Is this patient at risk of Klebsiella sepsis?

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Last updated: December 16, 2025View editorial policy

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Risk Assessment for Klebsiella Sepsis

Certain patient populations face substantially elevated risk for Klebsiella sepsis, and identifying these risk factors is critical for early recognition and prevention of this life-threatening infection.

High-Risk Patient Populations

Immunocompromised States

  • Neutropenic patients (absolute neutrophil count <500 cells/mm³) face dramatically increased susceptibility to Klebsiella infections, as this organism represents one of the most common gram-negative pathogens causing sepsis in this population 1
  • Uncontrolled diabetes mellitus significantly increases risk, with diabetic patients demonstrating higher rates of abscess formation, thrombotic complications, and septic emboli when infected with Klebsiella 2
  • HIV/AIDS and other immunosuppressive conditions substantially elevate susceptibility to recurrent gram-negative sepsis 3

Neonatal and Pediatric Risk Factors

  • Prematurity and low birth weight are independent risk factors, with greater gestational age and birth weight associated with lower infection risk (OR = 0.57,95% CI: 0.40-0.79) 4
  • Neonates in intensive care units are at particular risk, as Klebsiella pneumoniae accounts for a significant proportion of hospital-acquired infections in this setting, with healthcare worker hands and infant gastrointestinal tracts serving as transmission reservoirs 5

Healthcare-Associated Risk Factors

  • Indwelling devices dramatically increase risk, including central venous catheters, urinary catheters, and dialysis catheters 3
  • Prolonged mechanical ventilation is associated with increased Klebsiella infection rates 4
  • Extended antibiotic exposure (particularly third-generation cephalosporins) increases risk of multidrug-resistant Klebsiella infection (OR = 1.37,95% CI: 1.01-1.89) 4
  • Prolonged parenteral nutrition is an independent risk factor for MDR Klebsiella (OR = 1.39,95% CI: 1.01-1.89) 4
  • Intensive care unit admission, especially in units with high endemic rates of resistant organisms 1

Chronic Medical Conditions

  • Chronic kidney disease and end-stage renal disease substantially increase susceptibility 3
  • Chronic organ dysfunction (liver failure, renal failure) compromises defense mechanisms against infection 1

Geographic and Institutional Risk Factors

Endemic Areas

  • Facilities in regions where carbapenem-resistant Enterobacteriaceae (CRE) are endemic (notably New York City and other high-prevalence areas) require heightened surveillance 1
  • Units with previous CRE cases identified warrant point prevalence surveys to detect colonization 1

Healthcare Exposure History

  • Recent hospitalization (within 3 months) increases risk of colonization with resistant strains 1
  • Chronic care facility residence elevates risk compared to community-dwelling patients 1
  • Prior colonization or infection with Klebsiella or other resistant organisms is a critical predictor of subsequent infection 3

Specific Clinical Scenarios Requiring Heightened Vigilance

Septic Shock Predictors

  • Unknown-focus bacteremia represents the most frequent source (47.7% of cases) in ICU patients with carbapenem-resistant Klebsiella septic shock 6
  • Intra-abdominal source of infection is associated with increased mortality (HR 2.92,95% CI: 2.11-4.12) 6
  • Colistin-resistant strains dramatically increase mortality risk (HR 8.09,95% CI: 3.14-11.23) 6

Resistance Pattern Risk Factors

  • Previous colistin use is an independent risk factor for carbapenem resistance (OR = 19.108,95% CI: 2.027-180.133) 7
  • Previous aminoglycoside use increases carbapenem resistance risk (OR = 12.189,95% CI: 1.256-118.334) 7
  • Extended-spectrum beta-lactamase (ESBL) producing strains are increasingly common and limit treatment options 5

Critical Surveillance Indicators

When to Implement Active Surveillance

  • Perform rectal/perirectal swab surveillance cultures in patients with healthcare exposures in high-risk units to detect asymptomatic colonization, as colonization precedes infection 3
  • Conduct point prevalence surveys in intensive care units, units with previous cases, and units with high broad-spectrum antimicrobial exposure when CRE is detected 1
  • Review microbiology records for the preceding 6-12 months when a new case is identified to ensure previously unrecognized cases haven't occurred 1

Common Pitfalls to Avoid

  • Do not overlook device-related sources: All indwelling catheters must be evaluated as potential infection sources, and catheter removal is mandatory for Klebsiella catheter-associated bloodstream infections 3
  • Do not delay carbapenem susceptibility testing: All Klebsiella isolates require testing for carbapenem resistance and carbapenemase production, as this mandates enhanced infection control measures 3
  • Do not underestimate mortality risk: The 28-day mortality rate for carbapenem-resistant Klebsiella pneumoniae septic shock reaches 39.6-71.9%, with colistin resistance further increasing this risk 7, 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Recurrent Klebsiella Septicemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Predictors of outcome in ICU patients with septic shock caused by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2016

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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