Cruz Dinna N, Bellomo Rinaldo, Ronco Claudio
Department of Nephrology, Ospedale San Bortolo, Vicenza, Italy.
Contrib Nephrol. 2007;156:444-51. doi: 10.1159/000102138.
Endotoxin is one of the principal biological substances that cause gram-negative septic shock. Lack of clinical success with antiendotoxin or anticytokine therapy has shifted interest to extracorporeal therapies to reduce circulating levels of the mediators of sepsis. Direct hemoperfusion with polymyxin-B-immobilized fiber (PMX-F) is a promising treatment of gram-negative sepsis in critically ill patients. Because of the high affinity of polymyxin B for endotoxin, the rationale underlying extracorporeal therapy would be to remove circulating endotoxin by adsorption, thus preventing progression of the biological cascade of sepsis. In a systematic review of 28 studies (pooled sample size 1,390 patients), the preliminary results of which are described here, PMX-F therapy appeared to significantly lower endotoxin levels, improve blood pressure, and reduce mortality. However, publication bias and lack of blinding need to be considered. These encouraging results need to be verified with large-scale controlled clinical trials.
内毒素是导致革兰氏阴性菌败血症休克的主要生物物质之一。抗内毒素或抗细胞因子疗法在临床上未取得成功,这使得人们将兴趣转向体外疗法,以降低败血症介质的循环水平。用多粘菌素B固定化纤维(PMX-F)进行直接血液灌流是治疗重症患者革兰氏阴性菌败血症的一种有前景的方法。由于多粘菌素B与内毒素具有高亲和力,体外疗法的基本原理是通过吸附去除循环中的内毒素,从而防止败血症生物级联反应的进展。在对28项研究(汇总样本量为1390例患者)的系统评价中(此处描述了其初步结果),PMX-F疗法似乎能显著降低内毒素水平、改善血压并降低死亡率。然而,需要考虑发表偏倚和缺乏盲法的问题。这些令人鼓舞的结果需要通过大规模对照临床试验来验证。