Sepsis guidelines 2021 Flashcards

(31 cards)

1
Q

Definition of sepsis

A

Dysregulated host response to infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Against using qSOFA

qSofa: GCS <15, RR >=22, SBP <=100
Positive qSofa 2

A

over SIRS, NEWS and MEWS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

At least 30 ml/kg of IV crystalloid should be given within the first 3 hours of resuscitation

A

WEAK

Dynamic measures: better diagnostic accuracy in predicting fluid responsiveness
example
1. Passive leg raising combined with cardiac output measurement
2. Fluid challenges against stroke volume
3. Systolic pressure or pulse pressure
4. Increases of SV in response to changes in thoracic pressure

**>15% increase in pulse pressure could indicate that the patient is fluid responsive using a passive leg-raise test for 60-90 seconds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Lactate

can be used to screen for the presence of sepsis among undifferentiated adult patients with clinically suspected sepsis

A

Lactate cut off 1.6-2.5 mmol/L

Lactate is a biomarker for tissue hypoxia and dysfunction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Guiding resuscitation to decrease serum lactate

A

Capillary refill time to guide resuscitation as an adjunct

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Initial target MAP

A

65 mmHg

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Admit patient to ICU

A

within 6 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Adults with possible septic shock or HIGH likelihood for sepsis

A

Administer antimicrobials within 1 hour of recognition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Adults with possible sepsis WITHOUT shock

A

Administration of antimicrobials within 3 hours from the time sepsis was first recognized

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Patients at high risk for MRSA

Patients at risk for MRSA
1. Prior history of MRSA infection or colonization
2. Recent IV antibiotics
3. History of recurrent skin infections or chronic wounds
4. Presence of invasive devices
5. Hemodialysis
6. Recent hospital admission and severity of illness

A

Recommend using emperic antimicrobials with MRSA coverage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

For adults with sepsis or septic shock and high risk for MDR

Risk factors for MDR infection
1. Proven infection or colonization with an antibiotic-resistant organism within preceeding year
2 Local prevalence of antibiotic- resistant organism
3 Hospital-acquired/health care associated
4 Broad-spectrum antibiotic use within the preceeding 90 days
5 Concurrent use of selective digestive decontamination
6 Travel to highly endemic country preceding the 90 days
7 Hospitalization abroad preceding the 90 days

A

2 antimicrobials with gram negative coverage

**Local information about the resistance patterns of the most common causative agents of sepsis: essential to choose the most appropriate empirical antibiotic therapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Emperic double coverage of gram negeative bacilli is most important in patients

A

At high risk for resistant organisms with severe illness (septic shock)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

For adults with sepsis or septic shock at high risk for fungal infections

A

Using empiric antifungal therapy

Risk factors for fungal infection:
Febrile neutropenia patients who fail to defervesce after 4-7 days of broad-spectrum antibacterial therapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Optimizing dosing strategies based on

A

kinetic/pharmacodynamic (PK/PD) principles

Scenarios that affect the concentration of some antibiotics
1. Augmented renal clearance
2. AKI
3. Hypoalbuminemia
4. RRT
5. Extracorporeal membrane oxygenation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Daily assessment for de-esclatation of antimicrobials

A

Over fixed duration of therapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Patients with sepsis or septic shock and ADEQUATE source control where optimal duration of therapy is unclear

A

Use procalcitonin and clinical evaluation to decide when to discontinue antimicrobials

17
Q

First line fluid for resuscitation

A

balanced crystalloids (LR) over normal saline

Adverse effects of NSS
1. Hyperchloremic metabolic acidosis
2. Renal vasoconstriction
3. Increased cytokine secretion
4. AKI

18
Q

Use albumin in patients

A

Who received large volume of crystalloids

Effects of albumin :
1. Higher blood pressure at early and later time points
2. Higher static filling pressures
3. Lower net fluid balance

19
Q

Vasoactive management

1st line: norepinephrine (a-1 and b-1 adrenergic receptor agonist) vasoconstriction–> inc MAP with minimal effect on HR

2nd line: vasopressin

3rd line: epinephrine (b-1 and moderate b-2 and a-1 adrenergic receptor activity)
Low dose: b1: increased CO, decreased SVR, and variable effect on MAP
Higher dose: increase SVR and CO
SE: arrhythmia and impaired splanchnic circulation, increase aerobic lactate production via stimulation of skeletal b-2 adrenergic receptors

*Vasopressin is started when the dose of norepinephrine is 0.25-0.5 ug/kg/min
Fixed dose: 0.03 units/min
Ceiling 0.06 units/min
Produced in hypothalamus
Stored and released by the posterior pituitary gland
Binds to the V1 receptors on vascular smooth muscle thus increased arterial blood pressure
S/e: cardiac, digital and splanchnic ischemia

Dopamine: dose-dependent fasion on dopamine 1, a-1 and b-1 adrenergic receptors
Lower dose dopamine: vasodilation via dopamine 1 in renal, splanchnic, cerebral, and coronary beds
Higher dose: vasoconstriction and increased systemic vascular resistance via a1-receptor and b1-receptor activity can lead to dose-limiting arrhythmia

A

Inotropes

Patients with septic shock and cardiac dysfunction (low CO and elevated cardiac filling pressures) with persistent hypoperfusion

Noepinephrine+dobutamine
ORRRR
Epinephrine alone

Dobutamine
MOA: Increases CO and oxygen transport increases splanchnic perfusion and tissue oxygenation improves intramural acidosis and hyperlactatemia

S/e of dobutamine infusionL severe vasolatation–> result in lower MAP
>inotropic response may be blunted in sepsis with a preserved chronotropic effect causing tachycardia without an increase in stroke volume

20
Q

Suggest invasive monitoring of arterial blood pressure

A

Start vasopressors peripherally

21
Q

For sepsis-induced hypoxemic respiratory failure

A

Use high-flow nasal oxygen over NIV

HFNC:
warms and humidifiers secretions
High flow rates better match patient demand
Washout of nasopharyngeal dead space
Modest positive airway pressure effect

**allows airflow as high as 60L per minute to achieve Fio2 95-100%

NIV
Main risk: delaying need for intubation and increasing the risk of an interval aspiration events

Other S/E
Increased risk for gastric insufflation and aspiration, facial skin breakdown, excessively high tidal volumes, discomfort related to the inability to eat or effectively phonate

22
Q

Protective ventilation in ARDS

BERLIN definition of ARDS
Mild PaO2/Fio2 <=300 mmHg
Moderate PaO2/Fio2 <=200 mmHg
Severe PaO2/Fio2 <=100 mmHg

**Plateau pressure remain >30 cmH20 after reduction of TV to 6 ml/kg PBW, TV maybe reduced to as low as 4 mg/Kg

RR should be increased to a max of 35 breaths/min during TV reduction to maintain minute ventilation

*No single mode of ventilation is shown to be advantageous

A

Low TV ventilation 6 mL/kg

Upper limit goal for plateau pressure 30 cm H20

Higher PEEP (may open lung units to participate in gas exchange and may increase PaO2)
*PEEP >5 cm H20 is required to avoid lung collapse

Low TV (without ARDS)

Using traditional recruitment maneuvers

Using prone ventilation for greater than 12 hours daily

Using intermittent NMBA boluses

Veno-venous (VV) ECMO when conventional mechanical ventilation fails (severe ARDS)

23
Q

On going requirement for vasopressor therapy

A

IV corticosteroids

24
Q

Restrictive transfusion therapy over

25
Have risk factors for GI bleeding
Stress ulcer prophylaxis
26
Recommend pharmacologic venous thromboembolism (VTE) prophylaxis (Low molecular weight heparin)
unless contraindication to therapy exist
27
Initiating insulin therapy at a glucose level
>= 180 mg/dl
28
Septic shock severe metabolic acidemia ph <=7.2 Acute kidney injury (AKIN score 2 or 3)
Use sodium bicarbonate therapy
29
Enteral feeding
Early within 72 hours initiation of enteral nutrition
30
Discussing goals of care
Early within 72 hours
31
If patients are on MV >48 hours or an ICU stay >72 hours
Referral to a post-hospital rehabilitation program