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Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Catheter-Associated Vancomycin-Resistant Enterococcus faecium Ventriculitis and Multidrug-Resistant Acinetobacter
Kyle M Rei1, Vedhika Reddy1, Christopher Andraos2
1Neurosurgery, California University of Science and Medicine, Colton, USA.
Abstract:
Ventriculitis is associated with cerebrospinal fluid (CSF) shunts, and rare microorganisms associated with infection include vancomycin-resistant Enterococcus (VRE) faecium and Acinetobacter baumannii. Both organisms are known to cause nosocomial infections, and the emergence of multidrug-resistant (MDR) strains presents a treatment challenge. There is a lack of consensus on antimicrobial agent selection for ventriculitis involving VRE faecium or MDR A. baumannii, which are life-threatening conditions. We present a case of a 59-year-old male presenting with CSF catheter-associated VRE faecium ventriculitis and MDR A. baumannii pneumonia who subsequently developed a nosocomial MDR A. baumannii ventriculitis. Both instances of ventriculitis were successfully treated with combination antibiotic therapy. VRE faecium ventriculitis was successfully treated with linezolid and intrathecal daptomycin. While daptomycin is not approved for Enterococcal infections, the synergistic effect of daptomycin in combination with linezolid proved effective. Although the MDR A. baumannii pneumonia was not cured with cefiderocol monotherapy, the MDR A. baumannii ventriculitis was successfully treated with combination therapy including cefiderocol, ampicillin/sulbactam, and intrathecal colistin. This highlights life-saving combination antibiotic therapies for ventriculitis caused by multiple rare and drug-resistant microorganisms.
Insights
Ventriculitis caused by rare, drug-resistant bacteria like vancomycin-resistant Enterococcus faecium and multidrug-resistant Acinetobacter baumannii can be life-threatening. Combination antibiotic therapies, including novel agents, offer successful treatment options for these challenging infections.
Area of Science:
- Infectious Diseases
- Clinical Microbiology
- Neurocritical Care
Background:
- Ventriculitis, an inflammation of the brain's ventricles, is often associated with cerebrospinal fluid (CSF) shunts.
- Infections caused by rare microorganisms such as vancomycin-resistant Enterococcus faecium (VRE faecium) and multidrug-resistant (MDR) Acinetobacter baumannii pose significant treatment challenges due to antimicrobial resistance.
- A lack of established treatment guidelines exists for ventriculitis involving VRE faecium or MDR Acinetobacter baumannii.
Observation:
- A case study involving a 59-year-old male with concurrent VRE faecium ventriculitis and MDR Acinetobacter baumannii pneumonia is presented.
- The patient subsequently developed nosocomial MDR Acinetobacter baumannii ventriculitis, indicating the potential for cross-infection and progression of resistant organisms.
- Initial treatment of MDR Acinetobacter baumannii pneumonia with cefiderocol monotherapy was unsuccessful.
Findings:
- VRE faecium ventriculitis was effectively treated with a combination of linezolid and intrathecal daptomycin, demonstrating a synergistic effect despite daptomycin's non-approved status for enterococcal infections.
- MDR Acinetobacter baumannii ventriculitis was successfully managed using a combination regimen including cefiderocol, ampicillin/sulbactam, and intrathecal colistin.
- These findings highlight the efficacy of tailored combination antibiotic therapies in combating rare and extensively drug-resistant pathogens in the central nervous system.
Implications:
- The successful treatment of rare and MDR ventriculitis underscores the critical role of combination antibiotic strategies in neurocritical care.
- This case provides valuable insights into potential therapeutic options for life-threatening infections caused by VRE faecium and MDR Acinetobacter baumannii.
- Further research into synergistic antibiotic combinations is warranted to establish evidence-based guidelines for managing these challenging nosocomial infections.
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