Identification of the septic patient is the important first step. All other critical actions are missed if this does not occur.
Lactate measurement is critical to determining sepsis severity, response to therapy, and prognosis.
Early administration of appropriate antimicrobials and early goal-directed therapy are the mainstays of treatment.
Resuscitation of the critically ill septic patient should occur concurrent or before diagnostic evaluation.
Sepsis is now defined as “infection plus systemic manifestations of infection” (Table 34-1). Systemic inflammatory response syndrome is no longer a strict criteria. There are 3 sepsis syndromes (stages): uncomplicated sepsis, severe sepsis, and septic shock. Sepsis becomes severe sepsis when there is tissue hypoperfusion or organ dysfunction (Table 34-2). Septic shock is defined as a systolic blood pressure (SBP) <90 mmHg or 40 mmHg below one’s baseline blood pressure, despite two 20- to 30-mL/kg boluses.
Diagnostic criteria for sepsis.
Infection, documented or suspected, and some of the following: |
General variables
|
Inflammatory variables
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Hemodynamic variables
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Organ dysfunction variables
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Tissue perfusion variables
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Diagnostic criteria for severe sepsis.
Severe sepsis is sepsis with tissue hypoperfusion or organ dysfunction as defined by the following criteria: |
Hypotension |
Lactate greater than the upper limits of normal laboratory results |
Urine output <0.5 ml/kg/hr for >2 hrs, despite adequate fluid resuscitation |
ALI with PaO2/FIO2 <250 in the absence of pneumonia |
ALI with PaO2/FIO2 <200 in the presence of pneumonia |
Creatinine >2.0 mg/dL |
Bilirubin >2 mg/dL |
Platelet count <100,000/μL |
Coagulopathy (INR >1.5) |
Sepsis affects 751,000 patients per year, with an annual mortality that exceeds that of AIDS and breast cancer and approaches that of myocardial infarction. The lungs, abdomen, and urinary tract are the most frequent source of infection, but sepsis can come from anywhere in the body. In approximately 20% of cases, the etiology cannot be determined. Risk factors for the development of sepsis syndromes are extremes of age, immunosuppression (chemotherapy, organ transplantation, steroid use, HIV, etc.), severe comorbid disease, exposure to multiple drug-resistant organisms, vascular catheters and other indwelling devices, intravenous (IV) drug abuse, trauma, and burns.
Any patient presenting with an infectious syndrome should be considered for potential sepsis. Those at the extremes of age or the immunosuppressed may not mount a fever. Other patients may have defervescenced before triage vital signs. High clinical suspicion will be required in properly identifying these patients. Furthermore, patients with reduced physiologic reserve are at risk for rapid clinical deterioration.