重症COVID-19患者在DMCH ICU接受恢复期血浆(CP)治疗后的预后

Ferdous Rahman, Md. Tariqul Islam, M. Ashrafuzzaman, Tofazzel Hossain, Benzir Shafi, A. Ahmed
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摘要

到目前为止,还没有批准的针对COVID-19的特异性抗病毒药物或疫苗。本研究前瞻性纳入10例经实时病毒RNA检测确诊的危重患者。作为最大限度的支持治疗和抗病毒药物的补充,向患者输注来自中和抗体滴度高于1:160的近期康复供者的200mL恢复期血浆(CP)。本研究的目的是观察CP输注的结果。有40%(04)例患者可减少氧支持(降压),10%(01)例患者参数不变,50%(05)例患者需要更多氧支持(降压),这与淋巴细胞计数的增量反应和炎症生化参数的有害反应有关,其中70%(07)例患者接受机械通气治疗后,30%(03)例患者从机械通气转向高流量鼻插管。10%(01)患者停止使用高流量鼻插管。未观察到严重的不良反应。该研究表明,CP治疗耐受性良好,并可能通过中和covid -19危重病例的病毒血症来改善临床结果。最佳剂量和时间点,以及CP治疗的临床益处,需要在更大规模的良好对照试验中进一步研究。JBSA 2021;34 (1): 20 - 25
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcome of Critically Ill COVID-19 Patients After Getting Convalescent Plasma (CP) in ICU of DMCH
There are no approved specific antiviral agents or vaccines against COVID-19 till now. In this study, 10critically ill patients confirmed by real-time viral RNA test were enrolled prospectively. One dose of 200mL of convalescent plasma (CP) derived from recently recovered donors with the neutralizing antibodytiters above 1:160 was transfused to the patients as an addition to maximal supportive care and antiviralagents. The aim of this study is to see the outcome of CP transfusion. It was possible to reduce oxygensupport (step down) of 40%(04) patients, 10% (01) patient’s parameters was unchanged and 50% (05)patients were need more oxygen support (step up) after getting CP which correlate with incrementalresponse of lymphocyte counts and detrimental response of biochemical parameters of inflammation.70%(07)patients of total who received mechanical ventilation, after treatment with CP, 30%(03) patients wereweaned from mechanical ventilation to high-flow nasal cannula, and 10%(01) patient discontinued highflownasal cannula to NRM.No severe adverse effects were observed. This study showed CP therapy waswell tolerated and could potentially improve the clinical outcomes through neutralizing viremia in criticalCOVID-19 cases. The optimal dose and time point, as well as the clinical benefit of CP therapy, needsfurther investigation in larger well-controlled trials. JBSA 2021; 34(1): 20-25
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