Lecture 18 & 19: Locoregional Anesthesia (Exam 3) Flashcards
(65 cards)
Why should I use a local block
- General ax prevent the perception of pain but it doesn’t stop the transduction, transmission, & modulation of pain
- LA block the initiation & conduction of action potentials in nerve fibers
T/F: LA should always be considered as part of a multi-modal analgesic plan
True
Describe the admin of LA
- Can be pr, intra, or post op
- Administering prior to sx will decrease the stress response
- Often allows sx to be performed in a px w/o the use of general x (more used in Large animals)
- Reduces the amount of induction & maintenance drugs req if given before surgical stimulation
- When given prior to surgical stimulation it can reduce the potential for dev of “wind up” pain
What is the MOA of LA
- Analgesia is a direct result of the NA ion channel being blocked & the membrane being stabilized
- Blockade occurs from inside the nerve cell
- Nerve cell depolarization is prevented which block the conduction of nerve impulses
What happens to the px when given LA
- Has a dose dep loss of sensory, motor, & autonomic fxn
- This effect is transient as the local ax is metabolized or hydrolyzed
What do LA do to small diameter (C & Ag) nerve fibers
- Blocks preferentially prior to large myelinated fibers
- Loss of sensation occurs w/ varying degrees of loss of motor fxn
- C > Ag > Ay / Ab / Aa
What is the order that sensation disappears
- Pain
- Cold
- Warmth
- Touch
- Joint
- Deep pressure
How does the lipid solubility of an LA changes its effects
- High lipid soluble = more potent effects
- Increased solubility = increased duration of effect
- Speed of onset of the LA is inversely proportional to the drugs lipid solubility & pKa
How does the protein binding ability of an LA changes its effects
More highly protein bound LAs have a longer duration of action
T/F: Decreasing the concentration of LA in a given area will increase the duration of analgesia
False; increasing the concentration
How does the systemic absorption of an LA changes its effects
- As systemic absorption increases (like due to vasodilation) the duration of the effect decreases
- Lidocaine causes vasodilation so it has a shorter duration of action
List some ester local ax
- Procaine
- Tetracaine
- Benzocaine
List some amide local ax
- Lidocaine
- Mepivacaine
- Bupivacaine
- Ropivacaine
- Lidocaine + prilocaine
Describe lidocaine
- Commonly used LA w/ a fast onset time (low pKa of 7.9)
- Short duration of action b/c of low protein binding & ability to cause vasodilation
- Min damage or irritation to tissue
- Safe to give IV @ clinical doses
- Effects when given IV: ax sparing, augments analgesia, antiarrhythmic, GI promotility, anti inflammatory, & antishock
What is pKa (dissociation constant)
The pH @ which 50% of an acid or base is in the ionized state
What is the pKa of most LAs
They are mostly bases w/ a pKa btw/ 8 & 9 so they are mostly ionized @ a pH of 7.4
What happens to LAs in an acidic environment? What about alkaline?
- Acidic: The drug shifts to the ionized
- Alkaline: Drug shifts to an unionized form
Describe Mepivacaine
- Commonly used LA in equine for diagnostic nerve blocks in lameness exams
- Faster onset time compared to lidocaine (pKa of 7.6)
- Highly protein bound so longer duration of action than lidocaine
- Less irritation or tissue damage
- Absence of vasodilator effects so no need to use w/ epinephrine
Describe Bupivacaine
- Longer time to onset compared to lidocaine b/c of high pKa (8.1) & increased lipid solubility
- Longer duration of action b/c of high protein binding
- Margin of safety is the lowest compared to lidocaine, mepivacaine, & ropivacaine
- Greater concern for system cardiotoxicity so it should never be given IM
Describe bupivacaine liposome injectable suspension
- Nocita provides extended release of bupivacaine for up to 72 hours
- FDA approved in 2016 to control pain in dogs having cranial cruciate ligament sx
- Use a moving needle infiltration tech being sure to inject in all layers of tissue
Describe ropivacaine
- Similar chemical properties as bupivacaine (is the pure s-(-) enantoiomer)
- Less CV & CNS toxicity than bupivacaine
- Concentration dep onset time (low -> similar to bupivacaine & high -> similar onset to mepivacaine)
- Similar duration of action to bupivacaine
- More expensive the bupivacaine
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What happens if you combine local anesthetics
- Results can be unpredictable & duration of action shorter
- Need to pay attention to toxic Dosages
- Don’t do it
What can be additives to LAs
- Opioids
- Alpha 2 agonists
- Ketamine