Table 3.
Current knowledge gap: | Studies should address: |
---|---|
The role of gut microbiome alteration on sepsis predisposition | • Longitudinal microbiome changes in groups at high risk for sepsis |
• Microbiome characteristics that indicate high risk for sepsis, including whether these can be used for prediction/diagnosis | |
• Mechanisms linking increase or decrease of specific taxa to sepsis risk | |
• How gut microbiome alterations with loss of protective taxa impacts immune dysregulation predisposing to sepsis | |
• Impact of SCFAs on protection from sepsis | |
• If altering the gut microbiome can decrease sepsis risk | |
How the gut microbiome impacts sepsis outcomes | • Correlation of markers of gut microbiome alteration with end-organ dysfunction and mortality |
• Whether specific patterns of alteration can predict adverse outcomes in sepsis | |
• Gut microbiome changes that contribute to dysregulated immune responses of sepsis | |
• Role of pathobionts and antibiotic resistance genes in antibiotic selection | |
Whether microbiome-directed therapeutics can impact sepsis outcomes | • Which patients with microbiome alteration may benefit from attempting to restore the gut microbiome to lower risk of sepsis |
• Which patients with sepsis may benefit from microbiome-directed therapeutics to improve sepsis outcomes | |
• The ideal method of gut microbiome therapeutics (i.e., probiotics, FMT) | |
• The specific dose, timing, and frequency of FMT that may benefit patients in these groups |
FMT fecal microbiota transplant, SCFA short-chain fatty acid