# Prevalence, microbiological profiles, and determinants of hospital-acquired pneumonia in Addis Ababa: A focus on Pseudomonas aeruginosa and its antimicrobial resistance patterns in three hospitals

**Authors:** Etsub Brhanesilassie Hailemichael, Adey Feleke Desta, Girma Taye, Sirak Robele Gari, Etsehiwot Adamu, Zeleke Ayenew, Wondwossen Amogne

PMC · DOI: 10.1371/journal.pone.0340680 · PLOS One · 2026-01-20

## TL;DR

This study examines hospital-acquired pneumonia in Addis Ababa, focusing on Pseudomonas aeruginosa and its resistance to antibiotics, revealing high rates of multidrug resistance and risk factors like aspiration.

## Contribution

The study provides new insights into the prevalence and antimicrobial resistance patterns of Pseudomonas aeruginosa in hospital-acquired pneumonia in Addis Ababa.

## Key findings

- Pseudomonas aeruginosa isolates showed high resistance to ceftazidime and cefepime but remained susceptible to amikacin.
- Aspiration was independently associated with the presence of pneumonia-associated pathogens.
- Multidrug-resistant ESKAPE pathogens were found to contribute significantly to hospital-acquired pneumonia.

## Abstract

Hospital-acquired pneumonia is typically polymicrobial; nevertheless, Pseudomonas aeruginosa is a principal causative pathogen, attributable to its link with poor clinical prognoses and extensive antimicrobial resistance. Our study aims to assess the prevalence, microbiological profiles and determinants of hospital-acquired pneumonia with a focus on antibiotic-resistant P. aeruginosa across three hospitals in Addis Ababa. A cross-sectional study was conducted in which 1,800 patients were screened, and 298 cases of hospital-acquired pneumonia were identified between September 2022 and April 2024. Patient interviews and microbiological analysis of lower respiratory tract samples were performed. We detected a 17% prevalence of hospital-acquired pneumonia and 19% prevalence of ventilator-associated pneumonia across the study hospitals. Our patient profiles indicated a predominance of males (59%), with the largest proportion aged 30–39 years (28%), most were married (71%) and had attained secondary-level education (33%). Over half of the patients were admitted to the adult ICU (55%), 60% had a history of prior hospitalization and respiratory disease was the leading cause of admission (30%). Acinetobacter baumannii (n = 24) was the most frequently isolated pathogen, followed by Pseudomonas aeruginosa (n = 21) and Staphylococcus aureus (n = 13). Compounding these challenges, the P. aeruginosa isolates (7%) exhibited high resistance to ceftazidime and cefepime (89% resistance), while retaining relatively high susceptibility to amikacin (90%); notably, 67% of the isolates were multidrug resistant. We tested several patient-level vulnerabilities, only aspiration remained independently associated with presence of pneumonia-associated pathogen in patient samples (AOR = 4.43, 95% CI: 1.74–11.24, p = 0.002). This study demonstrates a substantial burden of multidrug resistance hospital-acquired pneumonia by ESKAPE pathogens that indicate deficiencies in hospital defences against hospital-acquired pathogens and risk of adverse patient outcomes. There is an urgent need to shift infection prevention strategies, emphasizing aspiration prevention measures and strengthened diagnostic stewardship.

## Linked entities

- **Species:** Pseudomonas aeruginosa (taxon 287), Acinetobacter baumannii (taxon 470), Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** ventilator-associated pneumonia (MESH:D053717), infection (MESH:D007239), pneumonia (MESH:D011014), respiratory disease (MESH:D012140)
- **Chemicals:** ceftazidime (MESH:D002442), amikacin (MESH:D000583), cefepime (MESH:D000077723)
- **Species:** Acinetobacter baumannii (species) [taxon 470], Staphylococcus aureus (species) [taxon 1280], Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12818687/full.md

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Source: https://tomesphere.com/paper/PMC12818687