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Treatment with Delipid Extracorporeal Lipoprotein Filter from Plasma after Intravenous Thrombolysis for Acute Ischemic Stroke: A Single-Center Experience

机译:急性缺血性脑卒中静脉溶栓后血浆醇体外脂蛋白过滤器治疗:单中心经验

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Introduction: The delipid extracorporeal lipoprotein filter from plasma (DELP) has been approved for the treatment of acute ischemic stroke (AIS) by the China Food and Drug Administration, but its effectiveness and mechanism are not yet fully determined. The purpose of this study was to evaluate the effect of DELP treatment on AIS patients after intravenous thrombolysis. Methods: A retrospective study was performed on AIS patients with no improvement within 24 h after intravenous thrombolysis who were subsequently treated with or without DELP. Primary outcome was the proportion with a modified Rankin scale (mRS) of 0–1 at 90 days. Secondary outcomes were changes in National Institute of Health Stroke Scale (NIHSS) score from 24 h to 14 days after thrombolysis, and the rate of improvement in stroke-associated pneumonia (SAP). The main safety outcomes were the rates of symptomatic intracranial hemorrhage and mortality. To investigate its mechanisms, serum biomarkers were measured before and after DELP. Results: A total of 252 patients were recruited, 63 in the DELP group and 189 matched patients in the NO DELP group. Compared with the NO DELP group, the DELP group showed an increase in the proportion of mRS 0–1 at 90 days (p = 0.042). More decrease in NIHSS from 24 h to 14 days (p = 0.024), a higher rate of improvement in SAP (p = 0.022), and lower mortality (p = 0.040) were shown in DELP group. Furthermore, DELP decreased levels of interleukin (IL)-1β, E-selectin, malondialdehyde, matrix metalloprotein 9, total cholesterol, low-density lipoprotein, and fibrinogen, and increased superoxide dismutase (p 0.05). Conclusions: DELP following intravenous thrombolysis should be safe, and is associated with neurological function improvement, possibly through multiple neuroprotective mechanisms. Prospective trials are needed.
机译:简介:从血浆(DELP)的Delipid体外脂蛋白过滤器已被中国食品和药物管理局批准治疗急性缺血性卒中(AIS),但其有效性和机制尚未完全确定。本研究的目的是评估Delp治疗对静脉溶栓后AIS患者的影响。方法:在静脉注射溶栓后24小时内没有改善的AIS患者进行回顾性研究,随后用或没有DELP治疗。主要结果是在90天时0-1的改进的Rankin规模(MRS)的比例。二次结果是国家健康卒中规模(NIHSS)的变化从溶解后24小时到14天的评分,以及中风相关肺炎(SAP)的改善速度。主要安全结果是症状颅内出血和死亡率的率。为了研究其机制,在DELP之前和之后测量血清生物标志物。结果:招募了252名患者,德尔普集团63名,No Delp组中的189名患者。与NO DELP组相比,DELP组在90天时显示MRS 0-1的比例(P = 0.042)。从24小时到14天的NIHS减少(P = 0.024),SAP的更高改善速率(p = 0.022),并且在delp组中显示了降低的死亡率(p = 0.040)。此外,德普素(IL)-1β,E-SELITIN,丙二醛,基质金属蛋白9,总胆固醇,低密度脂蛋白和纤维蛋白原的水平降低,以及升高的超氧化物歧化酶(P <0.05)。结论:静脉内溶栓后德普应安全,与神经功能改善有关,可能通过多种神经保护机制。需要预期试验。

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