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24 Cards in this Set

  • Front
  • Back
No ceiling effect (codeine? Fx dose ceiling w/constip take ....
<400mg day
<100mg dose
Pure (Full) Agonists
Fentanyl, Hydrocodone, Morphine, Methadone, Oxycodone, Oxymorphone
Agonist-Antagonists
butorphanol,nalbuphine, pentazocine
block mu, activate kappa
Partial Agonist
Buprenorphine
celing, reverse pure ag effects
Antagonists
Reverse or block agonist effects of pure opioids
Advantage of Time-Contingent Dosing
Prevents need for routine PRN use

Minimizes centrally mediated pain processese
Long Acting Oral Opioids (3)
methadone
levorphanol
morphine
MS contin
Kadian
Morphine ER
OxyContin
Adjust opioid dose ____ (once steady state reached)
2-4 days
Adjust methadone dose no more frequently than ____ days in most patients
4–7 days
Guideline for increasing opioid dose w/uncontrolled pain....say 10mg MSContin
Increase total daily dose of opioid by 25-50%.

BTP 10% of daily dose
Dose escalation

Mild to moderate pain continues after 24 hours
increase the routine dose by ____

Severe or uncontrolled pain
Adjust more quickly for severe uncontrolled pain
6 is top of moderate pain, maybe severe
Can increase after 1 or 2 doses (eg, crescendo pain)
Increase the routine dose by ____

If using time contingent approach with PRN analgesics
Increase by an amount at least equal to the total dose of PRN medication used during the previous ____.
25% to 50%
50% to 100%
24 hrs
Opioid Hypersensitivity

Phenylpiperidines =?

Phenylheptylamines =?

Could have x-hypersensitivity with these
Mixed Agonist-Antagonist
Meperidine like: synthetic
Meperidine, Fentanyl, Sufentanil, Alfentanil

methadone-like: synthetic
methadone, propoxyphene

Pentazocine
Butorphanol
Nalbuphine
Buprenorphine*
Dezocine
Explain

Tolerance to Analgesia, Resp depression, and constipation
Tolerance to Analgesia
may occur in first DAYS to WEEKS of therapy; rare after pain relief achieved with consistent dosing without increasing or new pathology.

Tolerance to Respiratory Depression and Sedation
occurs predictably after 5-7 DAYS of consistent opioid administration

Tolerance to Constipation
does not occur; scheduled stimulating laxatives are indicated with regularly scheduled opioids
Opioid-Induced Neurotoxicity (OIN)
Neuropsychiatric syndrome characterized by:
Cognitive dysfunction
Delirium
Hallucinations
Myoclonus/seizures
Hyperalgesia/allodynia
if oliguria or anuria in morphine tx...what do you do?
STOP routine dosing of morphine
use ONLY prn
Opioid Metabolites, active and their effect

metabolites are primary cause for OIN
Morphine-6-glucuronide = analgesic
Morphine-3-glucuronide (antianalgesic – problem if renal or hep fail)
Normorphine-neurotoxic
Noroxycodone-neurotoxic
Oxymorphone-Opana
Norfentanyl

Nor = neurotoxic
OIN: Treatment

Two approaches

Primary drug changes
Opioid rotation
Change route

Primary drug changes
--Morphine / hydromorphone/oxycodone

Second line agents
Fentanyl/methadone


Reduce opioid dose
Hydration
Circadian modulation
Psychostimulants
Emerging TX’s
Tables do not account for incomplete cross-tolerance between opioids
25 - 50% dose reduction if changing drug where patient has had good analgesic response
No dose reduction may be necessary if patient with continuing pain problems or worsening in pain prior to conversion
Methadone is an exception!
Methadone
Extremely long half-life (24-36+ hours)
Use caution on days 2-5 of dosing
Generally not first line therapy
Morphine : Methadone 10+ : 1
Components to a PCA Order
Drug and Concentration
Route
Loading Dose
Demand or PCA Dose (mg)
Basal or Continuous Rate (mg/hr)
Demand Dose Lockout or Delay (min)
1 or 4 Hour Dose Limit
Lockout Interval:

Dose Limit:

Basal/Continuous Dose
Period during which the PCA will not deliver another dose despite demands by patient.

Amount of drug a patient can receive over typically 4 hours.

Acute Pain: Use 1/3 average hourly usage (>12hours)
Chronic Pain: Use up to 2/3 average hourly usage

Attempt to keep an average of 2-3 successful demand doses per hour
Spinal Opioid Administration

Epidural

Intrathecal
outside of the dura
epidural space is a vascular potential space
drug must crosses dura to reach CNS

subdural, subarachnoid
drug delivered directly into the cerebrospinal fluid
drug delivered very near to opioid receptors
Spinal Analgesic Duration & Spread
Determined by physicochemical characteristics of the drug

low lipophilicity

more lipophilic

high lipophilicity
prolonged and widespread activity drug, morphine

intermediate duration and spread, methadone

short duration and limited spread, fentanyl
Epidural approximately 1/10th IV dosing
Intrathecal (IT) approximately 1/10th Epidural dosing
10 mg IV = 1 mg Epidural = 0.1 mg IT
reminder only