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LOCAL
ANAESTHESIA
Kirti Ranka
Final Year BDS
Roll No- 17
CONTENTS
 Definition
 Requirements
 Structure
 Classification
 Composition
 Theories Of Action
 Technique
 Recent Trends
 Complications
DEFINITION
 Local Anaesthesia is defined as a loss of sensation
in a circumscribed area of the body caused by a
depression of excitation in nerve endings or an
inhibition of the conduction process in the peripheral
nerves.(Stanley F. Malamed, Handbook of Local
Anaesthesia 5TH ED)
 Local Anaesthetics are drugs which upon topical
application or local injection cause reversible loss of
sensory perception especially of pain in a restricted
area of the body. Not only sensory, but also motor
impulses are interrupted when applied to a mixed
nerve, resulting in muscular paralysis and loss of
autonomic control as well.
REQUIREMENTS
 Potent to give complete anaesthesia.
 Relatively free from producing allergic reactions
 Stable in solution form and should undergo
biotransformation in the body readily.
 Sterile or capable of being sterilized by heat without
deterioration
 Low degree of local toxicity
 Shouldn't irritate the tissues.
 Shouldn't alter nerve structure permanently
 Low systemic toxicity
 Versatile.
 Rapid onset and sufficient duration of action and
completely reversible.
STRUCTURE
LIPOPHILIC
AROMATIC
PROTEIN
HYDROPHILIC
AROMATIC
PROTEIN
Hydrocarbon Chain containing either
an ester or an amide linkage
CLASSIFICATION
SALTS
ESTERS
Benzoic acid
PABA
meta-
aminobenzoic
acid
AMIDES
QUINOLONES
Esters
Benzoic acid
Cocaine
Butacaine
Benzocaine
Piperocaine
Isobucaine
Meprylcaine
PABA
Chlorprocaine
Procaine
Propoxycaine
Butethamine
Tetracaine
Meta-aminobenzoic acid
Meta-butathamine
primacaine
Amides
Lidocaine
Bupivacaine
Mepivacaine
Dibucaine
Etiodocaine
Articaine
Prilocaine
Ropivacaine
Parethoxycaine
Pyrrocaine
Quinolone
Centbucridine
INJECTABLE
High potency,Long
duration
Intermediate
Potency and
duration
Low potency, Short
duration
Tetracaine
Bupivacaine
Ropivacaine
Dibucaine
Procaine
Choloropro-
caine
Lidocaine
Prilocaine
SURFACE
ANAESTHETIC
Soluble Insoluble
Cocaine
Lidocaine
Tetracaine
Benzocaine
Butamben
Oxethazine
MECHANISM OF ACTION
MECHANISM OF ACTION
Altering the basic resting potential of
the nerve membrane
Altering the threshold potential(firing
level)
Decreasing the rate of depolarisation
Prolonging the rate of repolarisation
COMPOSITION
LOCAL ANAESTHETIC-Lignocaine,Lidocaine
VASOCONSTRICTOR-Epinephrine 1:200,000
REDUCING AGENTS-Sodium Metabisulphite
PRESERVATIVE-Methyl Paraben
FUNGICIDE-Thymol
VEHICLE-Ringers solution
THEORIES OF MECHANISM OF ACTION
 Acetylcholine Theory
 Calcium Displacement Theory
 Surface Charge(repulsion) Theory
 Membrane Expansion Theory
 Specific Receptor Theory
Now Discredited
MEMBRANE EXPANSION THEORY
SPECIFIC RECEPTOR THEORY
LA AGENTS
 Lidocaine
 Amide type.
 Onset-Rapid(2-3 min)
 Effective topically(5% concentration)
 Effective dental concentration-2%
 Metabolized in the liver to Monoethylglyceine and Xylidide
 Excretion via kidneys.
 Allergy is usually non-existant.
 Maximum recommended dose-3.2 mg/lb (Lidocaine with epinephrine)
- 4.4mg/lb (Lidocaine w/o epinephrine)
 Maximum dose should not exceed 300mg
-
 Benzocaine
 Ester type
 Onset-Prolonged; Duration of action-Prolonged
 Topical application only
 Allergic reactions are rare.
 Available as: Aerosols,Gels,Gel patches, Ointments,
Solutions.
 Maximum dose- topical 10% mucous membrane gel;
Apply topically to affected area(s) up to 4 times daily
with a cotton swab .
THE SYRINGE
 Types:
1. Non disposable syringes
a. Breech-loading,metallic,cartridge-type,aspirating
b. Breech-loading,plastic,cartridge-type,aspirating
c. Breech-loading,metallic,cartridge-type,self-aspirating
d. Pressure syringe for PDL injection
e. Jet Injector(“needleless syringe”)
2. Disposable syringes
3. “Safety” syringes
4. Computer controlled local anaesthetic delivery
system
DISPOSABLE SYRINGE
 These syringes contain a Luer-Lok screw-on needle
attachment but no aspirating tip.
 Aspiration can be done by pulling back the plunger
of the syringe before or during injection.
 The needle, attached to the syringe must be
inserted into a vial of LA drug and an appropriate
volume of solution is withdrawn
 Care should be taken to avoid contaminating the
vial.
 2-3 ml syringes with 23-or 25-gauge needles are
recommended.
 Single use,disposable
 Sterile until opened
 Lightweight
 Doesn’t except prefilled
dental cartridges
 Aspiration is difficult
ADVANTAGES DISADVANTAGES
COMPUTER CONTROLLED LOCAL
ANAESTHETIC DELIVERY SYSTEM(CCLAD)
 Introduced in 1997
 The Wand(The Wand/CompuDent)
 Improved ergonomics and precision of the dental syringe
 Enables a dentist to accurately manipulate needle placement with
fingertip accuracy and deliver LA with a foot-controlled device.
 The handpiece is held with a pen like grasp
 Flow rate is preprogrammed
 Precise control of flow
rate and pressure
produces a more
comfortable injection
even in tissues with low
elasticity
 Increased tactile
sensation and
ergonomics
 Non threatening
 Autonomic aspiration
 Rotational insertion
technique which
minimizes needle
deflection
 Requires additional
armamentarium
 Cost
ADVANTAGES DISADVANTAGES
THE NEEDLE
 Types: Stainless steel
Platinum
Iridium-Platinum Alloy
Ruthenium-Platinum Alloy
 Parts:
2 factors considered while selecting the needle-LENGTH and
GAUGE
GAUGE OF A NEEDLE
 Diameter of the lumen of the needle.
 Smaller the number = Greater the diameter of the lumen
 Most commonly used-27-gauge long and 30-gauge short
 25-gauge needle is most preferred for injections presenting a
higher risk of positive aspiration.
Advantages of a Large-Gauge Needles Over the Small-Gauge Needles
1)Less deflection, as needle advances through the tissues
2)Greater accuracy in injection
3)Less chance of needle breakage
4)Easier aspiration
5)No perceptual differences in patient comfort
LENGTH OF NEEDLE
 Long-32mm
 Short-20mm
TYPES OF INJECTION PROCEDURES
 1.Nerve block-depositing the LA solution within
close proximity to a main nerve trunk
 2).Field block-depositing a in proximity to the larger
nerve branches.
 3.Local infiltration-small terminal nerve endings are
anaesthetised.
INJECTION TECHNIQUES
 MAXILLARY
1) Supraperiosteal
2) PDL
3) Intraseptal Injection
4) Intracrestal Injection
5) Intraosseous Injection
6) PSA Nerve Block
7) MSA Nerve Block
8) ASA Nerve Block
9) Maxillary Nerve Block
10) Greater Palatine Nerve Block
11) Nasopalatine Nerve Block
12) AMSA Nerve Block
13) P-ASA Nerve Block
Supraperiosteal Injection Technique
Periodontal ligament
injection
Intraseptal injection Technique
POSTERIOR SUPERIOR ALVEOLAR NERVE BLOCK
(PSA)
 Nerves anaesthetized: Posterior superior alveolar nerve and its
branches
 Areas anaesthetized: Maxillary 3rd,2nd and 1st molars except the
mesiobuccal root of the maxillary 1st molar.
 Landmarks: Mucobuccal fold, Maxillary tuberosity,Zygomatic
process of maxilla
For Left PSA nerve block, a right handed administrator should face the patient
from the 10 o’clock;
For Right PSA nerve block a right handed administrator should face the patient
directly from the 8 o’clock position
Technique:
Prepare the tissues at the height of the mucobuccal fold
Orient the bevel towards the bone
Partially open the patient’s mouth; pulling the mandible to the side of
injection,retract the cheek with your fingers and pull the tissue taut.
Insert the needle into the height of the mucobuccal fold over the 2nd molar
Advance the needle in an upward, inward and backward direction(At once)
Slowly advance the needle through the soft tissue
Ensure the needle penetrates 10-14 mm depth.
Aspirate in 2 planes
If both aspirations are negative the deposit 0.9-1.8 ml solution over 30-60
seconds
Withdraw the syringe slowly
Wait for 3-5 minutes before commencing the dental procedure
ANTERIOR SUPERIOR ALVEOLAR OR INFRAORBITAL
NERVE BLOCK
(ASA)
 Nerves anaesthetized- Anterior superior alveolar
-Middle superior alveolar
-Infraorbital nerve
 Areas anaesthetized-
 Landmarks: Mucobuccal fold
Infraorbital notch
Infraorbital foramen
Assume 10 o’clock position either directly facing the patient or in the same
direction as the patient
Technique-
Position the patient supine or semisupine with the neck extended slightly
Prepare the tissue at the injection site
Feel the intraorbital notch,Move the finger inferiorly until a depression is felt.
Here the infraorbital foramen is located
Place the thumb over the infraorbital formen
Retract the lip, pull the tissues in the mucobuccal fold taut
Insert the needle into the height of the mucobuccal fold with the bevel facing
the bone
Orient the needle towards the Infraorbital foramen
The needle should be held parallel with the long axis of the tooth as it is
advanced to avoid premature contact with the bone.
Advance the needle slowly until the bone is contacted
Check the depth of needle penetration,lateral deviation of the needle from the
infraorbital foramen and the orientation of the bevel
Aspirate, then slowly deposit 0.9ml to 1.2ml(30-40 seconds).maintain firm
finger pressure at the injection site
Withdraw the syringe slowly
WAit for 3-5 minutes after the injection before comencing the dental procedure
MIDDLE SUPERIOR ALVEOLAR NERVE
BLOCK(MSA)
 Nerves anaesthetized: Middle superior alveolar and
terminal branches
 Areas anaesthetized:
 Landmarks: Mucobuccal fold over the
2nd premolar
For Right MSA nerve block, a right handed administrator should face the
patient from the 10 o’clock;
For Left MSA nerve block a right handed administrator should face the patient
directly from the 8 or 9 o’clock position
Prepare the tissue at the injection site
Stretch the patient’s upper lip to make the tissues taut and to gain visibility
Insert the needle into the height of the mucobuccal fold above the 2nd premolar
with the bevel facing the bone
Penetrate the mucous membrane and slowly advance the needle until its tip is
located well above the apex of the 2nd premolar
Aspirate
Slowly deposit 0.9ml-1.2ml in approx. 30-40 seconds
Withdraw the syringe slowly
Wait for 3-5 minutes before commencing the dental treatment
Techniques:
GREATER PALATINE NERVE BLOCK
 Nerves anaesthetized: Greater Palatine
 Areas anaesthetized:
 Landmarks: Greater palatine foramen
Junction of maxillary alveolar
process and palatine bone
NASOPALATINE NERVE BLOCK
 Nerves anaesthetized: Nasopalatine nerves
bilaterally
 Areas anaesthetized:
 Landmarks:Central incisors
Incisive papilla
 MANDIBULAR
1) IANB Nerve block
2) Buccal Nerve Block
3) Mental Nerve block
4) Incisive nerve block
INFERIOR ALVEOLAR NERVE BLOCK/
MANDIBULAR NERVE BLOCK
 Nerves anaesthetized: Inferior alveolar nerve
Incisive nerve
Mental nerve
Lingual nerve
 Areas anaesthetized: mandibular teeth till the
midline
body of mandible
Inferior portion of
Anterior 2/3rd of the tongue
Floor of the mouth
Lingual soft tissues and
periosteum
3 parameters considered during IANB
1. Height of injection
2. Anteroposterior site of injection
3. Penetration depth
LANDMARKS
Anatomical
Landmarks of Inferior
alveolar nerve block:
Mucobuccal fold.
Anterior border of
Mandibular ramus.
External oblique ridge.
Internal oblique ridge.
Retromolar triangle.
Pterygomandibular
ligament.
Buccal sucking pad.
Pterygomandibular space.
BUCCINATOR NERVE BLOCK/LONG
BUCCAL NERVE BLOCK
 Nerves anaesthetized: Buccal nerve
 Areas anaesthetized:Soft tissues and periosteum,
buccal to mandibular teeth
 Landmarks:Mandibular molars,Mucobuccal fold
MENTAL NERVE BLOCK
 Nerves anaesthetized: Mental nerve
 Areas anaesthetized:Soft tissues of the lower lip,
chin and buccal soft tissues anterior to the mental
foramen are anaesthetized
 Landmarks:Mandibular premolars,Mucobuccal
fold
INFILTRATION ANAESTHESIA
 Nerves anaesthetized:Large terminal branches of dental
plexus
 Areas anaesthetized: Pulp and root area of the tooth
Buccal periosteum
Connective tissue and mucous
membrane
RECENT ADVANCES
 Safety Syringes
 Computer controlled local
anaesthetic delivery
system
 Comfort Control Syringe
 Local Anaesthetics with
New Additives
 Eutectic mixture of LA
 Electronic Dental
Anaesthesia
 Vibraject
LOCAL
COMPLICATIONS
Needle breakage
Paresthesia
Facial nerve paralysis
Trismus
Soft tissue injury
Haematoma
Pain on injection
Burning on injection
Infection
Edema
Sloughing of the tissues
Post anaesthetic intraoral lesions
NEEDLE BREAKAGE
 Causes:
 Primary cause-Bending of the needle that causes
weakening.
 Sudden unexpected movement by the patient
 Manufacturing defects.
 Prevention
 Use longer needles for penetration of the tissue beyond
18mm
 Use larger-gauge needles
 Do not insert the needle upto its hub; rigid and weakest
point
 Do not redirect a needle after its insertion into the tissue
Management:
a. Remain calm; do not panic.
b. Instruct the patient to not move. Keep the patient’s mouth open or place a
bite block
c. If the fragment is visible then try to remove it with a small hemostat.
d. If the needle is lost and cannot be retrieved easily then do not proceed with
an incision or probing.
e. Inform your insurance company immediately.
f. Refer the patient to an OMFS for consultation.
PARAESTHESIA
 Persistant anaesthesia (extend well beyond the expected
duration)
 Cause:
 Trauma to any nerve
 Injection of LA solution contaminated by alcohol or a sterilizing
solution near a nerve produces irritation resulting in edema and
increased pressure in the region of the nerve.
 Haemorrhage in and around the nerve sheath,which increases the
pressure on the nerve
 Problems:
 Self-inflicted injury.
 Prevention
 Strict adherence to injection protocol
 Management
 Mostly resolves within approximately 8 weeks without treatment.
FACIAL NERVE PARALYSIS
 Cause:
 Administering LA into the capsule of the parotid gland
or place the tip within the parotid gland
 Problem
 Loss of motor function to the muscles of facial
expression
 Management
 The situation is transient so one must wait until the
effect of the nerve block wears off.
 Remove contact lenses if any
TRISMUS
 Tetanic spasm of jaw muscles by which the normal mouth opening is
restricted
 Causes:
 Trauma to muscles or blood muscles in the infratemporal fossa
 LA solutions into which alcohol or cold sterilizing solutions have
diffused produce irritation
 Haemmorhage
 Low-grade infection
 Prevention
 Use of sharp sterile needle
 Practice atraumatic insertion and injection technique
 Avoid multiple insertions
 Use minimum effective volumes of LA
 Management
 Heat therapy, warm saline rinse analgesics, muscle
relaxants
 Physiotherapy consists of opening and closing the
mouth, lateral excursions of the mandible for 5 minutes
every 3-4 hours, using sugarless chewing gum
 Antibiotics can also be prescribed for 7 days if the pain
doesn’t subside after 48-72 hours
 Refer to an OMFS if there is no improvement in pain or
dysfunction.
SOFT TISSUE INJURY
 Self-inflicted trauma to lips and tongue is frequently
caused by the patient inadvertently biting or chewing
these tissues while still anaesthetized.
 Cause: Trauma
 Problem: Swelling and significant pain after the effect of
anaesthesia wears off.
 Prevention: Place a cotton roll between lips and teeth if they
are still anaesthetized at the time of discharge.Secure this roll
with dental floss wrapped around the teeth
Warn the patient against eating or drinking hot
foods and biting on the lips or the tongue to test for anaesthesia
 MANAGEMENT
 Analgesics, for pain.
 Antibiotics if necessary
 Lukewarm saline rinses for decreasing any swelling.
 Petroleum jelly to cover lip lesions and minimize
irritation
HAEMATOMA
 The effusion of blood into the extravascular spaces that can result from
inadvertently nicking a blood vessel during the process of injecting the
local anaesthetic.
 Usually results due to the nicking of artery
 Cause: Haematomas after IANB are usually visible intraorally whereas
PAS haematomas are visible extraorally.
 Problems:Complications are trismus and pain
 Prevention:Modify the injection technique slightly as per the
patient’s facial characteristics.
-Minimize the number of needle penetrations into the
tissue.
Management : immediately, apply direct pressure to the site of the
bleeding for 2 mins. In case of IANB pressure is applied to the medial
aspect of the mandibular ramus. In case of ASANB pressure is applied
directly over the infraorbital foramen.
 Management: immediately, apply direct pressure to the site
of the bleeding for 2 mins. In case of
- IANB pressure is applied to the medial aspect of the
mandibular ramus.
- In case of ASA NB pressure is applied directly over the
infraorbital foramen.
- In case of PSA NB digital pressure can be applied to the
soft tissue in the mucobuccal fold as far distally as can be
tolerated. Apply pressure in the medial and superior
direction and if available apply ice.
- Subsequently after the treatment of hematomas slight
discolouration is likely to be seen. This is due to the
extravasated blood elements which will slowly resorb over
7-14 days. Heat should not be applied immediately though
it can be applied from the 2nd day onwards.
- Avoid any dental treatment until the hematoma resorbs.
PAIN ON INJECTION
 Causes - Careless injection technique, multiple
injections, rapid deposition of LA solutions
 Problems - Patient anxiety leading to sudden
unexpected movements increasing the risk of
needle breakage.
 Prevention - Adhere to proper injection techniques,
use sharp needles, use topical anaesthetic before
injecting, use sterile LA solutions, inject LA slowly
BURNING ON INJECTION
 Cause- pH of the solution, rapid injection of LA,
contamination of LA cartridges, solutions warmed to
normal room temperatures.
 Problems- tissue damage may result because of rapid
injection, contaminated tissue injection and overly warmed
LA solution.
 Complications- post anaesthetic trismus, oedema,
paraesthesia.
 Prevention- slow down the rate of injection to 1 ml per min.
 Management- It is a transient phase so management is
usually required for specific complications.
INFECTION
 Causes - Contamination of needle before
administrating LA, administrating LA into the area of
infection.
 Problems- Contamination of needles and solutions.
 Prevention- Use sterile disposable needles, handle
needles with care, prepare tissues properly before
injecting LA.
 Management- Trismus may be a complication which
must be treated using heat and analgesics and heat.
If there is no improvement the patient should be
started on a 7-10 day antibiotic course.
OEDEMA
 Causes- trauma during injection, infection, allergy-
angioedema, hemorrhage, injection of irritating solution.
 Problems- LA obstruction, pain and dysfunction of the
region, angioneurotic oedema.
 Prevention- proper care and handling LA armamentarium,
use atraumatic injection techniques.
 Management- prescribe analgesics for pain, antibiotic
therapy if the following persists –
-pain
-mandibular dysfunction
-oedema
-warmth.
 In case of allergy induced oedema prescribe
intramuscular and oral antihistamine agents if
breathing is not compromised.
 If breathing is compromised- P→A→B→C→D
 0.15mg epinephrine is injected every 10-15 mins
until respiratory distress resolves.
 Histamine blocker is administered either im or iv.
 Corticosteroid is administered either im or iv.
 Preparations are made for cricothyrotomy if
needed
 Thoroughly evaluate the patient before the next
appointment.
POST ANAESTHETIC INTRA-ORAL LESIONS
 Ulcerations seen 2 days after injection around the
site of the injection and presents with immense
pain.
 Recurrent apthous stomatitis on gingival tissues
that are not attached to the underlying bone and the
buccal mucosa.
 Herpes simplex seen on tissues attached to
underlying bone. Trauma to tissues by needles, LA
solutions, cotton swab or any other instrument may
activate latent form of diseased processes that
were present in the tissues before injection.
 Problems- acute sensitivity in ulcerated area.
 Prevention- antiviral agents can be used for
extraoral herpes simplex infections.
 Management- topical anaesthetic solutions,
mixture of equal amounts of diphenhydramine
and milk of magnesia is rinsed in he mouth.
 Ulcerations last for 7-10 days with or without pain.
SYSTEMIC COMPLICATIONS
 Overdose- results due to:
- biotransformation of drug is unusually slow.
- the unbiotransformed drug is too slowly eliminated
from the body through the kidneys.
- too large a total dose is administered.
- absorption from the injection site is unusually rapid.
- inadvertent intravascular administration occurs.
 Management- most of the LA overdose reactions are
self-limiting because the blood level in target organs
continues to decrease as the reaction progresses and
redistribution and biotransformation take place.
Rarely, drugs other than oxygen are necessary.
ALLERGY
 Allergic responses to LA- dermatitis
- bronchospasm
- systemic anaphylaxis
 Of special interest with regard to allergy is the
bacteriostatic agent- methylparaben.
 Other causes- sodium bisulfite allergy, epinephrine
allergy, latex allergy, topical anaesthetic allergy.
 Prevention- P→A→B→C→D
THANKYOU

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Local anaesthesia in dentistry

  • 2. CONTENTS  Definition  Requirements  Structure  Classification  Composition  Theories Of Action  Technique  Recent Trends  Complications
  • 3. DEFINITION  Local Anaesthesia is defined as a loss of sensation in a circumscribed area of the body caused by a depression of excitation in nerve endings or an inhibition of the conduction process in the peripheral nerves.(Stanley F. Malamed, Handbook of Local Anaesthesia 5TH ED)  Local Anaesthetics are drugs which upon topical application or local injection cause reversible loss of sensory perception especially of pain in a restricted area of the body. Not only sensory, but also motor impulses are interrupted when applied to a mixed nerve, resulting in muscular paralysis and loss of autonomic control as well.
  • 4. REQUIREMENTS  Potent to give complete anaesthesia.  Relatively free from producing allergic reactions  Stable in solution form and should undergo biotransformation in the body readily.  Sterile or capable of being sterilized by heat without deterioration  Low degree of local toxicity  Shouldn't irritate the tissues.  Shouldn't alter nerve structure permanently  Low systemic toxicity  Versatile.  Rapid onset and sufficient duration of action and completely reversible.
  • 8. INJECTABLE High potency,Long duration Intermediate Potency and duration Low potency, Short duration Tetracaine Bupivacaine Ropivacaine Dibucaine Procaine Choloropro- caine Lidocaine Prilocaine
  • 11. MECHANISM OF ACTION Altering the basic resting potential of the nerve membrane Altering the threshold potential(firing level) Decreasing the rate of depolarisation Prolonging the rate of repolarisation
  • 12. COMPOSITION LOCAL ANAESTHETIC-Lignocaine,Lidocaine VASOCONSTRICTOR-Epinephrine 1:200,000 REDUCING AGENTS-Sodium Metabisulphite PRESERVATIVE-Methyl Paraben FUNGICIDE-Thymol VEHICLE-Ringers solution
  • 13. THEORIES OF MECHANISM OF ACTION  Acetylcholine Theory  Calcium Displacement Theory  Surface Charge(repulsion) Theory  Membrane Expansion Theory  Specific Receptor Theory Now Discredited
  • 16. LA AGENTS  Lidocaine  Amide type.  Onset-Rapid(2-3 min)  Effective topically(5% concentration)  Effective dental concentration-2%  Metabolized in the liver to Monoethylglyceine and Xylidide  Excretion via kidneys.  Allergy is usually non-existant.  Maximum recommended dose-3.2 mg/lb (Lidocaine with epinephrine) - 4.4mg/lb (Lidocaine w/o epinephrine)  Maximum dose should not exceed 300mg -
  • 17.  Benzocaine  Ester type  Onset-Prolonged; Duration of action-Prolonged  Topical application only  Allergic reactions are rare.  Available as: Aerosols,Gels,Gel patches, Ointments, Solutions.  Maximum dose- topical 10% mucous membrane gel; Apply topically to affected area(s) up to 4 times daily with a cotton swab .
  • 18. THE SYRINGE  Types: 1. Non disposable syringes a. Breech-loading,metallic,cartridge-type,aspirating b. Breech-loading,plastic,cartridge-type,aspirating c. Breech-loading,metallic,cartridge-type,self-aspirating d. Pressure syringe for PDL injection e. Jet Injector(“needleless syringe”) 2. Disposable syringes 3. “Safety” syringes 4. Computer controlled local anaesthetic delivery system
  • 19. DISPOSABLE SYRINGE  These syringes contain a Luer-Lok screw-on needle attachment but no aspirating tip.  Aspiration can be done by pulling back the plunger of the syringe before or during injection.  The needle, attached to the syringe must be inserted into a vial of LA drug and an appropriate volume of solution is withdrawn  Care should be taken to avoid contaminating the vial.  2-3 ml syringes with 23-or 25-gauge needles are recommended.
  • 20.  Single use,disposable  Sterile until opened  Lightweight  Doesn’t except prefilled dental cartridges  Aspiration is difficult ADVANTAGES DISADVANTAGES
  • 21. COMPUTER CONTROLLED LOCAL ANAESTHETIC DELIVERY SYSTEM(CCLAD)  Introduced in 1997  The Wand(The Wand/CompuDent)  Improved ergonomics and precision of the dental syringe  Enables a dentist to accurately manipulate needle placement with fingertip accuracy and deliver LA with a foot-controlled device.  The handpiece is held with a pen like grasp  Flow rate is preprogrammed
  • 22.
  • 23.  Precise control of flow rate and pressure produces a more comfortable injection even in tissues with low elasticity  Increased tactile sensation and ergonomics  Non threatening  Autonomic aspiration  Rotational insertion technique which minimizes needle deflection  Requires additional armamentarium  Cost ADVANTAGES DISADVANTAGES
  • 24. THE NEEDLE  Types: Stainless steel Platinum Iridium-Platinum Alloy Ruthenium-Platinum Alloy  Parts: 2 factors considered while selecting the needle-LENGTH and GAUGE
  • 25. GAUGE OF A NEEDLE  Diameter of the lumen of the needle.  Smaller the number = Greater the diameter of the lumen  Most commonly used-27-gauge long and 30-gauge short  25-gauge needle is most preferred for injections presenting a higher risk of positive aspiration. Advantages of a Large-Gauge Needles Over the Small-Gauge Needles 1)Less deflection, as needle advances through the tissues 2)Greater accuracy in injection 3)Less chance of needle breakage 4)Easier aspiration 5)No perceptual differences in patient comfort
  • 26.
  • 27. LENGTH OF NEEDLE  Long-32mm  Short-20mm
  • 28. TYPES OF INJECTION PROCEDURES  1.Nerve block-depositing the LA solution within close proximity to a main nerve trunk  2).Field block-depositing a in proximity to the larger nerve branches.  3.Local infiltration-small terminal nerve endings are anaesthetised.
  • 29. INJECTION TECHNIQUES  MAXILLARY 1) Supraperiosteal 2) PDL 3) Intraseptal Injection 4) Intracrestal Injection 5) Intraosseous Injection 6) PSA Nerve Block 7) MSA Nerve Block 8) ASA Nerve Block 9) Maxillary Nerve Block 10) Greater Palatine Nerve Block 11) Nasopalatine Nerve Block 12) AMSA Nerve Block 13) P-ASA Nerve Block
  • 32. POSTERIOR SUPERIOR ALVEOLAR NERVE BLOCK (PSA)  Nerves anaesthetized: Posterior superior alveolar nerve and its branches  Areas anaesthetized: Maxillary 3rd,2nd and 1st molars except the mesiobuccal root of the maxillary 1st molar.  Landmarks: Mucobuccal fold, Maxillary tuberosity,Zygomatic process of maxilla
  • 33. For Left PSA nerve block, a right handed administrator should face the patient from the 10 o’clock; For Right PSA nerve block a right handed administrator should face the patient directly from the 8 o’clock position Technique: Prepare the tissues at the height of the mucobuccal fold Orient the bevel towards the bone Partially open the patient’s mouth; pulling the mandible to the side of injection,retract the cheek with your fingers and pull the tissue taut. Insert the needle into the height of the mucobuccal fold over the 2nd molar Advance the needle in an upward, inward and backward direction(At once) Slowly advance the needle through the soft tissue Ensure the needle penetrates 10-14 mm depth. Aspirate in 2 planes If both aspirations are negative the deposit 0.9-1.8 ml solution over 30-60 seconds Withdraw the syringe slowly Wait for 3-5 minutes before commencing the dental procedure
  • 34.
  • 35. ANTERIOR SUPERIOR ALVEOLAR OR INFRAORBITAL NERVE BLOCK (ASA)  Nerves anaesthetized- Anterior superior alveolar -Middle superior alveolar -Infraorbital nerve  Areas anaesthetized-  Landmarks: Mucobuccal fold Infraorbital notch Infraorbital foramen
  • 36. Assume 10 o’clock position either directly facing the patient or in the same direction as the patient Technique- Position the patient supine or semisupine with the neck extended slightly
  • 37. Prepare the tissue at the injection site Feel the intraorbital notch,Move the finger inferiorly until a depression is felt. Here the infraorbital foramen is located Place the thumb over the infraorbital formen Retract the lip, pull the tissues in the mucobuccal fold taut Insert the needle into the height of the mucobuccal fold with the bevel facing the bone Orient the needle towards the Infraorbital foramen The needle should be held parallel with the long axis of the tooth as it is advanced to avoid premature contact with the bone. Advance the needle slowly until the bone is contacted Check the depth of needle penetration,lateral deviation of the needle from the infraorbital foramen and the orientation of the bevel Aspirate, then slowly deposit 0.9ml to 1.2ml(30-40 seconds).maintain firm finger pressure at the injection site Withdraw the syringe slowly WAit for 3-5 minutes after the injection before comencing the dental procedure
  • 38. MIDDLE SUPERIOR ALVEOLAR NERVE BLOCK(MSA)  Nerves anaesthetized: Middle superior alveolar and terminal branches  Areas anaesthetized:  Landmarks: Mucobuccal fold over the 2nd premolar
  • 39. For Right MSA nerve block, a right handed administrator should face the patient from the 10 o’clock; For Left MSA nerve block a right handed administrator should face the patient directly from the 8 or 9 o’clock position Prepare the tissue at the injection site Stretch the patient’s upper lip to make the tissues taut and to gain visibility Insert the needle into the height of the mucobuccal fold above the 2nd premolar with the bevel facing the bone Penetrate the mucous membrane and slowly advance the needle until its tip is located well above the apex of the 2nd premolar Aspirate Slowly deposit 0.9ml-1.2ml in approx. 30-40 seconds Withdraw the syringe slowly Wait for 3-5 minutes before commencing the dental treatment Techniques:
  • 40.
  • 41. GREATER PALATINE NERVE BLOCK  Nerves anaesthetized: Greater Palatine  Areas anaesthetized:  Landmarks: Greater palatine foramen Junction of maxillary alveolar process and palatine bone
  • 42.
  • 43. NASOPALATINE NERVE BLOCK  Nerves anaesthetized: Nasopalatine nerves bilaterally  Areas anaesthetized:  Landmarks:Central incisors Incisive papilla
  • 44.
  • 45.  MANDIBULAR 1) IANB Nerve block 2) Buccal Nerve Block 3) Mental Nerve block 4) Incisive nerve block
  • 46. INFERIOR ALVEOLAR NERVE BLOCK/ MANDIBULAR NERVE BLOCK  Nerves anaesthetized: Inferior alveolar nerve Incisive nerve Mental nerve Lingual nerve  Areas anaesthetized: mandibular teeth till the midline body of mandible Inferior portion of Anterior 2/3rd of the tongue Floor of the mouth Lingual soft tissues and periosteum
  • 47. 3 parameters considered during IANB 1. Height of injection 2. Anteroposterior site of injection 3. Penetration depth LANDMARKS Anatomical Landmarks of Inferior alveolar nerve block: Mucobuccal fold. Anterior border of Mandibular ramus. External oblique ridge. Internal oblique ridge. Retromolar triangle. Pterygomandibular ligament. Buccal sucking pad. Pterygomandibular space.
  • 48.
  • 49.
  • 50. BUCCINATOR NERVE BLOCK/LONG BUCCAL NERVE BLOCK  Nerves anaesthetized: Buccal nerve  Areas anaesthetized:Soft tissues and periosteum, buccal to mandibular teeth  Landmarks:Mandibular molars,Mucobuccal fold
  • 51.
  • 52. MENTAL NERVE BLOCK  Nerves anaesthetized: Mental nerve  Areas anaesthetized:Soft tissues of the lower lip, chin and buccal soft tissues anterior to the mental foramen are anaesthetized  Landmarks:Mandibular premolars,Mucobuccal fold
  • 53.
  • 54. INFILTRATION ANAESTHESIA  Nerves anaesthetized:Large terminal branches of dental plexus  Areas anaesthetized: Pulp and root area of the tooth Buccal periosteum Connective tissue and mucous membrane
  • 55. RECENT ADVANCES  Safety Syringes  Computer controlled local anaesthetic delivery system  Comfort Control Syringe  Local Anaesthetics with New Additives  Eutectic mixture of LA  Electronic Dental Anaesthesia  Vibraject
  • 56. LOCAL COMPLICATIONS Needle breakage Paresthesia Facial nerve paralysis Trismus Soft tissue injury Haematoma Pain on injection Burning on injection Infection Edema Sloughing of the tissues Post anaesthetic intraoral lesions
  • 57. NEEDLE BREAKAGE  Causes:  Primary cause-Bending of the needle that causes weakening.  Sudden unexpected movement by the patient  Manufacturing defects.  Prevention  Use longer needles for penetration of the tissue beyond 18mm  Use larger-gauge needles  Do not insert the needle upto its hub; rigid and weakest point  Do not redirect a needle after its insertion into the tissue
  • 58. Management: a. Remain calm; do not panic. b. Instruct the patient to not move. Keep the patient’s mouth open or place a bite block c. If the fragment is visible then try to remove it with a small hemostat. d. If the needle is lost and cannot be retrieved easily then do not proceed with an incision or probing. e. Inform your insurance company immediately. f. Refer the patient to an OMFS for consultation.
  • 59. PARAESTHESIA  Persistant anaesthesia (extend well beyond the expected duration)  Cause:  Trauma to any nerve  Injection of LA solution contaminated by alcohol or a sterilizing solution near a nerve produces irritation resulting in edema and increased pressure in the region of the nerve.  Haemorrhage in and around the nerve sheath,which increases the pressure on the nerve  Problems:  Self-inflicted injury.  Prevention  Strict adherence to injection protocol  Management  Mostly resolves within approximately 8 weeks without treatment.
  • 60. FACIAL NERVE PARALYSIS  Cause:  Administering LA into the capsule of the parotid gland or place the tip within the parotid gland  Problem  Loss of motor function to the muscles of facial expression  Management  The situation is transient so one must wait until the effect of the nerve block wears off.  Remove contact lenses if any
  • 61. TRISMUS  Tetanic spasm of jaw muscles by which the normal mouth opening is restricted  Causes:  Trauma to muscles or blood muscles in the infratemporal fossa  LA solutions into which alcohol or cold sterilizing solutions have diffused produce irritation  Haemmorhage  Low-grade infection  Prevention  Use of sharp sterile needle  Practice atraumatic insertion and injection technique  Avoid multiple insertions  Use minimum effective volumes of LA
  • 62.  Management  Heat therapy, warm saline rinse analgesics, muscle relaxants  Physiotherapy consists of opening and closing the mouth, lateral excursions of the mandible for 5 minutes every 3-4 hours, using sugarless chewing gum  Antibiotics can also be prescribed for 7 days if the pain doesn’t subside after 48-72 hours  Refer to an OMFS if there is no improvement in pain or dysfunction.
  • 63. SOFT TISSUE INJURY  Self-inflicted trauma to lips and tongue is frequently caused by the patient inadvertently biting or chewing these tissues while still anaesthetized.  Cause: Trauma  Problem: Swelling and significant pain after the effect of anaesthesia wears off.  Prevention: Place a cotton roll between lips and teeth if they are still anaesthetized at the time of discharge.Secure this roll with dental floss wrapped around the teeth Warn the patient against eating or drinking hot foods and biting on the lips or the tongue to test for anaesthesia
  • 64.  MANAGEMENT  Analgesics, for pain.  Antibiotics if necessary  Lukewarm saline rinses for decreasing any swelling.  Petroleum jelly to cover lip lesions and minimize irritation
  • 65. HAEMATOMA  The effusion of blood into the extravascular spaces that can result from inadvertently nicking a blood vessel during the process of injecting the local anaesthetic.  Usually results due to the nicking of artery  Cause: Haematomas after IANB are usually visible intraorally whereas PAS haematomas are visible extraorally.  Problems:Complications are trismus and pain  Prevention:Modify the injection technique slightly as per the patient’s facial characteristics. -Minimize the number of needle penetrations into the tissue. Management : immediately, apply direct pressure to the site of the bleeding for 2 mins. In case of IANB pressure is applied to the medial aspect of the mandibular ramus. In case of ASANB pressure is applied directly over the infraorbital foramen.
  • 66.  Management: immediately, apply direct pressure to the site of the bleeding for 2 mins. In case of - IANB pressure is applied to the medial aspect of the mandibular ramus. - In case of ASA NB pressure is applied directly over the infraorbital foramen. - In case of PSA NB digital pressure can be applied to the soft tissue in the mucobuccal fold as far distally as can be tolerated. Apply pressure in the medial and superior direction and if available apply ice. - Subsequently after the treatment of hematomas slight discolouration is likely to be seen. This is due to the extravasated blood elements which will slowly resorb over 7-14 days. Heat should not be applied immediately though it can be applied from the 2nd day onwards. - Avoid any dental treatment until the hematoma resorbs.
  • 67. PAIN ON INJECTION  Causes - Careless injection technique, multiple injections, rapid deposition of LA solutions  Problems - Patient anxiety leading to sudden unexpected movements increasing the risk of needle breakage.  Prevention - Adhere to proper injection techniques, use sharp needles, use topical anaesthetic before injecting, use sterile LA solutions, inject LA slowly
  • 68. BURNING ON INJECTION  Cause- pH of the solution, rapid injection of LA, contamination of LA cartridges, solutions warmed to normal room temperatures.  Problems- tissue damage may result because of rapid injection, contaminated tissue injection and overly warmed LA solution.  Complications- post anaesthetic trismus, oedema, paraesthesia.  Prevention- slow down the rate of injection to 1 ml per min.  Management- It is a transient phase so management is usually required for specific complications.
  • 69. INFECTION  Causes - Contamination of needle before administrating LA, administrating LA into the area of infection.  Problems- Contamination of needles and solutions.  Prevention- Use sterile disposable needles, handle needles with care, prepare tissues properly before injecting LA.  Management- Trismus may be a complication which must be treated using heat and analgesics and heat. If there is no improvement the patient should be started on a 7-10 day antibiotic course.
  • 70. OEDEMA  Causes- trauma during injection, infection, allergy- angioedema, hemorrhage, injection of irritating solution.  Problems- LA obstruction, pain and dysfunction of the region, angioneurotic oedema.  Prevention- proper care and handling LA armamentarium, use atraumatic injection techniques.  Management- prescribe analgesics for pain, antibiotic therapy if the following persists – -pain -mandibular dysfunction -oedema -warmth.
  • 71.  In case of allergy induced oedema prescribe intramuscular and oral antihistamine agents if breathing is not compromised.  If breathing is compromised- P→A→B→C→D  0.15mg epinephrine is injected every 10-15 mins until respiratory distress resolves.  Histamine blocker is administered either im or iv.  Corticosteroid is administered either im or iv.  Preparations are made for cricothyrotomy if needed  Thoroughly evaluate the patient before the next appointment.
  • 72. POST ANAESTHETIC INTRA-ORAL LESIONS  Ulcerations seen 2 days after injection around the site of the injection and presents with immense pain.  Recurrent apthous stomatitis on gingival tissues that are not attached to the underlying bone and the buccal mucosa.  Herpes simplex seen on tissues attached to underlying bone. Trauma to tissues by needles, LA solutions, cotton swab or any other instrument may activate latent form of diseased processes that were present in the tissues before injection.
  • 73.  Problems- acute sensitivity in ulcerated area.  Prevention- antiviral agents can be used for extraoral herpes simplex infections.  Management- topical anaesthetic solutions, mixture of equal amounts of diphenhydramine and milk of magnesia is rinsed in he mouth.  Ulcerations last for 7-10 days with or without pain.
  • 74. SYSTEMIC COMPLICATIONS  Overdose- results due to: - biotransformation of drug is unusually slow. - the unbiotransformed drug is too slowly eliminated from the body through the kidneys. - too large a total dose is administered. - absorption from the injection site is unusually rapid. - inadvertent intravascular administration occurs.  Management- most of the LA overdose reactions are self-limiting because the blood level in target organs continues to decrease as the reaction progresses and redistribution and biotransformation take place. Rarely, drugs other than oxygen are necessary.
  • 75. ALLERGY  Allergic responses to LA- dermatitis - bronchospasm - systemic anaphylaxis  Of special interest with regard to allergy is the bacteriostatic agent- methylparaben.  Other causes- sodium bisulfite allergy, epinephrine allergy, latex allergy, topical anaesthetic allergy.  Prevention- P→A→B→C→D