What are the management strategies for septic shock?

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Last updated: October 14, 2025View editorial policy

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Management of Septic Shock

The management of septic shock requires immediate implementation of a structured approach focusing on early fluid resuscitation, antimicrobial therapy, source control, vasopressor support, and ongoing monitoring to reduce mortality and improve outcomes. 1, 2

Initial Resuscitation

  • Administer at least 30 mL/kg of IV crystalloid fluid within the first 3 hours of resuscitation, using balanced solutions or normal saline as first-choice fluids 1, 2
  • Continue fluid administration using a challenge technique as long as hemodynamic parameters improve, with dynamic measures of fluid responsiveness preferred over static measures 1
  • Target an initial mean arterial pressure (MAP) of 65 mmHg in patients requiring vasopressors 1, 3
  • Consider normalizing lactate levels as a marker of tissue hypoperfusion in patients with elevated lactate 1, 2
  • Avoid hydroxyethyl starches due to increased risk of acute kidney injury and mortality 1, 2

Antimicrobial Therapy

  • Administer broad-spectrum antimicrobials within the first hour of recognition of septic shock, after obtaining appropriate cultures if this doesn't significantly delay therapy 1, 3
  • Consider empiric combination therapy (using at least two antibiotics of different antimicrobial classes) aimed at the most likely bacterial pathogens for initial management 1, 4
  • De-escalate with discontinuation of combination therapy within the first few days in response to clinical improvement and/or evidence of infection resolution 1, 2
  • Optimize antimicrobial dosing based on pharmacokinetic/pharmacodynamic principles and specific drug properties 1, 5
  • Reassess antimicrobial regimen daily for potential de-escalation once pathogen identification and sensitivities are established 1, 2

Source Control

  • Identify specific anatomic diagnosis of infection requiring source control as rapidly as possible 1, 3
  • Implement required source control interventions as soon as medically and logistically practical, ideally within 12 hours of diagnosis 1, 3
  • Promptly remove intravascular access devices that are a possible source of sepsis after establishing alternative vascular access 1, 2

Vasopressor Therapy

  • Initiate norepinephrine as the first-choice vasopressor if the patient remains hypotensive despite adequate fluid resuscitation 1, 3
  • Add vasopressin (0.03 U/min) to norepinephrine to either raise MAP to target or decrease norepinephrine dose, but don't use it as the initial vasopressor 1, 3
  • Consider epinephrine when an additional agent is needed to maintain adequate blood pressure 1, 5
  • Avoid dopamine except in highly selected circumstances with low risk of tachyarrhythmias and absolute or relative bradycardia 1, 3
  • For norepinephrine administration, dilute in dextrose-containing solutions and administer through a large vein, preferably centrally placed 6, 4

Management of Refractory Shock

  • Administer hydrocortisone (200-300 mg/day) if adequate fluid resuscitation and vasopressor therapy are unable to restore hemodynamic stability 1, 3
  • Consider adding dobutamine infusion in the presence of myocardial dysfunction (elevated cardiac filling pressures and low cardiac output) or ongoing signs of hypoperfusion despite adequate intravascular volume and MAP 1, 5
  • Evaluate for and reverse pneumothorax, pericardial tamponade, or endocrine emergencies in patients with refractory shock 3, 7
  • Consider ECMO for refractory septic shock, particularly in pediatric patients 3, 7

Supportive Care

  • Target a hemoglobin of 7-9 g/dL in the absence of tissue hypoperfusion, ischemic coronary artery disease, or acute hemorrhage 1
  • Use low tidal volume (6 mL/kg predicted body weight) and limitation of inspiratory plateau pressure strategy for patients with ARDS 1, 8
  • Maintain blood glucose <180 mg/dL after initial stabilization 1, 9
  • Provide thromboprophylaxis with unfractionated or low-molecular-weight heparin unless contraindicated 1, 5
  • Consider enteral nutrition when feasible rather than parenteral nutrition 1, 7

Ongoing Monitoring and Reassessment

  • Perform frequent reassessment of hemodynamic status through clinical examination and available physiologic variables 1, 2
  • Consider further hemodynamic assessment (such as cardiac function evaluation) to determine the type of shock if clinical examination doesn't lead to a clear diagnosis 1, 3
  • Monitor for signs of fluid overload, including hepatomegaly and rales, especially in pediatric patients 1, 2

Pitfalls and Caveats

  • Avoid delays in antimicrobial administration; consider intraosseous access or intramuscular administration if vascular access is difficult 2, 4
  • Avoid fluid overresuscitation as it can delay organ recovery, prolong ICU stay, and increase mortality 3, 7
  • Don't rely solely on static measures like central venous pressure to guide fluid therapy 1, 8
  • Remember that the standard 30 mL/kg fluid recommendation may need modification based on individual patient characteristics, particularly cardiac function 3, 2
  • Avoid abrupt withdrawal of vasopressors; reduce gradually when discontinuing 6, 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Septic Shock

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Refractory Septic Shock

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Emergency medicine updates: Management of sepsis and septic shock.

The American journal of emergency medicine, 2025

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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