# Clinical and Microbiological Profile of Hospital-Acquired and Ventilator-Associated Pneumonia in Critically Ill Patients: A Retrospective Observational Study

**Authors:** Mihnea Miron, Anca Irina Ristescu, Mihaela Blaj, Diana Gabriela Iosep, Alexandru-Florinel Oancea, Gabriel Iosep, Radu Crișan-Dabija, Daniela Diculencu, Costin Damian, Mihaela Cătălina Luca

PMC · DOI: 10.3390/antibiotics15020232 · Antibiotics · 2026-02-22

## TL;DR

This study examines the causes and outcomes of severe lung infections in ICU patients, finding that drug-resistant bacteria are a major cause and are linked to poor health outcomes.

## Contribution

The study provides a detailed profile of hospital-acquired and ventilator-associated pneumonia in critically ill patients, focusing on local epidemiology and antimicrobial resistance patterns.

## Key findings

- Gram-negative bacteria, especially Acinetobacter baumannii and Pseudomonas aeruginosa, were the most common causes of infection.
- High resistance rates were observed among the isolated pathogens.
- Acute kidney injury was associated with higher severity scores and worse outcomes.

## Abstract

Background/Objectives: Severe respiratory infections remain a major cause of morbidity and mortality in critically ill patients admitted to an intensive care unit (ICU), particularly in the context of increasing antimicrobial resistance (AMR). This study aimed to describe the clinical, microbiological and resistance profiles of ICU patients diagnosed with hospital-acquired or ventilator-associated pneumonia. Methods: We conducted a retrospective, single-center observational study including adult ICU patients admitted between January and December 2025, with clinically significant positive endotracheal aspirates. Clinical severity scores (APACHE II, SOFA, SOFA-2), inflammatory biomarkers (neutrophil-to-lymphocyte ratio—NLR, platelets-to-lymphocyte ratio—PLR, C-reactive protein—CRP), microbiological findings, antimicrobial resistance patterns and ICU-related outcomes were analyzed. Results: Out of the 606 endotracheal aspirates collected, 76 (12.5%) were culture-positive and 62 (10.2%) patients met the final inclusion criteria. Ventilator-associated pneumonia accounted for 90% of infections, 25 episodes (44.6%) being classified as early-onset and 31 cases (55.4%) as late-onset, without significant differences in bacterial distribution between the two subtypes. In total, 85.5% of infections were monomicrobial, with Gram-negative bacteria representing 76% of isolates. Acinetobacter baumannii and Pseudomonas aeruginosa were the most frequently isolated pathogens, with high resistance rates. Acute kidney injury occurred in 25.8% of patients and was associated with higher APACHE II, SOFA, and SOFA-2 scores. Conclusions: Severe respiratory infections in critically ill patients were predominantly caused by Gram-negative, frequently drug-resistant pathogens and were associated with high disease severity and poor outcomes. These findings provide insight into the local epidemiology and antimicrobial resistance patterns of severe respiratory infections in critically ill patients.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249), acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** chronic kidney disease:6.4 (MESH:D051436), MRSA (MESH:D060467), cancer (MESH:D009369), lung cancer:38.7 (MESH:D008175), MDR (MESH:D018088), respiratory diseases (MESH:D012140), PLR (MESH:D001791), NLR (MESH:D015467), Critically Ill (MESH:D016638), injury to (MESH:D014947), Polymicrobial Respiratory Infections (MESH:D012141), Inflammatory (MESH:D007249), acute illness (MESH:D000208), VAP (MESH:D053717), AKI (MESH:D058186), pneumonia (MESH:D011014), infectious and non-infectious respiratory diseases (MESH:D000073296), chronic obstructive pulmonary disease:38.7 (MESH:D029424), cachexia:12.9 (MESH:D002100), Organ Failure (MESH:D009102), HAP (MESH:D000077299), immune (MESH:D007154), XDR (MESH:D054908), Infection (MESH:D007239), parenchymal (MESH:D002543), Death (MESH:D003643), Kocuria rosea (MESH:D017515), nosocomial infections (MESH:D003428), sepsis (MESH:D018805), infectious (MESH:D003141), CAP (MESH:D003147), septic shock (MESH:D012772), diabetes mellitus:16.1 (MESH:D003922), Gram-negative infections (MESH:D016905), chronic heart failure:29 (MESH:D006333)
- **Chemicals:** methicillin (MESH:D008712), meropenem (MESH:D000077731), carbapenem (MESH:D015780), imipenem (MESH:D015378)
- **Species:** Klebsiella pneumoniae (species) [taxon 573], Enterococcus durans (species) [taxon 53345], Nakaseomyces glabratus (species) [taxon 5478], Pseudomonas aeruginosa (species) [taxon 287], Pichia kudriavzevii (species) [taxon 4909], Escherichia coli (E. coli, species) [taxon 562], Candida albicans (species) [taxon 5476], Enterobacterales (order) [taxon 91347], Streptococcus pneumoniae (species) [taxon 1313], Homo sapiens (human, species) [taxon 9606], Haemophilus influenzae (species) [taxon 727], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Stenotrophomonas maltophilia (species) [taxon 40324], Corynebacterium striatum (species) [taxon 43770], Proteus vulgaris (species) [taxon 585], Kocuria rosea (species) [taxon 1275], Enterococcus faecium (species) [taxon 1352], Serratia marcescens (species) [taxon 615], Acinetobacter baumannii (species) [taxon 470]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938439/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938439/full.md

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Source: https://tomesphere.com/paper/PMC12938439