Pharm pain

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kellyw2417  on July 23, 2011

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Pharm pain

A pain fibers
-contain a myelin sheath, have a fast conduction speed
-large
1/33
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A pain fibers -contain a myelin sheath, have a fast conduction speed
-large
C pain fibers -contain no myelin sheath
-small
-pain travels here mostly
Endogenous neurotransmitters**enkephalins
-found in thalamus in brain
-bind to opioid receptors
-inhibit transmission of pain by closing gate
**endorphins
-produced in cells of nervous system
-binds with phetitive receptors, relieves common pain
-very powerful, not addictive
-control stress/frustration/addictions/eating disorders
-inhibit transmission of pain by closing gate
Acute pain -sudden in onset
-sharp and localized
-usually subsides once treated
Chronic pain -slow onset
-long duration (more than 6 weeks)
-dull persistent aching (recurring)
-often difficult to treat
Pain: somatic -from skeletal muscles, ligaments, joints
Pain: visceral -from organs, smooth muscles in abdomen
Pain: superficial -from skin
Pain: vascular -from inflammation of vasculature
Pain: referred -from somewhere pain is not originating from
-example is left arm pain during an MI and appendicitis
Pain: neuropathic -from fingers/feet from decreased sensation of nerves
Pain: phantom -from lost limbs
Pain: cancer -from wherever the cancer is
-bone cancer is most painful of all cancers
Pain: psychogenic -from procedures or other traumas
Pain: central -from CNS
Opioid receptors 1. Mu1, Mu2, Kappa
Mu1 binding -analgesia
-causes greatest improvement and less consequences
Mu2 binding -analgesia, respiratory depression, constipation, addiction
Kappa binding -analgesia, dysphoria (depression)
Opioids (enhances receptors ability to produce natural response)
1. prototypes
2. route/duration
3. indications
4. MOA
1. codeine sulfate, fentanyl citrate, morphine sulfate (and CR), oxycodone CR, meperidine HCL, methadone HCL
2. -morphine: IV and PO, lasts 5hr
-codeine: PO, lasts 4-6hr
-fentanyl: IV, transdermal, lasts 1 hr with IV,
13-40 with transdermal
**transdermal fentanyl works well with bone
cancer pain
3. to alleviate moderate-severe pain, cough center suppression, diarrhea
4. mimics actions of endogenous opioid peptides, primarily at Mu1 and Mu2 sites
Opioids
1. contraindications
2. ADR
1. allergy, severe asthma/respiratory insufficiency, increased intracranial pressure, pregnancy
2. CNS depression, euphoria, pupil constriction, diaphoresis, flushing, hypotension, bradycardia, RESPIRATORY DEPRESSION, N/V, constipation, urinary retention, itching, wheal formation
Opiate Antagonists
1. prototypes/ route/duration
2. indications
3. MOA
1.- naloxone (drug of choice). IV only. lasts 2hr
-Good for reversing respiratory depression
-naltrexone. PO only. Lasts 1-3 days
2. used for complete or partial reversal of opioid-induced respiratory depression
3. they bind to opiate receptors and prevent a response
Opioid tolerance -result of chronic opioid treatment
-larger and larger doses are needed to produce therapeutic response
-receptors are down-regulated
Opioid physical dependence -body's adaptation to opioid
-once drug is withdrawn, body craves the drug and withdrawal symptoms present
-most dangerous for patient
Opioid psychological dependence -pattern of compulsive drug use
-craving for drug for uses other than pain relief: euphoria
-ADDICTION
Narcotic withdrawal opioid abstinence syndrome characteristics -anxiety, irritability, chills/hot flashes, joint pain, excessive lacrimation, rhinorrhea, diaphoresis, N/V, abdominal cramps/pain, diarrhea
-In infants whose mothers were dependent: don't eat, cry, rub limbs until raw.
Non-opioids/NSAID
1. prototypes
2. route/duration
3. indications
4. MOA
5. toxicity
6. antidote
7. interactions
8. contraindications
1. acetominophen (tylenol)
2. PO. Lasts 3-4hr. Rectal suppositories for infants/elderly
3. mild-moderate pain, fever, alternative for those who can't take aspirin (people on anticoagulants)
4. blocks pain impulses peripherally by inhibiting prostaglandin synthesis
5. -lethal when overdosed: causes hepatic necrosis.
-Long-term ingestion of large doses causes
nephropathy, oxidative damage, inflammation
-4,000mg/day=max dosage
6. acetylcysteine
7. -alcohol
-other hepatotoxic drugs
8. liver dysfunction, and possible liver failure
Analgesics: Nursing Implications 1. pain assessment: LOCSTAAM
2. medicate patient before pain is severe
3. pain management includes drug and non-drug measures (massage, distractions, music...)
4. instruct patient to tell doctor if signs of allergic reaction or ADR present
5. take vitals and I&O
Opioid Analgesics: Nursing Implications1. withhold dose and call doctor if there's a decline in condition/VS, especially if respiratory rate is less than 12 breaths/minute
2. check dosages carefully
3. fentanyl given IV quickly=chest wall rigidity.
4. can be taken with food
5. patients should re-position themselves slowly b/c of hypotension
6. Monitor for VS change, continuance of pain: call doctor
7. monitor for therapeutic effects: decreased severity and complaints of pain, decreased fever (acetaminophen)
Signs of respiratory depression 1. respiratory rate of less than 12 per minute, dyspnea, diminished breath sounds, or shallow breathing
NSAIDS 1. inhibit cyclooxygenase 1 and 2
2. treat inflammatory disorders: rheumatoid arthritis, osteoarthritis, bursitis
3. alleviate mild-moderate pain, and menstrual pain
4. suppress fever
5. suppress inflammation
NSAIDS: 1st generation
1. prototypes/indications
2. route/duration
4. MOA
5. toxicity
6. antidote
7. interactions
8. contraindications
1. Propionic acid derivatives: ibuprofen (pain/fever), naproxen (inflammation of joints), indomethacin (arthritis), ketorolac (severe pain)
2. PO, lasts 4-6hr
3.
NSAIDS: 2nd generation
1. prototypes
2. route/duration
3. indications
4. MOA
5. ADR
6. contraindications
7. interactions
1. cyclooxygenase inhibitors: celecoxib (Celebrex)
2. PO, lasts 4-8hr
3. -suppresses inflammation/pain
-osteoarthritis/ rheumatoid arthritis
-dysmenorrhea
-familial adenomatous polyposis
4. -reversible inhibition of leukotriene and/or
-prostaglandin pathway
-blocks the action of cyclooxygenase2
5. -lower risk for GI side effects than other NSAIDS
-impairs renal function, hypertension, edema
-increases the risk for MI/stroke
6. sulfa allergy, pregnancy (NSAIDS close ductus arteriosis)
7. increase effects of warfarin, decreases diuretic effect of furosemide, decrease antihypertensive agents, may increase levels of lithium

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