IV Induction Agents Flashcards

1
Q

WHAT IS AN INDUCTION AGENT?

A

Produces loss of consciousness within one arm-brain time–> approximately 30 seconds
Induction agents induces anaesthesia

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2
Q

List 4 rapidly acting, true IV induction agents

A

Thiopentone
Etomidate
Propofol
Ketamine

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3
Q

List 3 slower acting IV induction agents

A

Benzodiazepines
Neuroleptic-anaesthetics
Opioids

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4
Q

What are the benefits of IV agents?

A

Rapid onset of action
More pleasant & acceptable for the patient
Pollution free
Low incidence of side-effects
Smooth induction with rapid transfer through the classic stages of anaesthesia

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5
Q

What are the disadvantages of IV agents

A

Requires intravenous access
It is easy to give too much …. side-effects
No removal of drug via the lungs as with inhalationals
-Recovery requires
*Redistribution
*Metabolism
*Excretion
Sudden loss of normal protective reflexes

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6
Q

Explain the mechanism of action for IV agents.

A

Most sedative hypnotics exert their effect via the inhibitory GABAA receptors
GABA – γ (gamma)-aminobutyric acid
Increased chloride conductance → hyperpolarisation → neuronal inhibition
Some inhibit the release of glutamate, an excitatory amino acid, in brain

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7
Q

Explain the pharmacokinetics of intravenous anaesthetics

A

The onset of action depends on the drug reaching the effect site (the brain) by crossing the Blood-Brain Barrier
Arm-brain circulation time is determined by:
Speed of injection
Lipid solubility
Protein binding
Blood flow to brain

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8
Q

List the characteristics of the ideal IV induction agent

A
Smooth and rapid onset of action 
Inexpensive 
Rapid recovery 
Minimal side effects 
No pain on injection
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9
Q

How would one reduce pain on injection?

A

IV lignocaine 10-20mg when giving propofol

New, large bore free running IV line

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10
Q

What are the international colour codings for all true IV induction agents and IV sedatives.

A

Yellow for true IV induction agents

Orange for IV sedatives

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11
Q

What are the physical properties of propofol?

A

It is hydrophobic 1%. Also known as 2,6 di-isoprophylphenol.
Most commonly used IV induction agent

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12
Q

Pharmacodynamics of Propofol

A

Can be infused for long periods with rapid emergence. Sequesters in fat

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13
Q

Effects of Propofol on the CNS

A

Rapid loss of consciousness and rapid recovery (3-6 min. Complete in 3 hours)
Less hangover.
No antanalgesia, no analgesic
Antipruritic

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14
Q

Effects of propofol on the CVS

A

Cardiovascular depression. Less compensatory tachycardia = greater hypotensive effect

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15
Q

Effects of propofol on the respiratory system

A

Respiratory depression with 100% incidence of apnoea, depresses laryngeal reflexes. Does not release histamine.

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16
Q

Indications for propofol

A
Porphyria
Asthma
Day-case
Conscious sedation 
Hx of malignant Hyperthemia
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17
Q

Contraindications for propofol

A

Avoid in elderly, heart failure, hypovolaemia, fixed cardiac output

18
Q

Physical properties of thiopentone

A

Barbiturate, precipitates when mixed with muscle relaxants. 2.5%

19
Q

Pharmacodynamics of thiopentone

A

Long elimination half-life – induction only
3-5mg/kg in adults

Children: 5-6mg/kg

Caution in elderly

20
Q

CNS effects of thiopentone

A
Rapid LOC (30 seconds)  Recovery 5-10 min. antanalgesia. Anticonvulsant
Possible protection with decreased cerebral metabolic rate and intracranial pressure
21
Q

CVS effects of thiopentone

A

Decreases cardiac output – peripheral vasodilation, negative inotropic effect, decrease in central catecholamine release. Compensatory tachycardia. CVS depression exaggerated in heart failure, hypovolaemia, fixed cardiac output

22
Q

Resp effects of thiopentone

A

Potent depressant. Laryngeal reflexes not depressed until deeply anaesthetised. Histamine release and active respiratory reflexes = avoid in asthmatics

23
Q

Oher effects of thiopentone

A

Irritant to tissues – venous thrombosis. Intra-arterial injection = precipitation

24
Q

Indications for thiopentone

A

Golden standard

25
Contraindications for thiopentone
Porphyria, known allergy, CVS disorders, asthma
26
Etomidate- Physical properties
2mg/ml – mix to 1 mg/ml
27
Pharmacodynamics of etomidate
Repeated doses not cumulative. Not used as infusion because of adrenal cortical depression Induction: 0.2-0.3mg/kg
28
Etomidate- CNS effects
Rapid onset. Rapid recovery 6-8 min. high incidence of involuntary movements and myoclonus – reduced by opiates and midazolam
29
Etomidate- CVS effects
Very stable, may cause bradycardia when mixed with opioids and sux.
30
Etomidate- Resp effects
Very little respiratory depression No release of histamine.
31
Etomidate- Metabolic effects
Inhibits cortisol and aldosterone synthesis
32
Etomidate- Pain on injection? Yes/no?
Yes
33
Etomidate- Indications
Cardiac Patient s
34
Ketamine- Physical properties
10mg.ml and 100 mg/ml. acidic. IV, intramuscular and oral. Derived from phencyclidine
35
Ketamine- Pharmacodynamics
50-60% of drug remains after recovery – protracted emergency Induction: 1-2 mg/kg onset 30-60 sec. lasts 5-15 min Maintenance – 0.5mg/kg boluses, 1-4mg/kg/hr infusion. Analgesia 0.2-0.4mg/kg IM followed by 0.2-0.3 mg/kg/hr infusion.
36
Ketamine- CNS effects
Dissociative anaesthetic – complete analgesia and amnesia. Involuntary movements, nystagmus, vocalisation. Psychic reactions – hallucinations. Place in darkened area. Tolerance.
37
Ketamine- CVS effects
Raise in BP, pulse, peripheral resistance, CO. Dysrrhythmias due to stimulation of central catecholamine release. Myocardial depressant.
38
Ketamine- Resp Effects
Minimal respiratory depression. Pharyngeal reflexes are preserved with good airway control. Bronchodilation. Increase in secretions – administer with antisialogogue
39
Ketamine- GIT effects
Post operative N&V
40
Ketamine- other effects
Uterine contraction in first trimester
41
Ketamine- indications
Poor risk surgical patients, paediatric surgery, debridement, painful dressings or skin grafts, short procedures, analgesia, field-work, status asthmaticus
42
Ketamine Contraindications
Aspiration risk. Shock, hypertension, IHD, aortic aneurysms, severe heart failure, raised ICP, cerebral aneurysms, open eye injuries, increased intraocular pressure, psychiatric patients, epileptics, thyrotoxicosis. Early pregnancy