Septic shock in obstetrics: the role of efferent techniques for endotoxin removal in Gram-negative sepsis

Q3 Medicine
A. Bayalieva, V. R. Davydova
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Abstract

Aim: to assess the sorption capacity of various devices for endotoxin removal modelled in in vitro patient with septic shock experiment.Materials and Methods. Endotoxin adsorption was evaluated in vitro by using circulating endotoxin solution in bovine serum in a closed circuit. The following columns were chosen for the experiment: Toraymyxin PMX-20R (РМХ), Alteco® LPS Adsorber, Efferon LPS, Toray Filtryzer BK-2.1U. Lipopolysaccharide (LPS) doses corresponding to severity of the septic process were sequentially added to a column pre-washed with physiological solution. The first LPS dose of 12.5 μg was added to a flask containing 1500 ml (1.5 L) of fetal bovine serum, a second LPS dose of 37.5 μg was added to the serum samples collected before the onset of experiment, as well as 30, 60, 120 (before the second dose), 120 (after the second dose), 150 and 240 minutes after the start of circulation. LPS measurement was carried out by mixing the prepared serum sample with LAL reagent at 1:1 ratio in a measuring tube.Results. All columns can reduce endotoxin levels below the 12.5 μg and even 50 μg levels, although none of devices were able to reduce the LPS level from “supercritical” 50 μg to “critical” 12.5 μg. However, at the same time, the capacity of the Toraymyxin PMX-20R column turned out to be 5–13 times greater than that of other products. This result suggests that while removing endotoxin under similar conditions, the Toraymyx in PMX-20R column will have a much higher reserve of sorption capacity and, therefore, greater opportunities for lowering a risk of septic shock progression.Conclusion. The work we presented provides insights into whether sorption capacity of the presented cartridges is sufficient to remove endotoxin at initial (12.5 μg) load that corresponds to the onset of systemic inflammatory response syndrome in a typical patient. Additionally, it elucidates to what extent a cartridge can reduce the endotoxin load in severe septic shock with a total LPS load of up to 50 μg.
产科脓毒性休克:传出技术在革兰氏阴性败血症中清除内毒素的作用
目的:在体外脓毒性休克患者实验中评估各种装置去除内毒素的吸附能力。通过在闭合回路中使用牛血清中的循环内毒素溶液,在体外对内毒素吸附能力进行评估。实验选用了以下色谱柱:Toraymyxin PMX-20R (РМХ), Alteco® LPS Adsorber, Efferon LPS, Toray Filtryzer BK-2.1U。将与败血症严重程度相对应的脂多糖(LPS)剂量依次添加到用生理溶液预洗过的色谱柱中。第一个 LPS 剂量为 12.5 μg,添加到装有 1500 毫升(1.5 升)胎牛血清的烧瓶中;第二个 LPS 剂量为 37.5 μg,添加到实验开始前、循环开始后 30 分钟、60 分钟、120 分钟(第二个剂量前)、120 分钟(第二个剂量后)、150 分钟和 240 分钟采集的血清样本中。将制备好的血清样本与 LAL 试剂按 1:1 的比例混合后放入测量管中进行 LPS 测量。尽管没有一种设备能将 LPS 水平从 "超临界 "50 微克降至 "临界 "12.5 微克,但所有色谱柱都能将内毒素水平降至 12.5 微克甚至 50 微克以下。但与此同时,东丽菌素 PMX-20R 柱的处理能力是其他产品的 5-13 倍。这一结果表明,在类似条件下清除内毒素时,PMX-20R 柱中的 Toraymyx 的吸附能力储备要高得多,因此有更多机会降低脓毒性休克恶化的风险。我们介绍的这项工作让我们深入了解了所介绍的滤芯的吸附能力是否足以去除典型病人在全身炎症反应综合征开始时的初始(12.5 微克)内毒素。此外,它还阐明了在 LPS 总负荷高达 50 μg 的严重脓毒性休克中,滤芯能在多大程度上减少内毒素负荷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
68
审稿时长
12 weeks
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