Blood Purification Techniques, Inflammatory Mediators and Mortality in COVID-19 Patients.
ARDS
Acute respiratory distress syndrome
COVID-19
Continuous renal replacement therapy
Coronavirus disease 2019
Cytokine
Hemoperfusion
Inflammatory marker
Mortality
Oxygenation
Journal
Tanaffos
ISSN: 1735-0344
Titre abrégé: Tanaffos
Pays: Iran
ID NLM: 101308232
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
entrez:
7
5
2021
pubmed:
8
5
2021
medline:
8
5
2021
Statut:
ppublish
Résumé
Inflammatory mediators are an important component in the pathophysiology of the coronavirus disease 2019 (COVID-19). This study aimed to assess the effects of reducing inflammatory mediators using hemoperfusion (HP) and continuous renal replacement therapy (CRRT) on the mortality of patients with COVID-19. Twelve patients with confirmed diagnosis of COVID-19 were included. All patients had acute respiratory distress syndrome (ARDS). Patients were divided into three groups, namely, HP, CRRT and HP+CRRT. The primary outcome was mortality and the secondary outcomes were oxygenation and reduction in inflammatory mediators at the end of the study. Patients were not different at baseline in demographics, inflammatory cytokine levels, and the level of acute phase reactants. Half of the patients (3 out of 6) in the HP+CRRT group survived along with the survival of one patient (1 out of 2) in the HP group. All four patients in the CRRT group died. Serum creatinine (SCr), Interleukin-1 (IL1), Interleukin-6 (IL6), Interleukin-8 (IL8), partial pressure of oxygen (PaO Combined HP and CRRT demonstrated the best result in terms of mortality, reduction of inflammatory mediators and oxygenation. Further investigations are needed to explore the role of HP+CRRT in COVID-19 patients.
Sections du résumé
BACKGROUND
BACKGROUND
Inflammatory mediators are an important component in the pathophysiology of the coronavirus disease 2019 (COVID-19). This study aimed to assess the effects of reducing inflammatory mediators using hemoperfusion (HP) and continuous renal replacement therapy (CRRT) on the mortality of patients with COVID-19.
MATERIALS AND METHODS
METHODS
Twelve patients with confirmed diagnosis of COVID-19 were included. All patients had acute respiratory distress syndrome (ARDS). Patients were divided into three groups, namely, HP, CRRT and HP+CRRT. The primary outcome was mortality and the secondary outcomes were oxygenation and reduction in inflammatory mediators at the end of the study.
RESULTS
RESULTS
Patients were not different at baseline in demographics, inflammatory cytokine levels, and the level of acute phase reactants. Half of the patients (3 out of 6) in the HP+CRRT group survived along with the survival of one patient (1 out of 2) in the HP group. All four patients in the CRRT group died. Serum creatinine (SCr), Interleukin-1 (IL1), Interleukin-6 (IL6), Interleukin-8 (IL8), partial pressure of oxygen (PaO
CONCLUSION
CONCLUSIONS
Combined HP and CRRT demonstrated the best result in terms of mortality, reduction of inflammatory mediators and oxygenation. Further investigations are needed to explore the role of HP+CRRT in COVID-19 patients.
Types de publication
Journal Article
Langues
eng
Pagination
291-299Informations de copyright
Copyright© 2020 National Research Institute of Tuberculosis and Lung Disease.
Déclaration de conflit d'intérêts
Competing interests Not applicable.
Références
Iran J Pharm Res. 2020 Winter;19(1):31-36
pubmed: 32922466
JAMA. 2020 Mar 17;323(11):1061-1069
pubmed: 32031570
Lancet. 1993 Mar 13;341(8846):643-7
pubmed: 8095568
BMC Infect Dis. 2020 Dec 21;20(1):963
pubmed: 33349241
Med Mal Infect. 2020 Jun;50(4):384
pubmed: 32240719
Nat Rev Microbiol. 2016 Aug;14(8):523-34
pubmed: 27344959
Lancet Respir Med. 2020 May;8(5):506-517
pubmed: 32272080
Am J Med Sci. 2015 Mar;349(3):199-205
pubmed: 25494217
Dis Markers. 2016;2016:3501373
pubmed: 26980924
Lancet Respir Med. 2020 May;8(5):475-481
pubmed: 32105632
Clin Exp Immunol. 2004 Apr;136(1):95-103
pubmed: 15030519
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
Lancet Respir Med. 2020 Mar;8(3):240-241
pubmed: 32035509
Lancet. 2020 Feb 22;395(10224):e35-e36
pubmed: 32035018
J Pathol. 2015 Jan;235(2):185-95
pubmed: 25270030
Lancet. 2020 Feb 15;395(10223):497-506
pubmed: 31986264
Autoimmun Rev. 2020 Jun;19(6):102537
pubmed: 32251717
Blood Purif. 2020 Dec 3;:1-8
pubmed: 33271549
J Inflamm (Lond). 2014 Aug 05;11:21
pubmed: 25110464