Chapter 10 pharm 343 Flashcards
*Acetaminophen (tylenol)
nonopioid analgesic. (APAP) management of pai especially pain with inflammation. avoid from alcoholics or who have hepatic disease. oral, rectal,and IV form. hydrocodone (vicodin) and oxycodone (percocet)
*Morphine Sulfate
naturally occuring alkaloid from opium poppy. schedule 11 drug. indicated for severe pain and has a high abuse potential. oral, injectable, and rectal forms. hydromorphone is 8 times more potent than morphine.
*Naloxone hydrochloride (narcan)
pure opioid antagonist. no agonist morphine-like properties and works as a blocking drug for opioids. does not cause anasthesia and resp depression. only injectable forms.
Agonist
a substance that bind to a receptor and causes a response.
mild- codeine, hydrocodone.
Severe- morphine, hydromorphine, levorphanol, oxycodone, oxymorphone, meperidine, fentanyl, and methadone.
Acute pain
pain that is sudden in onset, usually subsides when treated, and typically occurs over less than a 6-week period.
It is determined by its onset and duration, associated with disease or conditions and the way they treat.
Agonists-antagonists
substances that bind to a receptor and cause a partial response that is not as strong as that caused by an agonist.
(pentazocine and nalbuphine)
Addiction
A chronic, neurobiologic disease whose development is influenced by genetic,psycosocial, and environmental factors.
analgesic ceiling effect
what occurs when a given pain drug no longer effectively controls a patient’s pain despite the administration of the highest safety dose.
Adjuvant analgesics drugs
drugs that are added for combined therapy with a primary drug and may have additive or independent analgesic properties, or both.
drugs from other chemical categories are added to opioid regimen.
NSAIDS, antidepressants, antiepileptic drugs, and corticosteroids.
reduces some of the adverse effects that are seen with higher dosages of opioids, such as respiratory depression, constipation, and urinary retention.
analgesics
medications that relieve pain without causing loss of consciousness. (painkillers)
antagonist
a drug that binds to receptor and prevents a response.
it functions as a competitive antagonists bcuz it competes with and reverse the effects of agonist and agonist-antagonist drugs at the receptor sites.
Opioid antagonists-naloxone and naltrexone and bind to receptor sites. when treating overdose or toxicity, withdrawal may occur. severe resp depression, naloxone is given (shortlived and lasts abt 1hr.).
breakthrough pain
pain that occurs between between doses of pain meds.
it is becuz the analgesic effects wear off as the drug is metabolized and eliminated from body.
central pain
pain resulting from any disorder that causes central nervous system damage.
.
chronic pain
persistant or recurring pain that is often difficult to treat. pain lasting longer than 3-6months, longer than 1month after healing of an acute injury, or pain that accompanies a nonhealing tissue injury.
deep pain
pain that occurs in tissue below skin level.
gate theory
the most well-described theory of pain transmission and pain relief. it uses a gate model to explain how impulses from damaged tissues are sensed in the brain.
the tissue injury causes the release of several substances from injured cells, such as bradykinin, histamine, potassium, prostaglandins, and serotonin.
some pain meds work by altering the actions and levels of these substances.
the release if these initiates action potentials.
cancer pain
pain resulting from any of a variety of causes related to cancer and/or metastasis of cancer.
tumor mass against nerves, organs, or tissues.
include hypoxia from blockage of blood supply, metastasis, pathologic fractures, muscle spasms, and adverse effects of radiation and surgery and chemo.
narcotics
originally applied to drugs that produce insensibility or stupor, especially the opioids. currently used to refer to any medically used controlled substances and in legal setting to refer to any illicit or “street” drug.
neuropathic pain
pain that results from a disturbance of function or pathologic change in a nerve. could also be idiopathic (unexplained).
nociception
processing of pain signals in the brain that gives rise of the feeling of pain.
norciceptors
a subclass of sensory nerves that transmit pain signals to the central nervous system from other body parts. A&C fibers.
the nerve impulses are conducted along sensory nerve fibers and activate pain receptors in the dorsal horn of the spinal cord. the so-called gates are located.
the gates regulate the flow of sensory nerve impulses.
if impulses are stopped by gate, no impulses are transmitted to the higher centers of the brain.
if the gates permit sufficient number of action potentials to be conducted from the spine to the cerebral cortex, the pain is felt.
A fiber close gates. C fiber opens gates.
nonopioid analgesics
analgesics that are not classified as opioids.