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39 Cards in this Set

  • Front
  • Back

Acute pain


Usually predictable


common after surgery, trauma and medical problems


typically resolves as it heals


lasts less than 30 days


Chronic malignant pain

associated with progressive disease that is potentially life limiting


can have elements of acute pain when tissue damage continues from tumor infiltration

Chronic non-malignant pain

pain not associated with malignant disease


lasting greater than 6 months or beyond the healing period


associated with depression, insomnia, weight loss, etc.

tolerance

a state in which a larger dose is required to produce the same response that could formerly by elicited by a smaller dose

physical dependence

a state in which a withdrawal syndrome will occur if the drug is stopped abruptly or if dose is rapidly reproduced

addiction

compulsive need for and use of a habit forming substance characterized by tolerance and well-defined and physiological symptoms upon withdrawal

clinical presentation of somatic nociceptive pain

arising from skin, bone, joint, muscle or connective tissue


well-localized pain


dull, aching, throbbing pain

clinical presentation of visceral nociceptive pain

arising from internal organs (large intestine or pancreas)


referred or well-localized pain


deep, aching, squeezing pain

physical signs associated with acute pain

excessive cardiac activity (increased heart rate)


increased respiratory rate


hypertension


facial expression


diaphoresis (increased sweating)

5 pain assessment questions

palliative factors/ provocative factors (what makes the pain better/worse?)


quality


radiation


severity


temporal factors

somatic therapies for pain

heat/cold, exercise, massage/relaxation


TENS, acupuncture, ultrasound


surgery, radiation, nerve block

aspirin MOA

inhibits prostaglandin synthesis


inhibit platelet cyclooxygenase

aspirin adverse effects

GI upset, GI ulcers, GI bleeding

aspirin therapeutic effects

antipyretic


anti-inflammatory


analgesic


anti-platelet

acetaminophin MOA

inhibits COX in the brain but not at the peripheral sites

acetaminophen adverse effects

liver damage

acetaminophen therapeutic effects

analgesic, antipyritic

non-steroidal anti-inflammatory drugs (NSAIDS) MOA

inhibits prostaglandin synthesis via the inhibition of both COX 1 and COX 2

NSAIDS adverse effects

renal dysfunction, GI upset

NSAIDS therapeutic effects

analgesic, antipyretic, anti-inflammatory

ceiling effect

partial opioid agonists, NSAIDS



at a certain level of drug administered, the effects don't get stronger

cautions of aspirin

allergy, bleeding disorders or in combination with other anti platelets or anticoagulants, children under 16 for viral infection, pregnancy, history of GI disease, renal dysfunction

cautions of acetaminophin

hepatic impairment, heavy alcohol users

cautions of NSAIDS

allergy, combination with anticoagulants, decreased hepatic function, pregnancy

maximum dose of acetaminophen

acute- 4 grams


chronic- 2 grams


hepatic impairment or heavy alcohol users ≤ 2 grams/day


advantages of COX2 inhibitors

selectively inhibit COX 2, preserves protective effects of prostaglandins on GI mucosa

disadvantages of COX2 inhibitors

increased risk of adverse cardiac events

opioid analgesics MOA

binds to opiate receptors in the CNS altering the perception and response to pain

full agonist

sits on receptor and elicits a response

partial agonist

sits on receptor and results in activity that is less than full agonist



can act as antagonists in the presence of full agonists

antagonist

sit on receptor and blocks a response

morphine like analgesics

morphine, hydromorphone, oxycodone, codein, hydrocodone

toxicity associated with meperidine

active metabolite can cause tremor, muscle twitching and seizures

toxicity associated with the use of meperidine

active metabolite of meperidine can cause fatal seizures when converted by the liver

rationale for the use of methadone in narcotic treatment programs

it has a delayed onset and long duration of action


no highs or lows

advantages of partial opioid agonists

less additive and less respiratory depression

disadvantages of partial opioid agonists

ceiling effect


may precipitate withdrawal in opioid tolerant patients

utility of opioid antagonists

used for severe withdrawal reactions


rapidly reverses opioid induced respiratory depression

side effects associated with opioid use

respiratory depression, constipation, itching, nausea/vomiting, drowsiness/sedation