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PAIN
MANAGEMENT
Dr. Sameh Ahmad Muhamad abdelghany
Lecturer Of Clinical Pharmacology
Mansura Faculty of medicine
2
CONTENTS
1
4
5
3
2
PAIN
ASSESSMEN
T
TREATMENT
INTRODUCTION
CLASSIFICATION
TYPES
3
1 INTRODUCTION
4
Introduction
 Definition : An unpleasant sensory and
emotional experience associated with
actual or potential tissue damage.
 Pain may not be directly proportional to
amount of tissue injury.
 Highly subjective, leading to
undertreatment
5
 In cancer, the prevalence of pain in
advanced disease is 70-90%.
 " In HIV disease, pain prevalence is
about 50%.
 " Other illnesses may have significant
pain but no clear data.
6
2 CLASSIFICATION
7
Classification
I. Acute
II.Chronic :
i. Non malignant
ii. Malignant
8
 Injury, trauma, spasm or disease to skin, muscle, somatic
structures or viscera;
 Perceived and communicated via peripheral mechanisms
(pathways)
 Usually associated with autonomic response as well
(tachycardia, blood pressure, diaphoresis, pallor,
mydriasis (pupil dilation).
Acute Pain
9
 Usually subsides quickly as pain producing stimuli
decreases
 Associated with anxiety-(decreases rapidly)
 Can be understood or rationalized as part of the healing
process.
Cont.
10
i. Non-malignant
 Pain persists beyond the precipitating injury
 Rarely accompanied by autonomic symptoms
 Sufferers often fail to demonstrate objective
evidence of underlying pathology.
 Characterized by location-visceral, myofacial, or
neurologic causes.
II. Chronic Pain
11
ii. Malignant
 Has characteristics of chronic pain as well as
symptoms of acute pain (breakthrough pain).
 Has a definable cause, e.g. tumor recurrence
 In treatment, narcotic habituation is generally
not a concern.
II. Chronic Pain
12
3 TYPES OF PAIN
13
 Types of Pain
 Somatic
 Visceral
 Bone
 Neuropathic
 Emotional/Spiritual
14
I- Somatic Pain
 Aching, often constant
 May be dull or sharp
 Often worse with movement
 Well localized
 Skin, Muscle, Joints, superficial or deep.
 Eg:
o Bone & soft tissue
o chest wall
15
II- Visceral Pain
 Constant or crampy
 Aching, burning
 Poorly localized
 Referred
 Organs of Thorax & Abdominal Cavity.
 Usually as a result of stretching, infiltration and
compression
 Eg:
o Liver capsule distension
o Bowel obstruction
16
 Both Somatic & Visceral pain
travel along the same
pathways. Pain stimuli arising
from the viscera is perceived
as somatic in origin.
 This can be confused by the
brain and is often described as
referred pain.
17
III- Bone Pain
 Poorly localized, aching, deep, burning.
 Common with malignancy of Breast, Lung,
Prostate, Bladder, Cervical, Renal, Colon,
Stomach and Esophagus
 Can lead to pathological fractures.
 Vertebral Metastases can lead to cord
compression.
18
IV- Neuropathic Pain
 Caused by disturbance of function or pathological
changes in a nerve.
 May arise from a lesion or trauma, infection,
compression or tumour invasion.
 Described as burning, shooting, tingling.
 Does not respond well to standard analgesics.
19
 Categories of Pain
 Classified by inferred pathophysiology:
I. Nociceptive pain (stimuli from somatic and
visceral structures)
II. Neuropathic pain (stimuli abnormally
processed by the nervous system)
20
I. Nociceptive:
 Caused by invasion &/or destruction &/or pressure on
superficial somatic structures like skin, deeper skeletal
structures such as bone & muscle and visceral structures
and organs.
 Types: superficial somatic, deep somatic, & visceral.
21
II. Neuropathic:
 Caused by pressure on &/or destruction of peripheral,
autonomic or central nervous system structures.
 Radiation of pain along dermatomal or peripheral nerve
distributions.
 Often described as burning and/or deep aching &
associated with dysesthesia or lancinating pain.
22
Effects of pain
 Sympathetic responses
o Pallor
o Increased blood pressure
o Increased pulse
o Increased respiration
o Skeletal muscle tension
o Diaphoresis
23
Effects of pain
 Parasympathetic responses
o Decreased blood pressure
o Decreased pulse
o Nausea & vomiting
o Weakness
o Pallor
o Loss of consciousness
24
4 Pain Assessment
25
Pain History
 The site of pain
 Type of pain
 Exacerbating & Relieving factors
 How frequently
 Impact on daily life
26
Pain History
 Other important additional questions to be asked.
o What is the response to past and current analgesic
therapy?
o Any kind of diary or record about the pain?
o Fears they have about analgesics?
27
PAIN ASSESSMENT Tools
 Verbal Analogue Scales.
 Visual Analogue Scales.
 The Faces Scale
28
Factors to consider in choosing a
pain scale
1. Age of patient
2. Physical condition
3. Level of consciousness
4. Mental status
5. Ability to communicate
29
Numeric Pain Rating Scale
 Ask the patient to rate their pain intensity on a scale
of 0 (no pain) to 10 (the worst pain imaginable).
 Some patients are unable to do this with only verbal
instructions, but may be able to look at a number
scale and point to the number that describes the
intensity of pain.
30
Numeric Pain Rating Scale
31
Wong-Baker FACES Pain Rating
Scale
 Can be used with young children (sometimes as young as 3 years
of age)
 Works well for many older children and adults as well as for
those who speak a different language
 Explain that each face represents a person who may have no
pain, some pain, or as much pain as imaginable. Point to the
appropriate face and say the appropriate description. e.g. “This
face hurts just a little bit”
32
Wong-Baker FACES Pain Rating
Scale
 Ask the patient to choose the face that best matches how she or
he feels or how much they hurt.
33
Color Pain Rating Scale
 Ask the patient to point to the area on the scale that shows their
level of pain from white (no pain) to dark red (worst possible
pain).
 Obtain a number corresponding to the area where the patient
points.
34
Severity Assessment
 McGill Pain Questionnaire
 Scale from 0 to 5
 From None to Severe Pain
 for children or adults who understand numerical
relationships.
35
PAIN ASSESSMENT Tools
36
5 Pain Treatment
37
Goals of Pain Management Therapy
1) Decreased pain
2) Decreased healthcare utilization
o Decreased “shopping” for care
o Decreased emergency room visits
3) Improved functional status
o Increased ability to perform activities of daily living
o Return to employment
38
Management
 Non-Pharamcological treatment
 Pharmacological treatment:
 Analgesics
 Adjuvants
 Others
39
Non-pharmacological interventions
 Exercise
 Weight reduction
 Counseling
 Smoking cessation
 Massage ,Relaxation therapy
 Heat & cold applications
40
Non-pharmacological interventions
41
Analgesics
 Non-opioid
 e.g. aspirin,paracetamol
 Opioids
 e.g. codeine, morphine
 Adjuvant
 e.g. muscle relaxant, antidepressant, anti-epileptic
42
Choosing the Appropriate Analgesic
 Match the severity of pain to the strength of the
analgesic i.e. strong analgesics for severe pain.
 The WHO has developed 3-step model to guide
analgesic choice depending on the severity of the
patient’s pain.
43
WHO Pain Management Ladder
 Step I:
 NSAIDS ± adjuvants
 Step II:
 NSAID + Mild opioids ± adjuvant
 Step III:
 Strong opioids + NSAIDS ± adjuvants
44
Analgesics(Non-opioids)
 There are three types of non-opioid analgesics:
i. Salicylates
ii. Non-Steroidal Anti-Inflammatory Drugs
iii.Acetaminophen
45
Analgesics(Non-opioids)
 Used in full doses for the most part.
 All have a ceiling effect to their analgesia ( a
maximum dose past which no further analgesia can
be expected).
 COX-2 inhibitors may be associated with fewer
side-effects
46
Analgesics(Non-opioids)
 Use cytoprotection with NSAIDs only in patients
who have symptoms suggestive of GI distress or
who are at high risk of ulcer formation. For
cytoprotection use sulcrafate or misoprostol.
47
Analgesics(Weak Opioids)
 Useful drugs:
o Codeine & codeine combination products
o Oxycodone combination products.
 DO NOT USE:
o Dextropropoxyphene
48
Analgesics(Strong Opioids)
 Useful drugs:
o Morphine , hydromorphone, fentanyl, oxycodone ,
methadone.
 DO NOT USE:
o Meperidine , anileridine , pentazocine
49
Opioid Dosing
 Opioid analgesia is most effective when titrated to effect.
 Effective doses are highly variable between patients.
 “Standard” doses may be insufficient.
 When used properly for analgesia addiction occurs in less
than 1% of patients.
50
Opioid Side Effects
 Constipation :
o need proactive laxative use
 Nausea/vomiting:
o consider treating with dopamine antagonists and/or
prokinetics (metoclopramide, domperidone,
prochlorperazine, haloperidol)
 Urinary retention
51
Cont.
 Itch/rash
o worse in children; may need low-dose naloxone infusion. May
try antihistamines, however not great success
 Dry mouth
 Respiratory depression
o uncommon when titrated in response to symptom
 Neurotoxicity: delirium, myoclonus seizures.
 Drug interactions
52
Adjuvant analgesics (coanalgesics)
 Are medications that when added to primary
analgesics, further improve pain control.
 may themselves also be primary analgesics (e.g.
tricyclic antidepressant medications for postherpetic
neuralgia).
 They can be added into the pain management plan at
any step in the WHO ladder.
53
Adjuvants for Neuropathic Pain
 When pain is neuropathic there is good evidence for
treating with adjuvant medication rapidly.
 Always remember the potential of using radiotherapy,
chemotherapy and surgery as adjuvant modalities with
neuropathic pain but they should not replace drug adjuvants
completely.
 An adequate trial of 2-4 weeks at full dosage should be
tried for each drug
54
Adjuvants for Neuropathic Pain
 Cyclic Antidepressants:
o Amitriptyline - desipramine - nortriptyline –maprotiline
 Anticonvulsants:
o carbamazepine - valproic acid - gabapentin
 Local Anesthetics:
o mexiletine - lidocaine
55
Other modalities
 Nerve blocks, epidural blocks and ablative
neurosurgical procedures may be effective in pain
management.
 Such procedures may be associated with return of
pain after a number of months so that timing of
procedures may be important.
Thanks
for Coming

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pain-181012105908.pdf

  • 1. PAIN MANAGEMENT Dr. Sameh Ahmad Muhamad abdelghany Lecturer Of Clinical Pharmacology Mansura Faculty of medicine
  • 4. 4 Introduction  Definition : An unpleasant sensory and emotional experience associated with actual or potential tissue damage.  Pain may not be directly proportional to amount of tissue injury.  Highly subjective, leading to undertreatment
  • 5. 5  In cancer, the prevalence of pain in advanced disease is 70-90%.  " In HIV disease, pain prevalence is about 50%.  " Other illnesses may have significant pain but no clear data.
  • 7. 7 Classification I. Acute II.Chronic : i. Non malignant ii. Malignant
  • 8. 8  Injury, trauma, spasm or disease to skin, muscle, somatic structures or viscera;  Perceived and communicated via peripheral mechanisms (pathways)  Usually associated with autonomic response as well (tachycardia, blood pressure, diaphoresis, pallor, mydriasis (pupil dilation). Acute Pain
  • 9. 9  Usually subsides quickly as pain producing stimuli decreases  Associated with anxiety-(decreases rapidly)  Can be understood or rationalized as part of the healing process. Cont.
  • 10. 10 i. Non-malignant  Pain persists beyond the precipitating injury  Rarely accompanied by autonomic symptoms  Sufferers often fail to demonstrate objective evidence of underlying pathology.  Characterized by location-visceral, myofacial, or neurologic causes. II. Chronic Pain
  • 11. 11 ii. Malignant  Has characteristics of chronic pain as well as symptoms of acute pain (breakthrough pain).  Has a definable cause, e.g. tumor recurrence  In treatment, narcotic habituation is generally not a concern. II. Chronic Pain
  • 13. 13  Types of Pain  Somatic  Visceral  Bone  Neuropathic  Emotional/Spiritual
  • 14. 14 I- Somatic Pain  Aching, often constant  May be dull or sharp  Often worse with movement  Well localized  Skin, Muscle, Joints, superficial or deep.  Eg: o Bone & soft tissue o chest wall
  • 15. 15 II- Visceral Pain  Constant or crampy  Aching, burning  Poorly localized  Referred  Organs of Thorax & Abdominal Cavity.  Usually as a result of stretching, infiltration and compression  Eg: o Liver capsule distension o Bowel obstruction
  • 16. 16  Both Somatic & Visceral pain travel along the same pathways. Pain stimuli arising from the viscera is perceived as somatic in origin.  This can be confused by the brain and is often described as referred pain.
  • 17. 17 III- Bone Pain  Poorly localized, aching, deep, burning.  Common with malignancy of Breast, Lung, Prostate, Bladder, Cervical, Renal, Colon, Stomach and Esophagus  Can lead to pathological fractures.  Vertebral Metastases can lead to cord compression.
  • 18. 18 IV- Neuropathic Pain  Caused by disturbance of function or pathological changes in a nerve.  May arise from a lesion or trauma, infection, compression or tumour invasion.  Described as burning, shooting, tingling.  Does not respond well to standard analgesics.
  • 19. 19  Categories of Pain  Classified by inferred pathophysiology: I. Nociceptive pain (stimuli from somatic and visceral structures) II. Neuropathic pain (stimuli abnormally processed by the nervous system)
  • 20. 20 I. Nociceptive:  Caused by invasion &/or destruction &/or pressure on superficial somatic structures like skin, deeper skeletal structures such as bone & muscle and visceral structures and organs.  Types: superficial somatic, deep somatic, & visceral.
  • 21. 21 II. Neuropathic:  Caused by pressure on &/or destruction of peripheral, autonomic or central nervous system structures.  Radiation of pain along dermatomal or peripheral nerve distributions.  Often described as burning and/or deep aching & associated with dysesthesia or lancinating pain.
  • 22. 22 Effects of pain  Sympathetic responses o Pallor o Increased blood pressure o Increased pulse o Increased respiration o Skeletal muscle tension o Diaphoresis
  • 23. 23 Effects of pain  Parasympathetic responses o Decreased blood pressure o Decreased pulse o Nausea & vomiting o Weakness o Pallor o Loss of consciousness
  • 25. 25 Pain History  The site of pain  Type of pain  Exacerbating & Relieving factors  How frequently  Impact on daily life
  • 26. 26 Pain History  Other important additional questions to be asked. o What is the response to past and current analgesic therapy? o Any kind of diary or record about the pain? o Fears they have about analgesics?
  • 27. 27 PAIN ASSESSMENT Tools  Verbal Analogue Scales.  Visual Analogue Scales.  The Faces Scale
  • 28. 28 Factors to consider in choosing a pain scale 1. Age of patient 2. Physical condition 3. Level of consciousness 4. Mental status 5. Ability to communicate
  • 29. 29 Numeric Pain Rating Scale  Ask the patient to rate their pain intensity on a scale of 0 (no pain) to 10 (the worst pain imaginable).  Some patients are unable to do this with only verbal instructions, but may be able to look at a number scale and point to the number that describes the intensity of pain.
  • 31. 31 Wong-Baker FACES Pain Rating Scale  Can be used with young children (sometimes as young as 3 years of age)  Works well for many older children and adults as well as for those who speak a different language  Explain that each face represents a person who may have no pain, some pain, or as much pain as imaginable. Point to the appropriate face and say the appropriate description. e.g. “This face hurts just a little bit”
  • 32. 32 Wong-Baker FACES Pain Rating Scale  Ask the patient to choose the face that best matches how she or he feels or how much they hurt.
  • 33. 33 Color Pain Rating Scale  Ask the patient to point to the area on the scale that shows their level of pain from white (no pain) to dark red (worst possible pain).  Obtain a number corresponding to the area where the patient points.
  • 34. 34 Severity Assessment  McGill Pain Questionnaire  Scale from 0 to 5  From None to Severe Pain  for children or adults who understand numerical relationships.
  • 37. 37 Goals of Pain Management Therapy 1) Decreased pain 2) Decreased healthcare utilization o Decreased “shopping” for care o Decreased emergency room visits 3) Improved functional status o Increased ability to perform activities of daily living o Return to employment
  • 38. 38 Management  Non-Pharamcological treatment  Pharmacological treatment:  Analgesics  Adjuvants  Others
  • 39. 39 Non-pharmacological interventions  Exercise  Weight reduction  Counseling  Smoking cessation  Massage ,Relaxation therapy  Heat & cold applications
  • 41. 41 Analgesics  Non-opioid  e.g. aspirin,paracetamol  Opioids  e.g. codeine, morphine  Adjuvant  e.g. muscle relaxant, antidepressant, anti-epileptic
  • 42. 42 Choosing the Appropriate Analgesic  Match the severity of pain to the strength of the analgesic i.e. strong analgesics for severe pain.  The WHO has developed 3-step model to guide analgesic choice depending on the severity of the patient’s pain.
  • 43. 43 WHO Pain Management Ladder  Step I:  NSAIDS ± adjuvants  Step II:  NSAID + Mild opioids ± adjuvant  Step III:  Strong opioids + NSAIDS ± adjuvants
  • 44. 44 Analgesics(Non-opioids)  There are three types of non-opioid analgesics: i. Salicylates ii. Non-Steroidal Anti-Inflammatory Drugs iii.Acetaminophen
  • 45. 45 Analgesics(Non-opioids)  Used in full doses for the most part.  All have a ceiling effect to their analgesia ( a maximum dose past which no further analgesia can be expected).  COX-2 inhibitors may be associated with fewer side-effects
  • 46. 46 Analgesics(Non-opioids)  Use cytoprotection with NSAIDs only in patients who have symptoms suggestive of GI distress or who are at high risk of ulcer formation. For cytoprotection use sulcrafate or misoprostol.
  • 47. 47 Analgesics(Weak Opioids)  Useful drugs: o Codeine & codeine combination products o Oxycodone combination products.  DO NOT USE: o Dextropropoxyphene
  • 48. 48 Analgesics(Strong Opioids)  Useful drugs: o Morphine , hydromorphone, fentanyl, oxycodone , methadone.  DO NOT USE: o Meperidine , anileridine , pentazocine
  • 49. 49 Opioid Dosing  Opioid analgesia is most effective when titrated to effect.  Effective doses are highly variable between patients.  “Standard” doses may be insufficient.  When used properly for analgesia addiction occurs in less than 1% of patients.
  • 50. 50 Opioid Side Effects  Constipation : o need proactive laxative use  Nausea/vomiting: o consider treating with dopamine antagonists and/or prokinetics (metoclopramide, domperidone, prochlorperazine, haloperidol)  Urinary retention
  • 51. 51 Cont.  Itch/rash o worse in children; may need low-dose naloxone infusion. May try antihistamines, however not great success  Dry mouth  Respiratory depression o uncommon when titrated in response to symptom  Neurotoxicity: delirium, myoclonus seizures.  Drug interactions
  • 52. 52 Adjuvant analgesics (coanalgesics)  Are medications that when added to primary analgesics, further improve pain control.  may themselves also be primary analgesics (e.g. tricyclic antidepressant medications for postherpetic neuralgia).  They can be added into the pain management plan at any step in the WHO ladder.
  • 53. 53 Adjuvants for Neuropathic Pain  When pain is neuropathic there is good evidence for treating with adjuvant medication rapidly.  Always remember the potential of using radiotherapy, chemotherapy and surgery as adjuvant modalities with neuropathic pain but they should not replace drug adjuvants completely.  An adequate trial of 2-4 weeks at full dosage should be tried for each drug
  • 54. 54 Adjuvants for Neuropathic Pain  Cyclic Antidepressants: o Amitriptyline - desipramine - nortriptyline –maprotiline  Anticonvulsants: o carbamazepine - valproic acid - gabapentin  Local Anesthetics: o mexiletine - lidocaine
  • 55. 55 Other modalities  Nerve blocks, epidural blocks and ablative neurosurgical procedures may be effective in pain management.  Such procedures may be associated with return of pain after a number of months so that timing of procedures may be important.