Adult Hematology Department, Turgut Özal Medical Center, İnönü University, Malatya, Turkey.
Eur Rev Med Pharmacol Sci. 2022 Nov;26(21):8112-8117. doi: 10.26355/eurrev_202211_30165.
In this study, we aimed at evaluating the impact of HA330 hemoperfusion adsorbent application on inflammatory markers and end-organ damage markers in patients with sepsis/septic shock.
Patients who were diagnosed with sepsis/septic shock and treated with HA330 hemoperfusion adsorbent in addition to the standard treatment were included in this retrospective study conducted at Inonu University Turgut Ozal Medical Center between January 1, 2019 and January 1, 2021.
A total of 150 patients were included in the study. The mean±SD age of the patients was 51.9±17.7 years. 102 patients (68%) were in septic shock. Mean±SD APACHE II scores were 15.3±4.8. The need for mechanical ventilation was noted in 64 patients (42.7%). WBC, neutrophil count, hemoglobin, platelet count, BUN, creatinine, AST, ALT, CRP and procalcitonin levels were measured before and after the procedure. Overall, 104 patients (69.3%) died median (min-max) 2.5 (1-114) days after the cytokine adsorption, while 46 patients (30.7%) recovered from sepsis and were discharged. The increase in BUN levels and decrease in platelet count after the procedure were statistically significant (p≤0.001, 0.041, respectively) in the overall study population. The laboratory findings in 46 survivors indicated significantly decreased AST and ALT levels after cytokine adsorption compared to baseline pre-treatment levels. WBC, neutrophil count, CRP, procalcitonin, BUN and creatinine values were also decreased after cytokine adsorption in survivors, whereas the change was not statistically significant. There was also a non-significant tendency for an increase in platelet count and hemoglobin levels after cytokine adsorption compared to pre-treatment values in these patients.
Although no effect of HA330 hemoperfusion application on inflammatory markers and end-organ damage markers was demonstrated in our study, we used the HA330 hemoperfusion adsorbent method as a last resort in terminal patients with a mortality rate of approximately 90% and for whom antibiotic treatment did not benefit. Therefore, multicenter, prospective studies are needed to clarify the effect of early HA330 hemoperfusion use in the treatment of sepsis.
本研究旨在评估 HA330 血液灌流器吸附剂在脓毒症/脓毒性休克患者中的应用对炎症标志物和靶器官损伤标志物的影响。
本回顾性研究于 2019 年 1 月 1 日至 2021 年 1 月 1 日在因努大学图古特奥扎尔医疗中心进行,纳入了在标准治疗的基础上加用 HA330 血液灌流器吸附剂治疗的脓毒症/脓毒性休克患者。
本研究共纳入 150 例患者。患者的平均年龄(标准差)为 51.9±17.7 岁。102 例(68%)为脓毒性休克。平均(标准差)APACHE II 评分为 15.3±4.8。64 例(42.7%)需要机械通气。白细胞计数、中性粒细胞计数、血红蛋白、血小板计数、BUN、肌酐、AST、ALT、CRP 和降钙素水平在治疗前后均进行了检测。总体而言,104 例患者(69.3%)在细胞因子吸附后中位(最小-最大)2.5(1-114)天死亡,46 例患者(30.7%)从脓毒症中恢复并出院。在整个研究人群中,治疗后 BUN 水平升高和血小板计数降低均具有统计学意义(p≤0.001,0.041)。与治疗前相比,46 例存活者的 AST 和 ALT 水平在细胞因子吸附后显著降低。存活者的白细胞计数、中性粒细胞计数、CRP、降钙素、BUN 和肌酐值在细胞因子吸附后也有所降低,但差异无统计学意义。与治疗前相比,这些患者的血小板计数和血红蛋白水平在细胞因子吸附后也有升高的趋势,但无统计学意义。
虽然本研究未显示 HA330 血液灌流应用对炎症标志物和靶器官损伤标志物有影响,但我们在死亡率约为 90%且抗生素治疗无效的终末期患者中使用了 HA330 血液灌流吸附剂方法作为最后手段。因此,需要进行多中心、前瞻性研究以明确早期应用 HA330 血液灌流治疗脓毒症的效果。