How should I initially manage an adult with septic shock?

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Last updated: February 7, 2026View editorial policy

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Initial Management of Septic Shock in Adults

Immediately administer at least 30 mL/kg IV crystalloid within the first 3 hours, obtain blood cultures, and start broad-spectrum IV antibiotics within 1 hour of recognizing septic shock—each hour of antibiotic delay reduces survival by approximately 7.6%. 1

Immediate Resuscitation (First Hour)

Fluid Resuscitation

  • Administer a minimum of 30 mL/kg of IV crystalloid within the first 3 hours as the cornerstone of initial management 2, 1, 3
  • Use crystalloids (normal saline or balanced crystalloids) as first-line fluid choice 2
  • Avoid hydroxyethyl starch formulations completely—they increase acute kidney injury and mortality 2
  • Give fluid in rapid boluses of 500-1000 mL over 15-30 minutes, reassessing hemodynamic response after each bolus 1, 3

Antimicrobial Therapy

  • Administer broad-spectrum IV antibiotics within 1 hour of recognizing septic shock—this is the single most time-critical intervention 2, 1
  • Obtain at least two sets of blood cultures (aerobic and anaerobic) before antibiotics, but never delay antibiotics more than 45 minutes to obtain cultures 2, 1
  • Select empiric therapy covering all likely pathogens (bacterial, fungal if indicated) with good tissue penetration to the presumed source 2

Hemodynamic Targets (First 6 Hours)

  • Mean arterial pressure (MAP) ≥65 mmHg 2, 1
  • Central venous pressure 8-12 mmHg 2
  • Urine output ≥0.5 mL/kg/hour 2
  • Central venous oxygen saturation (ScvO₂) ≥70% or mixed venous oxygen saturation ≥65% 2

Lactate Monitoring

  • Measure serum lactate immediately at recognition of septic shock 2, 1, 3
  • Repeat lactate within 6 hours if initially elevated 1
  • Guide resuscitation to normalize lactate as rapidly as possible as a marker of tissue hypoperfusion 2, 1

Vasopressor Support

First-Line Agent

  • Initiate norepinephrine as the first-choice vasopressor if hypotension persists despite adequate fluid resuscitation 2, 1
  • Start at 0.05-0.1 mcg/kg/min and titrate every 10-15 minutes to maintain MAP ≥65 mmHg 1, 3

Additional Vasopressor Options

  • Add epinephrine when an additional agent is needed to maintain adequate blood pressure 2, 1
  • Vasopressin 0.03 U/min can be added to norepinephrine to raise MAP or decrease norepinephrine dose, but should not be used as the initial vasopressor 2
  • Avoid dopamine except in highly selected circumstances (e.g., patients with low risk of tachyarrhythmias and absolute or relative bradycardia) 2

Inotropic Support

  • Add dobutamine if myocardial dysfunction is present (elevated cardiac filling pressures with low cardiac output) or ongoing signs of hypoperfusion persist despite adequate intravascular volume and MAP 2

Source Control

  • Identify or exclude a specific anatomic diagnosis requiring emergent source control within 12 hours 2, 1
  • Implement required interventions (drainage, debridement, device removal) as soon as medically and logistically practical 2, 1
  • Obtain imaging studies promptly to confirm potential infection source 2

Antimicrobial De-escalation

  • Reassess antimicrobial therapy daily for potential de-escalation once pathogen identification and sensitivities are established 2, 1
  • Narrow to the most appropriate single therapy based on culture results and clinical improvement 2, 1
  • Plan for 7-10 days total duration for most serious infections; longer courses may be needed for slow clinical response, undrained foci, S. aureus bacteremia, or immunodeficiency 2, 1

Adjunctive Therapies

Corticosteroids

  • Avoid routine IV hydrocortisone in adult septic shock patients if adequate fluid resuscitation and vasopressor therapy restore hemodynamic stability 2
  • If hemodynamic stability cannot be achieved, consider hydrocortisone 200 mg/day 2

Blood Product Management

  • Target hemoglobin 7-9 g/dL in the absence of tissue hypoperfusion, ischemic coronary artery disease, or acute hemorrhage 2
  • Transfuse platelets prophylactically when counts <10,000/mm³ without bleeding, <20,000/mm³ with significant bleeding risk, or ≥50,000/mm³ for active bleeding or invasive procedures 2

Prophylaxis

  • Provide deep vein thrombosis prophylaxis with pharmacologic agents unless contraindicated 2, 1
  • Use stress ulcer prophylaxis (H2 blockers or proton pump inhibitors) in patients with bleeding risk factors 2, 1

Mechanical Ventilation (If Required)

  • Target tidal volume of 6 mL/kg predicted body weight for sepsis-induced ARDS 2
  • Maintain plateau pressures ≤30 cm H₂O in passively inflated lungs 2
  • Apply positive end-expiratory pressure (PEEP) to avoid alveolar collapse 2
  • Maintain head-of-bed elevation 30-45 degrees to prevent ventilator-associated pneumonia 2

Critical Pitfalls to Avoid

  • Do not delay antibiotics beyond 1 hour—each hour of delay decreases survival by 7.6% 1
  • Do not use hydroxyethyl starches for volume replacement 2
  • Do not rely solely on central venous pressure to guide fluid resuscitation; use dynamic measures of fluid responsiveness 3
  • Do not use dopamine as first-line vasopressor—norepinephrine has superior outcomes 2
  • Do not routinely use hydrocortisone if vasopressors and fluids achieve hemodynamic stability 2

Ongoing Monitoring

  • Continuously assess clinical markers of perfusion: mental status, capillary refill time, skin mottling, peripheral pulses, urine output 1, 3
  • Reassess hemodynamic response frequently and adjust therapy accordingly 1, 3
  • Address goals of care as early as feasible, but within 72 hours of ICU admission 2, 1

References

Guideline

Sepsis Management Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Initial Management of Shock

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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