Advanced Pharmacology Flashcards

1
Q

What is the onset of action for IV/IO administrated drugs

A

Onset: 30-60s

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2
Q

What is the onset of action for ETI administered drugs?

A

onset: 2-3min

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3
Q

Time of onset for IM and SC drug administration?

A

IM: 10-20Min
SC:15-30min

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4
Q

What is the “loading dose” for fentanyl in a patient presenting with severe pain? (IM/IV/IO)

A

-0.5-1.0mcg/kg to a max single dose of 100mcg. q-5 to a total of 300mcg

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5
Q

What is the intranasal dose for fentanyl?

A

-1.5 to 2.0mcg/kg.

Max single dose 100mcg

Max cumulative dose of 300mcg

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6
Q

When should ketamine be considered after fentanyl use?

A

-pain insufficiently managed after a total of 1-3mg/kg.

  • High opioid tolerance?
  • Patient request
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7
Q

What is the paediatric max single and cumulative dose of fentanyl IN/IV/IO

A

Max single IN: 100mcg

Max single IV/IO: 50mcg

Max cumulative dose: 200mcg

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8
Q

What is the SC dose for morphine?

A

0.1mg/kg SC or 2.5-5mg SC

May repeat every 10-30 min based on blood pressure >100mmHg

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9
Q

Describe the analgesic dose for Ketamine

A

IV/IO: 0.3mg/kg
-may repeat 1/2 (0.15mg/kg) after 5 min

IM-0.5mg/kg, may repeat 0.3mg/kg after 45 minutes

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10
Q

Describe the procedural sedation dose for ketamine

A

IV/IO: 0.1-0.5mg/kg slow push every 60 seconds to effect.

CONSIDER starting at 0.5mg/kg and use subsequent 0.25mg/kg doses as needed

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11
Q

Describe an induction dose of ketamine based on shock index

A

If SI is <1 use 2mg/kg

If SI is >1 use 1mg/kg

Half of induction dose every 10-15min as required

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12
Q

What are the doses for IM and IV/IO midazolam?

A

IV/IO 2-5mg

IM 5-10mg

MAX 30mg

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13
Q

What is the pediatric dose for midazolam?

A

IN 0.2mg/kg, max of 10mg

IV/IO 0.1mg/kg or max of 5mg

IM: 0.2mg/kg IM

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14
Q

Describe phase 0 of action potential

A
  • Depolarization phase

- Rapid influx of Na+ and Ca+

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15
Q

what is the resting membrane potential of a cardiac myocyte?

A

-90mv

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16
Q

Describe Phase 1 of action potential

A

Phase 1 consists of a transient efflux of K+

17
Q

Describe phase 2 of action potential

A

Phase 2 is the plateau phase, the efflux of K+ is balanced by the influx of Ca+

18
Q

Describe phase 3 of action potential

A

Phase 3 is the depolarization phase with an Efflux of K+

19
Q

Describe phase 4 of resting membrane potential

A

Consistent leak of K+

20
Q

Describe class one of Vaughn Williams classification

A
  • Sodium channel blockade
  • Reduces phase 0 slope and peak of action potential
  • broken up into 1A, 1B, 1C (moderate, weak, strong) Lido is 1B
21
Q

Describe class 2 of VW

A
  • Beta Blockade

- Block sympathetic activity; reducing HR and conduction.

22
Q

Describe class 3 of VW

A
  • Potassium channel blockade (Amio)

- Delays repolarization phase and increases action potential duration and the effective refractory period

23
Q

Describe class 4 of VW

A

Blocks L-type Ca+ channels, calcium channel blockers are most effect at the SA and AV nodes causing reduced HR and conduction.

24
Q

Describe MOA for Amioderone

A

Mainly a class 3 agent but has 1,2,4 class properties.

-Amio primarily blocks potassium channels lengthening the refractory period in all cardiac tissues

25
Q

Name three “Inoconstrictors”

Subset 1

A

Norepinephrine
Epinephrine
Dopamine

26
Q

Name two vasoconstrictors

A

Phenylephrine
Vasopressin (ADH)
subset 2

27
Q

Name three inodilators

A

Dobutamine
Milrinone

subset 3

28
Q

Name 3 Vasodilators

A

Nitroglycerin
Nitroprusside
Nesiritide

Subset 4

29
Q

What are the three stages of anaesthesia

A

Induction
Maintenance
Emergence