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. 2021 Aug 12;39:101074. doi: 10.1016/j.eclinm.2021.101074

Table 2.

Associations with time to clinical stability in CAP patients at admission.

Univariable Multivariable
Predictor Hazard Ratio (95% CI) p-value Hazard Ratio (95% CI) p-value
Age, y 1•00 (0•99–1•02) 0•616 1•00 (0•98–1•02) 0•955
Male sex 0•92 (0•56–1•52) 0•740 0•83 (0•48–1•44) 0•503
Caucasian ethnicity 0•70 (0•39–1•27) 0•24 0•67 (0.35–1.28) 0•225
Prior antibiotic usea 0•79 (0•39–1•60) 0•509 1•01 (0•47–2•18) 0•975
COPD 1•22 (0•70–2•12) 0•488 1•93 (0•92–4•03) 0•082
Immunosuppressedb 1•28 (0•74–2•21) 0•385 2•05 (1•03–4•05) 0•040
Severity of disease (PSI) 0•90 (0•71–1•13) 0•351 0•81 (0•63–1•06) 0•12
Microbiota features
Factor 1, high group 0•43 (0•20–0•93) 0•032 0•24 (0•09–0•66) 0•0055
Shannon diversity index, high groupc 0•67 (0•40–1•11) 0•118 •• ••

Univariable and multivariable Cox proportional hazards models were used to assess potential predictors of time to clinical stability.

Abbreviations: CI, confidence interval; COPD, chronic obstructive pulmonary disease; PSI, Pneumonia severity index.

a

Exposure to oral or systemic antibiotics between 90 days and 48 h prior to admission. b Immunosuppressive disease was defined as clinically suspected or proven immunodeficiency, the use of immunosuppressive therapy or immunomodulating medication in the past 3 months, including chemotherapy, or the use of more than 10 mg prednisone or equivalent each day for the past 3 months. c Group with a Shannon diversity index > 3•70.