Week 4 - READINGS Flashcards
Acute Pain
recent onset of pain that abates as healing occurs; serves as a warning signal that something is wrong or needs attention
Addiction
a chronic neurologic and biologic disease characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving to use the opioid for effects other than pain relief
Adjuvant Analgesic Agent
a drug that has a primary indication other than pain (e.g., anticonvulsant, antidepressant, sodium channel blocker, or muscle relaxant) but is an analgesic agent for some painful conditions; sometimes referred to as coanalgesic
Agonist Antagonist
a type of opioid (e.g., nalbuphine [Nubain] and butorphanol [Stadol]) that binds to the kappa opioid receptor site acting as an agonist (capable of producing analgesia) and simultaneously to the mu opioid receptor site acting as an antagonist (reversing mu agonist effects)
Allodynia
pain due to a stimulus that does not normally provoke pain, such as touch; typically experienced in the skin around areas affected by nerve injury and commonly seen with many neuropathic pain syndromes
Antagonist
drug that competes with agonists for opioid receptor binding sites; can displace agonists, thereby inhibiting their action
Breakthrough Pain
a transitory increase in pain that occurs on a background of otherwise controlled persistent pain
Ceiling EWffect
an analgesic dose above which further dose increments produce no change in effect
Central Sensitization
a key central mechanism of neuropathic pain; the abnormal hyperexcitability of central neurons in the spinal cord, which results from complex changes induced by the incoming afferent barrages of nociceptors
Chronic or Persistent Pain
pain that may or may not be time limited but that persists beyond the usual course/time of tissue healing
Comfort Function Goal
the pain rating identified by the individual patient above which the patient experiences interference with function and quality of life (e.g., activities the patient needs or wishes to perform)
Efficacy
the extent to which a drug or another treatment “works” and can produce the effect in question—analgesia in this context
Half Life
the time it takes for the plasma concentration (amount of drug in the body) to be reduced by 50% (after starting a drug, or increasing its dose, four to five half-lives are required to approach a steady-state level in the blood, irrespective of the dose, dosing interval, or route of administration; after four to five half-lives, a drug that has been discontinued generally is considered to be mostly eliminated from the body)
Hydrophilic
readily absorbed in aqueous solution
Intraspinal
“within the spine”; refers to the spaces or potential spaces surrounding the spinal cord into which medications can be given; synonymous with neuraxial
Lipophilic
readily absorbed in fatty tissues
Metabolite
the product of biochemical reactions during drug metabolism
Mu Agonist
ny opioid that binds to the mu opioid receptor subtype and produces analgesic effects (e.g., morphine); used interchangeably with the terms full agonist, pure agonist, and morphinelike drug
Neuraxial
of the central nervous system; synonymous with intraspinal