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Pain pathway.pptx

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Pain pathway.pptx

  1. 1. PAIN PATHWAY PRESENTED BY: DR. AMITHA PRAKASH POST GRADUATE STUDENT
  2. 2. 1. INTRODUCTION 2. DEFINITIONS 3. HISTORY 4. GLOSSARY 5. CLASSIFICATION OF PAIN 6. MECHANISM OF NERVE TRANSMISSION 7. PAIN PATHWAY 10. THEORIES OF PAIN 11. CLINICAL CONSIDERATION 12. METHODS TO CONTROL PAIN 13. CONCLUSION 14. REFERENCES CONTENTS
  3. 3. INTRODUCTION • Pain is almost an universal experience. • SUBJECTIVE sensation.
  4. 4. DEFINITIONS An unpleasant sensory or emotional experience associated with actual or potential tissue damage or described in terms of damage. IASP Definition The subject’s conscious perception of modulated nociceptive impulses that generate an unpleasant sensory & emotional experience associated with actual or potential tissue damage, or described in terms of such damage. Bell’s Orofacial Pain 5th ed Pain is defined as an “unpleasant emotional experience usually initiated by a noxious stimulus and transmitted over a specialized neural network to the central nervous system where it is interpreted as such”. Monheim’s Local anesthesia & pain control in dental practice. 7th ed
  5. 5.  Derived from Latin -“Poena” meaning Penalty/punishment from God.  JCAHO declared pain as fifth vital sign (1999). HISTORY
  6. 6. GLOSSARY OF PAIN ALLODYNIA ANALGESIA ANAESTHESIA DOLOROSA DYSAESTHESIA HYPERALGESIA PARESTHESIA NEURALGIA NEURITIS PAIN THRESHOLD
  7. 7. CLASSIFICATION OF PAIN • Based on duration  Acute Pain  Chronic pain • According to intensity  Mild pain  Moderate pain  Severe pain • According to onset  Spontaneous  Induced
  8. 8. • According to temporal relationship and duration  Intermittent  Continuous  Protracted  Intractable  Recurrent
  9. 9. • According to pain location  Localized  Diffused  Radiating  Lancinating  Migrating
  10. 10. CLASSIFICATION OF PAIN(BASED ON ORIGIN) PAIN SOMATIC VISCERAL SUPERFICIAL DEEP
  11. 11. • Results from stimulation of the pain receptors in the tissues. • Superficial pain- from skin and subcutaneous tissues. • Deep pain-from muscles, bones, joints, and periosteum. • Arises from viscera • From the heart –Angina pectoris • Stomach –peptic ulcer • Intestine –intestinal colic,renal colic SOMATIC PAIN VISCERAL PAIN
  12. 12. FAST PAIN • Begins after 1 sec or more and then increases slowly over many sec or min • It can occur both in the skin and in almost any deep tissue or organ • Associated with tissue destruction • Transmitted by C-fibres ,neurotransmitter – substance p SLOW PAIN • Felt within about 0.1 sec after a painful stimuli • Felt mainly in skin not felt in most deeper tissues of the body • Transmitted by A delta fibres,neurotransmitter – glutamate
  13. 13. BASIC STRUCTURE OF NEURONS
  14. 14. Depending on function Sensory Neuron Motor Neuron Depending on length of axons Golgi type 2 neurons Golgi type 1 neurons
  15. 15. MECHANISM OF NERVE TRANSMISSION
  16. 16. ELECTROCHEMISTRY OF NERVE CONDUCTION  RESTING STATE 1. Slightly permeable to Na+ ions 2. Freely permeable to K+ & Cl- ions  MEMBRANE EXCITATION a) Depolarization  Excitation of nerve increases permeability to sodium ions  influx of Na+ ions into nerve cell body- depolarization- -50 to -60mv  Decrease in negative electrical potential -55mv – firing threshold  When firing threshold is reached – rapid influx of Na+ ions – electrical potential of +40mv  This takes place within 0.3 msec.
  17. 17. b) Repolarization  Action potential terminates – membrane repolarizes  Due to inactivation of permeability to Na+ ions.  Increased permeability of K+ ions – efflux of K+ ions – rapid repolarization occurs.  Returns to resting potential  Movement of Na+ - depolarization & movement of K+ ions – repolarization – passive.  After reaching resting membrane potential – slight excess of Na+ ions & K+ions  Period of metabolic activity  Process requires 0.7 msec.
  18. 18. THEORIES OF PAIN 1. Intensity theory - PLATO 2. Specificity theory - VON FREY -1895 3. Pattern theory - JP NAFE 4. Gate control theory - RONALD MELZACK and 5. PATRICK WALL-1965
  19. 19. Intensity Theory • Fourth century by Plato • The theory defines pain, not as a unique sensory experience but rather, as an emotion that occurs when a stimulus is stronger than usual. • This theory is based on Aristotle’s concept that pain resulted from excessive stimulation of the sense of touch.
  20. 20. Limitation •The trigeminal system provides an example against this theory. •In case of trigeminal neuralgia the patient can suffer excruciating pain from a stimulus no greater than a gentle touch provided it is applied to a trigger zone. •Although, the intensity theory is not accepted, it remains true to say that intensity of stimulation is a factor in causing pain.
  21. 21. Specificity Theory (Von Frey, 1895) • Specific pain receptors transmit signals to a "pain center" in the brain that produces the perception of pain. • This theory considers pain as an independent sensation with specialized peripheral sensory receptors [nociceptors], which respond to damage and send signals through pathways (along nerve fibres) in the nervous system to target centers in the brain. • These brain centers process the signals to produce the experience of pain.
  22. 22. Specificity theory cannot explain •Any pathologic pain produced by mild noxious stimuli. • Referred pain that can be triggered by mild innocuous stimulation of normal skin. •Does not explain the paroxysmal episodes of pain produced by mild stimulation of trigger zone in trigeminal neuralgia.
  23. 23. PATTERN THEORY • In 1894, Goldscheider proposed that stimulus intensity and central summation are the critical determinant of pain. • Particular pattern of nerve impulses that evoke pain are produced by summation of sensory input within the dorsal horn of spinal cord (J.P. Nafe, 1929) • Pain results when the total output of the cells exceed a critical level.
  24. 24. • RONALD MELZACK and PATRICK WALL in 1965 GATE CONTROL THEORY
  25. 25. SIGNIFICANCE OF GATE CONTROL The gating of pain at spinal level is similar to presynaptic inhibition. It forms the basis for relief of pain through • rubbing • massage techniques • application of ice packs • Acupuncture • Electrical Analgesia . All these techniques relieve pain by stimulating the release of endogenous pain relievers ( opioid peptides ) which close the gate and block the pain signals.
  26. 26. REFERRED PAIN • Referred pain is the pain that is perceived at a site adjacent to or away from the site of origin. • The pain usually is initiated in one of the visceral organs are referred to an area on the body surface. • The pain may be referred to an area of the body not exactly coincident with the location of the viscus producing the pain. • For eg, a) Cardiac pain is felt at the inner part of left arm and left shoulder. b) Pain in diaphragm is referred to right shoulder
  27. 27. MECHANISM OF REFERRED PAIN Dermatomal Rule • According to it, pain is referred to a structure, which is developed from the same dermatome from which the pain producing structure is developed. • A dermatome includes all the structures or parts of the body, which are innervated by afferent nerve fibers of one dorsal root. For example, the heart and inner aspect of left arm originate from the same dermatome. So, the pain in heart is referred to left arm.
  28. 28. VISCERAL PAIN • A striking characteristic of the brain is that although it receives and processes nociceptive information, the brain itself has no sensation of pain. • The visceral organs themselves have no pain receptors, pain receptors are present , embedded in the walls of the arteries serving these organs.
  29. 29. • Visceral pain is characterized as diffuse and poorly localized and is often “referred to” and felt in another somatic structure distant or near the source of visceral pain. • General visceral afferent nociceptive information from visceral structures of the trunk is carried mostly by type C, Aδ, or Aβ fibers
  30. 30. NEURAL PAIN PATHWAY • Nociception is the neural mechanism by which an individual detects the presence of potentially tissue harming stimulus . • Nociceptive mechanism consists of: • Transduction • Transmission • Modulation • Perception
  31. 31. TRANSDUCTION • Involves conversion of signals from the environment , that is, light, taste, sound, touch smell, into electrical signals. • These signals are then collected and processed by the CNS. • Receptors are sensory nerve endings that terminates in the periphery and produces a series of impulses upon stimulation. • These impulses are transmitted through afferent nerves.
  32. 32.  There are two different types of receptors:- 1. Exteroreceptors 2. Interoreceptors  EXTEROCEPTORS are receptors which provides information from skin and mucosa.  Eg . Meissner’s corpuscles : tactile receptors in skin  Merkel’s corpuscles : tactile receptors in the submucosa of oral mucosa and tongue  Raffini’s end organ : warmth receptor  Pacinian corpuscle : pressure receptor  Krause’s end bulb : cold receptor  Free nerve ending : perceives superficial pain and touch
  33. 33.  INTEROCEPTORS  Interoceptors are the receptors which give response to stimuli arising from within the body.  For eg,  Baroreceptors – blood vessels  Chemoreceptors – GI tract  Osmoreceptors – urinary tract
  34. 34. TRANSMISSION MODULATION PERCEPTION
  35. 35. NEUROTRANSMITTER
  36. 36. CHEMICAL NEUROTRANSMITTERS
  37. 37. Neospinothalamic pathway • The fast type a-delta pain fibres transmit mainly mechanical and acute thermal pain. • They terminate mainly in lamina I (lamina marginalis of the dorsal horns) • These give rise to long fibers that cross immediately to the opposite side of the spinal cord through and then pass upward to the brain stem in anterolateral columns.
  38. 38. • These fibers terminate in the ventrobasal nucleus in thalamus. From the thalamic areas, signals are transmitted to cortex . • “glutamate” is the neurotransmitter for type A(δ) pain nerve fiber endings.
  39. 39. Paleospinothalamic pathway • The peripheral fibres terminate almost entirely in laminas II and III of the dorsal horns, which together are called as substantia gelatinosa. • The paleospinothalamic system transmits pain mainly carried in the peripheral slow-chronic type-C pain fibres, although it does transmit some signals from type A-delta fibers as well.
  40. 40. DENTAL PAIN PATHWAY • Trigeminal nerve is the mixed cranial nerve • It is the chief sensory nerve for face and the motor nerve for muscles of mastication • Trigeminal nerve carries somatosensory information from face , teeth , periodontal tissues , oral cavity and cranial dura mater to sensory cortex
  41. 41. Origin • Sensory fibers of trigeminal nerve arise from the trigeminal ganglion situated near temporal bone. • Peripheral processes of neurons in this ganglion form three divisions of trigeminal nerve, namely ophthalmic, mandibular and maxillary divisions. • Central processes from neurons of trigeminal ganglion enter pons in the form of sensory root.
  42. 42. Termination • After reaching the pons, fibers of sensory root divide into two groups, namely descending fibers and ascending fibers. • Descending fibers terminate on primary sensory nucleus and spinal nucleus of trigeminal nerve. Primary sensory nucleus is situated in pons. • Spinal nucleus of trigeminal nerve is situated below the primary sensory nucleus and extends up to the upper segments of spinal cord. • Ascending fibers of sensory root terminate in the mesencephalic nucleus of trigeminal nerve, situated in brainstem above the level of primary sensory nucleus.
  43. 43. Central Connections • Majority of fibers from the primary sensory nucleus and spinal nucleus of trigeminal nerve ascend in the form of trigeminal lemniscus and terminate in ventral posteromedial nucleus of thalamus in the opposite side. • From thalamus, the fibers reach the somatosensory areas of cerebral cortex. • Primary sensory nucleus and spinal nucleus of trigeminal nerve relay the sensations of touch, pressure, pain and temperature from the regions mentioned above.
  44. 44. • Fibers from mesencephalic nucleus form the trigeminocerebellar tract that enters spinocerebellum via the superior cerebellar peduncle of the same side. • This nucleus conveys proprioceptive impulses from facial muscles, muscles of mastication and ocular muscles.
  45. 45. CLINICAL CONSIDERATION PERIODONTAL PAIN ACUTE GINGIVAL OR PERIODONTAL ABSCESS PERICORONITIS
  46. 46. PERIODONTAL PAIN • Localized, deep throbbing pain • Involving inflammation of PDL around one or more teeth • Mobility • Localized bleeding • Presence of pocket • In radiograph loss of bone is present. • Pain last for hour or day • Involve tooth is tender on percussion • If pain involve multiple teeth including opposing teeth then occlusal trauma should considered
  47. 47. ACUTE GINGIVAL OR PERIODONTAL ABSCESS • Tooth is painful to bite on and is not so deep seated or throbbing as that of apical abscess. • Pain is spontaneous • Associated localized swelling • Presence of deep PDL pocket
  48. 48. PERICORONITIS • The pain can be severe, radiating in the posterior mouth region. • The patient mostly faces difficulty or inability to comfortably close or open the mouth. • The mucosa posterior to the erupting molar is very painful to touch.
  49. 49. Methods of pain control 1) Removing the cause 2) Blocking the pathway of painful impulses - Local anesthetic solution - Interferes with pain perception 3) Raising the pain threshold
  50. 50. MEDICATIONS  Non opioids • These include aspirin and NSAIDS, which have analgesic, anti-pyretic, anti-platelet, anti-inflammatory actions. • They differ from opioid analgesic in that they presumably prevent the formation of prostaglandin E1 by inhibitory action on enzyme, cyclooxygenase. • They don’t produce tolerance, physical dependence or addiction. • They have ceiling effect where by increases dose beyond peak point does not increase analgesic effect, but may effect duration of analgesic.
  51. 51.  Opiods  Includes morphine and morphine like drugs. They act by :- 1. Depressing nociceptive neurons while stimulate non-nociceptive Cells. 2. It elevates the threshold for painful stimuli. 3. It alters the emotional reaction to pain. 4. It produces sleep which also elevates the threshold. 5. Addition of codeine to NSAIDS increases analgesic effect.
  52. 52. NEW APPROACHES TO INHIBIT PAIN Transcutaneous Electrical Neural Stimulation (TENS) • With TENS, cutaneous bipolar surface electrodes are placed in the painful body regions and low voltage electric currents are passed. • Best results have been obtained when intense stimulation is maintained for atleast an hour daily for more than 3 weeks. • TENS portable units are in wider use in clinics throughout the world and has been proved most effective against neuropathic pain.
  53. 53. ACUPUNCTURE Method of inhibiting pain impulses. • Acupuncture theory is based on an invisible system of communication between various organs of the body that is distinct from circulatory, nervous and endocrine system. • Location of needle insertion depends on part of body acupuncturist wishes to anesthetize. • Eg : to pull a tooth – a needle is inserted in the web between thumb and index finger.
  54. 54. Conclusion
  55. 55.  ESSENTIALS OF PHYSIOLOGY SHEMBULINGAM  MONHEIMS LOCAL ANAESTHESIA AND PAIN CONTROL 7th EDITION  BELL’S OROFACIAL PAIN – JEFFREY 6th EDITION  TEXTBOOK OF PHARMACOLOGY – TRIPATHI 2nd EDITION  CARRANZA CLINICAL PERIODONTOLOGY 11th EDITION REFERENCES

Notas do Editor

  • Pain is difficult to define , for pain is a
  • INSP –THE INTERNATIONAL ASSOCIATION FOR THE STUDY OF PAIN

  • PAIN FIF
    FIFTHTH VITAL SIGN 2001- NUMERIC RATING SCALE
    JOINT COMMISION ON ACCREDITATION OF HEALTHCARE ORGANISATION
  • 1.Allodynia- pain due to non noxious stimulus to normal skin,non painful,eg;hair brushing against their skin-mechanical ,thermal ,tactile
    2.Analgesia-absence of pain on noxious stimulation
    3.Anesthesia dolorosa-pain in an area or region which is anesthetic
    5.Dysaesthesia-an unpleasant abnormal sensation of touch, persons may feel like as their skin is itiching or burning.this results from nerve damage,which results in inproper signaling.
    6.Hyperalgesia-increased sensitivity to noxious stimulation
    8.Neuralgia-pain in the distribution of nerve or nerves
    9.Neuritis-inflammation of nerve or nerves
    12.Pain threshold –the least stimulus intensity at which a subject perceives pain



  • Mild pain- Can be controled by analgesics
    Moderate pain -With narcotic analgesics
    Severe pain -Either elimination of cause or interuption of the pain pathway
    Chronic pain-defined as pain that persists longer than the normal course of time associated with a particular type of injury
    Spontaneous-without being provoked
    Induced-caused by provocation
    acute pain-suuden onset..clearly has a defined cause.
    Chronic pain-usually persist for weeks or months,and associated with underlying cause…arthritis.
    Heterotopic pain – defined by merskey and bogduk pain perceived in a region that has a nerve supply different from the source of pain.
  • Intermittent- Short duration and separated by pain free period

    Continuous- Longer duration

    Protracted- Lasts for several days

    Intractable- Does not respond to therapy

    Recurrent- Two or more similar episodes of pain

    Periodic- Regularly recurring episodes
  • Localized- patient is able to clearly and precisely define the pain

    Diffused- Less well define vague variable anatomically –fibromyalgia….widespread ..shifts in location….intensity throughout the body.

    Radiating-Rapidly changing pain

    Lancinating- Momentary cutting exacerbation,piercing or stabbing sensations…..clearly indicative of nerve irritation…journal of american medical association 19

    Migrating-If changes from one location to other
  • Type A – Alpha - + , 6-22 u , 30-120m/s motor, proprioception
    Beta - + 6- 22u, 30 – 120m/s motor, proprioception
    Gamma - + 3 – 6u, 15 – 35m/s muscle tone
    Delta - + 1 – 4u, 5 – 25m/s, pain, temperature touch

    Type B + <3u , 3 – 15m/s, various autonomic functions

    Type C -- 0.3 – 1.3u, 0.7 – 1.3m/s various autonomic functions
  • “Neurons are the fundamental unit of the nervous system specialized to transmit information to different parts of the body.
    Nerve cell body is also known as soma or perikaryon .it is irregular in shape and it is constituted by a mass of cytoplasm called neuroplasm which is covered by a cell membrane.it contains a large nucleus,nissl bodies,neurofibrils,mitochondria,and golgi apparatus
    Dendrite and axon together form the processes of neuron,in general the dendrites are shrt processes and the axons are are long processes. Dentrite is the branched processes of the neuron.dendrite is conductive in nature.it transmits impulses toward the nerve cell body
    Axon is longer than dendrites.each neuron has only one axon.the axon arises from axon hillock of nerve cell body
  • DEPENDING ON NUMBER OF POLES: unipolar – only one structure extending from the soma…seen in invertebrates.
    Bipolar –one axon and one dendrites arising from the soma
    Multipolar –one axon and many dendrites arising from the soma.
  • Sensory neurons carry signals from the outer parts of the body to cns .motor neurons carry signals from cns to the outer parts of the body.
    golgi type 1 neuron – neuron which has a long axon that begins in the grey matter of cns and may extend from there.and its called as projection neuron.they include the neurons forming peripheral nerves and long tracts of brain and spinal cord.
    Golgi type 2 neuron- no axon or short axon which does not extend branches out of the gray matter of cns.
  • Conduction of impulse depends upon the electrical potential that exists across the nerve membrane.
    Electrical poitential exists in the membrane of most cells but nerve cells posses the ability to transmit this impulse.
    This transmission occurs when during transition of nerve from resting to active state
  • Proposed by Descartes in 1664 , Muler 1840

    He proposed that pain occurs due to stimulation of specific pain receptors (Nociceptors)
    with transmission by nerves directly to brain

    The pain is purely an afferent sensory experience
  • Proposed that a gate mechanism exist within the dorsal horn of the spinal cord
    Small nerve ( pain receptors ) and large nerve fibres (normal receptors) synapse on projection cells (p) ,which go upto the spinothalamic tract , and inhibitory interneurons ( I )within the dorsal horn
  • According to dermatomal rule , pain is referred to a structure which is developed from the same dermatome from which the pain producing structure is developed

    A dermatome includes all the structures or parts of the body ,which are innervated by afferent nerve fibres of one dorsal root
  • Pain from internal organs.
    Two components of pain – fast pain – a delta
    slow – c fibre
  • Explain about each Aδ Mechanical Nociceptors

    C Polymodal Nociceptors

    C fibre mechanical nociceptors

    High threshold cold nociceptors
  • Process by which noxious stimuli leads to electrical activity in sensory nerve endings

    These are specialized sensory receptors distributed all over the body which respond to physical chemical stimuli

    Exteroceptors
    Interoceptors
    EXTEROCEPTORS are receptors which give response to stimuli arising from outside the body

    These receptors provide information from skin and mucosa

    Eg . Meissner’s corpuscles : tactile receptors in skin
    Merkel’s corpuscles : tactile receptors in the submucosa of oral mucosa and tongue
    Raffini’s end organ : warmth receptor
    Pacinian corpuscle : pressure receptor
    Krause’s end bulb : cold receptor
    Free nerve ending : perceives superficial pain and touch
    INTEROCEPTORS

    Interoceptors are the receptors which give response to stimuli arising from with in the body
  • TRANSMISSION

    Electrical events are transmitted along neuronal pathways, while molecules in the synaptic cleft transmit information from one cell surface to another.
    MODULATION

    The adjustment of events, by up- or down regulation. This can occur at all levels of the nociceptive pathway, from tissue, through primary (1°) afferent neurone and dorsal horn, to higher brain centres.
    PERCEPTION

    It determined by interaction of the (cortex, thalamus, and limbic system) higher centers.
  • Neurotransmitter is a chemical substance that acts as the mediator for the transmission of nerve impulse from one neuron to another neuron through a synapse.
  • Periphery to spinal cord-first order neuron located in the dorsal root ganglia
    Spinal cord to thalamus-second order neuron grey matter of spinal cord
    Thalamus to cortex –third order neuron posterolateral ventral nucleus of thalamus
  • First second third order neurons
    Pathways of pain sensation from skin and deeper structures
    All pain receptors are free nerve endings these endings use 2 separate pathways for transmitting pain signals into cns
  • 1/5th terminate at the ventral posterolateral nucleus of thalamus.
    Rest terminate in the nuclei of reticular formn in the brainstem
  • Localized, deep throbbing pain
    Involving inflammation of PDL around one or more teeth
    Mobility
    Localized bleeding
    Presence of pocket
    In radiograph loss of bone is there
    Pain last for hour or day
    Involve tooth is tender on percussion
    If pain involve multiple teeth including opposing teeth then occlusal trauma should considered

    Tooth is painful to bite on and is not so deep seated or throbbing as that of apical abscess.

    Pain is spontaneous

    Associated localized swelling is there

    Presence of deep PDL pocket


    Severe radiating pain in posterior mouth region and inability to comfortably close or open mandible.
    Tissue distal to erupting molar is most painful to touch.

  • Queen Victoria was the first one to have anaesthesia for pain control during childbirth
    chloroform was used



    Use of Willow bark & leaves by Hippocrates: Salicylic acid in willow plant of genus Salix is the active ingredient of ASPIRIN.

    Coca cola was initially sold as a cure for pain: concept of using cocaine as a pain reliever
  • Activation ogf acupoints
    Release of neuropeptides – vasodilation n increased circultn
  • Pain is a protective mechanism-causing the individual to react to remove the pain stimuli.
    Thus pain, although unpleasant, is a protective sensation.
    Every day patient seeks care for the reduction or elimination of pain.
    Nothing is more satisfying to the clinician than the successful elimination of pain.
    The most important part of managing pain is understanding the problem and cause of pain.
    This is possible through proper diagnosis and appropriate therapy.

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