Chapter 115-116: Local anesthetics- Flashcards

1
Q

What is the structure of a local anesthetic?

A

Aromatic lipophilic end connected to hydrophilic tertiary amine VIA AN INTERMEDIATE CHAIN that is either an ester or amide

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2
Q

Compare the differences between the ionized form and the nonionized form of a local anesthetic in terms of how each works to cause the desired effect of local anesthetics

A

The nonionized form will cross the lipid membrane. Because the intracellular pH is closer to 7, once the local anesthetic agent crosses the cell membrane it will become the ionized form. It is the ionized form that is able to bind with the alpha subunit of the na channel to inactive it.

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3
Q

Which properties of a local anesthetic will cause the onset time to be fast?

A

1) more lipophilic drugs have faster onset because they cross the cell membrane more readily.
2) Compounds have have pKA closer to physiologic pH will also have quicker onset.

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4
Q

How are ester local anesthetics metabolized?

A

pseudocholinesterases and partially be red blood cell esterases

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5
Q

How are amide local anesthetics metabolized?

A

hepatic pathway

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6
Q

What characteristic of local anesthetics are responsible for potency?

A

lipid solubility- the more soluble an agent is, the more readily it crosses into the axon

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7
Q

Which class of local anesthetic are there more allergic reactions?

A

The ester class because pseudocholinesterase causes hydrolysis to occcr and yields para-amiobenzoic acic (PABA)

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8
Q

How do the following ester local anesthetics compare in terms of duration? Tetracaine, procaine, chloroprocaine

A

Chloroprocaine is hydrolyzed 4x faster than procaine

Procaine is hydrolyzed 4x faster than tetracaine

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9
Q

How are amide local anesthetics metabolized?

A

Through the liver via 1) aromatic hydroxylation 2) N-dealkylation and 3) amide hydrolysis

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10
Q

Which amide local anesthetic has metabolism outside of the liver?

A

Prilocaine is metabolized by extrahepatic tissues

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11
Q

Which local anesthetics have had problems with methemoglobinemia? What is the treatment?

A

Benzocaine (because it insoluble in water, limited to topical use).
Prilocaine (used in EMLA)- metabolized to o-toluidine

Treatment is methylene blue- 1mg/kg.

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12
Q

Which locations are most worrisome for local anesthetic absorption?

A

Intravenous> Intercostal > Caudal > Lumbar epidural > brachial plexus > subcutaneous

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13
Q

What is the max dose and duration of effect of chloroprocaine?

A

12 mg/kg, up to 1 hour

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14
Q

What is the max dose and duration of effect of procaine?

A

12 mg/kg, up to 1 hour

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15
Q

What is the max dose and duration of effect of cocaine?

A

3 mg/kg, up to 1 hour

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16
Q

What is the max dose and duration of effect of tetracaine?

A

3 mg/kg up to 6 hour

17
Q

What is the max dose and duration of effect of lidocaine?

A

4.5 mg/kg without epi, 7 mg/kg with epi, 1.5 hours

18
Q

What is the max dose and duration of effect of prilocaine?

A

8 mg/kg, 1 hour

19
Q

What is the max dose and duration of effect of mepivicaine?

A

4.5 mg/kg without epi, 7 mg/kg with epi, 2 hours

20
Q

What is the max dose and duration of effect of bupivacaine?

A

3 mg/kg, 8 hours

21
Q

What is the max dose and duration of effect of ropivacaine?

A

3 mg/kg, 8 hours

22
Q

What is the cardiovasular effects of all local anesthetics?

A

decreased myocardial contractility and vasodilate (all except cocaine which causes vasoconstriction by acting as norephinepherine reuptake inhibitor)

23
Q

What is the dose of lipids that should be given for LA toxicity?

A

20% lipid infusion should be dose 1.5-4 mL/kg bolus then 0.5mL/kg infusion.

24
Q

Which LA have been implicated in cauda equina syndrome?

A

Chloroprocaine and lidocaine, especially with the intrathecal microcatheters

25
Q

What is transient neurologic symptoms, what are the associated factors and which drugs are implicated in this?

A

severe pan radiating down both legs
factors: lithotomy position, early ambulation, obesity
LA: lidocaine

26
Q

What does the American Academy of Dermatology set as the max safe dose of lidocaine for liposuction? When is toxicity likely to occur?

A

55 mg/kg

Because absorption of lidocaine is delayed in the fatty tissue, most toxicity reactions occur 6-12 hours after the procedure.

27
Q

What are the 3 most common LA preservatives, what is their function and what are the possible toxic reactions associated with them?

A

Sulfite- antioxidant- arachnoiditis and anaphylactoid reaction

EDTA- chelating agent, low back pain at site of injection 2/2 to lumbar paraspinal muscle spasm

Parabens- antimicrobial- chemical structure similiar to PABA, may get anaphylactoid reaction