Opioid Agents Flashcards

1
Q

What is the typical IV bolus dose of fentanyl for analgesia during anesthesia?

A

25–50 mcg

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2
Q

What is the approximate onset of action of fentanyl when given intravenously?

A

30–60 seconds

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3
Q

What is the typical duration of action of IV fentanyl after a single dose?

A

30–60 minutes

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4
Q

What is the mechanism of action of fentanyl?

A

Mu-opioid receptor agonist

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5
Q

Which of the following is a notable side effect of fentanyl?

A

Chest wall rigidity

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6
Q

In which of the following clinical scenarios is fentanyl most appropriately used?

A

Adjunct to general anesthesia for intraoperative analgesia

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7
Q

Which of the following best describes fentanyl’s potency compared to morphine?

A

100 times more potent

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8
Q

Is Fentanyl a short-acting synthetic opioid?

A

True

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9
Q

Does Fentanyl provide both analgesia and amnesia?

A

No (It provides analgesia, not amnesia)

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10
Q

Does Fentanyl cause bradycardia and respiratory depression?

A

Yes

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11
Q

Does Fentanyl have a slower onset of action than morphine?

A

No, it is faster

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12
Q

Is Fentanyl commonly used in rapid sequence intubation protocols?

A

Yes

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13
Q

Is Fentanyl associated with histamine release and hypotension?

A

No (Unlike morphine, it causes minimal histamine release)

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14
Q

Can the duration of fentanyl’s effect be prolonged with repeated dosing?

A

Yes

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15
Q

What is a typical IV dose range of fentanyl for analgesia in adult patients?

A

25-50 mcg; however 50–100 mcg IV bolus is also common

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16
Q

What is the onset time of fentanyl after IV administration?

A

Within 30–60 seconds

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17
Q

What is the duration of action of a single IV dose of fentanyl?

A

Approximately 30–60 minutes

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18
Q

What receptor does fentanyl primarily act on?

A

Mu-opioid receptor (μ-opioid receptor)

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19
Q

List two common side effects of fentanyl.

A
  • Respiratory depression
  • Bradycardia
  • Chest wall rigidity
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20
Q

Why might fentanyl be preferred over morphine in a hemodynamically unstable patient?

A

Because it has minimal histamine release and less hypotension

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21
Q

When should fentanyl be used cautiously?

A

In patients with compromised respiratory function or those on other CNS depressants

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22
Q

What complication can occur if fentanyl is administered too rapidly in high doses?

A

Chest wall rigidity, which can impair ventilation

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23
Q

What is the typical IV dose of morphine for adult pain management?

A

2–5 mg

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24
Q

What is the approximate onset of action of morphine when administered intravenously?

A

5–10 minutes

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25
Q

What is the typical duration of action for IV morphine?

A

2–4 hours

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26
Q

Morphine primarily acts on which receptor type?

A

Mu-opioid

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27
Q

Which of the following is a common side effect of morphine?

A

Constipation

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28
Q

Which of the following makes morphine less desirable in patients with hemodynamic instability?

A

Histamine release

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29
Q

Which clinical scenario best describes appropriate use of morphine?

A

Pain management post major abdominal surgery

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30
Q

Does Morphine have a slower onset than fentanyl?

A

Yes

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31
Q

Does Morphine cause any histamine release?

A

Yes

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32
Q

Is Constipation a common side effect of morphine?

A

Yes

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33
Q

Does Morphine cross the blood-brain barrier slower than fentanyl?

A

Yes

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34
Q

Is Morphine safe for use in all renal-impaired patients?

A

No (Active metabolites can accumulate)

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35
Q

Is Morphine a full agonist at mu-opioid receptors?

A

Yes

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36
Q

Respiratory depression is a rare side effect of morphine?

A

No it is common

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37
Q

What is a typical IV dose of morphine for moderate to severe pain?

A

2–5 mg IV every 4 hours as needed

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38
Q

What is the onset time of IV morphine?

A

Approximately 5–10 minutes

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39
Q

How long does a single dose of IV morphine typically last?

A

2–4 hours

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40
Q

What is the mechanism of action of morphine?

A

Morphine is a full mu-opioid receptor agonist that inhibits pain signaling pathways

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41
Q

List three common side effects of morphine.

A
  • Nausea
  • Respiratory depression
  • Constipation
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42
Q

What major cardiovascular effect can be caused by histamine release with morphine use?

A

Hypotension

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43
Q

Why should morphine be used with caution in patients with renal impairment?

A

Its active metabolite (morphine-6-glucuronide) accumulates and may cause prolonged sedation or respiratory depression

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44
Q

When is morphine preferred over fentanyl in clinical use?

A

For longer-lasting pain relief in settings where slower onset and longer duration are desired

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45
Q

How much more potent is Sufentanil compared to fentanyl?

A

50–100 times

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46
Q

What is the typical IV bolus dose of Sufentanil for adult anesthesia induction?

A

0.05–0.2 mcg/kg

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47
Q

What is the approximate onset of action of Sufentanil?

A

30–60 seconds

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48
Q

What is the typical duration of action of a single IV dose of Sufentanil?

A

20–45 minutes

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49
Q

What is the primary mechanism of action of Sufentanil?

A

Mu-opioid receptor agonism

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50
Q

In which clinical setting is Sufentanil most commonly used?

A

Intraoperative analgesia in cardiac or major surgeries

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51
Q

What is a major side effect of Sufentanil that must be monitored closely?

A

Respiratory depression

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52
Q

Is Sufentanil more lipid-soluble than fentanyl?

A

Yes

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53
Q

Does Sufentanil have a longer duration of action than morphine?

A

No

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54
Q

Does Sufentanil cause histamine release?

A

No

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55
Q

Is respiratory depression caused by Sufentanil dose-dependent?

A

Yes

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56
Q

Can Sufentanil be reversed with naloxone?

A

Yes

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57
Q

Is Sufentanil commonly used in neuraxial anesthesia (e.g., epidural)?

A

Yes

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58
Q

Does Sufentanil provide both analgesia and amnesia?

A

No (It provides analgesia, not amnesia)

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59
Q

What is the usual bolus dose range of Sufentanil for general anesthesia in adults?

A

0.05-0.2 mcg/kg IV

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60
Q

What is the onset time of Sufentanil after IV administration?

A

Approximately 30–60 seconds

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61
Q

How long does a single dose of Sufentanil typically last?

A

Approximately 20–45 minutes

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62
Q

What receptor does Sufentanil act on?

A

Mu-opioid receptors

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63
Q

Name two clinical scenarios where Sufentanil would be an appropriate choice.

A
  • Cardiac surgery
  • Epidural analgesia during labor
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64
Q

List three common side effects of Sufentanil.

A
  • Respiratory depression
  • Bradycardia
  • Nausea/vomiting
65
Q

Why might Sufentanil be preferred over fentanyl for certain surgeries?

A

Greater potency and shorter duration allow for precise titration during major surgeries

66
Q

What is one major risk when Sufentanil is administered in high doses or too rapidly?

A

Chest wall rigidity or profound respiratory depression

67
Q

What is the typical bolus dose of Remifentanil for induction in general anesthesia?

A

0.25 mcg/kg

68
Q

What is the recommended maintenance infusion dose of Remifentanil during general anesthesia?

A

0.05–2 mcg/kg/min

69
Q

What is the typical onset of action of Remifentanil after IV administration?

A

15–30 seconds

70
Q

How long does the effect of Remifentanil last after discontinuation?

A

5–10 minutes

71
Q

Which enzyme is primarily responsible for the metabolism of Remifentanil?

A

Plasma cholinesterases

72
Q

Which clinical scenario best fits the use of Remifentanil?

A

TIVA (Total Intravenous Anesthesia) requiring rapid offset

73
Q

Which of the following is a major side effect associated with high-dose Remifentanil use?

A

Chest wall rigidity

74
Q

Does Remifentanil have a rapid onset and ultra-short duration of action?

75
Q

Does Remifentanil accumulate significantly with prolonged infusions?

76
Q

Is Remifentanil suitable for use in patients with hepatic or renal impairment?

77
Q

Can Remifentanil be administered via intramuscular injection?

78
Q

Do the effects of Remifentanil wear off quickly after stopping the infusion?

79
Q

Does Remifentanil act primarily on delta-opioid receptors?

A

No (It acts on mu-opioid receptors)

80
Q

Should Remifentanil be used for post-operative pain control due to its short action?

81
Q

What is the usual IV bolus dose of Remifentanil?

A

0.25 mcg/kg

82
Q

What is the typical onset time of Remifentanil?

A

30–60 seconds

83
Q

How long does Remifentanil’s effect last after discontinuation?

A

5–10 minutes

84
Q

What is the mechanism of action of Remifentanil?

A

It is a potent mu-opioid receptor agonist that modulates pain signaling in the CNS.

85
Q

Why is Remifentanil ideal for short surgical procedures?

A

Because it has a rapid onset and ultra-short duration, allowing tight control over analgesia with quick recovery.

86
Q

What enzyme breaks down Remifentanil in the body?

A

Plasma esterases (non-specific cholinesterases)

87
Q

List three side effects of Remifentanil.

A
  • Respiratory depression
  • Bradycardia
  • Chest wall rigidity
88
Q

Why is Remifentanil not used for post-operative pain management?

A

Because of its rapid clearance and short duration—it wears off quickly and lacks residual analgesia.

89
Q

What is the usual IV dose of Meperidine for moderate pain in adults?

90
Q

What is the typical onset of action for IV Meperidine?

A

1–5 minutes

91
Q

What is the typical duration of analgesia for a single dose of Meperidine?

A

2–4 hours

92
Q

Which neurotransmitter system is most directly affected by Meperidine’s mechanism of action?

A

Mu-opioid receptors

93
Q

Which serious side effect is associated with the accumulation of Meperidine’s metabolite, normeperidine?

94
Q

In what scenario might Meperidine be preferred over other opioids?

A

Treatment of rigors/shivering

95
Q

Does Meperidine have both analgesic and local anesthetic properties?

96
Q

Does Meperidine have a shorter half-life than morphine?

97
Q

Is Normeperidine an active metabolite of Meperidine that is neurotoxic?

98
Q

Should Meperidine be avoided in patients with renal failure?

99
Q

Is Meperidine a good choice for chronic pain management?

100
Q

Can Meperidine cause serotonin syndrome if combined with MAO inhibitors?

101
Q

Is Meperidine primarily metabolized by the kidneys?

A

No (Metabolized in the liver, excreted by kidneys)

102
Q

What is the typical IV dose of Meperidine for an adult patient in moderate pain?

A

12.5-25 mg IV

103
Q

What is the typical onset time of IV Meperidine?

A

1–5 minutes

104
Q

What is the duration of action of Meperidine?

A

2–4 hours

105
Q

What receptor does Meperidine primarily act on to produce analgesia?

A

Mu-opioid receptor

106
Q

What is the name of Meperidine’s neurotoxic metabolite?

A

Normeperidine

107
Q

List three common side effects of Meperidine.

A
  • Nausea
  • Respiratory depression
  • Dizziness
108
Q

Why should Meperidine be avoided in patients with renal impairment?

A

Because normeperidine can accumulate and increase the risk of seizures

109
Q

In what situation is Meperidine especially useful over other opioids?

A

For the treatment of post-anesthesia shivering or rigors

110
Q

What condition can result from combining Meperidine with MAO inhibitors?

A

Serotonin syndrome

111
Q

What is the typical IV dose of Hydromorphone for moderate to severe pain in adults?

A

0.25–0.5 mg

112
Q

What is the onset time for IV Hydromorphone?

113
Q

What is the duration of action for IV Hydromorphone?

A

3–4 hours

114
Q

Hydromorphone is how many times more potent than morphine?

115
Q

Which receptor does Hydromorphone primarily act on to exert its analgesic effects?

A

Mu-opioid receptor

116
Q

In which of the following scenarios is Hydromorphone most appropriate?

A

Moderate-to-severe post-operative pain

117
Q

Is Hydromorphone more potent than morphine?

118
Q

Does Hydromorphone have a slower onset than morphine?

A

No (It has a faster onset)

119
Q

Is Hydromorphone suitable for use in patients with opioid tolerance?

120
Q

Does Hydromorphone act primarily on the kappa-opioid receptor?

A

No (It acts on the mu-opioid receptor)

121
Q

Are common side effects of Hydromorphone include respiratory depression and constipation?

122
Q

Is Hydromorphone recommended for use in renal impairment?

A

Yes (It is generally preferred over morphine in renal impairment)

123
Q

Is Hydromorphone contraindicated in patients with a history of opioid addiction?

A

No (It must be used cautiously, not necessarily contraindicated)

124
Q

What is the typical IV dosage of Hydromorphone for an adult?

A

0.25–5 mg IV

125
Q

What is the onset time for IV Hydromorphone?

A

Approximately 5 minutes

126
Q

How long does the analgesic effect of Hydromorphone usually last?

A

3–4 hours

127
Q

Describe the mechanism of action of Hydromorphone.

A

It is a potent mu-opioid receptor agonist that inhibits pain transmission in the central nervous system.

128
Q

List three common side effects of Hydromorphone.

A
  • Respiratory depression
  • Nausea
  • Constipation
129
Q

Why might Hydromorphone be preferred over Morphine in patients with renal impairment?

A

Hydromorphone produces fewer active metabolites that accumulate in renal dysfunction.

130
Q

In what type of clinical setting is Hydromorphone commonly used?

A

For the management of moderate to severe acute or chronic pain, especially post-operative pain

131
Q

What is one major risk when using Hydromorphone at high doses or in opioid-naïve patients?

A

Respiratory depression

132
Q

What is the typical adult IV dose of Naloxone for opioid overdose?

A

1-4 mcg/kg

133
Q

What is the onset of action for IV Naloxone?

A

30 seconds to 2 minutes

134
Q

What is the typical duration of action of Naloxone?

A

1–4 hours

135
Q

Which receptor does Naloxone primarily antagonize?

136
Q

Which of the following is a possible effect of Naloxone in opioid-dependent patients?

A

Acute withdrawal symptoms

137
Q

In which of the following scenarios is Naloxone indicated?

A

Opioid-induced respiratory depression

138
Q

Is Naloxone effective at reversing benzodiazepine overdose?

139
Q

Does Naloxone have a shorter half-life than many opioids?

140
Q

Does Naloxone bind to mu-opioid receptors and activate them?

A

No (It is an antagonist, not an agonist)

141
Q

Will Naloxone need to be re-administered if opioid effects outlast it?

142
Q

Can Naloxone be given intranasally?

143
Q

Is one dose of Naloxone always sufficient to reverse all opioid overdoses?

144
Q

Does Naloxone have known side effects?

145
Q

What is the standard IV dose range of Naloxone for an adult opioid overdose?

A

1-4 mcg/kg IV

146
Q

What is the onset time for Naloxone when given IV?

A

30 seconds to 2 minutes

147
Q

How long does Naloxone typically last in the body?

A

1 to 4 hours

148
Q

Can Naloxone be given intranasally?

A

Yes

Naloxone can be administered via the nasal route for opioid overdose reversal.

149
Q

Is one dose of Naloxone always sufficient to reverse all opioid overdoses?

A

No

Some overdoses may require multiple doses due to the potency of the opioid involved.

150
Q

Does Naloxone have known side effects?

A

Yes

Side effects may include withdrawal symptoms in opioid-dependent individuals.

151
Q

What is the standard IV dose range of Naloxone for an adult opioid overdose?

A

1-4 mcg/kg IV

Dosing may vary based on clinical response.

152
Q

What is the onset time for Naloxone when given IV?

A

30 seconds to 2 minutes

Rapid onset is critical in emergency situations.

153
Q

How long does Naloxone typically last in the body?

A

1 to 4 hours

Duration of action may be shorter than some opioids.

154
Q

What is the mechanism of action of Naloxone?

A

It is a competitive antagonist at opioid receptors, especially mu-opioid receptors, blocking the effects of opioids

This mechanism helps to reverse the effects of opioid overdose.

155
Q

List two clinical situations where Naloxone is indicated.

A
  • Opioid overdose with respiratory depression
  • Post-operative opioid-induced sedation

Naloxone is used in emergencies and after surgeries to counteract sedation.

156
Q

What may occur if Naloxone is administered to an opioid-dependent patient?

A

Sudden and severe opioid withdrawal symptoms

Symptoms can include agitation, nausea, vomiting, and tachycardia.

157
Q

What is one possible side effect of Naloxone?

A
  • Hypertension
  • Agitation
  • Nausea
  • Vomiting
  • Tachycardia

These side effects may arise especially in opioid-dependent individuals.

158
Q

Why might repeat doses or a continuous infusion of Naloxone be necessary?

A

Because its duration of action is shorter than many opioids, leading to re-sedation

Continuous monitoring and administration may be required in severe overdoses.