pain management and sedation Flashcards

1
Q

morphine sulfate ; morphine

A

Classification: opioid analgesic, opioid agonist

MOA: binds to opiate receptors in the CNS, altering perception to pain

Pharmacokinetics: Onset Immediate IV, 10-30 min IM, Duration 4-5 hrs

Indications: severe pain, pulmonary edema, pain associated with MI

AR/SE: respiratory depression, hypotension, confusion, sedations, N/V, constipation

Contraindications: known allergy, known hypersensitivity to tartazins, bisulfites, or alcohol

Dosage: Adult: 2-5 mg IV (5-10mg IM) q10 min for desired effect Peds( or adults under 50 kg): 0.01mg/kg IV, SQ, IM may repeat for desired effect, max dose 15 mg.

Special Considerations: (P Class C) Use caution in patients with head trauma, increased ICP.

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2
Q

hydromorphone ; dilaudid

A

Classification: Opioid analgesic, opioid agonist

MOA: binds to opiate receptors in the CNS, altering perception to pain

Pharmacokinetics: Well absorbed, Onset 10-15 min IV, Duration 2-3 hrs IV

Indications: moderate to severe pain, used alone and in combination with nonopioid analgesics.

AR/SE: respiratory depression, hypotension, confusion, sedation, constipation, physical dependence

Contraindications: Known allergy; should not be used during pregnancy or lactation

Dosage: 1mg IV (2mg IM) initially, may be repeated as needed for desired effect

Special Considerations: (P Class C)Added CNS depression may occur if used with other CNS depressant drugs; avoid use in patient who have received MAOI’s within 14 days.

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3
Q

meperidine ; demerol

A

Classification: opioid analgesic, opioid angonist

MOA: binds to opiate receptors in the CNS, altering perception to pain

Indications: moderate to severe pain, used as analgesic during labor

AR/SE: respiratory depression, hypotension, bradycardia, seizures, confusion, sedation, constipation, N/V, anaphylaxis

Contraindications: known allergy, pts with recent MAOI therapy

Dosage: 50-100 mg IV

Special Considerations: (P Class C)

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4
Q

fentanyl ; sublimaze

A

Classification: Opioid analgesic; opioid antagonist

MOA: binds to opiate receptors in the CNS, altering perception to pain

Pharmacokinetics: Absorbs Immediate, Onset 1-2 minutes IV, Duration ½-1 hour IV

Indications: severe pain, maintenance of analgesia

AR/SE: Apnea, Laryngospasm, respiratory depression, bronchospasm, hypotension, physical dependence

Contraindications: known allergy

Dosage: 0.5-1 mcg/kg (Adult over 12); 1-2 mcg/kg (peds under 12)

Special considerations: (P Class C) Added CNS depression may occur if used with other CNS depressant drugs; avoid use in patient who have received MAOI’s within 14 days.

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5
Q

nitrous oxide ; nitronox

A

Classification: medicinal gas, analgesic

MOA: exact MOA unknown, inhalation of 50% mixture of nitrous oxide and oxygen produces CNS depression and rapid pain relief.

Pharmacokinetics: rapid onset (2 minutes), duration 2-5 min

Indications: moderate to severe pain

AR/SE: lightheadedness, N/V, drowsiness, decreased respirations

Contraindications: known allergy, pts with decreased LOC, thoracic trauma, respiratory compromise, abdominal distention, pts who cannot follow simple instructions

Dosage: Self-administered

Special considerations: do not administer for abdominal pain if intestinal blockage is a possibility, nitrous oxide may collect in the obstructed space and aggravate the obstruction.

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6
Q

ketorolac ; toradol

A

Classification: NSAID, nonopioid analgesic

MOA: inhibits prostaglandin synthesis producing peripherally mediated analgesia; also has
antipyretic and anti-inflammatory properties

Pharmacokinetics: Rapid absorption, Onset 10 min IV, IM Duration 6+ hours IM, IM

Indications: short term (less than 5 days) management of moderate-severe pain

AR/SE: GI Bleeding, drowsiness, life threatening dermatitis, anaphylaxis

Contraindications: known allergy, cross-sensitivity may exist with other NSAIDS including
ASA; should not be given to patients with know alcohol intolerance; may inhibit labor and increase bleeding at delivery

Dosage: 30mg IV (60 mg IM) every 6 hours. May start with 15 mg IV (30mg IM) for patients over 65 yrs.

Special Considerations: (P Class C)increased risk of hypersensitivity in “aspirin triad patients”. Use with caution in cardiovascular disease, history of GI bleeding, and pts with renal impairment.

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7
Q

ibuprofen ; motrin

A

Classification: Nonopioid analgesic, NSAID

MOA: Inhibits prostaglandin synthesis, decreasing pain and inflammation

Pharmacokinetics: Well absorbed, Onset within 2 hours, Duration 6 hours

Indications: mild to moderate pain and fever

AR/SE: Rash, GI Bleeding, Hepatitis, Anaphylaxis, constipation, dyspepsia, N/V, headache

Contraindications: Known allergy, active GI bleeding or ulcer disease, risk of anaphylaxis in “aspirin triad patients” (asthma, nasal polyps, ASA intolerance); cross-sensitivity may exist with other NSAIDS including ASA.

Dosage: (Adult) 400-800 mg every 6 hours prn. Do not exceed 3200 mg/day
Special considerations: (P Class C till 30 then D) may limit cardioprotective effects of ASA. May increase the hypoglycemic effects of insulin or oral hypoglycemic agents. Discontinue at first site of rash as it may be life threatening.

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8
Q

acetaminophen ; tylenol

A

Class: Nonopoid analgesic; antipyretic

MOA: Inhibits synthesis of protstaglandins to reduce pain and fever, does not have significant anti-inflammatory properties

Pharmacokinetics: Well absorbed orally, onset ½-1 hour, duration 3-8 hours

Indications: Mild pain, Fever

AR/SE: Liver Failure and Hepatotoxicity with overdose; renal failure with chronic use

Contraindications: Known hypersensitivity

Dosage: Adult- 325-650 mg PO every 4-6 hours Peds- age and weight based.

Special Considerations: (P Class B)

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9
Q

midazolam ; versed

A

Classification: benzodiazepine, antianxiety, sedative/hypnotic

MOA: Acts on CNS to produce generalized CNS depression via GABA

Pharmacokinetics: Onset IN 5 min, IM 15 min, IV 1.5-5 min, Duration IN ½-1 hr, IM/IV 2-6 hrs

Indications: seizure activity, anxiety, premedication before painful procedures

AR/SE: Apnea, laryngospasm, respiratory depression, cardiac arrest, phlebitis, hiccups

Contraindications: known allergy, preexisting CNS depression, uncontrolled severe pain or angle-closure glaucoma.

Dosage: 1-2.5mg IV, 5mg IN (for sedation/induction, initial dose of 2-4 mg IV/IO followed by 3-5 mg q 15 min to maintain sedation)

Special considerations: (P Class C) monitor vital signs continuously.

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10
Q

lorazepam ; ativan

A

Classification: anticonvulsant, antianxiety

MOA: Depresses CNS by potentiating GABA

Pharmacokinetics: Absorbed rapidly, onset 15-30 minutes IV, duration 8-12 hours

Indications: decrease anxiety and seizure activity

AR/SE: Apnea and cardiac arrest (rapid IV), dizziness, drowsiness, lethargy, slurred speech

Contraindications: known allergy, pre-existing CNS depression, uncontrolled severe pain, severe hypotension, angle-closure glaucoma.

Dosage: 1-2 mg IV/IO/IM/IN, may be repeated if necessary but not to exceed 8 mg in 12 hrs.

Special considerations: (P Class D) Flush line before administration if other drugs have been given. Use caution in pts with severe liver, renal, or pulmonary impairment.

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11
Q

ketamine ; ketalar

A

Classification: Anesthetic; analgesic agent

MOA: blocks afferent transmission of impulses associated with pain perception; causes short-acting amnesia without muscular relaxation

Pharmacokinetics: Well absorbed, onset 30 seconds, duration 10-15 minutes

Indications: sedation, pain control, induction agent for RSI

AR/SE: Apnea, Severe Respiratory depression, hallucinations, explicit dreams

Contraindications: known allergy, hypertensive patients or patients with increased ICP

Dosage: Adult- 1mg/kg over 1 min IV (2-4 mg/kg IM) Peds- 1-2 mg over 1 min IV (3-5 mg/kg IM)

Special considerations: (P Class C) prolonged recover time if used with other opioids or barbituates, monitor vital signs frequently.

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12
Q

etomidate ; amidate

A

Classification: Sedative/hypnotic

MOA: exact MOA is unknown; believed to enhance GABA neurotransmission.
GABA is an inhibitory neurotransmitter in the CNS.

Pharmacokinetics: Well absorbed IV, Onset 1 minute, Duration 4-15 minutes

Indications: induction of anesthesia; premedication before tracheal intubation or cardioversion

AR/SE: Apnea, N/V, involuntary muscle movement

Contraindications: Known allergy, pts in labor

Dosage: 0.3 mg/kg over 30-60seconds IV

Special considerations: (P Class C) increased risk of apnea if administered with verapamil; monitor vitals constantly

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13
Q

propofol ; diprivan

A

Class: General Anesthetic

MOA: unknown but produces amnesia, has no analgesic properties

Pharmacokinetics: complete absorption; onset 45 sec; duration 3-5 min

Indications: sedation of intubated & ventilated patients

AR/SE: apnea, bradycardia, hypotension, burning, pain, stinging, long term use can lead to refractory bradycardia then asystole.

Contraindications: known allergy including to soybean oil, egg lecithin, and glycerol

Dosage: 40 mg every 10 seconds until induction achieved, then 100-200 mcg/kg/min for maintenance.

Special Considerations: (P class B)

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14
Q

succinycholine ; anectine

A

Class: Depolarizing neuromuscular blocker

MOA: prevents muscle from contracting by prolonging time during which the receptors at the neuromuscular junction cannot respond to acetylcholine

Pharmacokinetics: rapid absorption; onset 30-60 sec; duration 2-3 min

Indications: facilitate ET intubation

AR/SE: bradycardia/asystole in pediatric patients, apnea, bradycardia, therapeutic
hyperthermia, hyperkalemia

Contraindications: known allergy, therapeutic hyperthermia pts, acute narrow angle glaucoma or penetrating eye injury.

Dosage: 1.0 mg/kg IV/IO max dose 150 mg

Special Considerations: (P class C) fractures can occur from severe muscle spasms in pediatric pts.

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15
Q

pancuronium ; pavulon

A

Class: Neuromuscular blocker

MOA: competes with acetylcholine for the receptor sites in the muscle cells, causing paralysis.

Pharmacokinetics: rapid absorption; onset 30-45 sec; duration 30-60 min

Indications: produce muscle relaxation and facilitate ET intubation

AR/SE: bronchospasm, apnea, tachycardia, hypotension

Contraindications: known allergy including to bromides

Dosage: 0.1 mg/kg IV

Special Considerations: (P class C) note that it does not effect consciousness!

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16
Q

vecuronium ; norcuron

A

Class: Neuromuscular blocker

MOA: competes with acetylcholine for the receptor sites in the muscle cells, causing paralysis.

Pharmacokinetics: rapid absorption; onset <1 min; duration 30-40 min

Indications: produce muscle relaxation and facilitate RSI or routine ET intubation

AR/SE: bronchospasm, apnea, arrhythmias including cardiac arrest, bradycardia

Contraindications: known allergy including to bromides

Dosage: 0.1 mg/kg IV induction and maintenance (15-45 minutes after induction)

Special Considerations: (P class C) note that it does not effect consciousness!

17
Q

rocuronium ; zemuron

A

Class: Neuromuscular blocker

MOA: competes with acetylcholine for the receptor sites in the muscle cells, causing paralysis.

Pharmacokinetics: rapid absorption; onset 2-8 min; duration 30 min

Indications: produce muscle relaxation and facilitate RSI or routine ET intubation

AR/SE: bronchospasm, apnea, arrhythmias, N/V

Contraindications: known allergy including to bromides

Dosage: 0.6 mg/kg IV induction and maintenance (15-45 minutes after induction)

Special Considerations: (P class B) note that it does not effect consciousness!