# Beyond bacteremia: clinical phenotypes and determinants of mortality in hospitalized adults with community-acquired urinary tract infection

**Authors:** Cihan Semet, Yusuf Görgülü

PMC · DOI: 10.3389/fmed.2026.1754663 · Frontiers in Medicine · 2026-02-11

## TL;DR

The study explores factors affecting mortality in adults hospitalized with urinary tract infections, finding that bacteremia and organ dysfunction are key predictors.

## Contribution

The study introduces an eight-item risk score for predicting bacteremia in urinary tract infection patients and identifies qSOFA as a key mortality predictor.

## Key findings

- Bacteremia was present in 32.7% of hospitalized adults with CA-UTI.
- qSOFA score ≥ 2 was the sole independent predictor of 30-day mortality in bacteremic patients.
- An eight-item risk score showed strong discrimination for predicting bacteremia (AUROC 0.80).

## Abstract

Community-acquired urinary tract infection (CA-UTI) is a leading source of bacteremia and sepsis in adults, yet the determinants of bloodstream invasion and short-term mortality remain incompletely defined. In particular, the relative contributions of age, comorbidity, antimicrobial resistance, and acute organ dysfunction are uncertain.

We conducted a retrospective cohort study of consecutive adults hospitalized with CA-UTI at a tertiary hospital in Türkiye between January 2023 and June 2025. Clinical, laboratory, microbiological, and outcome data were abstracted. Multivariable logistic regression was used to identify predictors of concomitant bacteremia and 30-day all-cause mortality in the overall cohort and in the bacteremic subgroup. An eight-item unweighted risk-factor count score (male sex, short symptom duration, prior extended-spectrum β-lactamase–producing and carbapenem-resistant organisms colonization or infection, Charlson Comorbidity Index (CCI) ≥ 2, diabetes mellitus, qSOFA ≥ 2, C-reactive protein > 100 mg/L, procalcitonin ≥ 0.5 ng/mL) was derived to predict bacteremia, and its discrimination was assessed with ROC analysis.

Among 358 adults with CA-UTI, 117 (32.7%) had concomitant bacteremia. In the multivariable model, independent predictors of bacteremia included male sex, shorter symptom duration, prior extended-spectrum β-lactamase–producing and carbapenem-resistant organisms colonization or infection, CCI ≥ 2, diabetes mellitus, qSOFA ≥ 2, C-reactive protein > 100 mg/L, and procalcitonin ≥ 0.5 ng/mL. The eight-item risk-factor count showed a strong gradient in bacteremia prevalence (3.8% with 0–1 factors, 24.7% with 2–3, and 75.0% with ≥ 4) and good discrimination (AUROC 0.83 for the full model and 0.80 for the simplified score; DeLong p ≈ 0.3). Overall, 30-day mortality was 6.1% (22/358) and higher in bacteremic than non-bacteremic CA-UTI (9.4% vs. 4.6%). In the whole cohort, both bacteremia and qSOFA score ≥ 2 were independent predictors of 30-day mortality. Within the bacteremic subgroup, qSOFA score ≥ 2 was identified as the sole independent predictor.

In adults hospitalized with CA-UTI, bacteremia identifies a high-risk clinical phenotype but is not the sole determinant of prognosis. Bacteremia is a marker of severity, whereas organ dysfunction, as captured by qSOFA, is the main driver of mortality. A simple eight-item bedside score demonstrated promising performance in predicting bacteremia but requires external validation before its routine use in clinical triage.

## Linked entities

- **Diseases:** urinary tract infection (MONDO:0005247), bacteremia (MONDO:0005229), diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Genes:** UROD (uroporphyrinogen decarboxylase) [NCBI Gene 7389] {aka PCT, UPD}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ESBL [NCBI Gene 13906541]
- **Diseases:** malignancy (MESH:D009369), Diabetes mellitus (MESH:D003920), chronic kidney disease (MESH:D051436), DM (MESH:D009223), hyperglycemia (MESH:D006943), Inflammatory (MESH:D007249), Comorbidity (MESH:D004194), Fever (MESH:D005334), cystitis (MESH:D003556), hypoxemia (MESH:D000860), Organ Failure (MESH:D009102), urinary stasis (MESH:D014647), Bacteremia (MESH:D016470), acute organ dysfunction (MESH:D019965), CRO infection (MESH:D007239), leukocytosis (MESH:D007964), prostatic hypertrophy (MESH:D011470), CA-UTI (MESH:D014552), E. coli infections (MESH:D004927), urinary retention (MESH:D016055), Mortality (MESH:D003643), Bacteremic (MESH:D016870), urinary tract abnormalities (MESH:D014570), oncologic (MESH:D000072716), septic shock (MESH:D012772), infectious (MESH:D003141), invasive (MESH:D009361), Sepsis (MESH:D018805), Community-acquired (MESH:D003147), colonization (MESH:D003108), bacterial infection (MESH:D001424), dementia (MESH:D003704)
- **Chemicals:** oxygen (MESH:D010100), carbapenem (MESH:D015780), CRO (-), creatinine (MESH:D003404)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Escherichia coli (E. coli, species) [taxon 562], Enterobacterales (order) [taxon 91347], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932189/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932189/full.md

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Source: https://tomesphere.com/paper/PMC12932189