimation 2, Centre Hospitalier Universitaire (CHU) de Bordeaux, 33000, Bordeaux, France.
Intensive Care Med. 2013 Sep;39(9):1535-46. doi: 10.1007/s00134-013-2967-z. Epub 2013 Jun 6.
Septic shock is a leading cause of death among critically ill patients, in particular when complicated by acute kidney injury (AKI). Small experimental and human clinical studies have suggested that high-volume haemofiltration (HVHF) may improve haemodynamic profile and mortality. We sought to determine the impact of HVHF on 28-day mortality in critically ill patients with septic shock and AKI.
This was a prospective, randomized, open, multicentre clinical trial conducted at 18 intensive care units in France, Belgium and the Netherlands. A total of 140 critically ill patients with septic shock and AKI for less than 24 h were enrolled from October 2005 through March 2010. Patients were randomized to either HVHF at 70 mL/kg/h or standard-volume haemofiltration (SVHF) at 35 mL/kg/h, for a 96-h period.
Primary endpoint was 28-day mortality. The trial was stopped prematurely after enrolment of 140 patients because of slow patient accrual and resources no longer being available. A total of 137 patients were analysed (two withdrew consent, one was excluded); 66 patients in the HVHF group and 71 in the SVHF group. Mortality at 28 days was lower than expected but not different between groups (HVHF 37.9 % vs. SVHF 40.8 %, log-rank test p = 0.94). There were no statistically significant differences in any of the secondary endpoints between treatment groups.
In the IVOIRE trial, there was no evidence that HVHF at 70 mL/kg/h, when compared with contemporary SVHF at 35 mL/kg/h, leads to a reduction of 28-day mortality or contributes to early improvements in haemodynamic profile or organ function. HVHF, as applied in this trial, cannot be recommended for treatment of septic shock complicated by AKI.
感染性休克是危重病患者死亡的主要原因,特别是当并发急性肾损伤(AKI)时。小型实验和人体临床研究表明,高容量血液滤过(HVHF)可能改善血流动力学特征并降低死亡率。我们旨在确定 HVHF 对伴有感染性休克和 AKI 的危重病患者 28 天死亡率的影响。
这是一项在法国、比利时和荷兰的 18 个重症监护病房进行的前瞻性、随机、开放、多中心临床试验。2005 年 10 月至 2010 年 3 月期间,共纳入了 140 例感染性休克和 AKI 发病时间不足 24 小时的危重病患者。患者被随机分配到 HVHF 组(70ml/kg/h)或标准容量血液滤过(SVHF)组(35ml/kg/h),治疗 96 小时。
主要终点是 28 天死亡率。由于患者入组缓慢且资源不再可用,该试验在纳入 140 例患者后提前终止。共分析了 137 例患者(2 例撤回同意,1 例排除);HVHF 组 66 例,SVHF 组 71 例。28 天死亡率低于预期,但两组之间无差异(HVHF 组为 37.9%,SVHF 组为 40.8%,对数秩检验 p=0.94)。两组间次要终点均无统计学差异。
在 IVOIRE 试验中,与当代 35ml/kg/h 的 SVHF 相比,70ml/kg/h 的 HVHF 并未显示出降低 28 天死亡率的证据,也没有改善血流动力学特征或器官功能的早期获益。在这项试验中应用的 HVHF 不能推荐用于治疗伴有 AKI 的感染性休克。