Volume 21, Issue 2 pp. 363-369
Original Article

Nosocomial Acinetobacter pneumonia: Treatment and prognostic factors in 356 cases

Tülay Özvatan

Tülay Özvatan

Department of Infectious Diseases and Clinical Microbiology, Uludag University, Bursa, Turkey

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Halis Akalın

Corresponding Author

Halis Akalın

Department of Infectious Diseases and Clinical Microbiology, Uludag University, Bursa, Turkey

Correspondence: Halis Akalın, Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Uludag University, Bursa 16059, Turkey. Email: [email protected]Search for more papers by this author
Melda Sınırtaş

Melda Sınırtaş

Department of Microbiology and Clinical Microbiology, Uludag University, Bursa, Turkey

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Gökhan Ocakoğlu

Gökhan Ocakoğlu

Department of Biostatistics, Uludag University, Bursa, Turkey

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Emel Yılmaz

Emel Yılmaz

Department of Infectious Diseases and Clinical Microbiology, Uludag University, Bursa, Turkey

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Yasemin Heper

Yasemin Heper

Department of Infectious Diseases and Clinical Microbiology, Uludag University, Bursa, Turkey

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Nermin Kelebek

Nermin Kelebek

Department of Anesthesiology and Reanimation, Faculty of Medicine, Uludag University, Bursa, Turkey

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Remzi İşçimen

Remzi İşçimen

Department of Anesthesiology and Reanimation, Faculty of Medicine, Uludag University, Bursa, Turkey

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Ferda Kahveci

Ferda Kahveci

Department of Anesthesiology and Reanimation, Faculty of Medicine, Uludag University, Bursa, Turkey

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First published: 03 December 2015
Citations: 33

Abstract

Background and objective

Acinetobacter baumannii and A. baumannii/calcoaceticus complex are commonly encountered pathogens in nosocomial infections. This study aimed to evaluate the treatment and prognostic risk factors in nosocomial pneumonia caused by these microorganisms.

Methods

The study was conducted retrospectively in Uludag University Hospital and included 356 adult non-neutropenic patients with nosocomial pneumonia.

Results

Of the subjects, 94.9% (n = 338) had ventilator-associated pneumonia. The clinical response rate was 57.2%, the 14-day mortality 39.6% and the 30-day mortality 53.1%. The significant independent risk factors for the 30-day mortality were severe sepsis (OR, 2.60; 95% CI: 1.49–4.56; P = 0.001), septic shock (OR, 6.12; 95% CI: 2.75–13.64; P < 0.001), APACHE II score ≥ 20 (OR, 2.12; 95% CI: 1.28–3.50; P = 0.003) and empiric monotherapy (OR, 1.63; 95% CI: 1.00–2.64; P = 0.048). Multi-trauma (OR, 2.50; 95% CI: 1.11–5.68; P = 0.028) was found to be a protective factor. In patients with a clinical pulmonary infection score (CPIS) > 6 on the third day of treatment, both the 14- and 30-day mortality rates were high (P < 0.001, P < 0.001). Also, the 14- and 30-day mortality rates were significantly higher in the patients treated with empiric monotherapy compared with combination therapy (48/93 (51.6%)–46/123 (37.4%), P = 0.037 and 62/93 (66.7%)–65/123 (52.8%), P = 0.041, respectively) in pneumonia caused by imipenem-resistant strains.

Conclusion

Mortality rates were high in pneumonia caused by imipenem-resistant A. baumannii or A. baumannii/calcoaceticus complex. In the units with a high level of carbapenem resistance, antibiotic combinations should be considered for empiric therapy.

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