Fig. 5From: Multidimensional analysis of the host response reveals prognostic and pathogen-driven immune subtypes among adults with sepsis in UgandaIllness severity scores, distributions of organ failures and pathogens, and outcomes stratified by transcriptional subtypes. a–c Modified Early Warning Score, Universal Vital Assessment score, modified systemic inflammatory response syndrome [mSIRS], and quick Sepsis-related Organ Failure assessment [qSOFA] scores stratified by transcriptional subtype; p-values in 5C represent Chi-squared test with continuity correction (N = 128). d Chord plot indicating proportion of patients with specific organ failures across each transcriptional subtype; a wider chord band indicates a greater proportion of patients with each corresponding organ failure (N = 128, proportions in subtype 2 vs. 1 as follows: shock: 21.4% vs. 11.0%; acute respiratory failure: 35.7% vs. 20.0%; severe anemia: 28.6% vs. 21.0%; encephalopathy: 25.0% vs. 12.0%). e Chord plot indicating proportion of patients with specific infections across each transcriptional subtype; a wider chord band indicates a greater proportion of patients with each corresponding infection (N = 128, proportions in subtype 2 vs. 1 as follows: HIV: 75.0% vs. 48.5%; tuberculosis: 35.7% vs. 10.0%; malaria: 11.5% vs. 24.5%; influenza: 0.0% vs. 2.4%). f Proportions of patients with HIV-infection (N = 127), HIV-associated TB (N = 127), and positive urine TB-LAM results (among those tested, N = 55) across each transcriptional subtype. g In-hospital outcome (N = 128), impaired functional status [Karnofsky Performance Status; KPS] (N = 108) among hospital survivors, and 30-day vital status across each transcriptional subtype (N = 117); p-values in 5F and 5G represent Chi-squared test with continuity correction. h Forest plot indicating univariable (unadjusted) odds ratios for in-hospital outcome and 30-day mortality among patients in transcriptional subtype 2 vs. subtype 1, stratified by key pathogen groups [patients with influenza omitted given small number of events in that pathogen group, odds ratio for in-hospital outcome omitted for patients with no pathogen detected as all events in transcriptional subtype 1; for visualization, upper limit of 95% confidence interval for in-hospital outcome truncated at 15 for patients with HIV-associated TB (upper limit 29.76) and malaria (upper limit 51.46), as well as for 30-day outcome for patients with no pathogen identified (upper limit 38.39) and malaria (upper limit 34.67)Back to article page