Local Anesthetics - dosages Flashcards
List max doses of LAs
Bupivacaine, cocaine, tetracaine, ropivacaine, etidocaine, lidocaine, mepivacaine, choroprocaine
Bupivacaine 2.5 mg/kg
Cocaine 3 mg/kg
Tetracaine 3 mg/kg
Ropivacaine 3 mg/kg (3.5 w epi)
Etidocaine 4 mg/kg
Lidocaine 4 mg/kg (7 w epi)
Mepivacaine 4 mg/kg (7 w epi)
Chloroprocaine 12 mg/kg
when do you redose lidocaine (epidural)?
lidocaine lasts about 1.5-2 hours etc
Chloroprocaine Max Dose
12 mg/kg
Lidocaine Max Dose
4 mg/kg
7 mg/kg with epi
Mepivacaine Max Dose
4 mg/kg
7 mg/kg with epi
Bupivacaine Max Dose
2.5 mg/kg
Ropivacaine Max Dose
3 mg/kg
3.5 mg/kg with epi
Etidocaine Max Dose
4 mg/kg
Cocaine Max Dose
3 mg/kg
Tetracaine Max Dose
3 mg/kg
Mepivacaine duration after infiltration
1.5 - 3 hr
Bupivacaine/Levobupivacaine/Ropivicaine
duration after infiltration
4-8 hrs
Ropivacaine duration after infiltration
4-8 hrs
Prilocaine duration after infiltration
1 -2 hrs
Chloroprocaine duration after infiltration
30 - 60 minutes
Procaine duration after infiltration
45 - 60 minutes
Arrange LAs in the order of non-ionization %
- cocaine
- lidocaine
- mepivacaine
- chloroprocaine
- prilocaine
- ropivacaine
- tetracaine
- procaine
- bupivicaine
- levobupivicaine
- Etidocaine
- Chloroprocaine 2%
- Procaine 3%
- Tetracaine and Cocaine 7%
- Bupivacaine / Levobupivacaine / Ropivacaine 17%
- Lidocaine/Prilocaine 24%
- Etidocaine 33%
- Mepivacaine 39%
LAs used topically
- Tetracaine- spinal corneal and topical
- Lidocaine - patches, creams, gel
- Cocaine - for ENT surgeries
LAs that can be given IV
Lidocaine
Prilocaine
LAs that cannot be given in a peripheral block
Tetracaine- high toxicity risk, profound mortor block- used in spinal, corneal anesthesia and topicallu
LAs that cannot be give epidurally
- Procaine - no longer used, was used for infiltration
- Tetracaine - high toxicity - spinal, corneal and topical
LAs that are still questionable for a spinal block
Chloroprocaine
Lidocaine
Mepivacaine
Prilocaine
LAs with pKa in the ≈7s
- Mepivacaine = 7.6
- Etidocaine = 7.7
- Lidocaine/Prilocaine = 7.9
LAs with pKa in the ≈ 8s
- Bupivacaine/Levobupivacaine/Ropivacaine = 8.1
- Cocaine/Tetracaine = 8.5
- Chloroprocaine = 8.7
- Procaine = 8.9
Its metabolite interferes with efficacy of sulfonamide antibiotics
Procaine
Lidocaine solution concentrations
- topical
- regional IV
- PNB
- Spinal
- Epidural
- topical: 4%
- regional IV: 0.25-0.5%
- PNB: 1-2 %
- Spinal: 1.5 - 5%
- Epidural:3 1.5 - 2%
LA not effective topically
Mepivacaine
which has more CNS toxicity poptential
lidocaine or mepivacaine
mepivacaine
LA great for differential nerve block (sensory>motor)
great for OB
Bupivacaine
most cardiotoxic LA
Bupivacaine
Bupivicaine E½t
3.5 hrs
Bupivicaine solution concentration
- Spinal
- Epidural
- Peripheral Nerve Block
- Spinal: 0.5 - 0.75%
- Epidural: 0.0625 - 0.5%
- Peripheral nerve block: 0.25 - 0.5%
Bupivicaine/Levobupivicaine/Ropivicaine max spinal dose
15-20 mg
Lidocaine max spinal dose
30-100 mg
Bupivacaine DOA after spinal
1.5 to 3.5 hr
Bupivacaine onset and DOA w/ epidural
onset 15-20 min
DOA 3 - 6 hrs
Lidocaine onset and DOA w/ epidural
onset 5-15 min
DOA 1.5-2 hours
Mepivacaine onset and DOA w/ epidural
onset 2-15 min
DOA 1 - 3 hrs
Shortest DOA for epidural
Chloroprocaine
Chloroprocaine onset and DOA w/ epidural
onset 5-15 min
DOA 30-90 min
Prilocaine max spinal dose
100-200 mg
Mepivacaine max spinal dose
40-80 mg
Tetracaine max spinal dose
5-20 mg
Ropivacaine max spinal dose
15-20
Long DOA for an ester
Tetracaine
1.5 - 3.5hrs
pt cannot have epi
what LA is best alternative
Mepivacaine
it doesn’t vasodilate like lidocaine so can be used when avoiding epi
Which LAs have slow, moderate, and fast onsets?
Slow Onset: procaine, tetracaine (esters)
Intermediate Onset: bupivacaine
Fast Onset: chloroprocaine, lidocaine, etidocaine, mepivacaine
Lidocaine uses?
- Regional/ neuraxial block
- Cough suppression
- Attenuate ICP/BP raise during laryngoscopy
- Attenuate reflex bronchospasm that may occur with airway instrumentation
- Suppress ventricular dysrhythmias
How is cocaine metabolized?
Liver, plasma esterases, and about 10-12% eliminated by kidney
careful with renal disease
NOT PAVA like the other esters
What is chloroprocaine used for?
OB epidurals
it has an ultra rapid serum hydrolysis (metabolism) which reduces toxicity risk to mom and baby
Does lidocaine have an active metabolite?
YES.
2 Monoethylglycinexylidide (80% activity)
(Mono-ethyl-glycine-xylidide)
xylidide (10% activity)
metabolism of prilocaine.
Rapid metabolism
TOXIC metabolite ortho-toluidine
Must be avoided in OB due to metabolite
Big doses will convert hgb to methemoglobin (treated with methylene blue)
What is the dose of Lidocaine for epidural placement?
It depends on the level of blockade required and the density of blockade required. If you want profound motor blockade at T4 for example and the epidural is placed at the L2-3 interspace that is about 10 segments. Say this person is average size – I would give 1.5ml per segments I wanted blocked – so I would give 15cc of 2% lidocaine. 15cc X 20mg/cc = 300mg of lidocaine. I would need to make sure that this amount did not exceed the maximum dose allowed which is 5mg/kg for plain lidocaine. If the patient was 70kg that is 350mg – so 15cc is O.K. If I wanted to give more I might add epi which would increase my maximum dose to 7mg/kg or 490mg.
LAs that come in racemic mixtures
Bupivacaine
Mepivacaine
LAs that come as pure enantiometrs
Ropivacaine
Levobupivacaine
*advantage = less toxic, easier to resuscitate in case of toxicity
what LAs are highly lipid soluble
Bupivicaine
Etidocaine
Tetracaine
BET
what LAs have significant 1st pass effect by the lungs
Bupivicaine
Lidoicaine
Prilocaine
Why is lidocaine avoided in spinals?
Linked to caudal equina syndrome
Epidural ok to use
Bupivacaine pros and cons?
Pro
highly protein bound
- low incidence of neuro complications with spinal
- longer DOA (good for post-op pain and labor)
Also, A alpha, beta, and gamma fibers are not completely blocked, so sensory is blocked and motor is not completely blocked.
Con
TOXICITY! very cardio toxic; pressure is still felt, that can freak people out
Cocaine toxicity sxs
cocaine ↓ reuptake of NE → leads to ↑ concentrations of NE
- restlessness, tremors, seizures & euphoria
- tachycardia/MI
LA toxicity s/s?
CNS
circumoral numbness, tinnitus, vision changes, dizzy, slurred speech, restless, muscle twitching (especially in the face), seizures (which cause CNS depression, apnea, hypotension)
CV
hypotension, myocardial depression, AV block
Note: bupivacaine is most CV toxic
S (or levo) enantiomer of bupivacaine
Ropivacaine
less cardio-toxic