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Vivek Narayan
Oral Medicine & Radiology
IASP defines pain as an unpleasant
sensory and emotional experience
associated with actual or potential
tissue damage or described in terms
of such damage.
 Algesia/algia – pain.
 Neuralgia - Pain in one or more nerves
and is described as electric shock like
pain with presence of trigger zones.
 Neuropathic pain - Constant burning
type of pain without presence of trigger
zones.
 Allodynia - Pain due to a stimulus which
does not normally provoke pain.
 Hyperalgesia - Extreme reaction to a
stimulus which is normally painful.
Medical management.
Physiatry/physiotherapy.
TENS.
Acupuncture.
Low level laser therapy.
Cognitive behavioral therapy.
Hypnosis.
 Analgesic – pain reliever, pain killer.
 Analgesics
1. NSAIDS (non opioid analgesics) –
mild to moderate pain.
2. Opioid analgesics – severe pain.
 Arachidonic acid pathway.
 COX converts arachidonic acid
to produce,
1. Prostaglandins
2. Thromboxane
3. Prostacyclin
 COX 1 – secretion of mucus,
hemostasis & renal functions –
house keeping functions.
 COX 2 – induced by cytokines &
other stimuli of inflammation.
Mediators of pain &
inflammation
NSAIDS
Non selective COX
inhibitors
Aspirin
Indomethacin
Ibuprofen
Diclofenac
Piroxicam
Ketorolac
Preferential COX 2
inhibitors
Nimesulide
Meloxicam
Nabumetone
Selective COX 2
inhibitors
Celecoxib
Rofecoxib
Analgesics with poor
anti-inflammatory
action
Acetaminophen
Nefopam
 Acetyl salicylic acid.
 Converted to salicylic acid by the body.
 Acts on peripheral pain receptors.
 Hyperglycemia at toxic doses.
 Hyperventilation, asthma.
 GI irritant, ulcers.
 Prolonged bleeding.
 Dosage - 325 to 650 mg orally every 4
hours as needed, not to exceed 4 g/day
 Less effective than aspirin.
 Inhibits PG synthesis.
 Prolongs bleeding time.
 Gastric discomfort.
 Nausea & vomiting.
 Precipitates asthma.
 Indicated in RA, osteoarthritis, soft tissue
injuries & after tooth extraction.
 Dosage – 400mg q4 – 6h. Maximum
2.4g.
 Has all analgesic, antipyretic & anti-
inflammatory actions.
 Inhibits PG synthesis.
 Short lasting anti platelet action.
 Good tissue penetration.
 Concentration is 3 times the plasma t1/2 in
synovial fluid .
 Nausea, headache & dizziness.
 Used in arthritis, ankylosing spondyltits.
 Dosage – 50mg – 100mg q4 – 6h not to
exceed 150mg.
 Paracetamol.
 Central action & increases pain
threshold.
 Good antipyretic.
 Poor anti-inflammatory.
 No significant adverse effects.
 Used as analgesic for headache &
musculoskeletal pain, osteoarthritis.
 Dosage – 500mg – 1000mg q4 – 6h
not to exceed 4g.
 Locally acting NSAIDS.
 Inhibits prostaglandin synthetase.
 Has analgesic & local anesthetic
properties.
 Used for inflammatory conditions
of mouth & throat.
 Contraindicated in hypersensitivity.
 Oral tissue numbness & stinging
sensation may occur.
 Dosage – 0.15% mouthwash to be
used TID.
 Available as TANTUM ORAL RINSE.
 Acts on the CNS produces
depression.
 Otherwise called narcotic analgesics.
 Morphine is the prototype drug &
principal opium alkaloid .
 Morpheus – ‘god of dreams’
 Indicated for severe pain conditions.
 Sedation, mental clouding,
constipation, respiratory depression,
tolerance & dependence.
Opioid
analgesics
Natural alkaloids
Morphine
Codeine
Semisynthetic
opiates
Heroin
Pholcodeine
Hydrocodone
Oxycodone
Synthetic opioids
Pethidine
Fentanyl
Tramadol
 Methyl morphine.
 Converted to morphine by the
body.
 Effective cough suppressant.
 Constipation occurs.
 Used after extraction along with
NSAIDS.
 Dosage – 30mg – 60mg q4 – 6h.
 To treat moderate to severe pain.
 As an antitussive to suppress
cough.
 Effect starts after 30 mins & lasts
for 4 – 8hrs.
 Common side effects are nausea,
vomiting, constipation, drowsiness,
dizziness, lightheadedness.
 Dosage – 5mg – 10mg q4 – 6h.
 Synthetic centrally acting
analgesic.
 Indicated for moderate to
severe pain.
 Nausea, vomiting, drowsiness,
sedation & fatigue.
 50mg – 100mg q4 – 6h
maximum 400mg.
 To use lower doses of drugs.
 Increasing range of action – fast
onset, short acting
(acetaminophen) with a slow
onset, long acting (codeine or
tramadol).
 Targeting different pain
pathways simultaneously.
 Eliminate the source of pain, if at all
possible.
 Individualize regimens based on pain
severity and medical history.
 Maximize the non opioid before adding
an opioid.
 Optimize dose and frequency before
switching.
 For NSAIDs, consider,
1. Preoperative dose.
2. Loading dose.
3. Prescribing round-the-clock.
 Avoid chronic use of any analgesic
whenever possible.
 Reduce the dose and duration of any
NSAID or opioid in the elderly.
SEVERE PAIN – strong
opioids (morphine, heroin,
oxycodone) + non opioids
MODERATE PAIN – weak
opioid (codeine, tramadol)
+ non opioids
MILD PAIN –
acetaminophen, NSAIDS
 Primarily used to treat epilepsy or
seizures.
 MOA – reduces neuronal
hyperexcitability that is fundamental to
seizures.
 Neuralgic & neuropathic pain is also
because of neuronal hyperexcitability.
 Anticonvulsants used,
1. Carbamazepine
2. Oxcarbazepine
3. Phenytoin
4. Valproic acid
5. Lamotrigine
6. Baclofen
 Odontogenic infection &
inflammation.
 Post extraction, post surgical pain.
 Cracked tooth syndrome.
 Eagle’s syndrome.
 Neuralgias,
1. Trigeminal neuralgia.
2. Glossopharyngeal neuralgia.
3. Post herpetic neuralgia.
 Fractures – odontogenic &
osteogenic.
 Pain in carcinoma.
 Oral mucosal lesions.

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Analgesics in dentistry

  • 2. IASP defines pain as an unpleasant sensory and emotional experience associated with actual or potential tissue damage or described in terms of such damage.
  • 3.  Algesia/algia – pain.  Neuralgia - Pain in one or more nerves and is described as electric shock like pain with presence of trigger zones.  Neuropathic pain - Constant burning type of pain without presence of trigger zones.  Allodynia - Pain due to a stimulus which does not normally provoke pain.  Hyperalgesia - Extreme reaction to a stimulus which is normally painful.
  • 4. Medical management. Physiatry/physiotherapy. TENS. Acupuncture. Low level laser therapy. Cognitive behavioral therapy. Hypnosis.
  • 5.  Analgesic – pain reliever, pain killer.  Analgesics 1. NSAIDS (non opioid analgesics) – mild to moderate pain. 2. Opioid analgesics – severe pain.
  • 6.  Arachidonic acid pathway.  COX converts arachidonic acid to produce, 1. Prostaglandins 2. Thromboxane 3. Prostacyclin  COX 1 – secretion of mucus, hemostasis & renal functions – house keeping functions.  COX 2 – induced by cytokines & other stimuli of inflammation. Mediators of pain & inflammation
  • 7.
  • 8. NSAIDS Non selective COX inhibitors Aspirin Indomethacin Ibuprofen Diclofenac Piroxicam Ketorolac Preferential COX 2 inhibitors Nimesulide Meloxicam Nabumetone Selective COX 2 inhibitors Celecoxib Rofecoxib Analgesics with poor anti-inflammatory action Acetaminophen Nefopam
  • 9.  Acetyl salicylic acid.  Converted to salicylic acid by the body.  Acts on peripheral pain receptors.  Hyperglycemia at toxic doses.  Hyperventilation, asthma.  GI irritant, ulcers.  Prolonged bleeding.  Dosage - 325 to 650 mg orally every 4 hours as needed, not to exceed 4 g/day
  • 10.  Less effective than aspirin.  Inhibits PG synthesis.  Prolongs bleeding time.  Gastric discomfort.  Nausea & vomiting.  Precipitates asthma.  Indicated in RA, osteoarthritis, soft tissue injuries & after tooth extraction.  Dosage – 400mg q4 – 6h. Maximum 2.4g.
  • 11.  Has all analgesic, antipyretic & anti- inflammatory actions.  Inhibits PG synthesis.  Short lasting anti platelet action.  Good tissue penetration.  Concentration is 3 times the plasma t1/2 in synovial fluid .  Nausea, headache & dizziness.  Used in arthritis, ankylosing spondyltits.  Dosage – 50mg – 100mg q4 – 6h not to exceed 150mg.
  • 12.  Paracetamol.  Central action & increases pain threshold.  Good antipyretic.  Poor anti-inflammatory.  No significant adverse effects.  Used as analgesic for headache & musculoskeletal pain, osteoarthritis.  Dosage – 500mg – 1000mg q4 – 6h not to exceed 4g.
  • 13.  Locally acting NSAIDS.  Inhibits prostaglandin synthetase.  Has analgesic & local anesthetic properties.  Used for inflammatory conditions of mouth & throat.  Contraindicated in hypersensitivity.  Oral tissue numbness & stinging sensation may occur.  Dosage – 0.15% mouthwash to be used TID.  Available as TANTUM ORAL RINSE.
  • 14.
  • 15.  Acts on the CNS produces depression.  Otherwise called narcotic analgesics.  Morphine is the prototype drug & principal opium alkaloid .  Morpheus – ‘god of dreams’  Indicated for severe pain conditions.  Sedation, mental clouding, constipation, respiratory depression, tolerance & dependence.
  • 17.  Methyl morphine.  Converted to morphine by the body.  Effective cough suppressant.  Constipation occurs.  Used after extraction along with NSAIDS.  Dosage – 30mg – 60mg q4 – 6h.
  • 18.  To treat moderate to severe pain.  As an antitussive to suppress cough.  Effect starts after 30 mins & lasts for 4 – 8hrs.  Common side effects are nausea, vomiting, constipation, drowsiness, dizziness, lightheadedness.  Dosage – 5mg – 10mg q4 – 6h.
  • 19.  Synthetic centrally acting analgesic.  Indicated for moderate to severe pain.  Nausea, vomiting, drowsiness, sedation & fatigue.  50mg – 100mg q4 – 6h maximum 400mg.
  • 20.  To use lower doses of drugs.  Increasing range of action – fast onset, short acting (acetaminophen) with a slow onset, long acting (codeine or tramadol).  Targeting different pain pathways simultaneously.
  • 21.  Eliminate the source of pain, if at all possible.  Individualize regimens based on pain severity and medical history.  Maximize the non opioid before adding an opioid.  Optimize dose and frequency before switching.  For NSAIDs, consider, 1. Preoperative dose. 2. Loading dose. 3. Prescribing round-the-clock.  Avoid chronic use of any analgesic whenever possible.  Reduce the dose and duration of any NSAID or opioid in the elderly.
  • 22. SEVERE PAIN – strong opioids (morphine, heroin, oxycodone) + non opioids MODERATE PAIN – weak opioid (codeine, tramadol) + non opioids MILD PAIN – acetaminophen, NSAIDS
  • 23.  Primarily used to treat epilepsy or seizures.  MOA – reduces neuronal hyperexcitability that is fundamental to seizures.  Neuralgic & neuropathic pain is also because of neuronal hyperexcitability.  Anticonvulsants used, 1. Carbamazepine 2. Oxcarbazepine 3. Phenytoin 4. Valproic acid 5. Lamotrigine 6. Baclofen
  • 24.  Odontogenic infection & inflammation.  Post extraction, post surgical pain.  Cracked tooth syndrome.  Eagle’s syndrome.  Neuralgias, 1. Trigeminal neuralgia. 2. Glossopharyngeal neuralgia. 3. Post herpetic neuralgia.  Fractures – odontogenic & osteogenic.  Pain in carcinoma.  Oral mucosal lesions.