TREATING SEPSIS

     
   

 

     
     

Conclusion

The management of the septic patient has evolved somewhat in recent years. Initial management involves protection of the airway and delivery of oxygen into the blood, with restoration of circulating volume, initially with fluids and, if necessary, vasoactive agents. The splanchnic circulation appears to be a particularly important site for resuscitation, as the physiological response to hypotension causes reduction in blood flow to this area. The result is gut ischemia, bacterial translocation, worsened sepsis and renal failure. Gut resuscitation involves the use of beta-adrenergic agonists and early enteral nutrition, preferably with immunomodulatory supplements. There is increasing interest in the interaction between inflammation and coagulation in severe sepsis, with compelling data for the use of activated protein C in this patient population.

Key Points

  1. Immediate resuscitative efforts involve maintaining patency and adequacy of the airway, and ensuring oxygenation and ventilation. Initial management of hypotension is by aggressive volume resuscitation, either with isotonic crystalloids, or in combination with crystalloids. Do not interfere with the heart rate: tachycardia is a compensatory maneuver.
  2. Take a history (or obtain a collateral one), examine the patient, and quantify the extent of sepsis: temperature, white cell count, acid-base status and cultures. The choice of antimicrobial is determined by the source of infection and a best guess of the organism involved.
  3. Vasoactive therapy is commenced after other measures have failed. There is no simple solution. Vasoactive medication must be aimed at restoring tissue perfusion without causing ischemia. Persistent requirement for vasopressors requires investigation of adrenal function.
  4. The systemic inflammatory response is driven along by persistent infection: you must find the source and remove it. This may involve extensive detective work.
  5. The use of activated protein C at 24 µg per kilogram per hour for 96 hours is associated with a significant reduction in mortality.
  6. Prevention of villous atrophy and bacterial translocation involves restoration of circulation and restoration of gut luminal nutrition. Secondary sources of sepsis (lines) and organ dysfunction (pulmonary embolism) must be avoided.
  7. Adequacy of resuscitation is evaluated by looking at endorgan perfusion – using clinical examination and interpretation of monitored variables. There is no ideal method.
  8. It is the second and subsequent hits that often kill patients: it is important that you prevent this from arising from an inatrogenic source. Minimize the amount of interventions involved and wean and remove therapies that are no longer beneficial.

       
   

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