# Variations in capillary and serum lactates levels based on different etiologies of septic patients in the emergency department

**Authors:** Matteo Guarino, Benedetta Perna, Giacomo Maroncelli, Paolo Baldin, Chiara Donati, Francesco Luppi, Alice Eleonora Cesaro, Chiara Pesci, Anna Costanzini, Martina Maritati, Paolo Clavenzani, Carlo Contini, Roberto De Giorgio, Michele Domenico Spampinato

PMC · DOI: 10.3389/fmed.2025.1536148 · Frontiers in Medicine · 2025-04-16

## TL;DR

This study found that capillary and serum lactate levels vary depending on the cause of sepsis in emergency department patients.

## Contribution

The study identifies specific biomarker variations linked to different sepsis etiologies for better early prediction and treatment.

## Key findings

- Capillary and serum lactate levels were highest in Gram-positive infections.
- Neutrophil-to-lymphocyte ratio was higher in Gram-negative infections.
- Diastolic shock index increased in fungal infections.

## Abstract

Sepsis is a life-threating and time-depending condition. This study examined the association between sepsis etiology and variations in capillary and serum lactate levels, neutrophil-to-lymphocyte ratio, and diastolic shock index in emergency department patients.

This study, conducted between 2021 and 2022 at the Emergency Department of Ferrara, included the following criteria: (i) clinical suspect of infectious disease; (ii) qSOFA ≥2; (iii) age ≥18 years; (iv) signed informed consent. Etiologies were: (i) negative cultures (NC); (ii) Gram positive (GP); (iii) Gram negative (GN); (iv) fungal infections (FI).

Among the 200 included patients, 104 (52.0%) had NC, 36 (18.0%) GP, 53 (26.5%) GN and 7 (3.5%) FI. CLs (p = 0.006) and SLs (p < 0.001) were different according to etiology being higher in GP infections. NLR (p = 0.035) was higher in GN infections, while DSI (p = 0.008) increased in FI. Mortality was not influenced by the etiology.

All parameters differed according to sepsis etiology, thus improving early prediction of sepsis etiology and its pharmacological management.

## Linked entities

- **Diseases:** infectious disease (MONDO:0005550)

## Full-text entities

- **Diseases:** GN infections (MESH:D016905), FI (MESH:D009181), SLs (MESH:C536329), infectious disease (MESH:D003141), septic (MESH:D001170), GP infections (MESH:D016908), shock (MESH:D012769), Sepsis (MESH:D018805)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12040905/full.md

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Source: https://tomesphere.com/paper/PMC12040905