Management of Pain Flashcards

1
Q

TYPES OF PAIN?

A
  • Nociceptive
  • Inflammatory
  • Neuropathic
  • Functional
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2
Q

What is NOCICEPTIVE PAIN?

A

• Nociceptive pain is pain in response to a
noxious stimulus.
• Can be either somatic or visceral.

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3
Q

What is INFLAMMATORY PAIN?

A

• When tissue damage occurs despite the
nociceptive defense system, inflammatory pain
ensues.

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4
Q

What is Neuropathic pain?

A

• Neuropathic pain results from damage to or

dysfunction of the peripheral or central nervous system, rather than stimulation of pain receptors.

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5
Q

What is functional pain?

A

• Functional pain is pain sensitivity due to an
abnormal processing or function of the central
nervous system in response to normal stimuli.

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6
Q

Define acute pain?

A

• Pain that occurs as a result of injury or surgery and is
usually self-limited, subsiding when the injury heals.
• Usually nociceptive, although it can be neuropathic.

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7
Q

Define chronic pain?

A

• Under normal conditions, acute pain subsides quickly.
However, in some instances pain persists for months to
years, leading to chronic pain.
• Chronic pain may be nociceptive, inflammatory,
neuropathic, or functional.

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8
Q

Differentiate chronic malignant and chronic non-malignant pain?

A

CHRONIC MALIGNANT PAIN
• Chronic malignant pain is associated with a
progressive disease like cancer or AIDS.

CHRONIC NON-MALIGNANT PAIN
• Pain not associated with a life-threatening disease and lasting longer than 6 months beyond the healing period.

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9
Q

Guidelines by the WHO for treatment of cancer pain?

A

• For mild pain (1–3/10), management should be
started at step 1.
• For mild to moderate pain (4–6/10), it should be
started at step 2.
• For moderate to severe pain (7–10/10), it should
be started at step 3.

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10
Q

Outline of how to treat mild, moderate, and severe pain?

A

• Mild pain is generally treated with nonopioid
analgesics.
• Mild to Moderate pain is treated with
combinations of medium-potency opioids +/-
nonopioid analgesics.
• Moderate to severe pain is treated with high
potency opioids +/- nonopioid analgesics .
• Adjuvant medications are added as needed to
manage adverse effects and/or to augment
analgesia

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11
Q

Which two drugs can be used for mild to moderate and added benefit?
Chronic pain?

A

• Acetaminophen and NSAIDs are often effective
for mild to moderate pain.
• Nonopioids do not cause physical dependence
or tolerance.
OPIOID ANALGESICS
• Agents of choice for the management of
moderate to severe acute and chronic pain.

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12
Q

Acetaminophen and NSAID’s role in the management of pain?

A

ACETAMINOPHEN
• Often selected as initial therapy for mild to
moderate pain.
• First-line for low back pain and osteoarthritis.
• Hepatotoxicity has been reported with excessive
use and overdose.
NSAIDs
• Used for the treatment of mild to moderate pain,
especially the pain of inflammation such as that
of arthritis and gout.

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13
Q

4 drugs for mild to moderate pain?

A
  • NSAIDs
  • Acetaminophen
  • Codeine
  • Tramadol
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14
Q

Drugs used for moderate to severe pain?

A
  • Morphine (DOC in severe pain)
  • Hydromorphone
  • Oxymorphone
  • Meperidine
  • Fentanyl
  • Levorphanol
  • Methadone
  • Oxycodone
  • Hydrocodone
  • Pentazocine (3rd line)
  • Butorphanol (2nd line)
  • Nalbuphine (2nd line)
  • Buprenorphine (2nd line)
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15
Q

Describe Analgesic dosing?

A

• Analgesics should be given orally and by the
clock, ie at fixed intervals of time.
• The dose should be gradually increased until the
patient is comfortable.
• The next dose should be given before the effect
of the previous one has fully worn off.
• As the pain subsides, as-needed schedules
may be appropriate.

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16
Q

Define breakthrough pain?

Treatment for breakthrough pain?

A

• Transitory severe acute pain that occurs on a
background of chronic pain that is adequately
controlled by an opioid regimen.

• Rescue doses are given for relief.
• Typically, a short-acting supplemental opioid is
used.
• A typical rescue dose is 5 to 15 % of the basal
daily requirement of opioid.

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17
Q

Breakthrough pain formulations?

A
• Breakthrough pain may be targeted with a transmucosal fentanyl formulation.
• Six formulations are available in the US:
• Oral transmucosal lozenge
• Immediate-release transmucosal tablet
• Effervescent buccal tablet
• Buccal soluble film
• Nasal spray
• Sublingual spray
• Fentanyl oral
transmucosal lozenge.
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18
Q

THE ANALGESIC CEILING EFFECT define?

A

• The analgesic ceiling effect of a drug refers to
the dose beyond which there is no additional
analgesic effect.
• Higher doses do not provide any additional pain
relief but may increase the likelihood of side
effects.

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19
Q

Analgesic ceiling effect with opiods and non-opioids?

A

• Nonopioids have an analgesic ceiling.
• Pure opioid agonists have no analgesic ceiling.
• When using a combination of an opioid with an
nonopioid, the analgesic ceiling of the nonopioid
should be the dose-limiting factor.
• Mixed agonist-antagonists, such as pentazocine,
butorphanol, nalbuphine, and buprenorphine, do
have a ceiling effect.
• They are poor choices for patients with severe
pain.

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20
Q

ROA for opiods?

A
  • Opioids may be administered in a variety of routes:
  • Oral (tablet and liquid)
  • Sublingual
  • Rectal
  • Transdermal
  • Transmucosal
  • Intravenous
  • Subcutaneous
  • Intraspinal
21
Q

ROA benefits of PCA?

A

• PCA allows patients to self-administer parenteral
analgesics.
• The patient depresses a button to activate the
PCA controller to deliver a preset dose of opiate
medication
• Patient-controlled IV delivery of opioids has
often been considered the gold standard for
management of acute postoperative pain.
• Opioids used in PCA devices include morphine,
hydromorphone, fentanyl, and methadone.

22
Q

NOT RECOMMENDED ANALGESICS

FOR ROUTINE DOSING opiod agonist?

A
MEPERIDINE
• Meperidine has a half-life of 3 h.
• Its principal metabolite, normeperidine, has a
half-life of 15-20 h.
• Normeperidine produces significant adverse
effects when it accumulates:
• Dysphoria
• Myoclonus
• Seizures
23
Q

Not recommended anaglesic for routine dosing mixed agonist-antagonist?

A

MIXED AGONIST-ANTAGONISTS
• Mixed agonist-antagonists are not recommended as routine analgesics, as their
dosing is limited by a ceiling effect.
• Additionally, pentazocine, nalbuphine and
butorphanol cause psychotomimetic adverse
effects.
• Mixed agonist-antagonists should not be used in
a patient already taking a pure agonist opioid.
• Competition for the opioid receptors may cause
a withdrawal reaction.

24
Q

why do COMBINATION THERAPY?

A

• The combination of opioid and nonopioid
analgesics often results in analgesia superior to
that produced by either agent alone.

25
Common adverse effects of opioids?
* Pruritus * Constipation * Nausea/Vomiting * Sedation
26
Managing pruritus as opioid ae? Nausea /vomitting?
Pruritus • Due to histamine release from mast cells. • Can be managed with hydroxyzine or diphenhydramine. ``` Nausea/vomiting • Usually disappears as tolerance develops within a few days. • It can be treated with hydroxyzine, metoclopramide or prochlorperazine ```
27
Managing constipation in opioid?
Constipation • Almost universal. • Tolerance to constipation may develop very slowly, if at all. • A laxative should be prescribed when opioid is started. • Usually a stimulant laxative is prescribed. • A combination stimulant/softener can be useful. • Bulk-forming agents require substantial fluid intake and are not recommended for patients with advanced disease and poor mobility.
28
MANAGING OPIOID sedation Ae?
Sedation • Usually disappears over a few days as tolerance develops. • Persistent opioid-induced sedation that limits activity can be managed with methylphenidate or modafinil.
29
Management of respiratory depression with opioids?
Respiratory depression • Many physicians have an exaggerated view of the risk of respiratory depression when using opioids to relieve pain. • Tolerance to respiratory depression develops quickly. • If respirations are compromised, naloxone may be necessary.
30
what are ANALGESIC ADJUNCTIVE AGENTS | (COANALGESICS)?
• Adjuvant analgesics are drugs which are useful in the management of pain but that are not primarily classified as analgesics. • They can be used as monotherapy or in combination with non-opioids and opioids.
31
List coanalgesics?
* ANTIDEPRESSANTS * ANTICONVULSANTS * GLUCOCORTICOIDS * OTHER DRUGS
32
What are 2 mainstay of treatment for several neuropathic pain syndromes?
ANTIDEPRESSANTS AND ANTICONVULSANTS
33
What are NEUROPATHIC PAIN: MAIN CAUSES
* Diabetic peripheral neuropathy * Postherpetic neuralgia * Cancer * Spinal cord injury * Multiple sclerosis * Trigeminal neuralgia
34
moa of antidepressant action in adjuvant of pain?
• Serotonin and norepinephrine mediate descending inhibition of ascending pain pathways in the brain and spinal cord. • Antidepressants that enhance both serotonergic and noradrenergic transmission display significant analgesic effects. • Drugs with these actions are: • Tricyclic antidepressants (TCAs) • Serotonin and norepinephrine reuptake inhibitors (SNRIs). TCAs and SNRIs cause analgesia by inhibiting norepinephrine and serotonin reuptake. • Antidepressant agents that enhance only serotonergic transmission, such as the selective serotonin reuptake inhibitors (SSRIs) are less effective.
35
• TCAs commonly used as analgesics are:
* Amitriptyline * Imipramine * Desipramine * Nortriptyline
36
Tricyclic antidepressants AE?
• Most common adverse effects: constipation, dry mouth, blurred vision, cognitive changes, tachycardia, urinary hesitation. • Associated with their anticholinergic activity. • Other common adverse effects: sexual dysfunction, orthostatic hypotension, weight gain, sedation. • Secondary amines (desipramine, nortriptyline) exhibit fewer anticholinergic and sedative effects than do the tertiary amines (amitriptyline, imipramine). • Secondary amines are more desirable in the elderly population.
37
TCAs should be administered cautiously in | patients with:
* Angle-closure glaucoma * BPH * Urinary retention * Constipation * CV disease * Impaired liver function.
38
• TCAs should be avoided in patients with:
* Second- or third-degree heart block * Arrhythmias * Prolonged QT interval * Severe liver disease * Recent acute MI.
39
``` SEROTONIN & NOREPINEPHRINE REUPTAKE INHIBITORS (SNRIs) pain use and differences from TCAs? ```
• SNRIs selectively inhibit reuptake of serotonin and norepinephrine. • SNRIs lack the antihistamine, α-adrenergic blocking, and anticholinergic effects of TCAs. • Venlafaxine and duloxetine are effective for several types of neuropathic pain
40
SNRIs: ADVERSE EFFECTS?
* Nausea, sexual dysfunction, somnolence. | * SNRIs are better tolerated than TCAs.
41
ANTICONVULSANTS used for management of pain?
* Useful in the management of neuropathic pain. * Gabapentin & Pregabalin * Carbamazepine & Oxcarbazepine
42
moa and ae of Gabapentin and pregabalin?
MECHANISM OF ACTION • Block voltage-gated calcium-channels. This decreases release of glutamate, norepinephrine, and substance P. ADVERSE EFFECTS • Dizziness, somnolence, peripheral edema.
43
CARBAMAZEPINE & OXCARBAZEPINE uses?
• Carbamazepine is the DOC for treatment of pain due to trigeminal neuralgia. • Oxcarbazepine is also effective and better tolerated. • Trigeminal neuralgia is different from other types of neuropathic pain and responds to different pharmacologic agents
44
CARBAMAZEPINE & OXCARBAZEPINE moa?
MECHANISM OF ACTION • Voltage-gated sodium channels in sensory neurons play a crucial role in neuropathic pain. • Carbamazepine & oxcarbazepine block voltage gated sodium channels
45
AE of CARBAMAZEPINE & OXCARBAZEPINE
ADVERSE EFFECTS • Drowsiness, dizziness, nausea and vomiting. • Carbamazepine-induced leukopenia is not uncommon, but it is usually benign. • Aplastic anemia is a rare side effect. • Oxcarbazepine is better tolerated.
46
Topical Therapies used for pain?
Lidocaine Patches • Used for localized peripheral neuropathic pain (particularly postherpetic neuralgia). Capsaicin Patches • Capsaicin depletes substance P from the terminals of afferent C fibers. A high-concentration capsaicin patch is approved for postherpetic neuralgia. Clonidine • Can be administered orally, transdermally, or intraspinally. May improve pain in sympathetically maintained pain.
47
Glucocorticoids role in pain management?
• Commonly used in advanced illness. • Useful for acute nerve compression, increased intracranial pressure, bone pain, visceral pain,anorexia, nausea, and depressed mood. • Dexamethasone is the DOC. • Prednisone and methylprednisolone can also be used. • Glucocorticoids have several other indications. • They can improve appetite, nausea, malaise, and overall quality of life.
48
Bisphosphonates role in pain management?
• Bisphosphonates have analgesic effects on pain of bony origin. • Efficacious particularly with bone metastasis and multiple myeloma. • The bisphosphonates that have shown efficacy in malignant bone pain conditions are zoledronate and pamidronate. • Zoledronate is the most commonly used