SPECIAL CARE pharmacology of conscious sedation Flashcards

(53 cards)

1
Q

what does the body do to a drug (4)?

A

absorption
distribution
metabolism
excretion

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

explain the pathway of midazolam with IV sedation?

A

rapid rise in plasma levels
drug passes through RHS heart, pulmonary circulation and the LHS heart
goes to the brain via arterial system
effects start once crossed blood brain barrier

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

what is the hand-heart-brain circulation time with IV midazolam?

A

25 seconds

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

what are the 2 ways a pt recovers from sedation?

A

a. redistribution of drug from CNS into body fat
b. uptake and metabolism of the drug by the liver and elimination by kidneys

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

what mechanism is responsible for the initial recovery from sedation?

A

redistrubition

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

what is the alpha half life?

A

the time taken for the serum concentration to drop by 50%
redistribution is responsible for this

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

what is the beta half life?

A

time taken to remove half the drug from the body
elimination of the remaining drug

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

beta half life of midazolam?

A

2 hours

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

what is used to compare the pharmacokinetic effects of sedation agents?

A

elimination half life (beta half life)

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

what does the drug (conscious sedation drugs) do to the body?

A

sedation
analgesia
anxiolysis

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

how are benzodiazepines differentiated?

A

affinity for receptors (potency)
half life
active metabolites

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

describe action potentials and sedation?

A

AP starts when sodium and potassium start moving along concentration gradient

Potassium out and chloride in - drops below 70 = hyperpolarisation = sedation - short acting

Want to extend the hyperpolarisation state during sedation

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

describe benzodiazepines mechanism of action?

A

GABA controlled synaptic flow of chloride ions
activation of benzodiazepine receptors enhances the flow of chloride ions

Chloride ions entering the cell make the resting membrane potential more negative - this makes it hard to fire APs which reduces:
- polysynaptic transmission
- depressing the uptake of sensory information

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

according to AAPD, what are the indications for nitrous oxide?

A

pt who are fearful, anxious, or uncooperative
pt with special health care needs
pt with gag reflexes that interferes with dental care
pt who do not respond adequately to LA
younger pts who must undergo lengthy dental procedures

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

describe the mechanism of action of nitrous oxide?

A

enhance the activity of GABA
biphasic effect: initially enhances neuronal activity, followed by period of inhibition
effects are dose dependant

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

explain the effects of nitrous oxide at low and high doses?

A

low concentration: reduce anxiety and produce a sense of relaxation
high concentration: deeper level of sedation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

how much nitrous oxide is mixed with 02 for the desired level of sedation?

A

20-50%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

contraindications of nitrous oxide?

A

1st trimester pregnancy
history of COPD
vit B12 deficiency
substance abuse hx
history of mental health conditions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

why is diazepam no longer used for IV sedation?

A

causes vein damage: pain, thrombophlebitis, skin ulceration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

diazepam half life?

A

30 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

what is the max dose of midazolam for an adult pt?

A

10mg

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what is the max dose of midazolam for an elderly pt?

23
Q

what must a drug be to reach the brain?

A

lipid soluble

24
Q

elimination half life of midazolam?

25
what are the effects of midazolam
conscious sedation with acute detachment for 20-30 mins post administration a period of relaxation which may last another hour anterograde amnesia - loss of memory muscle relaxant anticonvulsant activity
26
where is midazolam metabolised?
in the liver, some taking place in the bowel
27
what metabolite does midazolam produce which is lipid soluble? and what is its half life?
alpha-hydroxymidazolam 1.2 hours half life
28
what is the titrations measurements of midazolam for an adult?
2-2.5mg 5-10mins before procedure (2mg/min) increase in steps of 1mg if required usual total dose = 3.5-5mg
29
what is the titration measurements for midazolam for an elderly pt?
initially 0.5-1mg 5-10 mins before procedure (2mg/min) increase by 0.5-1mg if required
30
at what time can you discharge a pt after IV midazolam?
2 hours (could be less than) after completion of tx
31
what is the impact of liver dysfunction on midazolam pharmacokinetics during IV infusion for conscious sedation?
decreased metabolism; reduced hepatic clearance of midazolam, prolonging its half life increased plasma levels: with impaired metabolism, there is a high risk of midazolam accumulating in the bloodstream potential for prolonged sedative effects
32
pre-cautions of midazolam?
- no analgesia - for a short time after injection, laryngeal reflexes may be dulled - too rapid injection can cause respiratory depression and apnoea - overdose may produce profound resp depression in pts with impaired respiratory function/ taking depressants i.e., alcohol - possibility of disinhibition (adverse reactions) - once reached end point do not give any more
33
what are the drug drug interactions of benzodiazepines?
opioids - increase risk of resp depression, sedation and hypotension propofol - increase risk of resp depression and hypotension
34
what are the drug drug interactions of nitrous oxide?
opioids - increase risk of resp depression and hypotension
35
what medications may interfere with sedation?
antidepressants antibiotics antifungals anti-seizure blood pressure meds narcotic antagonists
36
what foods interact with benzodiazepines?
grapefruit juice - increases the level of drug in the blood
37
what is the effect of St Johns Wort on benzodiazepines?
plasma concentrations of BZD decreases by half reduce the effect of BZD
38
side effects of BZDs?
resp depression hypotension ataxia and confusion (elderly) depression dizziness drowsiness and fatigue muscle weakness sleep disorder vision disorder tremor withdrawal syndrome
39
side effects of midazolam?
vomiting (very common) skin reactions
40
why is it mandatory for someone else to be in the room with dentist and pt during IV sedation?
sexual hallucinations
41
contraindications of BZDs?
allergy/ hypersensitivity severe resp depression / obstructive sleep apnoea glaucoma pregnancy/ breastfeeding concurrent use of alcohol/ CNS depressants
42
pre cautions for all BZDs?
avoid prolonged use and abrupt withdrawal elderly Hx of alcohol dependance/ abuse Hx of drug depednance and abuse personality disorder resp disease
43
pre cautions for midazolam?
cardiac disease debilitated pt (in children) - reduce dose
44
why is there a risk of potentially fatal resp depression when BZDs are used along side an opioid?
produce additive CNS depressant effects increasing risk of sedation, resp depression, coma and death
45
what does MHRA/CHM advise in regards to BZDs and sedation?
1. BZD and opioid interaction 2. BZDs should only be administered by experiences person with training in anaesthesia and airway management 3. for conscious sedation always 1mg/ml preparation 4. flumazenil must be available
46
what are the risks of taking BZDs when pregnant?
risk of neonatal withdrawal symptom high dose during late pregnancy/ labour = neonatal hypothermia, hypotonia, resp depression
47
can you give BZDs to pts with hepatic/ renal impairment?
mild to moderate hepatic impairment - advised caution severe hepatic impairment - avoid renal impairment - caution
48
what is the first choice of IV sedation for dentists?
Midazolam as a single drug
49
why should IV agents be used with great caution in the elderly?
altered drug distribution due to: - decreased total body fat water - increased body fat - decreased serum albumin - altered hepatic metabolism - altered renal excretion
50
why should IV agents be used with great caution in the young?
unpredictable and disinhibition
51
what is flumazenil?
a BZD antagonist
52
what are the effects of Flumazenil?
reverses the sedative, cardiovascular and resp depressant effects of midazolam
53
half life of flumazenil?
50 mins half life