|
Natural Opiates
|
Semi-Synthetic
|
Synthetic Opioids
|
|
Codeine
|
Burprenorphine
|
Fentanyl
|
|
Morphine
|
Heroin
|
Meperidine
|
|
Hydrocodone
|
Methadone
|
|
|
Hydromorphone
|
Sufentanil
|
|
|
Oxycodone
|
Sufentanil
|
|
|
Oxymorphone
|
||
|
Tramadol
|
||
|
Score
|
Severity
|
|
5 to 12
|
Mild
|
|
13 to 24
|
Moderate
|
|
25 to 36
|
Moderate to Severe
|
|
> 36
|
Severe
|
|
MOA
|
Opioid Antagonist
|
|
Warnings/ADRs
|
Cardiac or respiratory effects associated with rapid reversal of opioids
|
|
Aggression (from immediate withdrawal)
|
|
|
Administration
|
Call 911 FIRST
|
|
Administer
|
|
|
If no response after 3 minutes, administer 2nd dose
|
|
FIRST LINE
|
SECOND LINE
|
|
|
APA:
|
||
|
Buprenorphine
|
Naltrexone PO
|
|
|
Methadone
|
||
|
BAP:
|
||
|
Buprenorphine
|
Naltrexone PO
|
|
|
Methadone
|
||
|
VA/DOD:
|
||
|
Suboxone
|
Naltrexone
|
|
|
Buprenorphine
|
||
|
Methadone
|
||
|
Buprenorphine
|
Buprenorphine-Naloxone
|
|
|
Brand
|
Subutex
|
Suboxone, Zubsolv
|
|
MOA
|
Mu opiate receptor - partial agonist
|
Mu-partial agonist and opioid antagonists
|
|
Formulation
|
SL tablet
|
SL tablet, SL film; (4:1 ratio of bupren. and naloxone)
|
|
Dosing range
|
8 to 32 mg bupren./day
|
8 to 32 mg bupren/day
|
|
Warnings
|
initiation should not begin until pt is experiencing withdrawal
|
same
|
|
respiratory depression
|
same
|
|
|
risk of abuse or dependence
|
same
|
|
|
DDIs
|
CYP3A4 inhibitors/inducers
|
same
|
|
CNS depresants
|
same
|
|
|
Monitoring
|
Tolerability, resp. depression, (LFTs), urine drug screening, PMP, urine buprenorphine
|
same
|
|
Clinical Pearls
|
Preferred in pregnancy; higher abuse potential
|
naloxone added as an abuse deterrent; preferred formulation in non-pregnant patients
|
|
partial agonist activity results in ceiling effect, higher binding affinity than other opioids, newer formulation include sub-dermal implant, and subcutaneous injection
|
same
|
|
Dysphoric mood
|
Fever
|
|
Lacrimation or Rhinorrhea
|
Muscle aches
|
|
Yawning
|
Diarrhea
|
|
N/V
|
Insomnia
|
|
Pupillary Dilartion
|
Piloerection (goosebumps)
|
|
Sweating
|
|
|
Onset of withdrawal will depend upon the half-life of the opioid used (normally within 36 to 72 hours)
|
|
Completed within 7 days for short acting opioids (heroin) and 14 days for long-acting opioids (buprenorphine, methadone)
|
|
Methadone
|
buprenorphine
|
|
Chronic Pain
|
Prolonged QT interval
|
|
history or diversion or pilysubstance use
|
not able to attend daily clinic
|
|
requires closer monitoring
|
requires less monitoring and no untreated psychiatric comorbidities
|
|
pregnant women
|
dependent on lower doses of opioids (ceiling effect)
|
|
requires wide dosing range
|
|
|
Opioid Tolerance
|
Person using opioids begins to experience a reduced response to medication requiring more opioids to experience the same effect
|
|
Opioid Dependence
|
Occurs when the body adjusts its normal functioning around regular opioid use (unpleasant physical symptoms occurs when med is stopped)
|
|
Opioid Addiction
|
Occurs when attempts to cut down use are unsuccessful or when results insocial problems and a failure to fulfill obligations; often comes after person has developed opioid tolerance and dependence
|
|
A problematic pattern of substance use leading to clinically significant impairment or distress, manifested by ≥ 2 of the following over a 12-month period
|
|
⓵ Substance is taken in larger amounts or over a longer period than intended
|
|
⓶ Persistent desire or unsuccessful efforts to reduce or control use
|
|
⓷ A great deal of time is spent in activities necessary to obtain, use, or recover from effects
|
|
⓸ Cravings or a strong desire to use
|
|
⓹ Recurrent use resulting in a failure to fulfill major obligations
|
|
⓺ Continued use despite having persistent social or interpersonal problems caused by the substance
|
|
⓻ Important social, occupational, or recreational activities are given up or reduced
|
|
⓼ Recurrent use in situations that are physically hazardous
|
|
⓽ Recurrent use despite knowledge of having a persistent or recurrent physical or psychological problem due to use
|
|
⓾ Tolerance
|
|
⑪ Withdrawal
|
|
APA
|
British Association of Psychopharmacology
|
|
Buprenorphine
|
Alpha-2 agonist
|
|
Methadone
|
Buprenorphine
|
|
Methadone
|
|
Brand
|
METHADOSE
|
|
MOA
|
opioid agonist
|
|
Formulation
|
Liquid (opioid maintenance); tablets (pain only) | this is for pharmacies (methadone clinics do tabs)
|
|
Maintenance dose
|
80 to 120 mg daily
|
|
Warnings
|
QTc prolongation, respiratory depression, risk of abuse or dependence
|
|
DDI
|
QTc prolongating meds, CYP3A4 inhibitors or inducers, Medications that induce hypokalemia, hypocalcemia, or hypomagnesemia; CNS depressants
|
|
Monitoring
|
Tolerability, respiratory depression, HR/BP, EKG, electrolytes, UDS, urine methadone, PMP
|
|
Clinical Pearls
|
prolonged or delayed withdrawal due to long half-life; overdose risk is highest during initial 2 weeks of treatment
|
|
Pulillary Constriction
|
|
Slurred Speech
|
|
Drowsiness
|
|
Impaired attention or memory
|
|
Pupillary constriction
|
|
Shallow or slow respirations
|
|
Stupor
|
|
Coma
|
|
Hypothermia
|
|
Bradycardia
|
|
Naloxone
|
IM/IV/SQ
|
|
Naloxone
|
Intranasal
|
|
Evzio
|
IM auto-injector
|
|
Narcan
|
Intranasal
|
|
Medication
|
Class/MOA
|
Indication
|
|
Clonidine
|
Alpha-2 agonist reduced the noradrenergic hyperactivity associated with opioid withdrawal
|
Generalized Sx of opioid withdrawal
|
|
Loperamide
|
Anti-diarrheal
|
Diarrhea
|
|
Ondansetron
|
Antiemetic
|
N/V
|
|
Trazodone
|
Sedatine antidepressant
|
Insomnia
|
|
Hydroxyzine
|
Antihistamine/anxiolytic
|
Anxiety
|
|
Ibuprofen
|
NSAID
|
muscle pain
|
|
Cyclobenzaprine
|
skeletal muscle relaxant
|
muscle cramps
|
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