Analgesics Flashcards
Define analgesia.
insensibility to pain without loss of consciousness.
Describe the MOA, therapeutic and adverse actions of opioid agonist analgesics, and opioid antagonists.
Agonist - full activation of receptor, dose increases and so does resp depression threshold inccreases.
Antagonist - binds to opiate receptor and blocks it. does not cause respiratory depression - reversal of overdose and allows breathing
Describe the MOA, therapeutic and adverse actions and nursing considerations of opioids
Opioids / mOrphine, cOdeine / Analgesic action of opioids include inhibition of substance P, closing the gate in the dorsal horn, thus inhibiting afferent transmission and altering perception and emotional responses to pain.
AR - vitals low [HR, RR, BP], sedating, high abuse potential, physical and mental dependence, CNS depressent
Nursing indic
WH for RR below 12
Vitals monitor incl sedation score
Constipation - laxatives, high fibre diet
Describe the MOA, therapeutic and adverse actions and nursing considerations, contra and pt education of NSAIDS
NSAIDS(ibuprofen, celecoxib) NON opioid analgesic
Antipyretic(for fever) and anti flammatory. MOA the inhibition of the enzyme COX which inhibits prostaglandins decreasing inflammation, pain and fever [prostaglandin functions]
Dec pain, inflammation and fever
Contra
Dec renal/liver function
Inc bleeding risk
AR GI bleeding HTN Causing bronchospasm Blood clots Inc bleeding risk Dec kidney function
Pt education
Take w food never on empty stomach
If pt has tinnitus then sign of toxicity on NSAIDS.
Hydration to assist kidneys
Nursing cons
Monitor kidney function and platelets
Encourage adequate hydration
Discuss lifespan considerations for pain management
Opioids - sedating, check for elferly, constipation
Discuss the WHO analgesic ladder and side effects to step 2 and 3 and its purpose
Purpose: framework used to guide the pharmacological treatment of pain in chronic pain and palliative care patients.
Step 1 [mild 1-3] non opiod (NSAID or paracetamol) + non pharm adjuvents Step 2 [moderate 4-6] non opioids (paracetamol + NSAID + weak opioid like codeine or tramadol) + non pharm adju Step 3 (severe 7-10) Strong opioids (morphine, fentanyl, oxy) non pharm adju.
Side effects to 2 and 3 - constipation, nausea and vomiting, sedation, resp depression.
Three primary types of opioid receptors and the main one
Mu*
Kappa*
Delta*
Main one is MU
What is responsible for this mechanism
stimulation of opioid receptors in the dorsal horn in the spinal cord inhibits the release of substance P
Decreased substance P inhibits the afferent transmission of pain signals to the cortex
“closes the gate”
Alters the perception of pain
Opioid agonists
function of prostaglandin
- prosta are a group of lipids made up @ site of tissue damage. metabolised by cox enzyme and action in pain is to dec threshold of nociceptors. physiological function - inflammation through vasodilation, platelet aggregation, maintain renal blood flow.
NSAIDs should be avoided in late pregnancy due to:
the prolongation of gestation and labour
Opioid analgesics are best used in which type of pain?
Opioid analgesics are effective and commonly used for the management of severe acute pain.
Opioids can induce the following adverse effects
biliary colic, constipation, pruritus (itching)
Stimulation of the following opioid receptors is associated with analgesia
Mu, Kappa (K) and Delta (D)
The synthetic analgesic tramadol acts by
binding to the mu opioid receptors
inhibiting the reuptake of noradrenaline
inhibiting the reuptake of 5-HT (serotonin)
Tissue injury or tissue inflammation is most likely to cause which type of pain
nociceptive