Volume 13 Supplement 1

Proceedings of the 9th Edition of the Scientific Days of the National Institute for Infectious Diseases “Prof Dr Matei Bals”

Open Access

Microbiological profile and multidrug resistant bacteria in pneumonia

  • Adriana Slavcovici1Email author,
  • Cristina Cismaru1,
  • Mihaela Sabou1,
  • Mirela Flonta2 and
  • Natalia Hagău3
BMC Infectious Diseases201313(Suppl 1):O13

https://doi.org/10.1186/1471-2334-13-S1-O13

Published: 16 December 2013

Background

Currently accepted classifications of pneumonia include community acquired pneumonia (CAP), healthcare-associated pneumonia (HCAP), hospital-acquired pneumonia (HAP), and ventilator-associated pneumonia (VAP). Previous studies have shown a high rate of patients with HCAP or HAP caused by multidrug-resistant bacteria (MDR). Our aim was to determine the differences in etiology and antibiotic-resistant bacteria between CAP, HCAP and HAP groups.

Methods

We performed a retrospective study in which we included patients over 18 years old, with culture-positive pneumonia, between 2008 and 2011, from 3 clinical hospitals. The patients were classified as having CAP, HCAP or HAP. We recorded the bacteriologic results for the following samples: blood culture, sputum, bronchial aspirate, bronchoalveolar lavage. The statistical analysis was carried out using Graph Pad Prism 5.

Results

A total of 340 patients were recorded (160 with CAP, 39 with HCAP and 141 with HAP). Streptococcus pneumoniae and Haemophilus influenzae were seen more frequently in CAP (33%, 14.4%) than in HCAP or HAP (1.4%, 0%; p<0.0001). The most common pathogens in HAP were MRSA (27.7%), Acinetobacter spp. (26.2%), Klebsiella pneumoniae (19%). Compared to the HCAP, Acinetobacter spp. and MRSA were significantly associated with HAP (OR 54.8, p<0.0001, LR 3.9). Compared to the HAP P aeruginosa and E coli were more common in HCAP (36%, p 0.04, OR 2; respectively 23%, p 0.001, OR 7). Among Gram-negative bacilli, resistance to ceftazidime was higher (86%) and significantly associated with HAP (OR 14.3, p<0.0001, LR 2.7). The extended-spectrum β-lactamase-producing Enterobacteriaceae, were more frequent in HAP (67.7%). However, no differences were found regarding ESBL producing Enterobacteriaceae between HAP and HCAP (p=0.06). MDR bacteria, including MRSA and gram-negative bacilli, were identified more frequently in HAP versus HCAP (78.7% vs. 12.8%; p<0.0001, OR 25, LR 6).

Conclusion

S pneumoniae was the main causative pathogen in CAP. Despite the higher frequency of P aeruginosa in the HCAP group, the MDR bacteria were associated with the HAP group. Our results reveal important differences between HAP and HCAP concerning the etiology and antibiotic resistance patterns.

Authors’ Affiliations

(1)
Department of Infectious Diseases, Clinical Hospital of Infectious Diseases, Iuliu Hațieganu University of Medicine and Pharmacy
(2)
Clinical Laboratory, Clinical Hospital of Infectious Diseases
(3)
Department of Anesthesiology and Intensive Therapy, Iuliu Hațieganu University of Medicine and Pharmacy, University Emergency County Hospital of Cluj

Copyright

© Slavcovici et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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