Inflammatory Biomarkers Affecting Survival Prognosis in Patients Receiving Veno-Venous ECMO for Severe COVID-19 Pneumonia

Author:

Drmić Željka1ORCID,Bandić Ivan1,Hleb Sonja1ORCID,Kukoč Andrea1,Sakan Sanja1,Sojčić Nataša1,Kristović Darko1,Mikecin Verica1,Presečki Ivana1,Oremuš Zrinka Šafarić1ORCID,Bradić Nikola12,Peršec Jasminka123ORCID,Šribar Andrej13ORCID

Affiliation:

1. Clinical Department for Anesthesiology, Reanimatology and Intensive Care Medicine, University Hospital Dubrava, Avenija Gojka Šuška 6, 10000 Zagreb, Croatia

2. Department of Health Studies, University North, 42000 Varaždin, Croatia

3. School of Dental Medicine, University of Zagreb, 10000 Zagreb, Croatia

Abstract

Severe COVID-19 pneumonia in which mechanical ventilation is unable to achieve adequate gas exchange can be treated with veno-venous ECMO, eliminating the need for aggressive mechanical ventilation which might promote ventilator-induced lung injury and increase mortality. In this retrospective observational study, 18 critically ill COVID-19 patients who were treated using V-V ECMO during an 11-month period in a tertiary COVID-19 hospital were analyzed. Biomarkers of inflammation and clinical features were compared between survivors and non-survivors. Survival rates were compared between patients receiving ECMO and propensity matched mechanically ventilated controls. There were 7 survivors and 11 non-survivors. The survivors were significantly younger, with a higher proportion of females, higher serum procalcitonin at ICU admission, and before initiation of ECMO they had significantly lower Murray scores, PaCO2, WBC counts, serum ferritin levels, and higher glomerular filtration rates. No significant difference in mortality was found between patients treated with ECMO compared to patients treated using conventional lung protective ventilation. Hypercapnia, leukocytosis, reduced glomerular filtration rate, and increased serum ferritin levels prior to initiation of V-V ECMO in patients with severe COVID-19 pneumonia may be early warning signs of reduced chance of survival. Further multicentric studies are needed to confirm these findings.

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference42 articles.

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