Hemodynamic efficacy and safety of using modified gelatin solution and polyhydric alcohol solution for fluid resuscitation of patients with septic shock

Tinglan Zuo, F. Glumcher, S. Dubrov
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Abstract

Objective ‒ to compare the hemodynamic effects and safety of the infusion of succinylated gelatin solution, sorbitol-containing solution, and 0.9 % normal saline (0.9 % sodium chloride), analyze their effect on the treatment of septic shock and mortality.Materials and methods. A prospective randomized clinical trial that included 94 adult patients with an active surgical infection and septic shock was conducted. There were 34 (36.2 %) male and 60 (63.8 %) female patients aged between 19 and 96 years, mean age was (66.51 ± 17.06) years. An appropriate solution in a volume of 500 ml was used for resuscitation, then hemodynamic and other clinical and laboratory parameters were monitored.Results. There was no significant difference in mean arterial pressure (MAP) between the 3 groups until the 40th minute (p>0.05). At the 45th minute MAP in the NS group differed only from MAP in the Gel group (p=0.007). At the 50th minute MAP in the NS group did not differ from the baseline (p=0.139). From the 50th minute to 2 hours, MAP in the Gel and Sorb groups was higher than in the NS group in all measurements (p<0.05). There was no statistically significant difference in heart rate (HR) in any measurement (p>0.05). Cardiac output (CO) did not differ up to the 30th minute (p>0.05), at the 35th minute, CO differed only between Gel and NS groups (p=0.019), from the 40th minute to 2 hour CO in Gel and Sorb groups were significantly higher than in NS group in all measurements (p<0.05). Oxygen delivery (DO2) also did not differ up to the 30th minute (p>0.05), from the 35th minute to the 45th minute a significant difference was found only between Gel and NS groups (p<0.05), from the 50th minute to 2 hour DO2 in Gel and Sorb group was significantly higher than in NS group in all measurements (p<0.05). After infusion of the gelatin-containing solution and sorbitol-containing solution, the acid-base balance of the blood improved significantly. The dose of gelatin-containing and sorbitol-containing solutions applied in this study was safe for the renal function of the patients with septic shock. However, it is possible that a decrease in blood fibrinogen concentrations may be associated with the use of a gelatin-containing solution. Significant improvement in the Glasgow Coma Scale scores was observed only in patients in the group receiving the sorbitol-containing solution. The difference in 28-day mortality between the groups was not statistically significant (p=0.993).Conclusions. In our observations, when using these three types of solution in patients with septic shock, hemodynamic effects up to the 40th minute did not differ between groups. From the 40th minute to 2 hour, the volemic effect of 4 % succinylated gelatin solution and balanced polyionic solution with 6 % sorbitol was significantly better, compared to the 0.9 % sodium chloride solution. The volume of solutions used in these three groups did not affect renal function in patients with septic shock. The amount of balanced polyionic solution used with 6 % sorbitol and 0.9 % sodium chloride solution did not affect blood coagulation function. But the use of 4 % succinyl gelatin solution reduced the concentration of fibrinogen in the blood. After infusion of the gelatin-containing solution with buffer formulations and sorbitol-containing solution with buffer formulations, the acid-base status of the blood was significantly improved compared to 0.9 % sodium chloride solution. Infusion of the gelatin-containing solution and 0.9 % sodium chloride solution did not affect the Glasgow coma score in patients. After infusion of the sorbitol-containing solution, patients’ consciousness was improved by this scale. The 28-day mortality did not differ significantly between groups.
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改性明胶溶液与多羟基乙醇溶液用于感染性休克患者液体复苏的血流动力学疗效和安全性
目的比较琥珀酰明胶溶液、含山梨醇溶液和0.9%生理盐水(0.9%氯化钠)输注的血液动力学效果和安全性,分析它们对感染性休克和死亡率的治疗效果。材料和方法。进行了一项前瞻性随机临床试验,包括94名患有活动性外科感染和感染性休克的成年患者。年龄在19至96岁之间的患者有34名(36.2%)男性和60名(63.8%)女性,平均年龄为(66.51±17.06)岁。使用体积为500毫升的合适溶液进行复苏,然后监测血液动力学和其他临床和实验室参数。后果直到第40分钟,3组之间的平均动脉压(MAP)没有显著差异(p>0.05)。在第45分钟,NS组的MAP仅与凝胶组的MAP不同(p=0.007)。在50分钟,NS小组的MAP与基线没有差异(p=0.0139)。从第50分钟到2小时,Gel和Sorb组的MAP在所有测量中均高于NS组(p0.05)。心输出量(CO)在第30分钟没有差异(p>0.05),在第35分钟,CO仅在Gel和NS组之间存在差异(p=0.019),从第40分钟到2小时,Gel和Sorb组的CO在所有测量中均显著高于NS组,从第35分钟到第45分钟,Gel组和NS组之间只有显著差异(p<0.05),从第50分钟到第2小时,Gel和Sorb组的DO2在所有测量中都显著高于NS组(p<0.05)。本研究中使用的明胶和山梨醇溶液的剂量对感染性休克患者的肾功能是安全的。然而,血液纤维蛋白原浓度的降低可能与使用含有明胶的溶液有关。仅在接受含山梨醇溶液的组中的患者中观察到格拉斯哥昏迷量表评分的显著改善。两组之间28天死亡率的差异无统计学意义(p=0.993)。结论。在我们的观察中,当在感染性休克患者中使用这三种类型的溶液时,两组之间直到第40分钟的血液动力学效果没有差异。从第40分钟到2小时,与0.9%氯化钠溶液相比,4%琥珀酰化明胶溶液和含有6%山梨醇的平衡聚离子溶液的容量效应显著更好。这三组中使用的溶液体积不会影响感染性休克患者的肾功能。与6%山梨醇和0.9%氯化钠溶液一起使用的平衡聚离子溶液的量不影响凝血功能。但4%琥珀酰明胶溶液的使用降低了血液中纤维蛋白原的浓度。在输注含有缓冲制剂的明胶溶液和含有缓冲制剂山梨醇的溶液后,与0.9%氯化钠溶液相比,血液的酸碱状态显著改善。输注含明胶溶液和0.9%氯化钠溶液不会影响患者的格拉斯哥昏迷评分。在输注含有山梨醇的溶液后,患者的意识通过该量表得到改善。28天的死亡率在各组之间没有显著差异。
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