Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
63 Cards in this Set
- Front
- Back
what are some opiod analgesics that are Strong (Full) Agonists
|
Morphine (prototype)
Fentanyl Heroin Methadone Meperidine |
|
what are opioid analgesics that are weak agonists
|
Codeine
Hydrocodone Oxycodone (OxyContin, sustained release) Propoxyphene (caution) |
|
what are opioid analgesics that are mixes agonist and antagonists
|
Buprenorphine
Butorphanol Nalbuphine Pentazocine |
|
what are antitussitives
|
Codeine
Dextromethorphan |
|
what are non opioid analgesics
|
Acetaminophen, NSAIDs, & Selective COX-2 Inhibitors
|
|
what are some opioid antagonists
|
Naloxone
Naltrexone Nalmafene |
|
what are some weak agonist. reuptake inhibitors
|
Tramadol -(5-HT uptake blockade, NE uptake blockade, weak mu-receptor agonist) and Tapentadol -mu receptor agonist (?) & NE reuptake blocker
Antagonists |
|
what should you do for pain if the cause can not be identified
|
still treat agressively, but follow further pain symptoms
|
|
what drug is the first line of choice for acute severe pain and why
|
morphine bc it is as effective as other opioids with a similar adverse effect profile and comes in a large number of dosage forms.
|
|
when do you use Buprenorphine (Buprenex), Nalbuphine (Nubain), Butorphanol (Stadol)
|
when pt is allergic to merperidone and does not tolerate morphine
|
|
when is meperidine used
|
no unless pt has allergy to morphine, bc it has worse SEs than morphine and is highly ineffective orally
|
|
what is fenadyl and when is it used
|
a dermal patch may be as effective as sustained-release morphine but is difficult to titrate.
• advantage is Q72H dosing. • should likely be used only if patient has been stabilized on a regularly dosed opioid. |
|
what are Alfentanil (Alfenta), Remifentanil (Ultiva), and Sufentanil (Sufenta) used for
• |
use during general anesthesia and monitored anesthesia care
|
|
what is the top choice for post op pain
|
morphine
|
|
what do use use in post op when pt doesnt need reg dosing
|
move to acetometaphen with codeine
|
|
what is the only NSAID that is IV or IM
|
ketoralac
|
|
does clonidine supress general aches and opiod cravings
|
noooopppe
|
|
what can Administration of an opioid receptor antagonist in a subject physically dependent on opioids cause
|
an explosive abstinence syndrome, i.e., antagonist-precipitated withdrawal. Signs and symptoms of withdrawal can be seen within 3 minutes of injecting an antagonist.
|
|
when is morphine contraindicated
|
patients with hypotension,
head injury, compromised respiratory function, renal and hepatic disease use with extreme caution, can cause respiratory depression in neonate. |
|
what are the three major gastrointestinal effects of Aspirin,
|
dyspepsia, occult blood loss, and active GI hemorrhage.
|
|
____ has a much lower potential for GI irritation and bleeding complications and would be preferred agents in a patient with a history of GI bleeding.
|
Celecoxib
|
|
what does aspirin do to platlet aggregation
|
inhibits it
|
|
what are side effects of morphine that should be followed
|
Mental clouding, sedation, decreased GI motility with constipation and respiratory depression
|
|
what is oxycodon commonly used with
|
aspirin (Percodan) or acetaminophen (Percocet).
|
|
the term__ should never be used to replace dependence or tolerance
|
addiction
|
|
what is the method for treating opioid withdrawl and what is a specific drug that can be used
|
short-acting opioid such as morphine (or heroin) to a long-acting one such as methadone. The mu opioid receptor antagonist naltrexoneapproved
|
|
how is Buprenorphine taken?
|
sublingually
|
|
what is clonidine and what is it used for
|
α2-adrenergic agonist that decreases symp outflow, decreases many of the autonomic–mediated symptoms of wdrawal such as nausea, vomiting, cramps, sweating, tachycardia, and hypertension.
|
|
what is a downfall of fenydyl
|
do no provide sufficient flexibility in dosing to manage rapidly changing pain. delay of 6-12 hours in onset of analgesia after placement of the patch. On removal , the fentanyl continues to release active drug for about another 8-12 hours.
|
|
what pts is fenydyl best for
|
cancer pt with chronic pain
|
|
Intensity of pain is dramatically altered by
|
the level of anxiety and the stress response related to the original insult.
|
|
_____ is a term more legal than medical, referring to any substance producing stupor associated with analgesia (usually associated with derivatives of opium)
|
narcotic
|
|
what are three endogenous opioid peptide neurotransmitters
|
Endorphins
Enkephalins Dynorphins |
|
what do opioids do to signal transduction
|
Inhibit cyclic AMP production
Open G-protein modulated K+ channels allowing K+ efflux from the cell and hyperpolarization, slow IPSP Reduce presynaptic Ca++ influx which inhibits neurotransmitter release, glutamate, Substance P (which mediates pain perception) |
|
what are the main effects caused by opioid stim of K receptors
|
dysphoria, psychotomimetic responses (disoriented or depersonalized feelings), less miosis and respiratory depression than mu agonists, analgesia
|
|
what is the cause of death in opioid overdose
|
resp depression
|
|
what do opioids do to the pupils
|
miosis
|
|
why is miosis diagnostic of opioid development
|
bc OD of most other drugs that cause resp dep cause dilation
|
|
why are opiods contraindicated in pt with severe head injury
|
respiratory depression and carbon dioxide retention, cerebral vessels dilate and increase the cerebrospinal fluid (CSF) pressure.
|
|
what opioid has a high first pass metabolism
|
morphine- especially oral
|
|
is morphine highly addictive and abusable
|
yes
|
|
Partial agonists act as ____when given with a full agonist
|
antagonists
|
|
what is the main function of opioid agonist
|
analgesia
mu OD- resp dep K OD- hallucinations |
|
what is the main effect of opioid antagonist
|
precipitate withdrawal symptoms in physically dependent individuals
|
|
what drug is this mu effects seen starting with low doses; kappa effects at high dose
|
cocaine
|
|
what drug is thisrelatively pure mu; probably misclassified [a DEA Schedule-III agent]
|
hydrocodone
|
|
what opioid is a pure mu
|
oxycodone
|
|
what opioid antagonist is short acting and injected
|
naloxone
|
|
what opioid antagonist is long acting and oral
|
naltrexone
|
|
what drug percipitates withdrawal symptoms in opioid abusers
|
naloxone
|
|
tolerance to opioids does not occur to these symtpoms
|
Miosis
Constipation |
|
when does tolerance become clinically relevant
|
2-3 weeks
|
|
what is the primary triad of opioif overdose
|
lethargy or coma
depressed respiration pinpoint pupils (normoxic) |
|
opioid Relief from dyspnea associated with left ventricular failure may be due to:
|
reduced perception of shortness of breath, anxiolytic effects
reduction in cardiac preload and afterload |
|
what drug is the first line tx of pain assoc w acute MI
|
morphine
|
|
what two opioids can be used for cough suppression
|
Dextromethorphan (no analgesia)
Codeine (low doses) |
|
what opioids are used to treat diarrhea
|
Loperamide (Imodium)
Diphenoxylate (+ atropine) (Lomotil) Difenoxin (+ atropine) (Motofen) |
|
what opioid is 100 fold more potent than morphine,
|
fenadyl- short acting and rapid onset
|
|
what are side effects of meperidine
|
seizures and resp dep
|
|
what is meperidine used for
|
acute pain esp obstetrics
|
|
what is the major use of Buprenorphine
|
opioid detox
|
|
what drug is this: gets into brain more rapidly than morphine
More exaggerated euphoria Converted to morphine in the body but its effects last half as long |
heroin
|
|
what drug is this: it causes euphoria and has a longer duration of action than morphine,Used as an analgesic
Used for controlled withdrawal of dependent abusers of heroin and morphine |
methadone
|