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;
44 Cards in this Set
- Front
- Back
Antidote used for opioid toxicity
|
Naloxone (IV), naltrexone (PO)
|
|
Opioid associated with respiratory depression, but is used in high risk patients who may not survive full general anesthesia
|
Fentanyl
|
|
Inhibit synaptic activity of primary afferents and spinal cord pain transmission neurons
|
Ascending pathways
|
|
Activation of these receptors close calcium ion channels to inhibit neurotransmitter release
|
Presynaptic mu, delta, and kappa receptors
|
|
Activation of these receptors open potassium channels to cause membrane hyperpolarization
|
Postsynaptic mu receptors
|
|
Tolerance to all effects of opioid agonists can develop except to:
|
Miosis and constipation
|
|
All opioids except this agent(which has a muscarinic blocking action) cause pupillary constriction
|
Meperidine
|
|
SE of opioid analgesics
|
Dependence, withdrawal syndrome, sedation, euphoria, respiratory depression, nausea and vomiting, constipation, biliary spasm, increased urethral and bladder tone, and reduction in uterine tone
|
|
Morphine, methadone, meperidine, and fentanyl
|
Strong opioid agonists
|
|
Opioids used in anesthesia
|
Morphine and fentanyl
|
|
Opioid used in the management of withdrawal states
|
Methadone
|
|
Opioid available trans-dermally
|
Fentanyl
|
|
Opioid that can be given PO, by epidural and IV; helps to relieve the dyspnea of pulmonary edema
|
Morphine
|
|
Use of this opioid with a MAOI can lead to hyperpyrexic coma; use with SSRIs can lead to serotonin syndrome
|
Meperidine
|
|
Codeine, hydrocodone, and oxycodone
|
Moderate opioid agonists
|
|
Weak opioid agonist that is a poor analgesic; its overdose can cause severe toxicity, including respiratory depression, circulatory collapse, pulmonary edema and seizures
|
Propoxyphene
|
|
Partial opioid agonist, considered a strong analgesic, has a long DOA and is resistant to naloxone reversal
|
Buprenorphine
|
|
Opioid antagonist that is given IV and has a short DOA
|
Naloxone
|
|
Opioid antagonist that is given orally in alcohol dependency programs
|
Naltrexone
|
|
Opioids that are used as antitussives
|
Dextromethorphan, Codeine
|
|
Opioids used as antidiarrheals
|
Diphenoxylate, loperamide
|
|
Opioids that undergo extensive first pass metabolism
|
Morphine, hydromorphone, and oxymorphone
|
|
Toxic effect on fetus due to opioids' ability to cross the placental barrier
|
Respiratory depression and with continuous exposure physical dependence in neonates
|
|
Primary metabolite of opioids that is neuroexcitatory
|
morphine-3-glucuronide
|
|
Opioids that have a major increase in peak serum levels after ingestion of alcohol
|
Hydromorphone and oxymorphone
|
|
Metabolite of meperidine that may cause seizures at high plasma levels
|
Normeperidine
|
|
Opioid receptors located on neurons in the midbrain and medulla that function in pain modulation
|
Descending pathways
|
|
Opioid receptor whose activation plays a major role in the respiratory depressant actions of opioids
|
mu-receptor
|
|
Opioid receptor whose activation appears to be involved in sedative actions
|
kappa receptor
|
|
Opioid receptor whose activation may play a role in the development of tolerance
|
delta receptor
|
|
How opioid analgesics inhibit synaptic activity
|
Partly through direct activation of opioid receptors and partly through release of the endogenous opioid peptides, which are themselves inhibitory
|
|
Opioid actions in this part of the brain lead to inhibition of the respiratory center, with decrease in response to CO2 challenge
|
Medulla
|
|
Reason opioid analgesics are contraindicated in head injuries
|
Increase in PCO2 may cause cerebrovascular dilation resulting in increased blood flow and increased intracranial pressure
|
|
Causes the nausea associated with opioids
|
Activation of the chemoreceptor trigger zone
|
|
Basis for clinical use of opioids as antidiarrheal agent and adverse effects of constipation
|
Decreased intestinal peristalsis mediated by effects on opioid receptors in the enteric nervous system
|
|
Opioids (with the exception of meperidine) effects on smooth muscle
|
Contraction
|
|
Opioid antagonist that blocks miosis
|
naloxone (AKA atropine)
|
|
Block opioid tolerance
|
Antagonist of glutamate NMDA receptors and delta receptor antagonist
|
|
Intense form of withdrawal that results from admin of opioid antagonist to a physically dependent patient
|
Precipitated withdrawal
|
|
Large doses of this opioid used as an antitussive may cause hallucinations, confusion, excitation, changes in pupil size, nystagmus, seizures, coma and respiratory depression
|
Dextromethorphan
|
|
A triad of pupillary constriction, comatose state, and respiratory depression
|
Opioid overdose
|
|
Mixed action of buprenorphine
|
mu receptor agonist; kappa and delta antagonist
|
|
Adverse Effects of mixed agonist-antagonists
|
Dizziness, sweating, nausea, anxiety, hallucinations and nightmares
|
|
Opioid antagonists have the greatest affinity for this receptor
|
mu
|