Local Anesthetics Flashcards

1
Q

Name the esters (3)

A

Procaine
Chloroprocaine
Tetracaine

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2
Q

Name the amides (4)

A

Lidocaine
Mepivacaine
Ropivacaine
Bupivacaine

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3
Q

Procaine pka, ionized, protein binding, onset, DOA

A
8.9
97
6
Slow
60-90m
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4
Q

Chloroprocaine pka, onset, DOA

A

8.5
Fast
30 - 60m

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5
Q

Tetracaine pka, ionized, protein binding, onset, DOA

A
8.5
93
94
slow
180 - 600
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6
Q

Lidocaine pka, ionized, protein binding, onset, DOA

A
7.9
76
64
Fast
90 - 120
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7
Q

Mepivacaine onset, DOA

A

fast

120 - 240m

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8
Q

Ropivacaine onset, DOA

A

slow

180 - 600m

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9
Q

Bupivacaine pka, ionized, protein binding, onset, DOA

A
8.1
83
95
slow
180 - 600
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10
Q

Caudal epidural dosing

A

2 mL/segment

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11
Q

Lumbar epidural dosing

A

1 mL/segment

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12
Q

Thoracic epidural dosing

A

0.7 mL/segment

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13
Q

Epidural Epinephrine

A

alpha 1 agonist
1: 200,000 (5 mcg/mL)
prolong effect

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14
Q

Epidural Clonidine

A

selective alpha 2 agonist - potential direct action on nerves

synergism w/lidocaine or bupivacaine for labor analgesia

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15
Q

Opioids

A

must be preservative free

fentanyl or morphine!

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16
Q

Epidural Fentanyl

A

high lipid solubility
Dose: 50 - 100 mcg
Onset: 3 -5m
DOA: 1 -2h

17
Q

Epidural morphine

A

HIGHLY POLARIZED
Dose: 2 - 4 mg
Onset: 10 - 15m
DOA: 8 - 10h

18
Q

Morphine ADR

A

itching & urinary retention

19
Q

Epinephrine spinal

A

alpha 1 agonist
o 0.1 – 0.2 mL of 1: 1000 solution
o Greatest effect with tetracaine

20
Q

Phenylephrine spinal

A

alpha adrenergic agonist, slightly more effective than epi
o 0.05 – 0.2 mL of 1% (0.5 – 2 mg) added to LA
o Greatest effect with tetracaine

21
Q

Clonidine spinal

A

(NOT A VASOCONSTRICTOR)
o Used when epinephrine is c/i
o Synergism w/lidocaine & bupivacaine
o Central action helps with tourniquet pain

22
Q

Fentanyl spinal

A
high lipid solubility, binds directly to lipid elements of spinal cord. Less drug available to diffuse systemically
	Profound analgesia
	Dose: 12.5 – 25 mcg w/LA
	Onset: 5 – 10m
	DOA: 2 – 4h
23
Q

Morphine spinal

A

highly polarized, not lipid soluble. Drifts freely into CSF. 6 – 8 hours it will rise to respiratory center.
 Profound analgesia
 Dose: 0.1 – 0.25 mg mixed w/LA
 Onset: 60 – 90m
 DOA: 24h
 ADR: itching, urinary retention, delayed respiratory depression

24
Q

lidocaine max dosing

A

4/7 mg/kg

25
Q

mepivacain max dosing

A

4/7 mg/kg

26
Q

bupivacaine max dosing

A

3 mg/kg

27
Q

ropivacaine max dosing

A

3 mg/kg

28
Q

procaine

A

12 mg/kg

29
Q

chloroprocaine

A

11 / 14 mg/kg

30
Q

prilocaine

A

7/ 8.5 mg/kg

31
Q

tetracaine

A

3 mg/kg