EM Infectious 2 (Sepsis) Flashcards

1
Q

predominant pathogens of sepsis

A

gram-positive bacteria

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2
Q

QSOFA

A

Quick Sequential Organ Failure Assessment tool
-used to identify patients at higher risk of death

AMS
RR ≥22
SBP ≤100

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3
Q

Remarks on undifferentiated hypotension

A

in ED, 40% will ultimately have an infectious cause of symptoms

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4
Q

septic cardiomyopathy

A

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

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5
Q

the most common GI manifestation of sepsis

A

Ileus, which may persist for days after shock resolves

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6
Q

hematologic changes in sepsis

A

neutropenia and thrombocytopenia carries increased risk of mortality

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7
Q

the most common sepsis trigger

A

acute bacterial pneumonia

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8
Q

most common skin and soft tissue infection triggering a sepsis syndrome

A

cellulitis due to S aureus or S pyogenes

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9
Q

Those without an obvious source of septic shock may have

A

primary bacteremia or endocarditis

the most prevalent causes of primary baccteremia in outpatients are S aureus, S pneumoniae, and N meningitidis

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10
Q

community-acquired meningitis with shock is usually caused by

A

S pneumoniae or N meningitidis

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11
Q

In sepsis, there is no set amount of fluid, although most patients will require a total (bolus plus infusion) of

A

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

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12
Q

Once the patient is stabilized, other interventions that may improve patient outcomes

A

management of oxygenation and ventilation
fever control to reduce metabolic demand
control of hyperglycemia

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13
Q

remarks on refractory shock

A

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)

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14
Q

Describe early goal-directed therapy

A

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

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15
Q

remarks on lactate clearance

A

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

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16
Q

The important elements that improve outcomes in sepsis

A
  1. Early recognition of sepsis
  2. Administration of antimicrobials
  3. Adequate volume resuscitation
  4. 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

17
Q

the most important variable process in volume replacement in sepsis

A

determining wheter a patient is volume responsive

18
Q

remarks on vasopressors

A

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

19
Q

remarks on vasopressin

A

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

20
Q

if tachydysrhythmias are a problem, one option is:

A

phenylephrine, which as a pure a-adrenergic agonist

21
Q

what does Scvo2 <70% mean?

A

It implies a relative oxygen supply and demand mismatch

Central venous Oxygen saturation

22
Q

remarks on antibiotics

A

give ASAP in severe sepsis

combination antibiotic therapy as opposed to monotherapy leads to improved outcomes, potentially due to higher rates of bactericidal activity

23
Q

remarks on vancomycin

A

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

24
Q

glucose goals in sepsis

A

<180 mg/dL

hyperglycemia is associated with worsened outcomes in the setting of sepsis

25
Q

remarks on gentamicin

A

Consider use in
* adults with suspected urinary source

dose:
1.0 - 1.5 mg/kg every 8 hours

26
Q

antibiotics for sepsis with neutropenia

A

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

27
Q

what to give if patient is allergic to vancomycin>

A

linezolid 600 mg IV

28
Q

antibiotics to be added to regimen if patients have potential for legionella infection

A

Azithromycin 500 mg IV, then 250 mg IV q 24
or
Erythromycin 800 mg IV q6

29
Q

antibiotics to be added to regimen if patients with asplenia

A

Ceftriaxone 1 g IV q24
up to 2g IV q12 if meningitis