Endotoxemia in Critically Ill Patients with COVID-19.


Journal

Blood purification
ISSN: 1421-9735
Titre abrégé: Blood Purif
Pays: Switzerland
ID NLM: 8402040

Informations de publication

Date de publication:
2022
Historique:
received: 12 03 2021
accepted: 29 06 2021
pubmed: 14 9 2021
medline: 7 6 2022
entrez: 13 9 2021
Statut: ppublish

Résumé

Mechanism(s) mediating critical illness in coronavirus disease 2019 (COVID-19) remain unclear. Previous reports demonstrate the existence of endotoxemia in viral infections without superimposed gram-negative bacteremia, but the rate and severity of endotoxemia in critically ill patients with COVID-19 requires further exploration. This is a single-center cross-sectional study of 92 intensive care unit patients diagnosed with COVID-19 pneumonia. Endotoxin activity (EA) was measured in patients that met the following criteria: (1) age ≥18 years and (2) multi-organ dysfunction score >9 from March 24, 2020, to June 20, 2020. A total of 32 patients met the inclusion/exclusion criteria for measurement of EA. The median age of the study cohort was 60 years with a majority male (21/32, 65%) with hypertension (50%). A significant proportion of the patients exhibited either elevated EA in the intermediate range (0.40-0.59 EA units) (10/32, 31%) or high range (≥0.60 EA units) (14/32, 44%) or were nonresponders (NRs, low neutrophil response) to EA (6/32, 19%), with the presence of gram-negative bacteremia only in 2/32 (6%) patients. Low EA was reported in 2/32 patients. NRs (5/6, 83%) and patients with high EA (7/14, 50%) exhibited higher acute kidney injury (AKI) as compared to patients with low/intermediate EA level (1/12, 8.3%). Elevated EA was observed in a large majority of critically ill patients with COVID-19 and multi-organ dysfunction despite a low incidence of concurrent gram-negative bacteremia. While we observed that elevated EA and nonresponsiveness to EA were associated with AKI in critically ill patients with COVID-19, these findings require further validation in larger longitudinal cohorts.

Identifiants

pubmed: 34515062
pii: 000518230
doi: 10.1159/000518230
pmc: PMC8450835
mid: NIHMS1726210
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

513-519

Subventions

Organisme : BLRD VA
ID : I01 BX005300
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK112984
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007757
Pays : United States
Organisme : BLRD VA
ID : I01 BX003698
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK121846
Pays : United States

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Sobia Khan (S)

Department of Medicine, Stony Brook University, Stony Brook, New York, USA.

Olena Bolotova (O)

Department of Medicine, Stony Brook University, Stony Brook, New York, USA.

Haseena Sahib (H)

Department of Medicine, Stony Brook University, Stony Brook, New York, USA.

Debra Foster (D)

Spectral Medical Inc., Toronto, Ontario, Canada.

Sandeep K Mallipattu (SK)

Department of Medicine, Stony Brook University, Stony Brook, New York, USA.
Renal Section, Northport VA Medical Center, Northport, New York, USA.

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Classifications MeSH