Yamashita Chizuru, Hara Yoshitaka, Kuriyama Naohide, Nakamura Tomoyuki, Nishida Osamu
Department of Anesthesiology and Critical Care Medicine, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Ther Apher Dial. 2015 Aug;19(4):316-23. doi: 10.1111/1744-9987.12339.
Polymyxin B-immobilized fiber column direct hemoperfusion (PMX-DHP) therapy is widely used for the treatment of severe sepsis and septic shock, and is generally performed for 2 h. Although previous studies demonstrated the efficacy of PMX-DHP therapy, it currently remains unclear whether its optimal duration is 2 h. This retrospective study analyzed 37 patients with septic shock who showed a poor clinical response to 2 h of PMX-DHP, and underwent a longer duration of this therapy. The mean duration of PMX-DHP therapy was 15.8 ± 7.9 h, and none of the patients developed adverse events, which enabled the therapy to be performed safely. The pressure catecholamine index [CAIP = catecholamine index/mean arterial pressure; catecholamine index = dopamine + dobutamine + (adrenaline + noradrenaline) × 100 μg/kg per min], as an indicator of hemodynamics, improved significantly in the survival group in the period between the start and 24 h after the end of PMX-DHP therapy (P < 0.01), and between 2 h after the start of and the end of this therapy (P < 0.05). In addition, the P/F ratio improved significantly in the group of surviving patients with acute respiratory distress syndrome (ARDS) in the period between the start and 24 h after the end of PMX-DHP therapy (P < 0.01), and between 2 h after the start of and the end of this therapy (P < 0.01). These results suggest that a longer duration of PMX-DHP therapy can be expected to improve the hemodynamics and pulmonary oxygenation capacity of patients with severe sepsis/septic shock. Strict prospective studies are needed in the future.
多粘菌素B固定化纤维柱直接血液灌流(PMX-DHP)疗法广泛用于治疗严重脓毒症和脓毒性休克,通常进行2小时。尽管先前的研究证明了PMX-DHP疗法的疗效,但目前尚不清楚其最佳持续时间是否为2小时。这项回顾性研究分析了37例对2小时PMX-DHP临床反应不佳并接受更长疗程该疗法的脓毒性休克患者。PMX-DHP疗法的平均持续时间为15.8±7.9小时,且无患者发生不良事件,这使得该疗法能够安全进行。作为血流动力学指标的压力儿茶酚胺指数[CAIP =儿茶酚胺指数/平均动脉压;儿茶酚胺指数=多巴胺+多巴酚丁胺+(肾上腺素+去甲肾上腺素)×100μg/kg每分钟]在存活组中,于PMX-DHP治疗开始至结束后24小时期间显著改善(P<0.01),以及在该治疗开始后2小时至结束期间显著改善(P<0.05)。此外,在存活的急性呼吸窘迫综合征(ARDS)患者组中,于PMX-DHP治疗开始至结束后24小时期间(P<0.01),以及在该治疗开始后2小时至结束期间(P<0.01),P/F比值显著改善。这些结果表明,预计更长疗程的PMX-DHP疗法可改善严重脓毒症/脓毒性休克患者的血流动力学和肺氧合能力。未来需要进行严格的前瞻性研究。