Zan Mitrev Clinic, Republic of North Macedonia.
Braz J Cardiovasc Surg. 2022 Mar 10;37(1):35-47. doi: 10.21470/1678-9741-2020-0403.
Severe coronavirus disease 2019 (COVID-19) is characterised by hyperinflammatory state, systemic coagulopathies, and multiorgan involvement, especially acute respiratory distress syndrome (ARDS). We here describe our preliminary clinical experience with COVID-19 patients treated via an early initiation of extracorporeal blood purification combined with systemic heparinisation and respiratory support.
Fifteen patients were included; several biomarkers associated with COVID-19 severity were monitored. Personalised treatment was tailored according to the levels of interleukin (IL)-6, IL-8, tumour necrosis factor alpha, C-reactive protein (CRP), neutrophil-to-lymphocyte ratio, thrombocyte counts, D-dimers, and fibrinogen. Treatment consisted of respiratory support, extracorporeal blood purification using the AN69ST (oXiris®) hemofilter, and 300 U/kg heparin to maintain activation clotting time ≥ 180 seconds.
Ten patients presented with severe to critical disease (dyspnoea, hypoxia, respiratory rate > 30/min, peripheral oxygen saturation < 90%, or > 50% lung involvement on X-ray imaging). The median intensive care unit length of stay was 9.3 days (interquartile range 5.3-10.1); two patients developed ARDS and died after 5 and 26 days. Clinical improvement was associated with normalisation (increase) of thrombocytes and white blood cells, stable levels of IL-6 (< 50 ng/mL), and a decrease of CRP and fibrinogen.
Continuous monitoring of COVID-19 severity biomarkers and radiological imaging is crucial to assess disease progression, uncontrolled inflammation, and to avert irreversible multiorgan failure. The combination of systemic heparin anticoagulation regimens and extracorporeal blood purification using cytokine-adsorbing hemofilters may reduce hyperinflammation, prevent coagulopathy, and support clinical recovery.
严重的 2019 年冠状病毒病(COVID-19)的特征是炎症反应过度、全身凝血异常和多器官受累,特别是急性呼吸窘迫综合征(ARDS)。我们在此描述了我们对通过早期开始体外血液净化结合全身肝素化和呼吸支持治疗的 COVID-19 患者的初步临床经验。
共纳入 15 例患者;监测了与 COVID-19 严重程度相关的多种生物标志物。根据白细胞介素(IL)-6、IL-8、肿瘤坏死因子-α、C 反应蛋白(CRP)、中性粒细胞与淋巴细胞比值、血小板计数、D-二聚体和纤维蛋白原的水平,制定个体化治疗方案。治疗包括呼吸支持、使用 AN69ST(oXiris®)血液滤器进行体外血液净化以及给予 300 U/kg 肝素以维持激活凝血时间≥180 秒。
10 例患者表现为严重至危重症(呼吸困难、缺氧、呼吸频率>30 次/分、外周血氧饱和度<90%或 X 线成像显示>50%的肺部受累)。重症监护病房的中位住院时间为 9.3 天(四分位距 5.3-10.1);2 例患者发生 ARDS,并分别在 5 天和 26 天后死亡。临床改善与血小板和白细胞计数的正常化(增加)、IL-6 水平稳定(<50ng/mL)以及 CRP 和纤维蛋白原降低相关。
持续监测 COVID-19 严重程度的生物标志物和影像学表现对于评估疾病进展、失控的炎症和避免不可逆转的多器官衰竭至关重要。全身肝素抗凝方案与使用细胞因子吸附血液滤器的体外血液净化相结合可能会减轻炎症反应过度、预防凝血异常并支持临床恢复。