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23 Cards in this Set

  • Front
  • Back
- Opiod
- Opiate
- Narcotic
-Analgesic
- Opiod – any drug with actions similar to Morphine
- Opiate –those drugs present in opium: Morphine, Codeine, Heroin
- Narcotic – -drug capable of causing analgesia, CNS depression & physical depression
-Analgesic: pain relief without LOC
Opioid Receptors:
- mu
- kappa
- delta
- mu – most important – analgesia, ↓resp, euphoria, sedation, physical dependency, ↓GI motility
- kappa – mild/minor – sedation, analgesia, ↓GI motility
- delta/epsilon: Analgsia
Morphine Sulfate

Type:
Strong pure opioid agonists
Morphine Sulfate

Uses:
USES
Moderate to severe pain control
Sedation
Pulmonary edema

Relevance: standard others of its class measured
Morphine Sulfate

Pharmacokinetics
*routes
* Parenteral
* Enteral
*routes
-IV, IM, SubQ
-oral
-Epidural & Intrathecal: subarachnoid
* Parenteral
- fast onset
-effects can last up to 4-5 hrs
* Enteral
-slow onset
-higher doses needed – first pass effect
-effects can be 4-5 hours or 24 hours
Morphine Sulfate

INTERACTIONS (5)
*CNS depressants
-Benzodiazepines, Barbiturates, Alcohol
-↑sedation & respiratory depression
*Anticholinergic Drugs
-Atropine, Antihistamines
-↑constipation & urinary retention
*Antihypertensives
*MAOI
-excited delirium
*Opioid Antagonists
-Naloxone
Morphine Sulfate

Dose
Prep 10mg/ml – 1mlAmp
Dose (IV, IM, SubQ
Load- 0.1mg/kg
Main- 2.5-5mg PRN

2.5mg in 1 min
Administration
*IVP
*Supine
*Reversal agent & resp support on hand
Morphine Sulfate

Effects Caution (4)
CAUTION:
• Resp disorders
• Labor/pregnancy
• head injury
• hypotension
Morphine Sulfate

Adverse effects (10)
• Clinical Triad: Resp ↓, CNS depression, Pupil constriction miosis
• Hypotension: Histamine release, Baraceptor blockade
• Urinary retention
• Constipation
• Cough suppression amitussive
• Biliary Colic: Smooth muscle spasm within biliary ducts
• Emesis: Stimulation of chemoreceptor trigger zone
• ↑ ICP: Resp depression
• Euphoria/dysphoria
• Neurotoxicity
Fentanyl Citrate

Trade name:
Type:
Sublimaze©
Strong opioid agonists
Fentanyl Citrate

USED FOR:
For breakthrough/rapid pain control
Induction/maintenance of anesthesia
RAPID onset & SHORT duration
Fentanyl Citrate

Dose:
Dose (IV, IM )
PAIN:
1mcg/kg
INDUCTION:
3mcg/kg (max single 250mcg)
50mcg/min
Fentanyl Citrate

Compared to Morphine
100x more potent than morphine
Meperidine

Trade name:
Type:
Demerol©
Strong opioid agonists
Meperidine

Interactions
facts
Less potent than morphine and Shorter half life
Many drug interactions: MAOI, SSRI, TCA’s
May lead to neurotoxicity
Is narcotic of “exclusion”
Good for biliary related pain
Hydromorphone

Trade name
Type
Dilaudid©
Strong opioid agonists
Hydromorphone

Uses
Moderate to severe pain control
Alternative to Morphine for pain control
Often used as antitussive
Hydromorphone

Compared to morphine
10x more potent than morphine
Naloxone

Trade
type
Narcan©
Opioid antagonists
Naloxone

Used for
Reversal of opioid overdose
Focus on reversal of Respiratory depression
Careful with dosing as withdrawal can be caused
Mixed OD?
Naloxone

Pharmacodynamics
-competitive antagonist of opioid receptors
-will antagonize actions of opioids
Naloxone

Dose
Prep 0.4mg/ml – 10 ml Vial

Dose:( IV, IM, SubQ)
0.4mg-2mg Max total 10mg

Overall max 10mg 0.4mg/min
Naloxone

Pharmacokinetics
-IV, IM, SubQ
-immediate IV onset with effects lasting an hour
-IM/SubQ onset is 2-5 min with effects lasting hours
-2 hr half life
-cannot be administered orally- first pass effect