Critical Care

Sepsis & Septic Shock — Surviving Sepsis Campaign

By Dr. Sonu Lakeshar

Sepsis is a life-threatening organ dysfunction caused by a dysregulated host response to infection. It kills more people globally than heart attack and is the leading cause of in-hospital mortality. India carries a disproportionate sepsis burden due to high rates of infectious diseases, antimicrobial resistance, and limited ICU access. The Surviving Sepsis Campaign (SSC) 2021 update provides the standard-of-care bundle that, when delivered within 1 hour, can reduce mortality by 25-40%.

On This Page
  1. Overview
  2. Sepsis-3 Definition
  3. Diagnosis & qSOFA
  4. 1-Hour Bundle
  5. Vasopressors & Steroids
  6. FAQs

Sepsis is the leading cause of in-hospital death worldwide. Global incidence is approximately 49 million cases per year, with 11 million sepsis-related deaths (20% of all global deaths). In India, sepsis accounts for an estimated 30-50% of ICU admissions and carries mortality of 30-50% in septic shock despite optimal care. Common sources: pneumonia (50%), urinary tract infection, intra-abdominal infection, skin/soft tissue, central line-associated bloodstream infection.

The Sepsis-3 definition (2016) replaced the older SIRS-based definition with organ dysfunction assessment using SOFA score. The operational implication is that sepsis should be suspected in any patient with suspected infection AND organ dysfunction — and treatment should begin immediately without waiting for confirmation.

TermDefinition
InfectionSuspected or proven microbial invasion of normally sterile host tissue
BacteraemiaPresence of bacteria in blood (may be transient)
SepsisLife-threatening organ dysfunction caused by dysregulated host response to infection. SOFA score ≥ 2 points
Septic shockSepsis with circulatory and cellular/metabolic abnormalities severe enough to substantially increase mortality. Clinical criteria: vasopressor requirement to maintain MAP ≥ 65 mmHg AND serum lactate > 2 mmol/L despite adequate fluid resuscitation

qSOFA (quick SOFA) — bedside screen for sepsis in non-ICU patients:

  • Respiratory rate ≥ 22/min
  • Altered mentation (GCS < 15)
  • Systolic BP ≤ 100 mmHg

2 of 3 positive → high risk of poor outcome → initiate sepsis workup.

SOFA (Sequential Organ Failure Assessment) — formal scoring:

  • Respiratory: PaO2/FiO2 ratio
  • Coagulation: Platelet count
  • Liver: Bilirubin
  • Cardiovascular: MAP, vasopressor requirement
  • CNS: Glasgow Coma Scale
  • Renal: Creatinine, urine output

SOFA ≥ 2 points or acute change ≥ 2 points = sepsis.

Lactate: Lactate > 2 mmol/L indicates tissue hypoperfusion. Lactate > 4 mmol/L is severe. Serial lactate measurements guide resuscitation — clearance target is ≥ 10% per hour. Persistent hyperlactataemia predicts mortality.

Within 1 hour of recognition, ALL of the following should be done:

  1. Measure lactate (if initial > 2 mmol/L, re-measure at 2-4 hours)
  2. Obtain blood cultures x 2 sets BEFORE antibiotic administration (do not delay antibiotics beyond 45 min for cultures)
  3. Administer broad-spectrum antibiotics — cover Gram positives, Gram negatives, and anaerobes. Empiric regimens:
    • Community-acquired: Ceftriaxone 2 g IV ± Azithromycin 500 mg IV
    • Hospital-acquired: Piperacillin-Tazobactam 4.5 g IV OR Meropenem 1 g IV + Vancomycin 1 g IV (if MRSA risk)
    • Source-specific: add Metronidazole 500 mg IV for intra-abdominal; add Fluconazole for suspected fungal sepsis
  4. Begin rapid crystalloid resuscitation: 30 mL/kg IV crystalloid (Normal Saline or Ringer's Lactate) within first 3 hours. Ringer's Lactate preferred (less hyperchloraemic acidosis). Avoid hydroxyethyl starch (renal toxicity).
  5. Apply vasopressors if BP remains low despite fluids — target MAP ≥ 65 mmHg. Norepinephrine is first-line.

Vasopressor ladder:

  1. Norepinephrine (first-line): 0.05-0.5 mcg/kg/min. Alpha > beta agonist — increases SVR without much tachycardia.
  2. Vasopressin (second-line): 0.03 units/min fixed dose (not titrated). Add when NE dose exceeds 0.25 mcg/kg/min.
  3. Epinephrine (third-line): 0.05-0.5 mcg/kg/min. Add if NE+vasopressin insufficient.
  4. Dopamine: Avoid in septic shock (higher arrhythmia risk vs NE). Use only for select bradycardia-induced shock.
  5. Phenylephrine: Pure alpha — useful in tachyarrhythmia but reduces stroke volume.

Corticosteroids: Hydrocortisone 200 mg/day (50 mg IV 6-hourly OR continuous infusion) IF vasopressor requirement is rising or sustained despite adequate fluid resuscitation. Do NOT use for sepsis without shock. Steroids reduce vasopressor duration but not 28-day mortality (ADRENAL, APROCCHSS, CAPECHT trials).

Source control: Drain abscess, remove infected lines, debride necrotic tissue — within 6-12 hours of recognition.

What is the 1-hour sepsis bundle?
Within 1 hour of sepsis recognition: (1) measure lactate, (2) obtain blood cultures x 2 sets before antibiotics, (3) administer broad-spectrum antibiotics (e.g., Ceftriaxone for community-acquired, Pip-Tazo or Meropenem for hospital-acquired), (4) begin rapid crystalloid resuscitation 30 mL/kg, (5) apply vasopressors (Norepinephrine first-line) if MAP &lt; 65 despite fluids. Each hour of delay in antibiotics increases mortality by 7.6%.
What is the difference between SIRS, sepsis, and septic shock?
SIRS (Systemic Inflammatory Response Syndrome) = body's inflammatory response to any insult (infection, trauma, pancreatitis). Sepsis (Sepsis-3 definition, 2016) = life-threatening organ dysfunction from dysregulated host response to infection, SOFA &ge; 2. Septic shock = sepsis with circulatory and metabolic abnormalities requiring vasopressors to maintain MAP &ge; 65 AND lactate &gt; 2 mmol/L despite fluid resuscitation. Mortality rises with each stage: SIRS ~10%, sepsis ~20%, septic shock ~40-50%.
What is qSOFA?
quick SOFA — bedside 3-item screen for sepsis in non-ICU patients: (1) Respiratory rate &ge; 22/min, (2) Altered mentation (GCS &lt; 15), (3) Systolic BP &le; 100 mmHg. 2 of 3 positive &rarr; high risk of poor outcome &rarr; initiate sepsis workup and treatment. Replaced SIRS criteria in Sepsis-3 definition due to higher specificity for poor outcomes.
Why is Norepinephrine the first-line vasopressor in septic shock?
Norepinephrine is predominantly an alpha-adrenergic agonist with some beta activity. It increases systemic vascular resistance (raising BP) without significantly increasing heart rate — making it ideal for distributive shock (vasodilatory). Compared to dopamine (the older first-line), NE causes fewer arrhythmias (notably AF) and reduces mortality. Dopamine is now reserved only for bradycardia-associated shock.
When are steroids indicated in septic shock?
Hydrocortisone 200 mg/day (50 mg IV 6-hourly or continuous infusion) is indicated in septic shock IF vasopressor requirement is rising or sustained despite adequate fluid resuscitation. NOT recommended for sepsis without shock. Steroids reduce vasopressor duration and may reduce mortality in the sickest patients, but do not reduce 28-day mortality overall (ADRENAL, APROCCHSS trials).

Sepsis management is a clinical emergency where protocolised bundle therapy saves lives. For UPSC CMS aspirants, Sepsis-3 definitions, qSOFA, the 1-hour bundle, and vasopressor selection are extremely high-yield clinical topics.

🎓 Explore More on CMS Prep
CMS Prep covers UPSC CMS previous year questions, NEET PG, INICET, FMGE, AFMS, and complete careers-after-MBBS guidance — all free, no login.