Pharm exam II- opiods Flashcards

0
Q

What is the induction dose for Alfentanil?

A

50-300mcg/kg

think approx 150mcg/kg

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1
Q

What is the induction dose for Morphine?

A

1mg/kg (titrated to 1mg/kg)

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2
Q

What is the induction dose for Fentanyl?

A

5-40mcg/kg

Think approx 20mcg/kg

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3
Q

What is the induction/loading dose for Remifentanil (Ultiva)?

A

0.5-1mcg/kg over 30 sec

Think approx 0.75mcg/kg

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4
Q

What is the induction dose for Sufentanil?

A

2-10mcg/kg

Think approx 6mcg/kg

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5
Q

What is the induction dose for Etomidate (Amidate)?

A

0.1-0.4mg/kg

Think approx 0.2mg/kg

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6
Q

What is the induction dose for Ketamine (Kerolar)?

A

1-2.5mg/kg

Think approx 1.75 mg/kg

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7
Q

What is the induction dose for Propofol (Diprivan)?

A

2-2.5mg/kg

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8
Q

What is the induction dose for Methohexital (Brevital)?

A

1.5-2.5mg/kg

Think approx 2mg/kg

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9
Q

What is the induction dose for Thiopental (Pentothal)?

A

3-5mg/kg

Think approx 4 mg/kg

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10
Q

What is the induction dose for Diazepam (Valium)?

A

0.3-0.5mg/kg

Think 0.4mg/kg

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11
Q

What is the analgesic dose for Ketamine (Kerolar)?

A

0.5-1mg/kg

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12
Q

What is the analgesia dose for Afentanil (Afental)?

A

250-500mcg
or
5-10mcg/kg

(Think 375mcg or 7mcg/kg)

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13
Q

What is the analgesia dose for Fentanyl?

A

0.7-2mcg/kg

Think 1mcg/kg

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14
Q

What is the analgesia dose for Meperidine (Demerol)?

A

25-100mg

12.5-25 for post-op shivers

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15
Q

What is the analgesia dose for Acetaminophen (Tylenol) IV?

A

1000mg IV q6hr (give infusion over 15min)

650mg IV q4hr

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16
Q

What is the analgesia dose for Morphine?

A

2-15mg

titrate in increments of 1-2mg doses

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17
Q

What is the analgesia dose for Ketorlac (Toradol)?

A

15-30mg q6hr

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18
Q

What is the analgesia dose for Hydromophone (Dilaudid)?

A

0.2-0.6mg IV (q2-3hrs)

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19
Q

What is the infusion dosing for Sufentanil?

A

0.1-0.5mcg/kg/min

Think approx 0.3mcg/kg/min

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20
Q

What supplement bolus dose would you give for Sufentanil?

A

0.6mcg-4mcg/kg

Think 2mcg/kg

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21
Q

What is the infusion dosing for Remifentanil (Ultiva)?

A

0.05 - 2mcg/kg (supplemented with prop, N2O, or Forane because such short acting)

(Think approx 1mcg/kg)

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22
Q

What is the infusion dosing for Propofol (Diprivan)?

A

20-75mcg/kg/min (titrate to response)

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23
Q

What dosage would you give for a Propofol bolus for sedation?

A

25-50mg
or
0.5 - 1mg

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24
Q

What is the infusion dosing for Methohexital (Brevital)?

A

50-150mcg/kg/min

Think approx 100mcg/kg/min

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25
Q

What is the TIVA dose for Propofol?

A

100-200 mcg/kg/min

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26
Q

What is the TIVA dose for Fentanyl?

A

50-150mcg/kg

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27
Q

What is the TIVA dose for Sufentanil?

A

10-30mcg/kg

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28
Q

What is the induction dose for Midazolam (Versed)?

A

0.1-0.2mg/kg

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29
Q

What is the sedation dose for Midazolam (Versed)?

A

0.5 - 5mg (titrated)

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30
Q

What is the infusion dosing for Midazolam (Versed)?

A

0.25 - 5mcg/kg/min

Think approx 2mcg/kg/min

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31
Q

What dose of Versed would you give to stop a seizure?

A

2-5mg

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32
Q

What Lorazepam (Ativan) dose would you give?

A

0.5 - 1mg

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33
Q

What is Clonidine when considering receptor type to cause its effects?

A

Alpha 2 agonist (presynaptic = neg feedback)

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34
Q

What effects can be seen with Clonidine?

A

Analgesia (useful to augment morphine and LA blocks)
Sedation (hyperpolarizes A2 receptor)
bradycardia
hypotension

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35
Q

What is a N-methyl-D-aspartate receptor?

A

It is the receptor that glutamate binds to to cause excitatory pain response

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36
Q

How does Ketamine cause it analgesic effects?

A
  • It is a noncompetitive antagonist at the NMDA receptor which blocks glutamate and pain transmission
  • Also interacts with mu, delta, and kappa opiod receptors
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37
Q

What type of surgical case should ketamine not be used during?

A

Neuro cases because it can cause increased cerebral blood flow, increased ICP, and increased CMR02, myoclonus, nystagmous, and seizure-like activity.

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38
Q

What can you pretreat a patient with to prevent some of the CNS/Delirium side effects of Ketamine?

A

Benzo’s such as versed

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39
Q

Which cyclooxygenase enzyme would you want to block to prevent unwanted side effects found in many NSAIDs?

A

COX2 (ex- Celebrex is a COX2 inhibitor and will not cause decreased platelet aggregation, renal dysfunction, and GI ulcers whereas nonselective COX inhibitors will have these side effects)

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40
Q

What are some of the effects of NSAIDs?

A
  • Decreased pain receptor activation from prostaglandins
  • Reduced inflammation
  • Inhibition of platelet aggregation
  • Inhibition of prostaglandin formation causing reduced protection of GI tract and renal function
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41
Q

How does regional blockades or wound infiltration with local anesthetics prevent pain?

A

They inhibit transmission of nerve impulses by blocking sodium channels. (This slows the rate of depolarization so that threshold is not reached and action potentials are not propagated)

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42
Q

What group of drugs can provide anti-inflammatory and analgesic properties to supplement anesthesia?

A

NSAIDs

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43
Q

What is the safest NSAID for pts with renal impairment?

A

Aspirin

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44
Q

What are the max daily doses for adults and peds of Acetominophen?

A
Adults = 4gm/day
Peds= 75mg/kg
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45
Q

What meds should you be cautious of when considering liver toxicity from Acetaminophen?

A

opiod-nonopioid compounds containing acetaminophen

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46
Q

Is Ibuprofen a selective or nonselective COX inhibitor?

A

nonselective (therefore unwanted side effects= bleeding, ulcers, kidney failure)

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47
Q

What type of NSAID is Ketorolac (Tordal)?

A

Nonselective COX inhibitor (will have unwanted side effects)

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48
Q

In comparison to morphine what does 30mg of Ketorolac equivalent to?

A

9mg morphine

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49
Q

What patient populations would you not want to use Ketorolac (NSAIDs)?

A
  • Asthmatics
  • Renal impairment
  • Post-op bleeding concerns
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50
Q

What is recommended length of use for Ketorolac when considering renal impairment?

A

no longer than 5 days

51
Q

What type of NSAIDs can cause cardiac toxicity?

A

COX-2 selective agents

52
Q

Which two NSAIDS should not be taken together to prevent cardiac toxicity?

A

Aspirin and Ibuprophen

53
Q

How do opioid receptors cause analgesic effects?

A
  • agonists pre-synaptic (A2 neg feedback=decrease Ca++= decrease NT)
  • agonist post synaptic (inhibits membrane depolarization)
54
Q

What side effects are seen with opioid agonist activity (A2 neg feedback)?

A
  • Analgesia
  • Sedation
  • Miosis (pinpoint pupils)
  • Bradycardia
  • Resp depression
  • Euphoria/Dysphoria
55
Q

Where can opioid receptors be found?

A

Supraspinal=brain

Spinal= Spinal cord (dorsal horn)

56
Q

Supraspinal analgesia is mediated by which opioid receptors and which one one is most important?

A
  • All opioid receptors except Mu-2

- Mu-1 is most important in the brain

57
Q

Spinal analgesia is mediated by which opioid receptors and which one is most important?

A
  • All opioid receptors are found in the spinal cord

- Mu-2 is most important

58
Q

Which opioid receptor is more important in the periphery?

A

Delta receptors

59
Q

Which opioid receptor does not contribute to dependence?

A

Kappa

60
Q

What does neuraxial analgesia refer to?

A

Opiates given via Epidural or Spinal (intrathecal) methods

61
Q

Neuraxial analgesia from opioids have same potential side effects as any other route but which side affects seem to be increased?

A

Pruritis and urinary retention (> than when given IV route)

62
Q

Why are smaller doses used when a spinal (intrathecal) opiate is given compared to epidural dose?

A

Venous plexus in epidural space causes systemic absorption

63
Q

What CNS effects can be seen with morphine-like opioids?

A
  • Analgesia
  • Euphoria (when in pain)
  • dysphoria (when not in pain)
  • Sedation
  • Resp depression
  • **decreased stress response to surgical stimulation (incision)
  • **decreased MAC of volatile agents (ED50 of gas)
64
Q

What GI effects can be seen with morphine-like opioids?

A
  • Biliary tract-spasm of sphincter of odi
  • Delayed gastric emptying (constipation)
  • N&V
65
Q

What meds are used to treat biliary sphincter of Odi spasm?

A

Narcan

Glucagon 2mg

66
Q

What GU effects can be seen with morphine-like opioids?

A
  • Urinary retention (Antidiuretic effect)

- Increased detrussor muscle tone and sphincter tone

67
Q

What cutaneous effects can be seen with morphine-like opioids?

A
  • vessel dilation
  • localized histamine (non-allergic) release = decrease bp
  • Pruritis
  • Erythema
68
Q

Do morphine-like opioids cross the placenta/BBB?

A

Yes, morphine (most lipophobic opiod) less than Phenylpiperidines (more lipid soluble)

69
Q

What meds can be given for pruritis from opioids?

A

Nubain
Zofran
Prop 10mg

70
Q

How is morphine metabolized?

A

Conjugation in the liver

71
Q

How is morphine excreted?

A

Mainly Kidney

Biliary (7-10%)

72
Q

What is important to consider when thinking about morphine metabolism and patients with kidney failure?

A

Morphine has active metabolites (morphine-3-etheral sulfate, morphine-3-glucuronide, morphine-6-glucuronide) which can cause prolonged sedation in renal pts

73
Q

What is Codeine metabolized into?

A

Morphine

74
Q

Fentanyl is how much more potent than morphine?

A

100 x’s

75
Q

Which is more lipid soluble morphine or fentanyl?

A

Fentanyl

76
Q

What is fentanyl’s DOA compared to morphine?

A

Fentanyl is DOA is shorter

77
Q

What is Fentanyl’s elimination time compared to morphine?

A

It is longer due to fentanyl’s large Vd and lipid solubility.

78
Q

Why does fentanyl have a rapid onset?

A

Rapid passage of BBB due to highly lipid soluble

79
Q

Which med is more protein bound and has a smaller Vd because of it? Fentanyl or Sufentanil

A
Sufentanil = 92% protein bound small Vd
Fentanyl= 80-87% protein bound larger Vd than sufentanil
80
Q

What is important to consider when thinking about fentanyl metabolism?

A
  • metabolized in liver by D-methylation into somewhat active metabolite norfentanyl
  • Significant first pass pulmonary effect
81
Q

Fentanyl is excreted by kidneys and can be found present in urine for how long?

A

72 hrs.

82
Q

What causes bradycardia that is sometimes seen with fentanyl?

A

marked depression of carotid sinus reflex

83
Q

What are some important side effects to consider when thinking about fentanyl?

A
  • Rigid chest
  • less histamine release than (morphine)
  • Slight increase in ICP
84
Q

What meds would you give to treat rigid chest?

A

NDMR (give slow)

85
Q

How much more potent is Sufentanil compared to Fentanyl?

A

10 x’s

86
Q

What side effects are commonly seen in Sufentanil?

A

Basically same as fentanyl:

-Brady, increased ICP, respiratory depression, rigid chest, decreased cmrO2

87
Q

What opioids have first pass pulmonary uptake?

A

Fentanyl

Sufentanil

88
Q

Fentanyl is approximately how much more potent than Alfentanil?

A

10 x’s

89
Q

How is Alfentanil’s context sensitive half time different than Sufentanil’s and why?

A

It is longer due to its smaller Vd and less redistribution out of plasma

90
Q

Alfentanil is more likely to cause what side effect in comparison to other phenylpiperdines?

A

Rigid chest

91
Q

What types of surgical cases is Remifentanil commonly used?

A

Neuro cases (Dr’s like to see pt awake shortly after surgery)

92
Q

What is unique about Remifentanil?

A

It is ultra short acting due to its ester linkage which allows for hydrolysis by plasma/tissue

93
Q

When comparing Remifentanil to Alfentanil and fentanyl what is its potency?

A

Remifentanil is about 15-20 x’s more potent than Alfentanil and about the same potency as fentanyl

94
Q

Since Remifentanil is hydrolyzed in the plasma so rapidly what characteristics does it have?

A
  • Small Vd
  • Easily titratable
  • no cumulative effects
  • rapid clearance
  • Rapid recovery
  • context sensitive half time approx 5 mins
95
Q

Are the effects of Remifentanil affected by kidney and liver failure?

A

No, it is mainly metabolized via hydrolysis to an inactive metabolite and excreted by kidney

96
Q

What should be considered postoperatively when Remifentanil is stopped?

A

Need to follow with longer acting analgesic because it does not provide post-op relief of pain

97
Q

Why is Remifentanil not recommended as sole agent for surgery?

A

Uncertain loss of consciousness so usually supplemented with propofol, N2O, or forane.

99
Q

Is Remifentanil used via neuraxial routes?

A

no, due to neurotoxicty caused

100
Q

Meperidine (Demerol) is a synthetic opiate active mainly at which opioid receptors?

A

Mu and Kappa

101
Q

What is the potency of Demerol compared to morphine**?

A

1/10th

102
Q

What is important to consider about dosing when giving Demerol**?

A
  • Should not be used >48hrs

- Max dose is 600mg/24hrs

103
Q

How is Meperidine metabolized?

A

It is extensively metabolized in the liver

104
Q

Demerol’s active metabolite normeperidine can cause what side effects?

A

CNS effects such as seizures by decreasing threshold

105
Q

What other group of meds should not be given with Meperidine?

A

MAO inhibitors (can cause seizures and death)

106
Q

What other side effects can be seen with Demerol?

A

Hyperpyrexia and dysphoria

107
Q

What is Meperidine commonly used for?

A

Post-op shivers and L&D

108
Q

How does Naloxone (Narcan) produce its effects at receptors?

A

It is a pure opioid antagonist at mu, delta, and kappa

109
Q

How can Narcan be used with patients experiencing shock?

A

May reverse hypotension form endogenous endorphins

110
Q

Where is Narcan metabolized

A

In the liver

111
Q

Why is Narcan usually giving IV route?

A

First pass effect orally causes it to be 1/5th as potent

112
Q

What effects/side effects can be seen with Naloxone (Narcan)

A
  • Recurrence of pain
  • N&V from rapid infusion
  • Pulmonary edema
  • Re-narcotization after med wears off
113
Q

Narcan is supplied in 0.4mg/ml how would you draw it up to get 0.1mg/ml solution?

A

Draw up the 1ml of 0.4 solution with 3ml of NS

114
Q

What is the oral opiate antagonist that lasts 24hrs?

A

Naltrexone

115
Q

How is Nalmefene different than Narcan?

A

Its half time is 10hrs so its duration of action is longer due to slower metabolism by liver

116
Q

What is Dilaudid mostly used for?

A

Post-op pain

117
Q

What drug is better for renal patients Dilaudid or Morphine?

A

Dilaudid

118
Q

What is a sedative?

A

Reduces anxiety, has calming effect with little or no effect on motor or mental function

119
Q

What is a hypnotic?

A

Produces drowsiness, encourages the onset and maintenance of sleep

120
Q

Opioid receptors are what type of receptor?

A

G-protein coupled receptor (intermediary in cell communication)

121
Q

Extracellular binding of opioid to G-protein coupled receptor will cause what intracellularly?

A

Inhibition of adenyl cyclase

122
Q

Which opioid receptor subsets add to dependence when activated?

A

Mu-2 & Delta

123
Q

Is Remifentanil’s duration affected when a person has a psuedocholinesterase deficiency (abnormality may be sensitive to certain anesthetic drugs such as muscle relaxants and ester local anesthetics)

A

No

124
Q

What are some excitatory NT’s (EPSP)?

A
  • Acetylcholine
  • NE at Alpha1 and Beta 1 (IPSP at Alpha 2)
  • Serotonin (IPSP also at different sites)
  • Glutamate
125
Q

What NT’s are inhibitory (IPSP)?

A
  • Dopamine
  • NE at Alpha 2 only
  • Serotonin (in some receptors)
  • GABA
  • Nitric Oxide (?)