Endotoxin Adsorbent Therapy in Severe COVID-19 Pneumonia

被引:13
|
作者
Peerapornratana, Sadudee [1 ,2 ,3 ,4 ,5 ]
Sirivongrangson, Phatadon [1 ,2 ,3 ]
Tungsanga, Somkanya [1 ]
Tiankanon, Kanitha [1 ]
Kulvichit, Win [1 ,2 ,3 ]
Putcharoen, Opass [6 ]
Kellum, John A. [5 ]
Srisawat, Nattachai [1 ,2 ,3 ,5 ,7 ,8 ]
机构
[1] Chulalongkorn Univ, Fac Med, Dept Med, Div Nephrol, Bangkok, Thailand
[2] King Chulalongkorn Mem Hosp, Excellence Ctr Crit Care Nephrol, Bangkok, Thailand
[3] Chulalongkorn Univ, Crit Care Nephrol Res Unit, Bangkok, Thailand
[4] Chulalongkorn Univ, Fac Med, Dept Lab Med, Bangkok, Thailand
[5] Univ Pittsburgh, Sch Med, Dept Crit Care Med, Ctr Crit Care Nephrol,CRISMA Ctr, Pittsburgh, PA USA
[6] Chulalongkorn Univ, Fac Med, Dept Med, Div Infect Dis, Bangkok, Thailand
[7] Chulalongkorn Univ, Trop Med Cluster, Bangkok, Thailand
[8] Royal Soc Thailand, Acad Sci, Bangkok, Thailand
关键词
Coronavirus disease 19; Endotoxemia; Endotoxin adsorbent; Acute respiratory distress syndrome; Critical care; Adsorption therapy; RESPIRATORY-DISTRESS-SYNDROME; B-IMMOBILIZED-FIBER; DIRECT HEMOPERFUSION; INFLUENZA; INFECTION; PATHOGENS; DEATH; ASSAY; ARDS;
D O I
10.1159/000515628
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Uncontrolled systemic inflammation may occur in severe coronavirus disease 19 (COVID-19). We have previously shown that endotoxemia, presumably from the gut, may complicate COVID-19. However, the role of endotoxin adsorbent (EA) therapy to mitigate organ dysfunction in COVID-19 has not been explored. Methods: We conducted a retrospective observational study in COVID-19 patients who received EA therapy at the King Chulalongkorn Memorial Hospital, Bangkok, Thailand, between March 13 and April 17, 2020. Relevant clinical and laboratory data were collected by inpatient chart review. Results: Among 147 hospitalized COVID-19 patients, 6 patients received EA therapy. All of the 6 patients had severe COVID-19 infection with acute respiratory distress syndrome (ARDS). Among these, 5 of them were mechanically ventilated and 4 had complications of secondary bacterial infection. The endotoxin activity assay (EAA) results of pre-EA therapy ranged from 0.47 to 2.79. The choices of EA therapy were at the discretion of attending physicians. One patient was treated with oXiris (R) along with continuous renal replacement therapy, and the others received polymyxin B hemoperfusion sessions. All patients have survived and were finally free from the mechanical ventilation as well as had improvement in PaO2/FiO(2) ratio and decreased EAA level after EA therapy. Conclusions: We demonstrated the clinical improvement of severe COVID-19 patients with elevated EAA level upon receiving EA therapy. However, the benefit of EA therapy in COVID-19 ARDS is still unclear and needs to be elucidated with randomized controlled study.
引用
收藏
页码:47 / 54
页数:8
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