Abstract
Methods: We conducted a prospective observational study of all episodes of bacteremic, community-onset, and radiologically confirmed pneumonia due to Acinetobacter species at a tertiary referral hospital in tropical Australia from 1997 to 2012 following the introduction of routine empirical treatment protocols covering Acinetobacter . Demographic, clinical, microbiologic, and outcome data were collected.
Results: There were 41 episodes of bacteremic community-onset Acinetobacter pneumonia, of which 36 had no indicators suggesting health-care-associated infection. Of these, 38 (93%) were Indigenous Australians, one-half were men, the average age was 44.1 years, and 36 episodes (88%) occurred during the rainy season. All patients had at least one risk factor, with hazardous alcohol intake in 82%. Of the 37 isolates available for molecular speciation, 35 were Acinetobacter baumannii and two were Acinetobacter nosocomialis . All isolates were susceptible in vitro to gentamicin, meropenem, and ciprofloxacin, but only one was fully susceptible to ceft riaxone. ICU admission was required in 80%. All 41 patients received appropriate antibiotics within the first 24 h of admission, and 28- and 90-day mortality were both low at 11%.
Conclusions: Community-acquired Acinetobacter pneumonia is a severe disease, with the majority of patients requiring ICU admission. Most patients have risk factors, particularly hazardous alcohol use. Despite this severity, correct initial empirical antibiotic therapy in all patients was associated with low mortality.
| Original language | English |
|---|---|
| Pages (from-to) | 1038-1045 |
| Number of pages | 8 |
| Journal | Chest |
| Volume | 146 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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Dive into the research topics of 'A 16-Year Prospective Study of Community-Onset Bacteremic Acinetobacter Pneumonia: Low mortality with appropriate initial empirical antibiotic protocols'. Together they form a unique fingerprint.Projects
- 3 Finished
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Improving outcomes of severe bacterial infections in Northern Australia
Davis, J. (Principal Investigator/Chief Investigator A)
1/01/11 → 31/12/14
Project: Research
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Pathophysiology and treatment of malaria and other tropical infectious diseases prevalent in our region
Anstey, N. (Principal Investigator/Chief Investigator A)
1/01/13 → 31/12/17
Project: Research
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Tropical Disease - immunity, pathogenesis and vaccine development: global translation
GOOD, M. (Principal Investigator/Chief Investigator A), MCMANUS, D. P. (Co Investigator/Chief Investigator B), TOTH, I. (Chief Investigator C), Anstey, N. (Chief Investigator D), DOOLAN, D. (Chief Investigator E), Engwerda, C. (Chief Investigator F), LOUKAS, A. (Chief Investigator G), McCarthy, J. (Chief Investigator H), Price, R. (Chief Investigator I) & Murphy, A. (Project Manager)
1/01/13 → 31/12/17
Project: Research
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