1 Sepsis Flashcards
The cornerstones of the initial treatment and stabilization of severe sepsis
- Early recognition
- Early reversal (or prevention) of hemodynamic compromise
- Early infection control
predominant pathogens of sepsis
gram-positive bacteria
QSOFA
Quick Sequential Organ Failure Assessment tool
-used to identify patients at higher risk of death
AMS
RR ≥22
SBP ≤100
Remarks on undifferentiated hypotension
in ED, 40% will ultimately have an infectious cause of symptoms
septic cardiomyopathy
a reversible process with impaired systolic function and diastolic relaxation
the combination of intravascular volume depletion and septic cardiomyopathy may manifest as “cold shock”, impaired peripheral perfusion and cool extremities
the most common GI manifestation of sepsis
Ileus, which may persist for days after shock resolves
hematologic changes in sepsis
neutropenia and thrombocytopenia carries increased risk of mortality
the most common sepsis trigger
acute bacterial pneumonia
most common skin and soft tissue infection triggering a sepsis syndrome
cellulitis due to S aureus or S pyogenes
Those without an obvious source of septic shock may have
primary bacteremia or endocarditis
the most prevalent causes of primary baccteremia in outpatients are S aureus, S pneumoniae, and N meningitidis
community-acquired meningitis with shock is usually caused by
S pneumoniae or N meningitidis
In sepsis, there is no set amount of fluid, although most patients will require a total (bolus plus infusion) of
2-5 liters of crystalloid in the first 6 hours to achieve optimal outocmes
similarly do not delay vasopressors when blood pressure does not respond to volume or if volume overload seems likely
Once the patient is stabilized, other interventions that may improve patient outcomes
management of oxygenation and ventilation
fever control to reduce metabolic demand
control of hyperglycemia
remarks on refractory shock
consider corticosteroids
hydrocortisone 50mg IV
*“Hydrocortisone shortens time to shock reversal in refractory hemodynamic shock (i.e., requiring more than on evasopressor after adequate volume restoration)
Describe early goal-directed therapy
Titration of
* Fluids to CVP
* Vasopressors to MAP
* Blood transfusion and inotropes to central venous oxygen saturation (Scvo2)
This protocol decreased mortality when compared with standard care, although all patients had central venous catheters placed early
Follow-up uncontrolled observaton studies confirmed that even partial use of this approach lowered mortality
remarks on lactate clearance
If initial lactate is elevated (>2 mmol/L), repeat lactate required prior to 6 hours
Lactate clearance of ≥10% was noninferior to continuous Scvo2 monitoring in the setting of ED-based resuscitation of septic shock
measure lactate using the same method 1-2 hours apart
The important elements that improve outcomes in sepsis
- Early recognition of sepsis
- Administration of antimicrobials
- Adequate volume resuscitation
- Assessment of adequacy of circulation
not any specific path of resuscitation
mandatory central venous catheterization and monitoring of CVP or Scvo2 are not necessary for all patients with sepsis
the most important variable process in volume replacement in sepsis
determining wheter a patient is volume responsive
remarks on vasopressors
Peripheral vasopressor use to start care is safe
High-dose and prolonged infusions are better deployed using a central venous line to limit extravasation and resultant tissue necrosis
When using **peripheral catheters, make sure they are large, secured, and not distal
remarks on vasopressin
give at constant infusion at a rate of 0.03 or 0.04 U/min.
Do NOT titrate the dose, because higher rates are associated with vasospasm and high morbidity
if tachydysrhythmias are a problem, one option is:
phenylephrine, which as a pure a-adrenergic agonist
what does Scvo2 <70% mean?
It implies a relative oxygen supply and demand mismatch
Central venous Oxygen saturation
remarks on antibiotics
give ASAP in severe sepsis
combination antibiotic therapy as opposed to monotherapy leads to improved outcomes, potentially due to higher rates of bactericidal activity
remarks on vancomycin
15 mg/kg loading dose
Vancomycin is often underdosed in clinical practice, and guidelines suggest an initial dose of 25-30 mg/kg in critically ill patients
Use also in patients with indwelling vascular devices
glucose goals in sepsis
<180 mg/dL
hyperglycemia is associated with worsened outcomes in the setting of sepsis
remarks on gentamicin
Consider use in
* adults with suspected urinary source
dose:
1.0 - 1.5 mg/kg every 8 hours
antibiotics for sepsis with neutropenia
Ceftazidime/Cefepime 2g IV q8
or Pip-Taz
+
Levofloxacin 750 mg IV q24
or moxifloxacin 400 mg IV q24
+
Vancomycin 15 mg/kg LD
and consider
Fluconazole 400 mg IV q24
or micafungin 100 mg Q24
what to give if patient is allergic to vancomycin>
linezolid 600 mg IV
antibiotics to be added to regimen if patients have potential for legionella infection
Azithromycin 500 mg IV, then 250 mg IV q 24
or
Erythromycin 800 mg IV q6
antibiotics to be added to regimen if patients with asplenia
Ceftriaxone 1 g IV q24
up to 2g IV q12 if meningitis