Introduction: Currently, the effect of hemoperfusion on outcome in severe COVID-19 patients is still unknown. Therefore, we aimed to investigate the effects of early HA-330 hemoperfusion in severe COVID-19 patients. Methods: We conducted a single center, prospective cohort study on patients who were diagnosed with severe COVID-19 patients and admitted to ICU. Patients in hemoperfusion group (defined as patients who were treated with hemoperfusion therapy at least 3 sessions in combination with standard therapy) were compared with the control group (defined as patients who received standard treatment alone or received less than 3 sessions of hemoperfusion therapy). The primary outcome was daily sequential organ failure assessment (SOFA) scores. Secondary outcomes were all-cause mortality at 28 days, mechanical ventilator-free day, daily C-reactive protein (CRP), oxygenation (defined by PaO2/FiO2 ratio), and severity score of lung infiltration on the chest X-ray (CXR RALE score). All outcomes were adjusted by regression analysis to reduce the confounders due to some difference in baseline characteristics. Results: A total number of 29 severe and critical COVID-19 confirmed patients were enrolled. Fifteen patients were defined as hemoperfusion group and 14 were control group. The median of CRP and SOFA score at the baseline (the day after severe pneumonia diagnosis or before hemoperfusion) in hemoperfusion and control groups were comparable, 96.79 mg/L and 87.3 mg/L, p = 0.53, 3.53 ± 0.99 versus 4.3 ± 1.89, p = 0.15, respectively. Clinical improvement associated with decreased SOFA score and improvement of CXR RALE score were found in hemoperfusion group compared to control group (p = 0.008 and p = 0.005, respectively). The 28-day mortality rate was significantly lower in hemoperfusion group compared to control group (6.67% vs. 85.71%, p < 0.001) and the adjusted hazard ratio of death was 0.017 (95% confidence interval = 0.008–0.351, p = 0.008). Conclusions: The addition of early HA-330 hemoperfusion to standard therapy improved severity of organ failure and might reduce the mortality rate. However, the results were affected by the baseline confounders and limited sample size.

1.
Huang
C
,
Wang
Y
,
Li
X
,
Ren
L
,
Zhao
J
,
Hu
Y
,
Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China
.
Lancet
.
2020
;
395
(
10223
):
497
506
.
2.
Fajgenbaum
DC
,
June
CH
.
Cytokine storm
.
N Engl J Med
.
2020
;
383
:
2255
73
. .
3.
RECOVERY Collaborative Group
.
Dexamethasone in hospitalized patients with Covid-19
.
N Engl J Med
.
2021
;
384
:
693
704
.
4.
Clark
EG
,
Hiremath
S
,
McIntyre
L
,
Wald
R
,
Hundemer
GL
,
Joannidis
M
.
Haemoperfusion should only be used for COVID-19 in the context of randomized trials
.
Nat Rev Nephrol
.
2020
;
16
(
12
):
697
9
. .
5.
Nkawi
G
,
Fan
W
,
Pomarè Montin
D
,
Lorenzin
A
,
Neri
M
,
Caprara
C
,
A new series of sorbent devices for multiple clinical purposes: current evidence and future directions
.
Blood Purif
.
2019
;
47
(
1–3
):
94
100
.
7.
Alhazzani
W
,
Evans
L
,
Alshamsi
F
,
Møller
MH
,
Ostermann
M
,
Prescott
HC
,
Surviving sepsis campaign guidelines on the management of adults with coronavirus disease 2019 (COVID-19) in the ICU: first update
.
Crit Care Med
.
2021
;
49
(
3
):
e219
34
.
8.
Setiawati
R
,
Widyoningroem
A
,
Handarini
T
,
Hayati
F
,
Basja
AT
,
Putri
ARDS
,
Modified chest X-ray scoring system in evaluating severity of COVID-19 patient in Dr. Soetomo General Hospital Surabaya, Indonesia
.
Int J Gen Med
.
2021
;
14
:
2407
12
.
9.
Peng
Z
,
Srisawat
N
,
Ratanarat
R
.
A collection of case reports from China, Thailand and Iran of HA330 or HA380 haemoperfusion cartridges to treat people with COVID-19. 2020
.
Available form:
http://www.jafron.com/index.php?m=content&c=index&a=show&catid=96&id=1027.
10.
Li
H
,
Liu
L
,
Zhang
D
,
Xu
J
,
Dai
H
,
Tang
N
,
SARS-CoV-2 and viral sepsis: observations and hypotheses
.
Lancet
.
2020
;
395
:
1517
20
.
11.
Ronco
C
,
Bagshaw
SM
,
Bellomo
R
,
Clark
WR
,
Husain-Syed
F
,
Kellum
JA
,
Extracorporeal blood purification and organ support in the critically ill patient during COVID-19 pandemic: expert review and recommendation
.
Blood Purif
.
2021
;
50
(
1
):
17
27
.
12.
Kaçar
CK
,
Uzundere
O
,
Kandemir
D
,
Yektaş
A
.
Efficacy of HA330 hemoperfusion adsorbent in patients followed in the intensive care unit for septic shock and acute kidney injury and treated with continuous venovenous hemodiafiltration as renal replacement therapy
.
Blood Purif
.
2020
;
49
(
4
):
448
56
.
13.
Darazam
IA
,
Kazempour
M
,
Amin
M
,
Hatami
F
,
Rabiei
MM
,
Gharehbagh
FJ
,
Efficacy of hemoperfusionin severe and critical cases of COVID-19
.
2021
. Epub ahead of print. .
14.
Shadvar
K
,
Tagizadiyeh
A
,
Gamari
AA
,
Soleimanpour
H
,
Mahmoodpoor
A
.
Hemoperfusion as a potential treatment for critically ill COVID-19 patients with cytokine storm
.
Blood Purif
.
2021
;
50
(
3
):
405
7
. .
15.
Esmaeili Vardanjani
A
,
Ronco
C
,
Rafiei
H
,
Golitaleb
M
,
Pishvaei
MH
,
Mohammadi
M
.
Early hemoperfusion for cytokine removal may contribute to prevention of intubation in patients infected with COVID-19
.
Blood Purif
.
2021
;
50
(
2
):
257
60
. .
16.
De Rosa
S
,
Cutuli
SL
,
Ferrer
R
,
Antonelli
M
,
Ronco
C
,
Group
CEC
,
Polymyxin B hemoperfusion in COVID-19 patients with endotoxic shock: case series from EUPHAS II registry
.
Artif Organs
.
2021
;
45
(
6
):
E187
94
.
17.
Supady
A
,
Weber
E
,
Rieder
M
,
Lother
A
,
Niklaus
T
,
Zahn
T
,
Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
.
Lancet Respir Med
.
2021
;
9
(
7
):
755
62
.
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