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ADVANCED LOCAL ANAESTHESIA
CROWN & BRIDGE STUDY CLUB
APRIL 16, 2021
PETER NKANSAH
PHARMACOLOGYANATOMYTECHNIQUESTIPS, TRICKS & GADGETS
OUTLINE
HISTORY OF LOCAL ANAESTHETICS
• LOCAL ANAESTHETICS (LA) HAVE BEEN ISOLATED SINCE THE 1860S
(COCAINE)
• SENSORY NERVE BLOCKADE WAS FIRST DESCRIBED BY HALSTED IN 1884
• “NOVOCAINE” (PROCAINE) WAS THE FIRST COMMONLY USED LOCAL
ANAESTHETIC IN DENTISTRY
• LIDOCAINE IS THE ORIGINAL AMIDE LA
• COMMERCIALLY AVAILABLE IN 1948
• ARTICAINE IS THE NEWEST POPULAR LA
• RELEASED IN CANADA IN 1982 (US IN 2000)
PURPOSE OF LA
• TO STOP THE GENERATION AND CONDUCTION OF NERVE IMPULSES
• TO ABORT IMPULSES FROM STIMULI
• TO DECREASE POSTOPERATIVE PAIN
MECHANISM OF ACTION
• LOCAL ANAESTHETICS BIND TO
SITE ON NA+ CHANNEL
• INHIBITS THE PERMEABILITY
TO NA+
• BLOCK PROPAGATION OF
ACTION POTENTIALS
STRUCTURE
3 COMMON FEATURES:
• LIPOPHILIC (AROMATIC)
GROUP
• INTERMEDIATE CHAIN
WITH AMIDE OR ESTER
LINKAGE
• HYDROPHILIC (TERTIARY
AMINE) GROUP
LA SOLUTIONS
• BY THEMSELVES, LA SOLUTIONS ARE WEAKLY BASIC, POORLY
SOLUBLE IN WATER AND UNSTABLE
• USED AS SALT SOLUTIONS (USUALLY HCL) WHICH ARE WATER-
SOLUBLE AND STABLE
• WITH THE ADDITION OF VASOPRESSORS, THE SOLUTIONS BECOME
ACIDIC
• TRUE ALLERGY IS POSSIBLE BUT RARE
• < 1% OF REPORTED REACTIONS
BIOTRANSFORMATION & ELIMINATION
• AMIDE LAS ARE PRIMARILY BIOTRANSFORMED IN THE LIVER
• CYTOCHROME P450 CYP3A4
• ARTICAINE HAS THE SHORTEST HALF-LIFE
• MEDICAL HISTORY CONCERNS:
• SEVERE LIVER DYSFUNCTION
• PSEUDOCHOLINESTERASE DEFICIENCY (FOR ESTERS)
LA PROPERTIES
Characteristic Factor(s)
Onset time Concentration
pKa
Lipid solubility
Duration Concentration
Protein binding
Potency Lipid solubility
pKa
COMMON LA PREPARATIONS
• ARTICAINE
• BUPIVACAINE
• LIDOCAINE
• MEPIVACAINE
• PRILOCAINE
PKA OF LOCAL ANAESTHETICS
pKa % base at pH
7.4
Time to onset
(min)
Mepivacaine 7.6 40 2-4
Articaine 7.8 29 2-4
Lidocaine 7.9 25 2-4
Prilocaine 7.9 25 2-4
Bupivacaine 8.1 18 5-8
Procaine 9.1 2 14-18
DURATION OF ACTION
Maxillary Paraperiosteal (min) IAN Block (min)
Preparation Pulp Soft Tissue Pulp Soft Tissue
Lidocaine w epi 60 150 75 180-300
Articaine w epi 60 120-360 75 120-360
Prilocaine w epi 40 120 75 180
Prilocaine plain 15 60-90 60 150
Mepivacaine w levo 50 180-300 75 180-300
Mepivacaine plain 20 120-180 40 120-180
Bupivacaine w epi 60 240-540 180 240-540
COMFORTABLY NUMB
GRADE “A” ANAESTHESIA
GRADE “B” ANAESTHESIA
GRADE “C” ANAESTHESIA
REASONS FOR FAILURE
• PRACTITIONER IMPATIENCE
• PRESSURE SENSATION = PAIN
• PRESENCE OF INFECTION
• IMPROPER EQUIPMENT/TECHNIQUE
• ANXIETY/FEAR
• ANATOMIC VARIABILITY
PRACTITIONER IMPATIENCE
• DEPENDING ON THE TOOTH, MANDIBULAR TOOTH PULPAL NUMBNESS
CAN TAKE FROM 5.2 (2ND MOLAR) TO 13.6 (CANINE) MINUTES TO SET
IN
• POSSIBLE EXCEPTION FOR BUFFERED LOCAL ANAESTHETIC SOLUTIONS
PRESSURE SENSATION AS PAIN?
• IS RESIDUAL PAIN THE RESULT OF PRESSURE AND ITS INTERPRETATION?
• VOLTAGE-GATED SODIUM CHANNELS CAN BE SUBDIVIDED
• USE-DEPENDENT CHANNELS
• TETRODOTOXIN-SENSITIVE AND TETRODOTOXIN-RESISTANT SODIUM
CHANNELS
• TETRODOTOXIN-RESISTANT CHANNELS ARE ABOUT 4X MORE RESISTANT TO THE
EFFECTS OF LIDOCAINE THAN TETRODOTOXIN-SENSITIVE CHANNELS
Ref.: Wells et al., JOE, 33(10): 1172, 2007
TESTING, TESTING…
• SOFT TISSUE NUMBNESS IS A GOOD (NOT EXCELLENT) INDICATOR OF
PULPAL ANAESTHESIA
• 23% FAILURE FOR THE LOWER FIRST MOLAR
• COLD TESTING OR ELECTRIC PULP TESTING ARE MORE RELIABLE
Ref.: Reader et al., Successful Local Anesthesia, 2017
HENDERSON-HASSELBALCH EQUATION
pKa – pH = log 10Ionized (BH+)Unionized (B)
DRUG IONIZATION
EXAMPLE: LIDOCAINE
• PKA – PH = LOG [IONIZED/UN-IONIZED]
• 7.9 – 7.4 = LOG [IONIZED/UN-IONIZED]
• 100.5 = IONIZED/UN-IONIZED
• ~3/1 = IONIZED/UN-IONIZED
DRUG IONIZATION
EXAMPLE: LIDOCAINE AT THE SITE OF INFECTION
• PKA – PH = LOG [IONIZED/UN-IONIZED]
• 7.9 – 4.9 = LOG [IONIZED/UN-IONIZED]
• 103 = IONIZED/UN-IONIZED
• 1,000/1 = IONIZED/UN-IONIZED
MANDIBULAR INFILTRATION ANAESTHESIA
• INFILTRATION/PARAPERIOSTEAL TECHNIQUES ARE SIMPLER, SAFER
AND MORE COMFORTABLE THAN BLOCK TECHNIQUES
• THICK CORTICAL PLATES ARE (SOMETIMES) BARRIERS TO LA DIFFUSION
• AMSA TECHNIQUE?
Ref.: J Meechan, JADA, 2011
MANDIBULAR INFILTRATION ANAESTHESIA
• SUPPLEMENTARY INFILTRATION CONSISTENTLY INCREASES
ANAESTHETIC EFFICACY
• PRIMARY INFILTRATION
• METHOD OF CHOICE FOR THE INCISORS
• ESPECIALLY WITH DOSE-SPLITTING
• WORKS BEST FOR THE MOLARS WHEN YOU THE MORE CONCENTRATED
SOLUTIONS
• SUCCESS RATES ALWAYS LOWER THAN WITH BLOCKS
Ref.: J Meechan, JADA, 2011
IMPROPER EQUIPMENT/TECHNIQUE
• REASONABLY COMMON PRACTICE TO USE 30-GAUGE AND/OR
SHORT NEEDLES FOR MANDIBULAR BLOCKS
• THIS IS A BAD IDEA
• NEEDLE DEFLECTION
• NEEDLE TIP DOESN’T REACH THE INTENDED END POINT
• UNRELIABLE ASPIRATION RESULTS
• NEEDLE BREAKAGE
SOLUTION DIFFERENCES
• MOST COMPARISONS IN THE LITERATURE ARE BETWEEN LIDOCAINE
AND ARTICAINE
• THE RESULTS ARE DIVIDED
• ARTICAINE IS MORE EFFECTIVE THAN LIDOCAINE IN THE MAXILLARY ARCH
• BOTH ARE VERY GOOD LOCAL ANESTHETICS
ANATOMY &ANATOMIC VARIABILITY
ANATOMY & ANATOMIC VARIABILITY
• MANDIBULAR FORAMEN LOCATION IS QUITE VARIABLE
• THE INFERIOR ALVEOLAR NERVE CAN BE BIFID OR TRIFID
• AND HAS A VARIETY OF WAYS TO ENTER THE MANDIBLE
• THE GREATER PALATINE FORAMEN IS OFTEN AT OR DISTAL TO THE
MAXILLARY SECOND MOLAR
• THE MENTAL FORAMEN IS USUALLY AT THE APEX OF THE SECOND
PREMOLAR
• AND ALMOST NEVER AT THE FIRST PREMOLAR
• THE MAXILLARY ARTERY IS (ALMOST) IN YOUR WAY
TROUBLESHOOTING
POSTERIOR SUPERIOR ALVEOLAR (PSA) NERVE BLOCK
• BRANCHES OF THE PSA CAN ENTER THE PALATAL ROOT OF THE
MOLARS OR THE LINGUAL ASPECT OF THE PREMOLARS OR BOTH
• CONSIDER SUPPLEMENTATION WITH A GREATER PALATINE BLOCK
Ref.: P Blanton and A Jeske, JADA, 134:753-760. (2003)
INFRAORBITAL BLOCK
• A.K.A. ASA NERVE BLOCK
• MUST INJECT CLOSE TO THE BONE IN ORDER TO AVOID CN VII (THE
FACIAL NERVE)
• THIS PROXIMITY IS REDUCED IN CHILDREN
Ref.: P Blanton and A Jeske, JADA, 134:753-760. (2003)
MAXILLARY (V2) NERVE BLOCK
MAXILLARY NERVE BLOCK
MAXILLARY NERVE BLOCK:HIGH TUBEROSITY APPROACH
MAXILLARY NERVE BLOCK:HIGH TUBEROSITY APPROACH
MAXILLARY NERVE BLOCK:HIGH TUBEROSITY APPROACH
MAXILLARY NERVE BLOCK:GREATER PALATINE CANAL APPROACH
MAXILLARY NERVE BLOCK:GREATER PALATINE CANAL APPROACH
MAXILLARY NERVE BLOCK:GREATER PALATINE CANAL APPROACH
MAXILLARY NERVE BLOCK:GREATER PALATINE CANAL APPROACH
MAXILLARY NERVE BLOCK:GREATER PALATINE CANAL APPROACH
MANDIBULAR BLOCKS
MANDIBULAR FORAMEN
WHERE IS THE MF?
• NICHOLSON (1985) DISSECTED 80 CADAVERS AND MEASURED THE
POSITION OF THE MANDIBULAR FORAMEN
• USUALLY ANTERIOR TO THE MIDPOINT OF THE RAMUS
• BELOW THE OCCLUSAL SURFACES OF THE MOLARS 75% OF THE TIME
Ref.: ML Nicholson, The Anatomical Record, 212:110-112 (1985)
WHERE IS THE MF?
• LASEMI ET AL. (2019) STUDIED THE MF LOCATION VIA 194
PANORAMIC RADIOGRAPHS
• MF = 5 MM ABOVE THE OCCLUSAL PLANE
• MF = 16.5 MM BEYOND THE ANTERIOR BORDER OF THE RAMUS
Ref.: E. Lasemi et al., Anesthesia Progress, 66:20-23. (2019)
HOW MANY NERVES ARE THERE?
• ONE OR TWO OR THREE
• BRANCHES CAN ARISE HIGH IN THE INFRATEMPORAL FOSSA
• AND CAN ENTER THE MANDIBLE ANYWHERE FROM THE BASE OF THE
CORONOID PROCESS TO THE RETROMOLAR FOSSA
• PLUS THE MYLOHYOID NERVE
• PROVIDES INNERVATION TO THE MOLARS 60% OF THE TIME
Ref.: P Blanton and A Jeske, JADA, 134: 753-760. (2003)
WHICH BLOCK IS BEST?
• GOLDBERG ET AL. (2008) COMPARED THE THREE MANDIBULAR BLOCK
TECHNIQUES TO COMPARE THE DEGREES OF PULPAL ANAESTHESIA,
THE PAIN ON INJECTION, AND THE EXTENT OF SOFT TISSUE
ANAESTHESIA
• 40 ADULT SUBJECTS IN GOOD HEALTH, EACH RECEIVED ALL THREE
BLOCKS (3.6 ML OF 2% LIDOCAINE W/ 1:100,000 EPINEPHRINE) FROM
A SINGLE PRACTITIONER
• MISSED BLOCKS WERE ELIMINATED (10 V-A, 8 G-G)
Ref.: Goldberg et al., JOE, 34(11): 1307, 2008
WHICH BLOCK IS BEST?
• STATISTICALLY SIGNIFICANT DIFFERENCES WERE SEEN IN:
• MEAN ONSET TIME BETWEEN IANB AND GOW-GATES
• MEAN ONSET TIME BETWEEN IANB AND VAZIRANI-AKINOSI
• CLINICAL STRATEGIES SHOULD ACKNOWLEDGE SUCCESS
PROBABILITIES
GOW-GATES MANDIBULAR BLOCK
• INDICATED FOR PATIENTS WITH:
• FAILURE HISTORIES
• SUSPECTED ACCESSORY INNERVATION
• A DESIRE TO BE PROFOUNDLY NUMB
GOW-GATES
GOW-GATES
Extraoral landmarking
Follow the extraoral landmark
line inside the mouth
Injection point
THE VAZIRANI-AKINOSI MANDIBULAR BLOCK
• INDICATED FOR PATIENTS WITH:
• TRISMUS
• MACROGLOSSIA
• HYPERACTIVE GAG REFLEX
• UNPOPULAR BECAUSE OF VISUAL CHALLENGES AND NO BONY
ENDPOINT FOR THE NEEDLE TO CONTACT
VAZIRANI-AKINOSI
ADVERSE REACTIONS
ADVERSE REACTIONS TO LA
• PSYCHOGENIC REACTIONS
• TOXICITY FROM LOCAL ANAESTHETIC OR THE VASOCONSTRICTOR
• ALLERGIC REACTIONS TO THE LOCAL ANAESTHETIC AGENT (OR TO
METABISULFITE)
• METHEMOGLOBINEMIA
• HEMATOMA
• PARAESTHESIAS
P Blanton & A Jeske. The Journal of the American Dental Association 2003 134, 888-893.
Copyright © 2003 American Dental Association
LA MAXIMUM DOSES (FOR ADULTS)
Drug Max
(mg/kg)
Max (mg) Max
(mg w/o
epi)
# cart. (for
70 kg adult)
Lidocaine 7 500 300 13
Articaine 7 500 300 7
Prilocaine 8 600 400 8
Bupivacaine 2 200 75 10
Mepivacaine 7 450 300 8
DOSAGE
• HOW MANY CARTRIDGES OF ARTICAINE CAN A 23-KG, 7-YEAR-OLD
HAVE?
DOSAGE
EXAMPLE: 2% LIDOCAINE
2% = 20 MG/ML
1 CARTRIDGE HAS 1.8 ML OF FLUID
= 36 MG OF DRUG/CARTRIDGE
PARAESTHESIAS
• THERE ARE NUMEROUS REPORTS REGARDING THE ASSOCIATION
BETWEEN 4% SOLUTIONS AND A HIGHER-THAN-EXPECTED INCIDENCE
OF PARAESTHESIAS
• NOTE THE RISK:BENEFIT EQUATION
• OVERALL PARAESTHESIA INCIDENCE IS 1:785,000 INJECTIONS (RARE)
• THERE HAS BEEN AN RCDSO ADVISORY REGARDING 4% SOLUTIONS
USED FOR BLOCKS
• UNIVERSITY OF TORONTO DENTAL STUDENTS
Ref.: Haas and Lennon, JCDA, 1995
PARASTHESIAS
• MOST ARE TRANSIENT, USUALLY RESOLVING WITHIN 8 WEEKS
• IF NOT, PROGNOSIS IS VERY POOR
• PRECISE CAUSE NOT KNOWN WITH CERTAINTY
• DIRECT NEEDLE TRAUMA
• HEMORRHAGE INTO NERVE SHEATH
• SCAR FORMATION
• NEUROTOXICITY (CONTROVERSIAL)
PARAESTHESIAS
• A 21-YEAR RETROSPECTIVE STUDY OF REPORTS OF PARESTHESIA
FOLLOWING LOCAL ANESTHETIC ADMINISTRATION
• HAAS AND LENNON, JCDA, 1995, 61:319-330
PARAESTHESIAS
• THE OVERALL INCIDENCE OF PARAESTHESIA FOLLOWING LOCAL
ANESTHETIC ADMINISTRATION FOR NON-SURGICAL PROCEDURES IN
DENTISTRY IS VERY LOW →1:785,000
• IF, HOWEVER, PARAESTHESIA DOES OCCUR, THE RESULTS SUGGEST
THAT IT IS MORE LIKELY IF EITHER ARTICAINE OR PRILOCAINE IS USED
• REASONS ARE SPECULATIVE ONLY
RESULTS (1973-1993)
0
10
20
30
40
50
60
Articaine Bupivacaine Lidocaine Mepivacaine Prilocaine
PARAESTHESIAS
• RETROSPECTIVE REVIEW OF VOLUNTARY REPORTS OF NON-SURGICAL
PARESTHESIA IN DENTISTRY
• GAFFEN AND HAAS, 2009, JOURNAL OF THE CANADIAN DENTAL
ASSOCIATION, 75(8): 579
• OBJECTIVES:
• TO ANALYZE CASES OF PARESTHESIA ASSOCIATED WITH LOCAL ANESTHETIC
INJECTION THAT WERE REPORTED TO THE PROVINCE OF ONTARIO’S
PROFESSIONAL LIABILITY PROGRAM (PLP) FROM 1999 TO 2008 INCLUSIVE
• TO UPDATE PREVIOUS STUDY (1995)
DISTRIBUTION OF PARESTHESIAS
0
10
20
30
40
50
60
70
articaine bupivacaine lidocaine mepivacaine prilocaine
Percentage
JADA (JULY 2010)
JADA (JULY 2010)
CONCLUSIONS
• INCIDENCE IS VERY LOW
• PRILOCAINE = 1:2,070,678 INJECTIONS
• ARTICAINE = 1:4,159,848 INJECTIONS
• LIDOCAINE = 1:181,076,673 INJECTIONS
• YET DATA ARE STRONGLY SUGGESTIVE OF AN ASSOCIATION
• NO PROOF OF CAUSE-EFFECT
• IT IS NOT THE DRUG PER SE
• HIGHER CONCENTRATIONS MAY SIMPLY PREDISPOSE TO GREATER EFFECT
STUDIES OF DOSE-DEPENDENT NEUROTOXICITY
• FINK AND KISH, ANESTHESIOLOGY, 1976
• BARSA ET AL, ANESTHESIA ANALGESIA, 1982
• RIGLER ET AL, ANESTHESIA ANALGESIA, 1991
• LAMBERT AND HURLEY, ANESTHESIA ANALGESIA, 1991
• KALICHMAN ET AL, JOURNAL OF NEUROPATHOLOGY, 1993
• SELANDER, REGIONAL ANESTHESIA, 1993
• LAMBERT ET AL, ANESTHESIOLOGY, 1994
• KANAI ET AL, ANESTHESIA AND ANALGESIA, 1998
• CORNELIUS ET AL, JOURNAL CRANIO-MAXILLOFACIAL SURGERY, 2000
• JOHNSON ET AL, ANESTHESIOLOGY, 2002
WHAT’S DIFFERENT?WHAT’S NEW?
THE WAND® COMPUTER GUIDED ANESTHESIA SYSTEM
CALAJECT
DENTAPEN
• MANUFACTURED AND
DISTRIBUTED BY
SEPTODONT
• USES REGULAR NEEDLES
• HAS A “STANDARD” FINGER
GRIP
• LIGHT (40 G IN WEIGHT)
DENTAPEN
• CORDLESS
• THREE INJECTION SPEEDS
• SLOW = 1 ML/90 SEC
• MEDIUM = 1 ML/60 SEC
• FAST = 1 ML/30 SEC
• AUTOMATIC ASPIRATION
DENTAPEN
DENTAPEN CONTROL PANEL
Aspiration button
Power button
Speed selection
Mode selection
Rewind
INTRAOSSEOUS ANESTHESIA
• DIRECT INJECTION IN THE SPONGY BONE,
CLOSE TO THE APEX.
QUICKSLEEPER 5
QUICKSLEEPER 5
• PAINLESS NEEDLES
• CUTTING EDGE BEVEL
• SPECIFIC INDICATOR
S TA N DA R D
N E E D L E S
P a i n l e s s& e f f i c i e n t
T r a u m a t i c
P E R I O S T E U M
H OW TO B E PA I N L E S S ?
ONSET®
• BUFFERED LA SOLUTIONS
• BRANDED AS ONSET
• USES NA(HCO3) AND CO2
TO RAISE THE PH LEVEL OF
THE LA SOLUTION
• THEORETICALLY RESULTS IN
FASTER ONSET AND LESS
DISCOMFORT DURING AND
AFTER INJECTIONS
• PULPAL ANAESTHESIA
TWO MINUTES AFTER
IAN BLOCK
BUFFERED LOCAL ANAESTHETICS
ORAVERSE®
• PHENTOLAMINE MESYLATE
• A NON-SELECTIVE Α-
ADRENERGIC ANTAGONIST
• INCREASES THE
REDISTRIBUTION OF LA
AWAY FROM INJECTION
SITE
• REDUCES DURATION OF
ANAESTHESIA BY 50%
• NON-TOXIC AND WELL-
TOLERATED < AGE 6 YEARS
NEVERMIND THE OPIOIDS…
• BENZOCAINE AND LIDOCAINE AS ADULTERANTS FOR COCAINE
• BENZOCAINE ADULTERANTS HAVE LEAD TO METHEMOGLOBINEMIA IN
THE ED
• LIDOCAINE INCREASES THE NASAL NUMBNESS ASSOCIATED WITH
SNORTING COCAINE
• LEADS TO SEIZURES IN THE ED
• VERY COMMON COCAINE ADULTERANT
Ref.: Saraghi & Hersh, JADA, March 2014
DEXAMETHASONE INJECTIONS
• CHEN ET AL. (2017) EXAMINED THE ABILITY OF SUBMUCOSAL
INJECTIONS TO REDUCE POSTSURGICAL DISCOMFORT (COCHRANE
REVIEW)
• MODEL USED WAS FOR THIRD MOLAR EXTRACTIONS
• REVIEWED 11 ARTICLES
• 4 MG OF DEXAMETHASONE SM REDUCES EDEMA AND EARLY TRISMUS
• NO STRONG EVIDENCE TO SUPPORT THE MINIMIZATION OF PAIN OR
LATE TRISMUS
Chen et al., JADA, 148(2): 81, 2017
LIPOSOMAL BUPIVACAINE(EXPAREL®)
INJECTABLE BUPIVACAINE LIPOSOME SUSPENSION
• TRADE NAME: EXPAREL® (PACIRA PHARMACEUTICALS INC.)
• MARKETED AS AN OPIOID-FREE WAY TO MANAGE POST-SURGICAL PAIN
• CONSISTS OF MULTIVESICULAR LIPOSOMES (DEPOFOAM®) THAT RELEASE
DOSES OF BUPIVACAINE AS THE CHAMBERS BREAK DOWN
• INJECTED INTO AND/OR AROUND THE SURGICAL SITE
• NOT USED FOR NERVE BLOCKS
• CAN PROVIDE UP TO 96 HOURS OF PAIN RELIEF
• IT’S EXPENSIVE
• $300 FOR A 20-ML VIAL
Ref.: https://www.exparel.com
EXPAREL® IN ORAL SURGERY
DOWN THE ROAD…
• PAIN-ONLY LA
• THE TRPV1 CHANNEL IS PRESENT ONLY IN PAIN-SENSING NEURONS
• THESE CHANNELS RESPOND TO NOXIOUS HEAT, PROTONS,
ENDOCANNABINOIDS, AND CAPSAICIN
• WHEN OPENED BY AN AGONIST, QX-314, A CHARGED LIDOCAINE
DERIVATIVE, CAN BE DELIVERED