LAs Flashcards

(44 cards)

1
Q

max dose: cocaine

A

3 mg /kg

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2
Q

anomalies with cocaine:

A

Heavily liver metabolized
Excreted unchanged by kidneys at higher percentage
Overall longer metabolism than most esters

Vasoconstriction! Unique among LAs

Causes SE of euphoria and increased SNS outflow

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3
Q

max dose: procaine

A

7 mg / kg

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4
Q

Special notes on procaine:

A

Increased incidence of CNS effects
increased PO-Nausea
Metabolites interfere with sulfa abx

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5
Q

max dose: Tetracaine

A

3 mg /kg

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6
Q

Special notes Tetracaine:

A

primarily used in spinal / corneal anesthesia

Very long DOA for ester r/t increased protein binding

Higher risk for TNS

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7
Q

max dose: chloroprocaine

A

12 mg/kg

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8
Q

onset of chloroprocaine:

pKa

A

onset: fast
pKa = 8.7

given at higher concentrations 2-3%

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9
Q

Notes on chloroprocaine:

A

great for OB anesthesia r/t minimal protein binding = rapid metabolism

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10
Q

Max dose: Mepivicane

A

max dose: 4mg/kg or with epi 7mg/kg

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11
Q

notes on Mepivicaine:

A

less vasodilatory than Lido but similar drug

more CNS effects than lido

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12
Q

Max dose: etidocaine

A

4 mg/kg

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13
Q

Max dose: lidocaine

A

4 mg/kg or with epi 7 mg/kg

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14
Q

Notes on lidocaine:

A

spinal use associated with CE

2 active metabolites !

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15
Q

Max dose: Prilocaine

A

600 mg

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16
Q

Notes on prilocaine:

A

toxic metabolite: ortho-tuolidine -> r/f metheglobinemia

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17
Q

Max dose: Bupivicaine

A

2.5 mg/kg

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18
Q

spinal dose: Bupivicaine

19
Q

Notes on bupivicaine:

A

low incidence of CNS effects

VERY CARDIOTOXIC

great at differential blocks

Long duration (95%) protein bound

20
Q

Max Dose: Levobupivicaine

A

Max dose: 2mg/kg

21
Q

Spinal dose: Levobupivicaine:

22
Q

Notes levobupivicaine

A

S enantiomer of bupivicane

less of a half life

less cardiotoxic

23
Q

Max dose: Ropivicaine

A

3 mg/kg, 3.5 mg/kg* with epi

24
Q

spinal dose: ROPIVICAINE

25
Notes on ropivicaine
s enantiomer of bupivicane homolog. less cardio toxic. more vasoconstriction 2 active metabolites *shortest half life of levo/bu/ro
26
mepivicaine has a longer DOA than lido because
it has less vasodilatory effects .
27
mepivicaine is structurally similar to
bupivicane
28
mepivicaine is clinically similar to
lidocaine
29
Spinal concentration, dose, volume, duration for lidocaine,
1.5% or 5% 30-100mg 1-2mL 30-90 min
30
spinal concentration, dose, volume, duration for mepivacaine
4% 40-80 mg 1-2 mL 30-90 min
31
spinal concentration, dose, volume, duration for tetracaine
0.25 - 1 % 5 - 20 mg 1 - 4 mL 90 - 200 min
32
spinal concentration, dose, volume, duration, for bupivacaine
0.5% 15-20 mg 3-4 mL 90-200 min
33
spinal concentration, dose, volume, duration, for ropivacaine
0.75% 15-20 mg 2-3 mL 90-200 min
34
spinal concentration, dose, volume, duration for levobupivacaine
0.75% 15-20 mg 2-3 mL 90-200 min
35
LAs: with active metabolites:
ropivicane (2) lidocaine (2) prilocaine (1)
36
higher concentration =
faster onset b/c more molecules
37
systemic effects are more likely with
amides
38
seizures in CNS toxicity are followed by
CNS depression | possibly hypotension, apnea
39
population at increased risk of CV collapse with bupivocaine
pregnancy hypoxia pH abnormalties CV modulating drugs [propofol, volatile agents]
40
lipid for bupivacaine
intralipid 20% 1.5 mL/lg rapid bolus immediately. follow with infusion 0.25 ml/kg/min x 10 minutes
41
drugs implicated in CE
lidocaine 5%, tetracaine, chloroprocaine (preservative?)
42
factors that increase the risk of CNS toxicity
hypercarbia (increases CBF) hyperkalemia (increases resting membrane potential) metabolic acidosis (decreases convulsions threshold and favors ion trapping in the brain)
43
difficulty of CPR with OD
bupivacaine > levobupivacaine > ropivacaine > lidocaine
44
site of injection and blood flow:
IV > tracheal > intrapleural > intercostal > caudal > epidural > brachial plexus > femoral > sciatic > SubQ