Week 7: Pain & Anesthetics Flashcards

1
Q

Immediate goal of pain management

–Reduce pain to level that allows patient to:

A

perform reasonable ADLs

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2
Q

Key principles of pain management

–Patient should be considered_______of their pain.
–Pain management is a patient _______.
–Nonpharmacologic interventions _____________.
▪Combination of therapies optimal

A

–Patient should be considered expert of their pain.
–Pain management is a patient right.
–Nonpharmacologic interventions encouraged.
▪Combination of therapies optimal

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3
Q

Acute vs Chronic pain

A

▪Acute pain = Abrupt onset but brief duration

▪Chronic pain = persists longer than 6 months
–Chronic nonmalignant pain
–Chronic malignant = Cancer pain

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4
Q

Nociceptor vs Neuropathic pain

A

▪Nociceptor = Responds well to analgesics
–Somatic = Localized muscles or joints
–Visceral = Organs

▪Neuropathic = caused by Injury or irritation to nerve tissue

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5
Q

Phases of pain physiology

  1. _____________: trauma stimulates ____________
  2. Transmission in ___________________
  3. Transmission in ____________________
  4. ______________ [cerebral cortex recognizes the pain stimulus]
  5. ____________: limbic system reacts to pain
A
  1. Transduction: trauma stimulates nociceptors
  2. Transmission in peripheral nerves
  3. Transmission in spinal tracts
  4. Perception [cerebral cortex recognizes the pain stimulus]
  5. Modulation: limbic system reacts to pain
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6
Q

Nonpharmacologic therapies are used to attain adequate pain relief in place of drugs
– Serve as adjuncts to analgesics

Improved comfort, lower doses, potential for fewer drug related
adverse events

Examples:

A

▪Acupressure and acupuncture
▪Hypnosis, massage, meditation
▪Application of cold or heat
▪Biofeedback therapy & Electrical nerve stimulation
▪Distraction = Art/music therapy/ Laughter
▪Physical therapy
▪Yoga

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7
Q

Drug classes for pain meds

A

▪Nonopioids
–NSAIDs, centrally acting agents, or acetaminophen
–Used for mild to moderate pain

▪Opioid drugs
–Used to treat severe pain

▪Adjuvant analgesics
–Used to treat chronic pain that’s neuropathic in nature

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8
Q

Combination drugs for pain

–Opioid & nonopioid drugs
–Available as fixed-dose tablets or capsules
–Dose ceiling due to toxicities of nonopioid analgesic
▪Such as risk of acute liver failure when taking acetaminophen

–Common examples: ?

A

–Opioid & nonopioid drugs
–Available as fixed-dose tablets or capsules
–Dose ceiling due to toxicities of nonopioid analgesic
▪Such as risk of acute liver failure when taking acetaminophen

–Common examples: Endocet, Norco, Percocet

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9
Q

Management of cancer pain

A

–Radiation therapy

–Nerve blocks
▪Alcohol / other neurotoxic substance
▪Local anesthetics / steroid hormones

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10
Q

Patient-controlled analgesia

A

–Infusion pump allows patient to self-administer.
–May reduce anxiety of waiting for drug administration
–Morphine usually used.
–Requires patient be conscious and capable of understanding pump operation

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11
Q

Opium (Papaver somniferum)
–Extracted from unripe :

A

poppy plant seeds

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12
Q

Opiates
–Natural substances obtained from:
–Include:

A

–Natural substances obtained from opium
–Include morphine and codeine

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13
Q

Opioid
–Synthetic drug with _____________ activity
–Can be _________ or __________

A

–Synthetic drug with morphine-like activity
–Can be natural or synthetic

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14
Q

Opioids are usually used for:

A

moderate to severe pain

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15
Q

Opioids when used for prolonged periods at high doses, can cause :

A

physical and psychological dependence

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16
Q

Narcotic: _________________ drug used to alleviate pain

A

Morphine-like

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17
Q

3 common receptors that opioids work with:

A

Mu
Kappa
Delta

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18
Q

Opioid agonists activate ___________________ receptors

A

mu and kappa

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19
Q

Opioid antagonists block _______________ receptors

A

mu and kappa

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20
Q

Mixed opioid agonist-antagonists work on one receptor but :

A

block or have no effect on another

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21
Q

Opioids
–Neither lower threshold for pain at nociceptor level nor _________________1_____________________
–Alter _______2_________, emotional response

▪Patient knows pain exists, but it does not cause concern or anxiety.

A

1- slow/block transmission of pain impulse

2- perception

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22
Q

Opioids Cause CNS depression:

A

Sedation, euphoria, intense relaxation

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23
Q

Opioids side effects

A

– GI side effects
▪Nausea, vomiting, constipation
– Urinary retention
– Pruritus
– Respiratory depression
– Orthostatic hypotension
– Increased intracranial pressure (ICP)
– Risk of physical and psychological dependence
– Dizziness, hallucinations, anxiety
– Tolerance

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24
Q

Prototype drug: Morphine sulfate (Astramorph PF, Duramorph RF, Roxanol)

–Therapeutic classification-
–Pharmacologic classification-

A

–Therapeutic classification
▪Narcotic analgesic

–Pharmacologic classification
▪Opioid agonist

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25
Q

Prototype drug: Morphine sulfate (Astramorph PF, Duramorph RF, Roxanol)

–Therapeutic effects and uses

▪Acute and severe _______________

▪Off label
–Preanesthetic __________ and to calm severely agitated patients
–Relieve _________________________ associated with end-stage cancer, heart failure, or pulmonary edema

A

▪Acute and severe chronic pain

▪Off label
–Preanesthetic sedation and to calm severely agitated patients
–Relieve shortness of breath associated with end-stage cancer, heart failure, or pulmonary edema

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26
Q

Prototype drug: Morphine sulfate (Astramorph PF, Duramorph RF, Roxanol)

–Mechanism of action

A

▪Occupies mu and kappa receptor sites in brain and dorsal horn of spinal cord that alter release of afferent neurotransmitters
▪Alters perception of and emotional response to pain
▪Produces analgesia and euphoria
▪Mimics actions of endogenous endorphins

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27
Q

Prototype drug: Morphine sulfate (Astramorph PF, Duramorph RF, Roxanol)

–Adverse effects
-Black box warning

A

▪CNS depression
▪Respiratory depression
▪Constipation, nausea, vomiting
▪Urinary retention
▪Sedation, dizziness, anxiety, disorientation
▪Orthostatic hypotension
▪Pruritus with IV or epidural route

–Black box warning
▪Schedule II controlled substance with high
potential for physical and psychologic dependence
▪Extended release forms prescribed for opioid tolerant patients only and are not intended for prn use

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28
Q

Prototype drug: Morphine sulfate (Astramorph PF, Duramorph RF, Roxanol)

–Contraindications/precautions

A

▪Hypersensitivity
▪Premature infants

▪Precautions
–Older adults
–Undiagnosed abdominal pain
–Hepatic/renal impairment
–Shock
–CNS depression
–Head injury/increased ICP
–COPD

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29
Q

Morphine sulfate
–Drug interactions

A

▪Increased sedation
–CNS depressants

▪Reversed effect with opioid antagonist
–Naloxone

▪Additive constipation
–Antidiarrheal

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30
Q

Morphine sulfate
–Herbal/food

A

▪Kava, valerian, or chamomile can increase CNS depression
▪St. John’s wort may decrease analgesic action

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31
Q

Morphine sulfate Treatment of overdose

A

▪Overdose can cause coma & respiratory depression
–Immediate treatment
–Naloxone for morphine intoxication

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32
Q

Mixed agonist-antagonist opioids

–Fewer ________ effects
▪Less ___________ depression
▪Lower potential for dependence
–Used to treat ____________ pain

A

–Fewer adverse effects
▪Less respiratory depression
▪Lower potential for dependence
–Used to treat moderate pain

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33
Q

Buprenorphine (Buprenex, Butrans, Suboxone)

–Partial agonist at ____ receptors
–Antagonist at _____ receptors

–Parenteral route
▪Relief of moderate to severe pain

–Sublingual route
▪Management of opioid withdrawal & dependence

–Schedule III drug

A

–Partial agonist at mu (μ) receptors
–Antagonist at kappa receptors

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34
Q

Butorphanol (Stadol)

–Agonist at ? receptors
–Weak antagonist at ? receptors

–IV or IM route
▪Moderate to severe pain
▪Preanesthesia or general anesthesia adjunct
–Nasal spray

–Schedule III drug

A

–Agonist at kappa receptors
–Weak antagonist at mu receptors

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35
Q

Nalbuphine (Nubain)

–Agonist at ? receptors
–Weak antagonist at ? receptors

–IV, IM, subcutaneous routes
▪Moderate to severe pain
▪Preanesthesia or anesthesia adjunct

–Not a scheduled drug

A

–Agonist at kappa receptors
–Weak antagonist at mu receptors

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36
Q

Pentazocine (Talwin)

–Agonist at ? receptors
–Weak antagonist at ? receptors
–PO and parenteral routes

▪Moderate to severe pain

A

–Agonist at kappa receptors
–Weak antagonist at mu receptors

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37
Q

NSAIDs (Aspirin, ibuprofen)

– Preferred medications ^^
– Have antipyretic and anti-inflammatory properties
– Act at ______________, inhibiting pain mediators at _______________ level

A

– Preferred medications
– Have antipyretic and anti-inflammatory properties
– Act at peripheral sites, inhibiting pain mediators at nociceptor level

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38
Q

NSAIDs (Aspirin, ibuprofen) do not produce severe adverse effects of narcotics

▪No physical or psychological dependence
▪Most prominent effects:

A

–GI related
* Ulceration of mucosa

–Dizziness, headache, and rash

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39
Q

Miscellaneous analgesics such as
▪Clonidine (Catapres, Duraclon)
▪Ziconotide (Prialt)

–Tramadol (Ultram, others)
▪More widely prescribed

–Act on : ?

A

CNS

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40
Q

Tramadol (Ultram, others)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Analgesic
–Pharmacologic classification
▪Mixed opioid-nonopioid analgesic

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41
Q

Tramadol (Ultram, others)
–Therapeutic effects and uses:

▪___________ pain

▪Off-label uses
–Neuropathic pain
–______________ ________ syndrome

A

▪Moderate pain

▪Off-label uses
–Neuropathic pain
–Restless leg syndrome

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42
Q

Tramadol (Ultram, others)
–Mechanism of action

▪Drug and one of metabolites bind to _______________ site
–Weak opioid agonist activity

▪Inhibits_________________________________________ reuptake in spinal neurons
–Inhibits transmission of pain impulses

A

▪Drug and one of metabolites bind to mu receptor site
–Weak opioid agonist activity

▪Inhibits norepinephrine and serotonin reuptake in spinal neurons
–Inhibits transmission of pain impulses

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43
Q

Tramadol (Ultram, others)
–Adverse effects

A

▪Vertigo / Dizziness
▪Headache
▪Nausea / Vomiting
▪Constipation
▪Lethargy
▪CNS stimulation effects
▪Seizures
▪Respiratory depression
▪Possible physical dependence

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44
Q

Tramadol (Ultram, others)
– Contraindications/precautions

A

▪Hypersensitivity
▪History of depression or suicidal ideation
▪Pregnancy

▪Precautions
–Codeine allergies
–History of drug abuse
–Chronic Obstructive Pulmonary Disease (COPD)
–Renal/hepatic impairment
–Increased ICP
–History of seizures
–Contraindicated in children younger than age 12

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45
Q

Tramadol (Ultram, others)
–Drug interactions

A

▪Increased risk of seizures
–Carbamazepine, certain antidepressants
–MAOIs

▪Sudden death if combined with ethanol
▪Reduced analgesic effect
–Inhibitors of CYP2D6 enzyme

▪Herbal/food
–Food significantly affects absorption of
extended release form
–St. John’s wort contraindicated; possibility of
serotonin syndrome
–Caution with valerian or kava; additive CNS
depressant effect

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46
Q

Tramadol (Ultram, others) –Treatment of overdose

A

▪Serious CNS depression, respiratory depression, death possible

▪Naloxone
–May precipitate convulsions

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47
Q

Adjuvant analgesics
–Diverse group of drugs used to : ?

A

enhance analgesia for specific indications

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48
Q
  • Adjuvant analgesics
    Primary indications
A

▪Pain refractory to opioids (such as intractable cancer pain)
▪Neuropathic pain

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49
Q

Preferred drugs for abusers:

A

Morphine, meperidine, and heroin

  • OxyContin
    –Major drug of abuse in recent years
    –Long-acting form of oxycodone
    ▪Beneficial to patients with chronic pain
    ▪Can be crushed, injected, snorted
    –Potent and dangerous
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50
Q

Acute opioid intoxication - Respiratory depression

▪Treat with : ?
▪Repeat small doses until patient exhibits opioid withdrawal symptoms
–Maintain patent ____________
–Have resuscitation equipment available

A

▪Treat with naloxone (Narcan)
▪Repeat small doses until patient exhibits opioid withdrawal symptoms
–Maintain patent airway
–Have resuscitation equipment available

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51
Q
  • Evzio
    –Handheld autoinjector containing naloxone to treat individual with :
A

known or suspected opioid overdose

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52
Q

–Tension headache

▪Muscles of head & neck tight due to :
▪Treat with :

A

▪Muscles of head & neck tight due to stress
▪Self-limiting
▪Treat with OTC analgesics

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53
Q

Migraine headache

▪Throbbing, pulsating pain
▪Preceded by aura
–Sensory warning of imminent attack
▪Patients appear to have___________________ that overreact to various triggers.
▪Neurotransmitter _______________ plays key factor.

A

▪Throbbing, pulsating pain
▪Preceded by aura
–Sensory warning of imminent attack
▪Patients appear to have blood vessels that overreact to various triggers.
▪Neurotransmitter serotonin plays key factor.

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54
Q

About ____ of patients with migraines have a first degree relative with a history of migraine.

A

70%

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55
Q

Before puberty, more boys have migraines than girls;

after puberty, women are _______ more likely to have migraines than men.

A

3 times

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56
Q

History of migraine is associated with an increased incidence of __________________________________, especially if the patient experiences migraines with aura.

A

major cardiovascular disease

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57
Q
  • Migraines are rare after age:
A

50

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58
Q

Mild migraine (occasional headaches with no other functional impairment) treatment

A

–NSAIDs
–Acetaminophen combined with NSAID and caffeine
–Oral serotonin 5-HT agonists
▪Triptans/ergot alkaloids

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59
Q

Moderate migraines (moderate headaches, nausea, some functional impairment) treatment

A

–Oral, intranasal, subcutaneous serotonin (5-HT) agonists
▪If contraindicated or ineffective, then dopamine agonists prescribed

60
Q

Severe migraine (severe headaches more than 3 times/month, marked nausea or vomiting, functional impairment) treatment

A

–Subcutaneous, IM or IV serotonin agonists
–Second-choice parenteral dopamine agonist
–Narcotic analgesics for refractory pain

61
Q

Triptans
–Selective for 5-HT1 receptor subtype
–Constrict certain intracranial vessels
–Effective in aborting migraines with or without auras
–Not effective at __________ migraines

A

preventing

62
Q

Ergot alkaloids

–For patients unresponsive to triptans
▪Separate use by 24 hours

–Constrict ________________________
–Regular daily use can cause physical dependence.

A

both arteries and veins

63
Q

Sumatriptan (Imitrex, Onzetra)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Antimigraine agent
–Pharmacologic classification
▪Serotonin (5-HT1) receptor agonist

64
Q

Sumatriptan (Imitrex, Onzetra)

Therapeutic effects and uses:

A

▪Acute migraine headaches

65
Q

Sumatriptan (Imitrex, Onzetra)
–Mechanism of action

▪Activates : 5-HT1 _______________________________ on intracranial and extracerebral blood vessels

–Cranial vessel constriction
–Reduced transmission in trigeminal pain pathways

A

▪Activates 5-HT1 serotonin receptors on intracranial and extracerebral blood vessels
–Cranial vessel constriction
–Reduced transmission in trigeminal pain pathways

66
Q

Sumatriptan (Imitrex, Onzetra)
–Adverse effects

A

▪Mild, transient dizziness
▪Nausea
▪Diarrhea
▪Myalgia
▪Inflammation or pain at injection site
▪Headache recurrence
▪Serious adverse cardiac effects

67
Q

Sumatriptan (Imitrex, Onzetra)
–Contraindications/precautions

A

▪Epilepsy
▪CAD
▪Cerebrovascular disease
▪Peripheral vascular disease
▪Uncontrolled hypertension, hypercholesterolemia
▪Family history of cardiovascular disease
▪Renal/hepatic impairment
▪Pregnancy

68
Q

Sumatriptan (Imitrex, Onzetra)
–Drug interactions

A

▪MAOIs, SSRIs- should not be used within 2 weeks of such drugs
▪Avoid use within 24 hours of ergot alkaloids or other 5-HT1 agonist
▪Serotonin syndrome possible
▪Drugs that increase serotonin levels or activity

–Herbal/food
▪St. John’s wort and feverfew avoided

69
Q

–Treatment of overdose
Sumatriptan (Imitrex, Onzetra)

A

▪Few recorded
▪Supportive of side effects

70
Q

Preventive treatment is recommended for headaches that occur 3 or more times a month.

– Identify personal triggers for migraines:

A

▪Foods/diet
▪Adopting regular sleep patterns and meals
▪Aerobic exercise
▪Avoiding alcohol (especially red wine)
▪Smoking cessation
▪Keeping a diary
▪Relaxation exercises
▪Meditation
▪Yoga
▪Progressive muscle relaxation

71
Q

Preventive treatment is recommended for headaches that occur 3 or more times a month.
–Pharmacologic treatment:

▪________________ blockers
▪_______________blockers
▪Anti____________
▪Anti____________

A

▪Beta-adrenergic blockers
▪Calcium channel blockers
▪Antidepressants
▪Antiseizure drugs

72
Q

General anesthesia

–Loss of ___________ throughout whole body
–Accompanied by loss of:

A

–Loss of sensation throughout whole body
–Accompanied by loss of consciousness (LOC)

73
Q

Local anesthesia
–Loss of __________ to limited body area without LOC

A

sensation

74
Q

Regional anesthesia
–Similar to local
–Encompasses :

A

larger body area, such as entire limb

75
Q

–Minimal sedation (anxiolysis)
▪Patient responds to

A

responds to verbal commands.

76
Q

Moderate (conscious) sedation
▪Patient responds to: ?

A

verbal or light tactile prompting

77
Q

–Deep sedation/analgesia
▪Patient aroused by : ?
▪Airway, ventilation interventions
▪Cardiovascular functions usually adequate

A

▪Patient aroused by repeated or painful stimulation
▪Airway, ventilation interventions
▪Cardiovascular functions usually adequate

78
Q

General Anesthesia
* Purposes

A

–Analgesia [blocks pain sensation]
–Relaxation [relieves anxiety]
–Hypnosis
–Amnesia
–Loss of reflexes

79
Q

Balanced anesthesia
–Combination of medications:
▪___________ blockers
▪Short-acting ___________
▪Opioids
▪General ___________

A

▪Neuromuscular blockers
▪Short-acting benzodiazepines
▪Opioids
▪General anesthetics

80
Q

4 stages of general anesthesia

  • Stage I
    –________ = lose sensation, but may remain awake
  • Stage II
    –______________ and ________________
    ▪May have irregular pulse and respirations with
    increased blood pressure
  • Stage III
    –Surgical ______________ = Skeletal muscle relaxation
  • Stage IV [avoided]
    –Paralysis of _____________ = Death could result
A
  • Stage I
    –Analgesia = lose sensation, but may remain awake
  • Stage II
    –Excitement and hyperactivity
    ▪May have irregular pulse and respirations with
    increased blood pressure
  • Stage III
    –Surgical anesthesia = Skeletal muscle relaxation
  • Stage IV [avoided]
    –Paralysis of medulla = Death could result
81
Q

Intravenous Anesthetics
* Commonly used classes :

A

–Opioids
–Benzodiazepines
–Miscellaneous agents

82
Q
  • Neurolept analgesia
    –Feelings of ______________ to patient’s surroundings
A

indifference

83
Q

Fentanyl (Sublimaze)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Analgesic
▪Anesthetic

–Pharmacologic classification
▪Opioid agonist

84
Q

Fentanyl (Sublimaze)
–Therapeutic effects and uses

A

▪Short-duration analgesia
▪Chronic, persistent pain

85
Q

Mechanism of action of Fentanyl (Sublimaze)

▪________________ against mu and kappa receptors
▪More _________onset of action than morphine

A

▪Opioid agonist against mu and kappa receptors
▪More rapid onset of action than morphine

86
Q

Fentanyl (Sublimaze)
–Adverse effects

A

▪Most common = Respiratory depression (5-15 min
after IV), apnea, skeletal muscle rigidity,
bradycardia, nausea, vomiting, constipation

▪Transdermal patches
–Localized pain
–Irritation
–Ulceration
–Bleeding

87
Q

Fentanyl (Sublimaze)
–Black box warning

A

▪High risk for misuse, abuse, or diversion
▪High risk for death due to overdose or respiratory
depression
▪Concurrent use with CYP450 3A4 inhibitors
–Increase fentanyl plasma concentrations
▪Concurrent use with CNS depressants
–Profound sedation, respiratory depression,
coma, and death

88
Q

Fentanyl (Sublimaze)
–Contraindications/precautions

A

▪Head trauma
▪Lactation
▪Respiratory impairment
▪Bradydysrhythmia
▪Hepatic or chronic kidney disease

89
Q

Fentanyl (Sublimaze)
–Drug interactions

A

▪Additive CNS depression
–Other CNS depressants
▪Interacts with drugs that induce/inhibit CYP450
enzyme
▪Cardiovascular depression
–Nitrous oxide

–Herbal/food
▪St. John’s wort may intensify or prolong effects.
▪Valerian or kava may cause additive CNS
depression.

90
Q

–Treatment of overdose for Fentanyl (Sublimaze)

A

▪Mechanical ventilation
▪Naloxone (Narcan) to reverse serious respiratory
depression

91
Q

Primary indication for benzodiazepine use is to treat symptoms of :

A

anxiety

92
Q

__________ most commonly used for surgical procedures

A

Midazolam

93
Q

______________ & ___________ have slower onset, longer duration.
–Used as anesthesia adjuncts

A

Diazepam and lorazepam

94
Q

Midazolam (Versed)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪IV anesthetic
–Pharmacologic classification
▪Benzodiazepine
▪GABA receptor agonist

95
Q

Midazolam (Versed)
Therapeutic effects and uses

A

▪Reduces anxiety and stress during surgery
▪Off-label use = Status epilepticus
▪Off-label use = Mechanically ventilated patients

96
Q

Midazolam (Versed)
–Mechanism of action

A

▪Produces CNS depression and skeletal muscle relaxation
▪Acts at limbic, thalamic, hypothalamic regions of brain

97
Q

Midazolam (Versed) –Adverse effects & black box warning

A

▪Drowsiness
▪Fatigue
▪Ataxia
▪Slurred speech
▪Tremor

–Serious adverse effects
▪Hypotension
▪Tachycardia
▪Cardiovascular collapse
▪Laryngospasm

–Black box warning
▪Respiratory depression and arrest

98
Q

Midazolam (Versed)
–Contraindications/precautions

A

▪Acute, closed-angle glaucoma
▪Acute alcohol intoxication
▪Shock
▪Coma
▪Depressed vital signs

99
Q

Midazolam (Versed)
–Drug interactions

A

▪Additive CNS depression
–Other CNS depressants

▪Increased serum phenytoin levels/additive CNS
depression
–Dilantin

▪Interactions with drugs that inhibit or induce
CYP3A4 enzyme

100
Q

Midazolam (Versed)
–Herbal/food interactions

A

▪Increased sedation with kava or valerian
▪Grapefruit juice may increase serum concentration
▪Melatonin may increase sedation

101
Q

–Treatment of overdose for Midazolam (Versed)

A

▪General supportive measures
▪Flumenazil (romazicon) - Benzodiazepine antagonist –May induce seizures with rapid reversal

102
Q

Propofol (Diprivan)

– Therapeutic classification
– Pharmacologic classification

A

– Therapeutic classification
▪IV anesthetic
▪Sedative–hypnotic drug
– Pharmacologic classification
▪N-methyl-D-aspartate (NMDA) receptor agonist

103
Q

Propofol (Diprivan)
– Therapeutic effects and uses

A

▪IV anesthetic

▪Off-label
–Refractory migraines
–Refractory status epilepticus
–Treatment of agitation associated with alcohol withdrawal

104
Q

Propofol (Diprivan)
–Mechanism of action

A

▪Exact mechanism not clear
▪Believed to activate GABA receptors, causing
general inhibition of CNS activity

105
Q

Propofol (Diprivan)
Adverse effects

A

▪Injection site pain
▪Apnea
▪Respiratory depression
▪Hypotension

–Serious adverse effects
▪Metabolic abnormalities
▪Propofol infusion syndrome (PRIS)

106
Q

Propofol (Diprivan)
–Contraindications/precautions

A

▪Hypersensitivity to soybean and egg products
▪Obstetric patients
▪Intracranial pressure
▪Cardiac or respiratory impairment

107
Q

Propofol (Diprivan)
–Drug interactions

A

▪Reduced dose in patients receiving preanesthetic
medications
▪Other CNS depressants can cause additive CNS
and respiratory depression

108
Q

Propofol (Diprivan) –Treatment of overdose

A

▪Mechanical ventilation
▪Increasing flow rate of IV fluids
▪Vasopressor agents

109
Q

_______ are given following administration of IV agents

A

Gases

110
Q

Today, _______________ is the only gaseous anesthetic in use.

A

nitrous oxide

111
Q

gaseous anesthetic in use.

Rapidly absorbed into general circulation
–Very _________ soluble
–Cross _________________ barrier

A

Rapidly absorbed into general circulation
–Very lipid soluble
–Cross blood–brain barrier

112
Q

Nitrous oxide

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Gaseous general anesthetic
–Pharmacologic classification
▪GABA-receptor agonist
▪Opioid agonist

113
Q

Nitrous oxide
Therapeutic effects and uses

A

▪Minor medical and surgical procedures

114
Q

Nitrous oxide
–Mechanism of action

A

▪Not fully known
▪Believed to be due to activation of opioid receptors in midbrain
▪Relaxation properties likely due to activation of GABA receptors

115
Q

Nitrous oxide

Adverse effects (at high doses)

A

▪Anxiety
▪Excitement
▪Combativeness
▪Alveolar hypoxia

116
Q

Nitrous oxide
–Contraindications/precautions

A

▪Inability to comply with instructions and/or Impaired LOC
▪Undiagnosed abdominal pain, abdominal distention, bowel obstruction, head injury,
pneumothorax
▪Hypotension
▪Shock
▪COPD
▪Chest pain
▪Cyanosis

117
Q

Nitrous oxide
–Drug interactions

A

▪Exacerbate dysrhythmias
–Adrenergic agonists or caffeine

▪Additive sedation and respiratory depression
–CNS depressants

▪Excessive hypotension
–Amiodarone or antihypertensive

▪Herbal/food
–St. John’s wort discontinued

118
Q

Treatment of overdose of Nitrous oxide

A

▪Metoclopramide or antiemetic to reduce
associated nausea, vomiting

119
Q

Volatile liquid general anesthetics

–_________________ pressure allows them to vaporize at low temperatures and pressures

▪Anesthesia machine delivers precisely controlled
amounts.
–Very potent but little analgesic effect

A

–Low vapor pressure allows them to vaporize at low temperatures and pressures

▪Anesthesia machine delivers precisely controlled
amounts.
–Very potent but little analgesic effect

120
Q

Isoflurane (Forane)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Inhaled general anesthetic
–Pharmacologic classification
▪GABA and glutamate receptor agonist

121
Q

Isoflurane (Forane)
Therapeutic effects and uses

A

▪Induction of general anesthesia

122
Q

Isoflurane (Forane)
–Mechanism of action

▪Unknown
▪Interacts with ________________________in brain, including glutamate and GABA receptors

A

▪Unknown
▪Interacts with multiple receptors in brain, including glutamate and GABA receptors

123
Q

Isoflurane (Forane)
–Adverse effects

A

▪Mild nausea
▪Vomiting
▪Tremor

–Serious adverse effects
▪Malignant hyperthermia
▪Respiratory depression
▪Reduction in blood pressure

124
Q

Isoflurane (Forane)
–Contraindications/precautions

A

▪Malignant hyperthermia
▪Head trauma
▪Brain neoplasms
▪Patient under age 18
▪Older patients
▪Prolonged QT interval

125
Q

Isoflurane (Forane)
– Drug interactions

A

▪Coughing, breath holding, laryngospasm
–With nitrous oxide

▪Skeletal muscle weakness, respiratory depression, apnea
–Systemic polymyxin, aminoglycosides

▪Additive effects
–Skeletal muscle relaxants

▪Additive hypotension
–Antihypertensive medications

▪Dysrhythmias with adrenergic agonists
▪Discontinue levodopa 6 to 8 hours prior

126
Q

Isoflurane (Forane)
–Treatment of overdose

A

▪Profound respiratory depression
▪Symptomatic until effects diminish

127
Q

Local Anesthetics
* Block pain transmission in :

  • Loss of sensation to small or limited area of the body
A

peripheral nerves

  • Loss of sensation to small or limited area of the body
128
Q

Local Anesthetics
* Methods of delivery:

A

–Topical (surface) anesthesia
–Nerve block
–Infiltration anesthesia
–Spinal anesthesia
–Epidural anesthesia

129
Q
  • Two major classes of Local Anesthetics
A

–Esters

–Amides
▪Lower incidence of allergic reaction

130
Q

Ester-type local anesthetics

–Act by decreasing the amount of ________ that enters neuron, depress polarization, prevent conduction of pain impulse

–May be administered with epinephrine as a
vasoconstrictor

–Limit blood loss at surgical site
–Decrease amount of anesthetic absorbed systemically

A

sodium

131
Q

Procaine (Novocaine)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Local anesthetic
–Pharmacologic classification
▪Ester
▪Sodium channel blocker

132
Q

Procaine (Novocaine)
–Therapeutic effects and uses

A

▪Spinal, epidural, and peripheral nerve blocks for
local anesthesia

133
Q

Procaine (Novocaine)
–Mechanism of action

A

▪Decreases influx of sodium into neuron
–Increases threshold for depolarization
–Prevents conduction of nerve impulse

134
Q

Procaine (Novocaine)
–Adverse effects

A

▪Rare

–Serious adverse effects
▪Respiratory arrest
▪Anaphylaxis

135
Q

Procaine (Novocaine)
–Contraindications/precautions

A

▪Hypersensitivity
▪Generalized septicemia
▪Inflammation
▪Sepsis
▪Heart block
▪Hypotension
▪Hypertension
▪Altered coagulation

136
Q

Procaine (Novocaine)
–Drug interactions

A

▪Antagonizes antimicrobial effects of sulfonamides
▪Increased risk of hypotension
–Antihypertensives
▪Incompatible
–Aminophylline, chlorothiazide, magnesium
sulfate, phenobarbital, phenytoin, secobarbital,
sodium bicarbonate

137
Q

Procaine (Novocaine)
–Treatment of overdose

A

▪Symptomatic
▪Cardiopulmonary resuscitation may be necessary

138
Q

Amide-type local anesthetics

–Less effect on : _______________
–Lower incidence of __________ reactions
–Metabolized by hepatic CYP450 enzymes
▪Exercise caution when administering large
amounts to patients with hepatic impairment

A

–Less effect on myocardial contractility
–Lower incidence of allergic reactions
–Metabolized by hepatic CYP450 enzymes
▪Exercise caution when administering large
amounts to patients with hepatic impairment

139
Q

Lidocaine (Anestacon, Dilocaine, Xylocaine)

–Therapeutic classification
–Pharmacologic classification

A

–Therapeutic classification
▪Local anesthetic
–Pharmacologic classification
▪Amide
▪Sodium channel blocker

140
Q

Lidocaine (Anestacon, Dilocaine, Xylocaine)

–Therapeutic effects and uses

A

▪Surface or infiltration local anesthetic agent
▪Caudal and spinal block anesthesia

141
Q

Lidocaine (Anestacon, Dilocaine, Xylocaine)

–Mechanism of action

A

▪Blocks conduction of action potentials by reducing
sodium permeability

142
Q

Lidocaine (Anestacon, Dilocaine, Xylocaine)
–Adverse effects
-Black box warning

A

▪Erythema
▪Pruritus
▪Dermatitis
▪Burning
▪Alteration in taste
▪Headache
▪Gingivitis

–Serious adverse effects
▪Hypotension
▪Dysrhythmias
▪CV collapse
▪Cardiac arrest

–Black box warning: significant systemic absorption
may occur with topical use.

143
Q

Lidocaine (Anestacon, Dilocaine, Xylocaine)

– Contraindications/precautions

A

▪Hypersensitivity
▪Seriously damaged skin from trauma, burns, eczema (topical)
▪Stokes-Adams syndrome
▪Untreated sinus bradycardia, sinoatrial, AV, or
intraventricular heart block
▪Liver or kidney disease
▪Myasthenia gravis
▪Hypovolemia
▪Debilitated patients
▪Older patients

144
Q

Lidocaine (Anestacon, Dilocaine, Xylocaine)
–Drug interactions

A

▪Toxic effects
–Tocainide, mexiletine

▪Decreased lidocaine activity
–Barbiturates

▪Increased pharmacologic effects
–Cimetidine, beta blockers, quinidine

145
Q

–Treatment of overdose for Lidocaine (Anestacon, Dilocaine, Xylocaine)

A

▪Symptom management

146
Q

Adjuncts to Anesthesia

Purpose:

A

–To enhance anesthesia
-make procedure safer/ less unpleasant

147
Q

Preoperative medications

–Reduce -
–Reduce -
–Reduce -

A

–Reduce anxiety
–Reduce gastric fluid volume and acidity
–Reduce salivary and airway secretions