Management of Septic Shock
Administer intravenous broad-spectrum antimicrobials within 1 hour of recognizing septic shock, initiate aggressive fluid resuscitation with 30 mL/kg crystalloids immediately, and start norepinephrine as the first-choice vasopressor if mean arterial pressure remains below 65 mmHg despite adequate fluid resuscitation. 1, 2
Immediate Resuscitation (First Hour)
Antimicrobial Therapy
- Administer IV antimicrobials within 1 hour of septic shock recognition using broad-spectrum antibiotics that cover all likely bacterial pathogens 1, 2
- Obtain at least two sets of blood cultures before starting antibiotics, but do not delay treatment beyond 45 minutes 2
- For septic shock specifically, use combination therapy with at least two antibiotics of different antimicrobial classes targeting the most likely pathogens 2
- Ensure adequate dosages with high likelihood of activity against suspected organisms 1
Fluid Resuscitation
- Administer a minimum of 30 mL/kg of crystalloid fluids rapidly for initial resuscitation in sepsis-induced hypoperfusion 1, 3, 2
- Use crystalloids as first-line therapy; colloids offer no superiority in bacterial sepsis and carry higher costs with potential adverse effects 1
- Target specific hemodynamic endpoints within the first 6 hours: central venous pressure 8-12 mmHg (12-15 mmHg if mechanically ventilated), mean arterial pressure ≥65 mmHg, urine output ≥0.5 mL/kg/hour, and central venous oxygen saturation ≥70% 3
Vasopressor Support
- Use norepinephrine as the first-choice vasopressor to maintain MAP ≥65 mmHg if hypotension persists despite adequate fluid resuscitation 1, 4, 3, 2
- In resource-limited settings where norepinephrine is unavailable, dopamine or epinephrine are acceptable alternatives for persistent tissue hypoperfusion 1
- Never delay vasopressor initiation if fluid resuscitation alone fails to restore adequate perfusion 1
Source Control and Diagnosis
Infection Source Identification
- Perform detailed patient history and thorough clinical examination to identify the infection source 1
- Sample fluid or tissue from the suspected infection site whenever possible without harming the patient 1
- Examine sampled material by Gram stain, culture, and antibiogram when available 1
- Use imaging techniques when available to localize infection 1
Source Control Interventions
- Implement source control interventions as soon as possible after diagnosis, ideally within 12 hours when anatomically feasible 4, 2
- Drain or debride the infection source whenever possible 1
- Remove any foreign body or intravascular device that may be the infection source after establishing alternative access 1, 2
Hemodynamic Monitoring and Optimization
Clinical Assessment of Tissue Perfusion
Monitor for these clinical indicators of adequate tissue perfusion 1:
- Normal capillary refill time (age-dependent: <2-3 seconds in adults <65 years, <4.5 seconds in elderly ≥65 years)
- Absence of skin mottling
- Warm and dry extremities
- Well-felt peripheral pulses (radial or dorsalis pedis)
- Return to baseline mental status
- Urine output >0.5 mL/kg/hour in adults
Blood Pressure Monitoring
- Measure arterial blood pressure frequently in hemodynamically unstable patients 1
- Maintain MAP ≥65 mmHg as the primary hemodynamic target 1, 4, 2
Respiratory Support
Oxygen Therapy
- Apply oxygen to achieve oxygen saturation ≥90% 1
- If pulse oximetry is unavailable, administer oxygen empirically in septic shock 1
- Maintain adequate oxygenation without hyperoxia 4
Positioning and Airway Management
- Place patients in semi-recumbent position with head of bed elevated 30-45 degrees 1, 4
- Position unconscious patients laterally and keep airway clear 1
Mechanical Ventilation (if required)
- Use non-invasive ventilation in patients with dyspnea and/or persistent hypoxemia despite oxygen therapy, if staff is adequately trained 1
- Apply lung-protective ventilation with tidal volumes 6 mL/kg predicted body weight if ARDS develops 4, 3, 2
- Maintain plateau pressure ≤30 cm H₂O 3
- Minimize sedation during mechanical ventilation 4, 3
- Conduct daily spontaneous breathing trials when patients are ready for weaning 4
Adjunctive Therapies
Corticosteroids
- Administer hydrocortisone or prednisolone to patients requiring catecholamines for hemodynamic support 1
Metabolic Management
- Target blood glucose 140-180 mg/dL using protocolized insulin therapy; avoid tight control <110 mg/dL 4, 3, 2
- Avoid hypoglycemia 1
- Measure serum lactate levels as a marker of tissue hypoperfusion 2
Blood Product Management
- Target hemoglobin 7-9 g/dL unless active myocardial ischemia, acute hemorrhage, or severe coronary artery disease is present 3, 2
- Transfuse red blood cells only when hemoglobin <7.0 g/dL 3
Thromboprophylaxis
Gastrointestinal Protection
- Use H2-blockers or proton pump inhibitors in patients with bleeding risk factors 3
Post-Acute Management
Antimicrobial Stewardship
- Regularly reassess antimicrobial therapy 1
- Administer antimicrobials for adequate but not prolonged duration 1
Nutritional Support
- Resume oral food intake after resuscitation and regaining of consciousness 1
Sedation Management
- Minimize sedation to the absolute minimum necessary 4
- Avoid benzodiazepines entirely in septic patients 4
- Use opioids and sedatives carefully 1
Mobilization
Critical Pitfalls to Avoid
The most common errors in septic shock management include:
- Delaying antimicrobial administration beyond 1 hour—this directly increases mortality 1, 2
- Inadequate initial fluid resuscitation—the 30 mL/kg bolus is a minimum, not a maximum 1, 2
- Failing to initiate vasopressors when MAP remains <65 mmHg despite fluids—this prolongs tissue hypoperfusion 1, 2
- Using excessive sedation, particularly benzodiazepines—this worsens delirium and outcomes 4
- Attempting extubation while patients still require vasopressors—this is an absolute contraindication 3
- Tight glucose control targeting <110 mg/dL—this increases hypoglycemia risk without benefit 4, 3