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Relationship Between Positive End-expiratory Pressure Levels, Central Venous Pressure, Systemic Inflammation and Acute Renal Failure in Critically Ill Ventilated COVID-19 Patients: a Monocenter Retrospective Study in France

Overview
Journal Acute Crit Care
Specialty Critical Care
Date 2023 Jun 14
PMID 37313663
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Abstract

Background: The role of positive pressure ventilation, central venous pressure (CVP) and inflammation on the occurrence of acute kidney injury (AKI) have been poorly described in mechanically ventilated patient secondary to coronavirus disease 2019 (COVID-19).

Methods: This was a monocenter retrospective cohort study of consecutive ventilated COVID-19 patients admitted in a French surgical intensive care unit between March 2020 and July 2020. Worsening renal function (WRF) was defined as development of a new AKI or a persistent AKI during the 5 days after mechanical ventilation initiation. We studied the association between WRF and ventilatory parameters including positive end-expiratory pressure (PEEP), CVP, and leukocytes count.

Results: Fifty-seven patients were included, 12 (21%) presented WRF. Daily PEEP, 5 days mean PEEP and daily CVP values were not associated with occurrence of WRF. 5 days mean CVP was higher in the WRF group compared to patients without WRF (median [IQR], 12 mm Hg [11-13] vs. 10 mm Hg [9-12]; P=0.03). Multivariate models with adjustment on leukocytes and Simplified Acute Physiology Score (SAPS) II confirmed the association between CVP value and risk of WRF (odd ratio, 1.97; 95% confidence interval, 1.12-4.33). Leukocytes count was also associated with occurrence of WRF in the WRF group (14 G/L [11-18]) and the no-WRF group (9 G/L [8-11]) (P=0.002).

Conclusions: In mechanically ventilated COVID-19 patients, PEEP levels did not appear to influence occurrence of WRF. High CVP levels and leukocytes count are associated with risk of WRF.

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References
1.
Hamilton P, Hanumapura P, Castelino L, Henney R, Parker K, Kumar M . Characteristics and outcomes of hospitalised patients with acute kidney injury and COVID-19. PLoS One. 2020; 15(11):e0241544. PMC: 7608889. DOI: 10.1371/journal.pone.0241544. View

2.
Hultstrom M, Lipcsey M, Wallin E, Larsson I, Larsson A, Frithiof R . Severe acute kidney injury associated with progression of chronic kidney disease after critical COVID-19. Crit Care. 2021; 25(1):37. PMC: 7829656. DOI: 10.1186/s13054-021-03461-4. View

3.
Yang X, Tian S, Guo H . Acute kidney injury and renal replacement therapy in COVID-19 patients: A systematic review and meta-analysis. Int Immunopharmacol. 2020; 90:107159. PMC: 7608016. DOI: 10.1016/j.intimp.2020.107159. View

4.
Lumlertgul N, Pirondini L, Cooney E, Kok W, Gregson J, Camporota L . Acute kidney injury prevalence, progression and long-term outcomes in critically ill patients with COVID-19: a cohort study. Ann Intensive Care. 2021; 11(1):123. PMC: 8343342. DOI: 10.1186/s13613-021-00914-5. View

5.
Legrand M, Bell S, Forni L, Joannidis M, Koyner J, Liu K . Pathophysiology of COVID-19-associated acute kidney injury. Nat Rev Nephrol. 2021; 17(11):751-764. PMC: 8256398. DOI: 10.1038/s41581-021-00452-0. View