Management of Different Types of Shock
Early recognition and targeted therapy based on shock type is essential for reducing mortality and improving outcomes in all shock states. 1, 2
Shock Classification and Recognition
Shock is characterized by inadequate tissue perfusion resulting in an imbalance between oxygen supply and demand. Clinical criteria for shock include:
- SBP <90 mmHg for 30 minutes or requiring vasopressors/inotropes
- Evidence of end-organ hypoperfusion
- Lactate >2 mmol/L 1
Four Major Categories of Shock:
- Hypovolemic Shock - Inadequate circulating volume
- Cardiogenic Shock - Primary cardiac dysfunction
- Distributive Shock - Pathological vasodilation (includes septic, anaphylactic, neurogenic)
- Obstructive Shock - Mechanical obstruction to circulation 3
Management by Shock Type
1. Hypovolemic Shock
Immediate volume resuscitation with balanced crystalloids is the cornerstone of hypovolemic shock management.
Initial resuscitation:
- Rapid infusion of 20-30 mL/kg balanced crystalloids
- Reassess after each bolus
- Control ongoing fluid losses (hemorrhage control, surgical intervention)
Vasopressors: Only if fluid resuscitation inadequate to maintain MAP ≥65 mmHg
- Norepinephrine: 0.01-3 μg/kg/min
- Vasopressin: 0.01-0.04 units/min can be added as second agent 4
Blood products: For hemorrhagic shock
- Packed RBCs for Hgb <7 g/dL
- Consider 1:1:1 ratio of RBCs:plasma:platelets for massive hemorrhage
2. Cardiogenic Shock
Cardiogenic shock requires a multidisciplinary approach focusing on improving cardiac output while maintaining adequate perfusion pressure.
Clinical criteria:
- SBP <90 mmHg for ≥30 min or requiring vasopressors
- CI <1.8 L/min/m² without vasopressors/inotropes
- CPO <0.6 W
- Evidence of end-organ hypoperfusion 1
Initial management:
- Identify and treat underlying cause (revascularization for AMI)
- Optimize preload (cautious fluid administration)
- Reduce afterload when appropriate
Pharmacologic therapy:
LV-dominant failure:
- Dobutamine: 2-20 μg/kg/min (first-line inotrope)
- Milrinone: 0.375-0.75 μg/kg/min (for high-afterload LV failure)
- Nitroprusside: 0.3-5 μg/kg/min (for normotensive hypoperfusion) 1
RV-dominant failure:
Mechanical circulatory support (MCS) for refractory shock:
- Intra-aortic balloon pump
- Impella devices
- VA-ECMO
- Selection based on shock phenotype (LV, RV, or biventricular failure) 1
3. Distributive Shock
Early antimicrobial therapy (for septic shock) and vasopressors to restore vascular tone are essential in distributive shock management.
Initial management:
- Identify and treat underlying cause (antibiotics within 1 hour for septic shock)
- Fluid resuscitation: 30 mL/kg balanced crystalloids
Vasopressor therapy:
- Norepinephrine: 0.01-3 μg/kg/min (first-line)
- Vasopressin: 0.01-0.07 units/min (second-line) 4
- Epinephrine: 0.01-0.5 μg/kg/min (third-line)
- Phenylephrine: 0.5-9 μg/kg/min (for tachyarrhythmias)
Adjunctive therapy:
- Hydrocortisone: 200 mg/day in divided doses for refractory shock
- Source control for septic shock
4. Obstructive Shock
Immediate identification and relief of the obstruction is critical in obstructive shock management.
Tension pneumothorax:
- Immediate needle decompression followed by chest tube placement
Cardiac tamponade:
- Pericardiocentesis or surgical drainage
Pulmonary embolism:
- Systemic thrombolysis for massive PE with hemodynamic compromise
- Surgical embolectomy or catheter-directed therapy for contraindications to thrombolysis
Supportive care:
- Judicious fluid administration
- Vasopressors to maintain perfusion until obstruction relieved
Monitoring and Reassessment
Hemodynamic monitoring:
- Continuous arterial pressure monitoring
- Central venous pressure
- Pulmonary artery catheter for complex cases
- Cardiac output monitoring
Tissue perfusion assessment:
- Lactate clearance
- Urine output
- Mental status
- Skin perfusion
Special Considerations
- Shock phenotyping: Use invasive hemodynamics to identify shock phenotype and tailor therapy 1
- Mechanical complications: Failure to recognize mechanical complications can be fatal 2
- Multidisciplinary approach: Shock teams and specialized shock centers improve outcomes 1, 2
Pitfalls to Avoid
- Delayed recognition - Mortality increases with delayed treatment
- Inappropriate fluid management - Over-resuscitation in cardiogenic shock; under-resuscitation in hypovolemic shock
- Failure to identify shock phenotype - Different types require different approaches
- Delayed source control - Particularly important in septic shock
- Overlooking mixed shock states - Multiple shock types can coexist
Despite advances in management, shock continues to carry high mortality rates (35-45% for cardiogenic shock) 2. Early recognition, appropriate monitoring, and phenotype-specific therapy remain the cornerstones of effective shock management.