Sublingual microcirculation in patients with SARS-CoV-2 undergoing veno-venous extracorporeal membrane oxygenation

Microvasc Res. 2020 Nov:132:104064. doi: 10.1016/j.mvr.2020.104064. Epub 2020 Aug 22.

Abstract

Veno-Venous Extracorporeal Membrane Oxygenation (VV-ECMO) is a rescue treatment for severe acute respiratory failure refractory to conventional ventilation. We examined the alterations of sublingual microcirculation in patients with SARS-CoV-2 during VV-ECMO treatment and assessed the relationship between microvascular parameters and ventilation, hemodynamics, and laboratory tests. Nine patients were included in the study and the following microcirculatory parameters were estimated: TVD 16.81 (14.46-18.6) mm/mm2; PVD 15.3 (14.09-17.96) mm/mm2; PPV 94.85% (93.82%-97.79%); MFI 2.5 (2.5-2.92); HI 0.4 (0.18-0.4). TVD and PVD were inversely related to D-dimer levels (rho = -0.667, p = 0.05 and rho = -0.733, p = 0.025 respectively), aspartate aminotransferase (AST) (rho = -0.886, p = 0.019 and rho = -0.886, p = 0.019 respectively) and alanine aminotransferase (ALT) (rho = -0.829, p = 0.042 and rho = -0.829, p = 0.042 respectively). Our results showed an altered sublingual microcirculation in patients receiving VV-ECMO for severe SARS-CoV-2 and suggest a potential contribution of endothelia dysfunction to determine microvascular alteration.

Keywords: Extracorporeal membrane oxygenation; Microcirculation; SARS-CoV-2.

MeSH terms

  • Betacoronavirus
  • COVID-19
  • Capillaries / physiopathology
  • Coronavirus Infections / blood*
  • Coronavirus Infections / therapy*
  • Endothelium, Vascular / physiopathology
  • Extracorporeal Membrane Oxygenation / methods*
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis
  • Hemodynamics
  • Humans
  • Male
  • Microcirculation*
  • Microscopy, Video
  • Middle Aged
  • Mouth Floor / blood supply*
  • Pandemics
  • Pneumonia, Viral / blood*
  • Pneumonia, Viral / therapy*
  • Retrospective Studies
  • SARS-CoV-2
  • Veins

Substances

  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D