Shock & Pressors Flashcards

1
Q

Criteria for ARDS Diagnosis

A
  1. Acute onset
  2. Chest X-Ray: Bilateral diffuse infiltrates of the lungs
  3. No cardiovascular lesion
  4. No evidence of left atrial hypertension: PaO2/FiO2 ratio equal to or less than 200 mmHg.
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2
Q

Definition of Shock

A

Failure of circulatory system to maintain adequate blood flow to end organs

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3
Q

3 most common forms of shock

A

Distributive, Hypovolemic, Cardiogenic

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4
Q

Common causes of distributive shock

A

Sepsis, Anaphylaxis, Neurogenic

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5
Q

Equation for MAP

A

MAP = CO * SVR = SV * HR * SVR

Use this to figure out how to treat shock in the short-term

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6
Q

3 Short-term interventions for shock

A

1) Fluids: inc SV –> inc CO –> inc MAP
2) Vasopressors: inc SVR –> inc MAP
3) Inotropes: inc CO –> inc MAP

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7
Q

Hypovolemic Shock - PCWP / CO / SVR

A

PCWP decreases
CO decreases
SVR increases

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8
Q

Cardiogenic Shock - PCWP / CO / SVR

A

PCWP increases
CO decreases
SVR increases

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9
Q

Distributive Shock - PCWP / CO / SVR

A

PCWP decreases
CO increases or decreases
SVR decreases

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10
Q

How to figure out PCWP and SVR of a patient clinically

A

Clinically dry - decreased PCWP
Clinically wet - increased PCWP
Cold extremities - increased SVR
Warm extremities - decreased SVR

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11
Q

3 Types of Vasoactive agents used in shock

A

Vasopressors
Inodilators
Inopressors

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12
Q

Receptors targeted by vasoactive agents

A
a1 - peripheral vasoconstriction
b1 - inotropy
b2 - peripheral vasodilation
V1 - peripheral vasoconstriction
D1 - selective vasodilation of renal, mesenteric, cerebral, coronary vasculature
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13
Q

Volume status and Pressors

A

Aggressive IVF is key 1st step. Pressors can cause decreased end-organ perfusion if there’s inadequate circulating volume

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14
Q

Name the 6 vasoactive agents commonly used

A
Dobutamine - ID
Epinephrine - IP
Dopamine - IP
Norepinephrine - IP
Phenylephrine - VP
Vasopressin - VP
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15
Q

Dobutamine

A

Inodilator
0-20 mcg/kg/min
b1, b2
inc CO, dec SVR

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16
Q

Epinephrine

A

Inopressor
0-10 mcg/kg/min
a1, b1, b2
inc CO, inc SVR

17
Q

Dopamine

A

Inopressor
0-20 mcg/kg/min (renal dose 0-2.5)
Renal dose: b1, D1 - inc CO, dec SVR
Higher doses: a1, b1, D1 - inc CO, inc SVR

18
Q

Norepinephrine

A

Inopressor
0-20 mcg/min
a1, b1
inc CO, inc SVR

19
Q

Phenylephrine

A

Vasopressor
0-200 mcg/kg/min
a1
inc SVR

20
Q

Vasopressin

A

Vasopressor
0.04 units/min
V1
inc SVR

21
Q

First line agents in shock

A

Norepinephrine and Dopamine
For both Cardiogenic and Septic shock
ACC/AHA and Surviving Sepsis Campaign

22
Q

SOAP II Trial (NEJM 2010)

A
Dopamine vs Norepinephrine
1679 pts in shock (cardiogenic & septic)
No mortality diff at 28 days
Dopamine had increased mortality at 28 days for pts in cardiogenic shock
Dopamine pts had more arrhythmic events
23
Q

Pressors in Sepsis Study (Chest 1993)

A

32 pts in septic shock randomized to NE vs DA. If no response, rescue w/ other agent.
DA response 31%; NE response 93%.
NE rescued 10/11 DA failures.
Survival NE 59%; DA 17%.

24
Q

Renal dose DA in sepsis study (Lancet 2000)

A

328 septic pts w/ early renal failure
Randomize to DA vs Placebo
Results: No difference in peak Cr or clinical outcomes

25
Q

Second-Line Agents for Shock

A

Phenylephrine and Epinephrine

26
Q

Phenylephrine - data for use

A

Less useful in cardiogenic shock (already increased SVR).
In sepsis, potential to lower SV b/c increases SVR w/o increasing CO
Possible dec splanchnic blood flow
May be useful in pts w tachyarrhythmia, esp if worsened with NE

27
Q

Epinephrine - data for use

A

First line for anaphylactic shock
Increases inotrophy more than NE, but more arrhythmias
Dec splanchnic Q, inc lactate

28
Q

Vasopressin - data for use

A

Only use as adjunctive agent
Studies show lower ADH lvls in sepsis
Better HD & end-organ perfusion, lower tachyarrhythmia, higher ischemic skin lesions
Use at fixed rate of 0.04u/h - no titration

29
Q

Dobutamine - data for use

A

Only use as adjunctive agent
Septic pts often have lower CO 2/2 endotoxins & cytokines.
Studies show no benefit and possibly harm (Systemic O2 delivery study NEJM 1994).
Never use only as lower SVR may reduce BP more than increased by higher CO.