Local Anesthesia Flashcards

1
Q

Actions of Local Anesthesia

A
  1. Block nerve conduction of sensory impulses from the periphery of the CNS
  2. Abolish sensation (Motor in high conc.) in a limited area w/o producing unconsciousness
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2
Q

Components of Local Anesthesia

A
  1. Lipophilic group - Aromatic ring
  2. Intermediate chain - Ester or Amide
  3. Ionizable group - Tertiary amine
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3
Q

Duration of action due to intermediate groups

A

Ester have a shorter duration of action

- more prone to hydrolysis than amide links

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4
Q

pK values of Local anesthetics

A

Weak bases w/ pK values around 8-9 = Faster onset

- larger fraction in body is in cationic form

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5
Q

Different form of Local anesthetics

A
  1. Cationic form - Most active at receptor site

2. Uncharged form - Important for penetration of biologic membranes

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6
Q

MOA of Local Anesthetics

A
  • Block voltage-gated Na channels
  • Binds to receptors near the intracellular end of the channel –> Blocks channel
  • Abolish Action potential when enough is applied to nerve fiber
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7
Q

Liposolubility, Potency, Duration of action, pKa & Onset of action

A

Liposolubility correlates w/ Potency & Duration of onset
- Inc liposolubility = Inc Potency, DOA and toxicity

pKa correlated w/ Speed of Onset of action
- Closer pKa to body pH = Faster onset

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8
Q

Prolongation of Action by Vasoconstriction

A

Vasoconstriction –> Dec blood flow –> Dec systemic absorption –> Keep drug @ nerve –> Inc neuronal uptake –> Prolongs action & Dec systemic toxic effects

  • Epinephrine
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9
Q

Prolongation of Action by vasoconstriction in Spinal Anesthesia

A

Epi acts on A2-adrenoceptors –> Inhibits Substance-P release –> Dec pain

vasoconstriction may have AEs:
- Delayed wound healing, tissue edema & necrosis

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10
Q

Vasoconstriction by Cocaine

A

Cocaine constricts Blood vessels by potentiating action of NE; preventing it’s own absorption

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11
Q

Metabolism of Local Anesthetics

A

Ester-linked –> Metabolized by tissue & plasma esterase (pseudo-cholinesterase) –> Shorter DOA

Amide-linked –> Metabolized by Liver microsomal Cytochrome P450 –> Longer DOA

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12
Q

Classification of Local Anesthetics by Duration of action

A

Short- acting

  • Procaine
  • Chloroprocaine

Intermediate- acting

  • Lidocaine
  • Mepivacaine
  • Prilocaine

Long-acting

  • Tetracaine
  • Bupivacaine
  • Etidocaine
  • Ropivacaine
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13
Q

CNS Toxicity of Local Anesthetics

A

CNS stimulation followed by CNS depression
Stimulation – Restlessness, tremor –> Clonic convulsions (high blood levels)

Depression – Resp. failure –>Death

Benzo is used as premedication to provide prophylaxis against seizures

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14
Q

Why is Benzodiazepine used when large doses of Local anesthetics?

A
  • Local anesthetics can cause clonic seizures; Benzos are given as prophylaxis against seizures.
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15
Q

PNS Toxicity of Local Anesthetics

A

Toxic to nerve tissue @ excessively high concentrations

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16
Q

CVS Toxicity of Local Anesthesia

A
  1. Block Na channels –> Dec cardiac pacemaker activity, excitability & conduction
  2. Dec strength of Cardiac contraction –> Arteriolar dilation –> Hypotension

BUPIVACAINE is most cardiotoxic local anesthetic
NOT COCAINE

17
Q

Most Cardiotoxic local anesthesia

A

Bupivacaine

18
Q

CVS effects of Cocaine

A
  • Vasoconstriction
  • HTN
  • Cardiac arrhythmias
19
Q

Blood Toxicity of Local Anesthetics

A

Prilocaine (large doses) –> Accumulation of metabolite o-toluidine (oxidizing agent) –> Converts Hemoglobin to Methemoglobin

20
Q

Allergic reactions of Local anesthetics

A

Ester-linked anesthetics are metabolized to P-aminobenzoic acid derivatives which cause allergic reaction in a small percentage of population

Amine-linked allergies are rare bc they are not metabolized to P-aminobenzoic acid

21
Q

Drug interactions of Local Anesthesia

A

Procaine (hydrolysis) –> Para-aminobenzoic acid (PABA)

PABA inhibits the action of Sulfonamides

22
Q

How to differentiate between Ester & Amide anesthetics by name?

A

Esters have 1 “i”

Amides have 2 “i”