Background: As a treatment method, considerable amounts of patients' blood are
transferred to absorbents to remove blood cytokines in hemoperfusion. The
present research studies the contribution of hemoperfusion to the outcomes
observed in patients with COVID-19. Methods: The present quasi-experimental
pilot trial recruited 80 patients hospitalized in intensive care units (ICU) suffering
from COVID-19 who received hemoperfusion. Hemoperfusion was conducted
for the patients in the study group in two 3-hour sessions. The requirement of
respiratory support and mortality were estimated. Results: The patients were
56.37±14.97 years old on average. 92.5% of patients were polymerase chain
reaction (PCR) positive, while the others showed the radiographic characteristic
of COVID-19. In total, 52.5% of the patients died. The most prevalent clinical
presentations were fever and cough. The average saturation of oxygen after and
before conducting the hemoperfusion was 81.41±10.92 and 77.84±13.33,
respectively. Most of those who died had an involvement higher than 75%. The
reductions observed in the platelet and hemoglobin levels following
hemoperfusion were recorded. In addition, urea and alanine aminotransferase
(ALT) levels increased following the hemoperfusion. Conclusions: Hemoperfusion
can result in decreased levels of platelet and hemoglobin and increased levels of
urea and ALT, indicating the adverse effects of hemoperfusion on the COVID-19
patients receiving this treatment. The most important predictive factor
determining the mortality rate of the COVID-19 patients receiving
hemoperfusion was intubation.
Keywords: Coronavirus Disease 2019, SARS-CoV-2, Hemoperfusion, COVID-19,
Pilot Study, Recovery