Lecture 24: CV Support Drugs & Basic CPR (Exam 3) Flashcards

1
Q

What should MAP & SAP be to prompt recognition & tx will ensure perfusion of vital organs

A
  • MAP > 60 - 70 mmHg
  • SAP > 80 - 90 mmHg
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2
Q

What are the common causes of CV depression during ax

A
  • Drugs
  • Equipment malfunction/misuse
  • Shock/sepsis
  • Hypovolemia
  • Mechanical ventilation
  • Surgical procedure
  • pre existing CV dx
  • Metabolic dx
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3
Q

What is the key to CV depression during ax

A

Treat the underlying cause of hypotension

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4
Q

What is the equation for CO

A

HR x SV

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5
Q

What is the equation for MAP

A

CO x SVR

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6
Q

List management options for CV depression

A
  • Adjustment to current ax manangement
  • Fluids
  • Anticholinergics
  • Vasopressors
  • Positive ionotrops
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7
Q

What are sympathomimetics that support CV

A
  • Positive ionotropes
  • Vasopressors
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8
Q

Describe sympathomimetics

A
  • Includes endogenous catecholamines, synthetic catecholamines, & synthetic non catecholamines
  • Have relative selectivity of sympathomimetics for various adrenergic receptors depends on the chemical structure of the drug
  • Act on alpha & beta adrenergic or dopaminergic receptors directly or indirectly & these receptors are coupled to G proteins
  • The density of alpha & beta adrenergic receptors in tissue determines the response of the drug
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9
Q

Fill out the following:

A
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10
Q

Describe dobutamine

A
  • Mostly beta 1 (+) ionotropic effects
  • Has dose dep beta 2 & alpha 1 agonist effects
  • Increase in myocardial contractility, stroke vol, & cardiac output
  • For px w/ dilated cardiomyopathy, heart failure, show, & low CO
  • CRI dose used for tx of hypotension in small animals
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11
Q

Describe dopamine

A
  • Endogenous catecholamines
  • Precursor to NE
  • Acts directly & indirectly on both a & B 1 receptors
  • Has dopaminergic (D1 & D2) effects
  • Increases CO, HR, BP, & SVR
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12
Q

What does dopamine tx? What about a low & high doses?

A
  • tx of acute heart failure & severe hypotension/shock
  • low dose d1 & d2 affects - dilation of renal, mesenteric, coronary, intracerebral vasular beds (can indirectly increase the production of urine in px w/ acute renal failure)
  • At higher doses of dopamine - increase SPR due to a1 receptor effect
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13
Q

Describe ephedrine

A
  • Mixed inotropic pressor agonist @ a1, a2, B1, & B2 receptors
  • Used for the management of hypotension during ax in horses
  • Can be used in dogs but effects may be short lived
  • Dose is species dep
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14
Q

Why is ephedrine used in horse to manage hypotension during gen ax

A

B/c it can be given as a bolus instead of a CRI due to its longer duration of action compared to other CV support drugs

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15
Q

Describe noreepinephrine

A
  • Agonist @ a1, a2, & B1 receptors
  • Has (=) potency to epinephrine for stimulation of B1 but has little effect on B2
  • Is a potent a-agonist that produces intense arterial & venous vasoconstriction in all vascular beds
  • Tends to decrease CO & may cause metabolic acidosis
  • Can cause necrosis
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16
Q

What is the main use of norepinephrine

A

Used as a CRI for the tx of refractory hypotension due to vasodilation from inhalant ax or sepsis b/c the effects are mostly on the a1 receptor @ the clinically used dose rate

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17
Q

Describe epinephrine

A
  • Has both vasopressor & inotropic effects by directly stimulating a1, B1, & B2 receptors
  • Most potent activator of a-adrenergic receptors
  • Reserved for use as a bolus during CPR
  • Can be given as a CRI as a last resort for tx of severe hypotension due to endotoxemia
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18
Q

What are the effects of epinephrine on a1 receptors

A

Intense vasoconstriction

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19
Q

What are the effects of epinephrine on B1 receptors

A

Increases SAP, HR, & CO

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20
Q

What are the effects of epinephrine on B2 receptors

A

Modest decrease in DAP due to vasodilation in skeletal m & bronchodilation

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21
Q

What are the net effects of epinephrine

A
  • Increase in pulse pressure
  • Min change in MAP
  • Preferential distribution of CO to skeletal m
  • Decreased SVR
  • Renal blood flow decreases
  • Coronary blood flow increases
  • Secretion of renin b/c of B stimulation in the kidneys
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22
Q

Describe phenylephrine

A
  • Increased peripheral vascular resistance by agonist effect on the a1 receptors
  • Can be used in px w/ severe vasodilation
  • Used in dogs/cats to increase BP
  • Generally recommended to avoid use in preg px
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23
Q

Why is phenylephrine not recommended to use w/ preg px

A

It decreases blood flow to the uterus & therefore impairs oxygen delivery to the fetus

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24
Q

Describe vasopressin

A
  • Works through stimulation of the V1 receptor located on vascular SM
  • Has no inotropic or chronotropic effects
  • Indicated for vasodilatory hypotension due to sepsis, prolonged hemorrhagic shock, or cardiac arrest
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25
Q

How is a infusion of dompaine or dobutamine made

A
  • Dobutamine must be diluted to a concentration of < 5 mg/mL
  • Dobutamine & dopamine are physically compaticle w/ DSw, 0.9% NaCl, dextrose-saline, & LRS
  • Desired infusion concentration can be made in a syringe & delivered by syringe pump if ava or can be place in a bag of IV fluids & del by calculated drops per second or an accurate fluid pump
  • Dobamine & dobutamine are stable for about 24 H @ room temp so it should not be made up in advance of anticipated use
26
Q

Answer the following case

27
Q

Answer the following case

28
Q

What are the key take aways of CPR

A
  • Cats are almost 5x more likely to survive to hospital discharge than dogs
  • Anesthetic related CPA events are almost 15x more likely to be discharged compared to other groups
29
Q

What are the goals of recover guidelines

A
  • Review of literature
  • Dev consensus on CPR guidelines
  • Provide education & training for vet medical care teams
30
Q

What is the “chain of survival”

A
  • Prevention/early recognition
  • Basic life support (BLS)
  • Advanced life support (ALS)
  • Post resuscitation care (post cardiac arrest care)
31
Q

What are the signs of cardiopulmonary arrest

A
  • Not responsive
  • Not breathing
  • No pulse detected
32
Q

What are the steps of basic life support

A
  1. Shake & shout (provide stimulation)
  2. If not breathing/responsive immediately start chest compressions @ 100 - 120 per min & depth of 1/3 to 1/2 chest width (don’t stop to check the pulse for 2 mins)
  3. Est airway & ventilate @ 10 bpm (give breath every 6 secs)
33
Q

Describe how chest compressions are given

A
  • px position: lateral recumbency
  • compressor position: stand behind the px (along the spine)
  • Hand position: hand over hand w/ interlaced fingers
  • Compressors stance: shoulders over elbows/hands, lock the elbows, & bend @ the waste
  • put the px on the floor or get on the table/stool if need be
34
Q

What are the different patient chest types

A
  • Large round chest (A)
  • Large keel chest (B)
  • Wide chest - bulldogs, dorsal recumbency, compress to 25% depth (C)
  • Cats & small dogs - circumferential, one handed palm, or one handed thumb to fingers (D)
35
Q

How many breath per min should be delivered? what is the wanted tidal vol, inspiratory time, & peak pressure

A
  • 10 bpm
  • TV = 10 ml/kg
  • Inspiratory time = 1 sec
  • Peak pressure < 40 cmH2O
36
Q

Describe airway & ventilation during CPR

A
  • Ideally intubated w/ appropriately sized ETT w/ the cuff inflated & the tube secured in place
  • Can use a tight fitting mask & self inflating bag to deliver breath (ambu bag)
  • Use of 100% O2 is reasonable
  • If not able to intubate do mouth to snout using a ratio of 30 compression to 2 ventilation tech
37
Q

What should be done during the 2 min cycle of compressions & ventilations

A
  • Hook up ECG leads
  • Place capnograph (ETCO2) @ the end o the ETT
  • Gain IV access (IO would be 2nd choice & some drugs can go IT if no other access ava)
  • Admin reversal agents if indicated (no cardiac sticks)
38
Q

How long should you take to stop compression long enough to feel for a femoral pulse & assess the ECG hook ups

A

No more than 10 secs

39
Q

If there is a pulse what should be done

40
Q

If there is no pulse when checked what should be done

A
  • Eval ECG to determine if there is a shockable or non shockable rhythm
  • Eval ETCO2 - if < 18 mmHg evaluate the quality of compressions
41
Q

What does this capnography wave form show

A

Cardiac arrest

42
Q

What does the capnography wave form show

A

Return of spontaneous circulation

43
Q

Which arrests rhythms are non shockable

A
  • Asystole
  • Pulseless electrical activity (PEA)
44
Q

Which arrest rhythms are shockable (rate > 200)

A
  • Pulseless ventricular tachycardia
  • Ventricular fibrillation
45
Q

Which arrest rhythm is this

46
Q

Which arrest rhythm is this

47
Q

Which arrest rhythm is this

A

Pulseless ventricular tachycardia

48
Q

Which arrest rhythm is this

A

Ventricular fibrillation

49
Q

What are the emergency drugs for non shockable rhythms

A
  • Vasopressors
  • Anticholinergics
50
Q

Describe vasopressors as a emergency drug

A
  • Epinephrine & vasopressin
  • 0.01 mg/kg every other cycle
51
Q

Describe anticholinergics as an emergency drug

A
  • Atropine & glycopyrrolate
  • Use one as early as possible & don’t reduce
  • Glycopyrrolate onset is too slow for CPR use
52
Q

What does the ratio expression of strength mean for epinephrine

A

This is the formulation used for life threatening anaphylaxis, CPR, & sometimes for extremely low blood pressure under ax

53
Q

What is the reversal agent for opioids

54
Q

What is the reversal agent for benzodiazepines

A

Flumazenil

55
Q

What is the reversal agent for Alpha 2 agonist

A

Atipamezole

56
Q

What is the reversal agent for local anesthetic toxicity

A

Lipid emulsion infusion + supportive care

57
Q

What drug is considered for use in prolonged CPR ( > 15 min & pH < 7)

A

Sodium bicarb @ 1 mEq/kg

58
Q

Describe defibrillation

A
  • 1st ling of tx for ventricular fibrillation or pulseless ventricular tachycardia
  • Immed after electrical defibrillation restart chest compression to replenish energy substrates & increase the chance of success before eval the ECG
59
Q

Describe the use of defibrillators

A
  • Biphasic defibrillator dose: 2 J/kg
  • Double the dose for subsequent shocks (4 J/kg)
  • Use conductive electrode gel
  • Use of biphasic is recommended over monophasic b/c of less risk of myocardial damage & it is more effective w/ lower joules
60
Q

T/F: RECOVER recommends the use of IV fluid boluses in euvolemic dogs & cats during CPR

A

False; recommends against the use

61
Q

What is the use of IV fluids if a px is hypovolemic or in distributive shock

A
  • use isotonic crystalloid during CPR
  • Hypertonic saline may be neuroprotective
  • Avoid synthetic colloids but blood products may be needed for significant hemorrhage
  • Manage electrolyte imbalance as needed
62
Q

What are some final takeaways that will help lead to a positive px outcome

A
  • A well prepared/trained team
  • Effective closed loop communication
  • Ability to meet afterwards to discuss what went well & what to work on for next time
  • Stocked & ready to go crash cart
  • Perform compressions & ventilations effectively