What are the criteria for diagnosing sepsis?

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Last updated: October 18, 2025View editorial policy

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Sepsis Diagnostic Criteria

Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host response to infection, with diagnosis based primarily on the Sequential Organ Failure Assessment (SOFA) score and clinical evidence of infection. 1, 2

Primary Diagnostic Tools

  • The Sequential Organ Failure Assessment (SOFA) score is the primary tool for diagnosing sepsis-related organ dysfunction, with a score increase of ≥2 points indicating organ dysfunction associated with >10% in-hospital mortality 1, 2
  • For rapid bedside assessment, the quick SOFA (qSOFA) score can be used, which includes three criteria: respiratory rate ≥22/min, altered mentation, and systolic blood pressure ≤100 mmHg 2, 3
  • The National Early Warning Score 2 (NEWS2) has been shown to be superior to qSOFA for detecting sepsis with organ dysfunction in emergency department settings 1, 4

Clinical Signs and Laboratory Markers

Infection Indicators

  • Fever (core temperature >38.3°C) or hypothermia (core temperature <36°C) 5, 6
  • Tachycardia (heart rate >90 beats/min or >2 SD above normal for age) 5, 6
  • Tachypnea (respiratory rate >20 breaths/min) 6
  • Altered mental status 5, 6
  • Significant edema or positive fluid balance (>20 mL/kg over 24h) 5, 6
  • Hyperglycemia (plasma glucose >140 mg/dL) in the absence of diabetes 5, 6
  • Leukocytosis (WBC >12,000/μL), leukopenia (WBC <4,000/μL), or normal WBC with >10% immature forms 5, 6
  • Elevated inflammatory markers: C-reactive protein or procalcitonin >2 SD above normal value 5, 6

Organ Dysfunction Markers

  • Arterial hypotension (SBP <90 mmHg, MAP <70 mmHg, or SBP decrease >40 mmHg) 5, 6
  • Arterial hypoxemia (PaO₂/FiO₂ <300) 5, 6
  • Acute oliguria (urine output <0.5 mL/kg/h for at least 2h despite adequate fluid resuscitation) 5, 6
  • Creatinine increase ≥0.5 mg/dL 5, 6
  • Coagulation abnormalities (INR >1.5 or aPTT >60s) 5, 6
  • Ileus (absent bowel sounds) 5, 6
  • Thrombocytopenia (platelet count <100,000/μL) 5, 6
  • Hyperbilirubinemia (plasma total bilirubin >4 mg/dL) 5, 6
  • Hyperlactatemia (>1 mmol/L) 5, 6
  • Decreased capillary refill or mottling 5, 6

Severe Sepsis and Septic Shock

  • Severe sepsis is defined as sepsis with evidence of organ dysfunction or tissue hypoperfusion 5, 6
  • Septic shock is defined as sepsis with persistent hypotension requiring vasopressors to maintain MAP ≥65 mmHg and serum lactate >2 mmol/L despite adequate fluid resuscitation 6, 2

Special Considerations

  • In neutropenic patients, white blood cell count cannot be used as a criterion to define sepsis 5, 6
  • The SOFA score has demonstrated superior predictive validity for in-hospital mortality in ICU patients compared to SIRS criteria and qSOFA 7, 3
  • For non-ICU patients, qSOFA has shown better predictive validity than SOFA for in-hospital mortality 3
  • When SOFA score is >11, sensitivity and negative predictive values for sepsis diagnosis approach 100% 7

Monitoring and Re-evaluation

  • Risk stratification should guide re-evaluation frequency: high-risk patients every 30 minutes, moderate-risk every hour, and low-risk every 4-6 hours 1
  • Deterioration or lack of improvement should prompt immediate re-evaluation 1
  • Regular assessment of vital signs, mental status, urine output, and peripheral perfusion is essential for monitoring sepsis progression 6

Pitfalls and Caveats

  • The previous SIRS criteria (from 1992) are overly sensitive and non-specific, which may lead to overdiagnosis 5, 2
  • The term "severe sepsis" is now considered redundant as sepsis itself implies organ dysfunction 2
  • Different scoring systems have varying performance depending on the clinical setting (ICU vs. non-ICU) 3
  • Delayed recognition of sepsis significantly increases mortality, emphasizing the importance of early screening with appropriate tools 4

References

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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