[Potential for infusion correction of COVID-19-associated endotheliopathy].

IF 0.7 0 RELIGION
I S Simutis, V A Ratnikov, A N Scheglov, O V Nikolaeva, G A Boyarinov, A A Sapegin, L B Gaikovaya, D A Evteeva, K N Zamyatina
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引用次数: 0

Abstract

Aim: To evaluate the relationship between the systemic inflammatory response and the severity of COVID-19-associated endotheliopathy and the effect of succinate-containing crystalloid solution (sodium meglumine succinate) on it in patients with severe COVID-19.

Materials and methods: Clinical and laboratory parameters of 53 intensive care unit's patients with COVID-19 complicated by community-acquired bilateral multisegmental pneumonia were analyzed. Intensive therapy complex of 27 patients (study group) included daily infusion of 1.5% solution of sodium meglumine succinate (Reamberin) in the daily dose of 10 ml/kg for at least 11 days (or during the whole stay in the unit). A similar volume of Ringer's solution was present in the control group of 26 patients. The levels of endotheliocytosis, homocysteine, and systemic inflammatory response were determined at all stages of the study.

Results: The evaluation of endotheliopathy degree in the meglumine succinate group showed a significant reduction of initially elevated levels of endotheliemia and homocysteinemia at all study stages. The pattern of changes in the study group was highly correlated (r=0.90-0.96) with the dynamics of systemic inflammatory response parameters-fibrinogenemia, C-reactive protein and interleukin-6 levels. As normalization of the immune imbalance, we regarded the termination of lymphopenia in the Reamberin group.

Conclusion: Early inclusion of Reamberin infusion into intensive therapy of severe COVID-19, in comparison with Ringer's solution, leads to significant and stable correction of the severity of systemic inflammatory response, which in turn is naturally reflected in the severity of endothelial dysfunction, multiple organ failure, and also leads to a decrease in 28-day mortality.

[输液纠正 COVID-19 相关内皮病变的潜力]。
目的:评估重症COVID-19患者全身炎症反应与COVID-19相关内皮细胞病变严重程度之间的关系,以及含琥珀酸盐的晶体液(琥珀酸兆葡胺钠)对其的影响:分析了 53 名合并社区获得性双侧多节段肺炎的 COVID-19 重症监护病房患者的临床和实验室参数。27名患者(研究组)的综合重症治疗包括每日输注1.5%的琥珀酸钠巨鲁明溶液(Reamberin),每日剂量为10毫升/千克,持续至少11天(或在整个住院期间)。由 26 名患者组成的对照组也使用了类似剂量的林格氏液。在研究的各个阶段都测定了内皮细胞病变、同型半胱氨酸和全身炎症反应的水平:结果:对琥珀酸葡甲胺组内皮细胞病变程度的评估显示,在所有研究阶段,最初升高的内皮细胞血症和同型半胱氨酸血症水平均显著降低。研究组的变化模式与全身炎症反应参数--纤维蛋白原血症、C 反应蛋白和白细胞介素-6 水平的动态变化高度相关(r=0.90-0.96)。作为免疫失衡的正常化,我们认为兰贝林组淋巴细胞减少症已经终止:结论:与林格氏溶液相比,在重症COVID-19的强化治疗中尽早输注兰贝林可显著、稳定地纠正全身炎症反应的严重程度,而这又自然反映在内皮功能障碍、多器官衰竭的严重程度上,同时还可降低28天的死亡率。
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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