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Serratia marcescens bacteremia.
W W Wong1, L S Wang, D L Cheng
1Department of Medicine, Veterans General Hospital, Taipei, Taiwan R.O.C.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|January 1, 1991
Summary
Serratia marcescens bacteremia is a serious concern, with a high fatality rate. Early recognition and appropriate antibiotic selection, such as amikacin or third-generation cephalosporins, are critical for effective treatment.
Area of Science:
- Clinical Microbiology
- Infectious Diseases
- Hospital Epidemiology
Background:
- Serratia marcescens bacteremia is increasingly recognized as a significant clinical issue.
- Both hospital-acquired and community-acquired infections warrant attention due to potential severity.
- Previous understanding of S. marcescens bacteremia's impact and treatment may be outdated.
Purpose of the Study:
- To analyze the clinical characteristics and outcomes of Serratia marcescens bacteremia.
- To evaluate the sources of infection and identify risk factors.
- To assess the efficacy of different antibiotic treatments for nosocomial S. marcescens bacteremia.
Main Methods:
- Retrospective review of 23 episodes of S. marcescens bacteremia occurring in 1985.
- Categorization of infections into hospital-acquired versus community-acquired.
- Analysis of infection sources, patient outcomes, and antibiotic susceptibility patterns.
Main Results:
- A high case fatality rate of 39% was observed among the 23 patients.
- Hospital-acquired infections predominated (74%), with a significant proportion (48%) having no clear source.
- Amikacin and third-generation cephalosporins demonstrated superior efficacy compared to gentamicin for nosocomial infections.
Conclusions:
- Serratia marcescens bacteremia is a critical condition requiring heightened clinical awareness.
- Effective management necessitates prompt diagnosis and appropriate antibiotic therapy, particularly in nosocomial settings.
- Antibiotic resistance patterns underscore the importance of selecting effective agents like amikacin or third-generation cephalosporins.