LOCAL ANAESTHETIC Flashcards

1
Q

for maxillary anaesthesia, what nerve are we achieving to block?

A

the trigeminal nerve trunk which then branches off to the posterior superior alveolar nerve, the middle superior alveolar nerve, the anterior superior alveolar nerve and then another small branch known as the infra orbital nerve

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2
Q

what teeth would we PALATALLY INFILTRATE due to the unique/difficult anatomy of the teeth

A

the UPPER 6’S due to the zygomatic arch and divergent roots
the UPPER 2’S due to the apex of the root lying palatally - APEX IS WHERE WE AIM FOR WHEN INJECTING LOCAL!!!!

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3
Q

what type of anaesthetic would we normally use when doing an infiltration (maxillary anaesthesia)

A

lidocaine (normally) - GOLD STANDARD

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4
Q

what, of the anatomy of the mandible, makes it difficult for anaesthetic to diffuse through

A

the thick outer cortical bone

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5
Q

what type of anaesthetic would we normally use for mandibular anaesthesia

A

articaine

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6
Q

for LA, what nerve are we anaesthetising

A

the TRIGEMINAL NERVE - MAXILLARY AND MANDIBULAR DIVISON!

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7
Q

PALATALLY, what are the nerves for anaesthesia

A

nasopalatine (incisive branch coming off of the nasopalatine nerve!), greater, lesser!

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8
Q

advantages of infiltrating rather than block

A

lower risk of intravascular administration, local haemostasis (wound healing/clot?), its local diffusion - accuracy is better as a smaller region to anaesthetise, it acts on nerve ENDINGS rather than the trigeminal trunk

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9
Q

advantages of ID BLOCK rather than infiltration

A

acts on nerve trunk, widespread effect from one single injection rather than many, can deposit away from infected areas?

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10
Q

what is aspiration?

A

it is a technique used to reduce the risk of intravascular injections.
if there is blood - then likely to be in a vessel, if no blood - then less likely to be in a vessel

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11
Q

what nerve(s) is involved in mandibular anaesthesia

A

the main nerve is the IAN (inferior alveolar nerve). branches off of this are the lingual, buccal, mental and incisive nerve.

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12
Q

explain the procedure for carrying out an IDB

A

patient should be supine (think vasovagal), place the thumb on coronoid notch of ascending ramus of mandible, inject lateral to the pterygomandibular raphe (soft tissue triangle sort of), leave 1cm out - 2-2.5cm in.

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13
Q

what is the KEY sign that the IDB has worked

A

a numb LOWER LIP!!!!!! (ipsilateral - whatever side you do your block on)

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14
Q

can we carry out bilateral blocks

A

NO! either infiltrations OR 1 block and 1 infiltration

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15
Q

what division of the trigeminal nerve are we blocking when carrying out a BLOCK (IDB)

A

the mandibular division

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16
Q

what are the nerves involved for mucosal innervation for mandibular LA

A

lingual nerve, long buccal and mental

17
Q

what is the minimum amount of LA we can inject when doing an IDB

A

half a cartilage - 1.5-2.2ml

18
Q

for the MANDIBULAR incisors, would we do a block?

A

NO - this is because there it crossover so luckily there is actually thinner bone here therefore we can carry out an infiltration quite nicely to anaesthetise that area.

19
Q

what makes up an LA cartilage

A

2.2ml
anaesthetic agent
vasoconstrictor
preservative for shelf life
isotonic carrier

20
Q

describe the structure of LA

A

has a lipophillic end and a hydrophillic end with an intermediate chain in the middle - there are two types of intermediate chains it can either be an ester or an amide

21
Q

name the types of LA under the ester group

A

procaine, benzocaine (topical)

22
Q

name the types of LA under the amide group

A

lidocaine, prilocaine, mepivicaine, bupivicaine, articaine

23
Q

describe how LA works

A

it works by REVERSIBLY blocking LA channels (no depolarisation or action potential)

24
Q

describe the specific receptor theory

A

LA binds to Na channels and inactivates the Na channels. Must be able to pass through lipid membrane, must be able to bind to Na channels (hydrophillic)

25
Q

what 2 states do anaesthetics exist?

A

UNCHARGED (lipophillic) and CHARGED (hydrophillic)

26
Q

what do we do if there is a site of infection

A

WE NEVER PUT LA IN AN INFECTED SITE. this is due to the fact that there is a low ph meaning an increased conc of hydrogen ions.

27
Q

what LA has the best lipid solubility?

A

articaine has increased lipid solubility

28
Q

what does LA cause

A

VASODILATION , increased blood flow (systemic uptake and decreased duration due to it being taken away from the site)

29
Q

process of LA/how it works

A

absorbed into blood stream, distributed INTO TISSUE ONLY, metabolised (mainly in the liver) - articaine is the exception as it is in liver and plasma!

30
Q

role of a vasoconstrictor in LA

A

counteracts vasodilation of LA , reduces blood flow, increases speed of onset, reduced haemhorrage

31
Q

what is the MAX doss when administering lidocaine (with adrenaline)

A

7 cartilages (300mg), 1 cartilage for every 10kg

32
Q

when would we avoid using lidocaine with adrenaline

A

avoid with cardiac (unstable angina) issues or allergy (use prilocaine)

33
Q

what LA’s would we use with pregnant mothers

A

mepivicaine

34
Q

what does the thiophene ring in articaine do

A

its part of the amide ring and ester group. it increases lipid solubility, meaning v good diffusion

35
Q

what are some problems with LA in terms of the anatomy of the patient

A

shape of the mandible - elongates with age, could have thicker cortical bone, divergent roots

36
Q

what happens when we do a facial nerve block

A

this happens if we inject too deep, there is a risk of injecting into parotid gland, loss of IPSILATERAL tone in facial expression!!! - they are unable to blind therefore we need to cover the eye, would keep these pts KUO !

37
Q

What would we carry out if the IDB wasnt working due to the patients obscured anatomy?

A

using ARTICAINE (not lidocaine), placed bucccally, lingually or use one of the supplemental techniques

38
Q

describe the membrane expansion theory

A

LA diffuses into axon membrane and prevents Na channels opening!

39
Q

Uncharged LA what…

A

passes through the membrane easier!!!!!! IT IS LIPID SOLUBLE