| Term 
 
        | What is the difference between acute and chronic pain? |  | Definition 
 
        | Acute - identified event, resolves in days/weeks Chronic - Cause often not easily identified, multifactorial; indeterminate duration; nociceptive and/or neuropathic  |  | 
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        | Term 
 
        | What is nociceptive pain? |  | Definition 
 
        | - Direct stimulation of intact nociceptors, transmits along normal nerves - Described as sharpe, aching, throbbin, somatic is easy to localize while visceral isn't - In this, tissue injury is apparent, and we will manage it with opiods and adjuvant/coanalgesics |  | 
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        | Term 
 
        | What is neuropathic pain? |  | Definition 
 
        | - From disordered peripheral or central nerves - Comes from compression, transection, infiltration, ischemia, or metabolic injury - Varied Types:  Peripheral, deafferentation, complex regional syndromes - Pain may exceed observable injury - Burning, tingling, shooting, stabbing, or electrical like pain - Management with opiods and/or adjuvant/coanalgesics |  | 
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        | Term 
 
        | What are some interventional means of neuropathic pain management? |  | Definition 
 
        | - Neuronal blockade (sympathetic nerve blocks) - Neurostimulatory techniques (spinal cord stimulation) - Intraspinal infusion |  | 
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        | Term 
 
        | What aer some pharmacologic therapies for neuropathic pain? |  | Definition 
 
        | - Gabapentin, Carbamazepine, lamotrigine, and new AED's - Antidepressants - Opioid analgesics - Lidocaine (Transdermal, IV, mexiletine) - Alpha-2 adrenergic agonists |  | 
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        | Term 
 
        | What are examples of different pain rating scales? |  | Definition 
 
        | - Visual Analog Scale - Graphic rating scale (verbal,numerical) - Numerical Rating Scale (initiate therapy at 3/4) - Wong-Baker (literally cartoon faces) - Color (blue is no pain, red is extreme pain) - Simple Descriptive pain intensity scale (No pain, mild, discomfort, distresssing, horrible, excruciating) - FLACC (Face, legs, activity, cry, consolability, useful in non-verbal patients, describes behavior in response to pain) |  | 
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        | Term 
 
        | What are some nonverbal signs of acute pain? |  | Definition 
 
        |   •Diaphoresis •Decreased food digestion •Tachycardia •Hypertension •Mydriasis  •Hormone release  |  | 
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        | Term 
 
        | What are some nonverbal signs of chronic pain? |  | Definition 
 
        |   •Aggressive behavior •Changes in daily activities •Facial expression •Bodily movements •Vocal •Mood •Change in vital signs |  | 
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        | Term 
 
        | What are the general guidelines for treating chronic pain? |  | Definition 
 
        | - Easier to prevent than relieve - Keep pain diary - Dose meds around the clock - Long acting for continuous pain, intermediate for breakthrough pain (look for end of dose failure, incident prophylaxis) - Dose sliding scales and freq. ranges |  | 
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        | Term 
 
        | What are medications for mild pain? |  | Definition 
 
        | - APAP - NSAIDS - ASA - Adjuvants |  | 
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        | Term 
 
        | What are medications for moderate pain? |  | Definition 
 
        | APAP with...... - Codeine - Hydrocodone - Oxycodone - Dihydrocodeine     - Tramadol - +/- adjuvants |  | 
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        | Term 
 
        | What are medications for severe pain? |  | Definition 
 
        | - Morphine - Hydromorphone - Methadone - Levorphanol - Fentanyl - Oxycodone - +/- adjuvants |  | 
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        | Term 
 
        | What two drugs are best for muscoskeletal pain? |  | Definition 
 
        | - APAP and ASA - Both 325-650 q4-6h or 1000mg tid or qid - Max dose of 4000mg - Apap drug of choice, potential liver toxicity - ASA ADR's could be bleeding, ulcers, stomach upset, tinnitus, intx |  | 
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        | Term 
 
        | What is significant regarding NSAIDS? |  | Definition 
 
        | - inflammatory disease use or unresponsive APAP therapy - OTC - Ceiling effect (wtf is this?) - Avoid in high risk patients such as elderly and those with heart/renal problems - Cox 1 inhibition: bleeding, GI, kidney, liver problems - Cox 2 inhibition:  Decreases inflammation, pain, fever - Celexicob has same efficacy but less bleeding, ulcers,similar renal effects |  | 
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        | Term 
 
        | What is significant regarding Ultram? |  | Definition 
 
        | - Moderate-severe pain - Duel mechanism with mu-opioid receptor and then NE and 5-HT reuptake - Usual dose = 50-100 q4-6h - Onset is 60 minutes - Also available with APAP - ADR's include n/v, dizziness, CNS stimulation, constipation, potential for seizures |  | 
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        | Term 
 
        | Classify the opiod analgesics by their chemical class |  | Definition 
 
        | 
•Phenanthrenes 
–Morphine
–Codeine
–Hydromorphone *
–Levorphanol *
–Oxycodone *
–Oxymorphone *
–Buprenorphine *
–Nalbuphine 
–Butrorphanol *
 
•Benzomorphans 
–Pentazocine 
•Phenylpiperidines 
–Meperidine 
–Fentanyl 
–Alfentanyl 
–Sufentanyl 
•Diphenylheptanes 
–Methadone
–Propoxyphene 
 |  | 
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        | Term 
 
        | What are the benefits of opiods? |  | Definition 
 
        | - No ceiling effect - Titratable - No irreversible or life-threatening end-organ problems - Wide variety of formulations,strengths, dosage forms - Titrate q1-2 days, either by 25%, 25-50%, or 50-100% depending on mild, moderate, or unrelieved severe pain, respectively - Increase dose when B/T medication used > 3 times/24 hours for 2-3 days   |  | 
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        | Term 
 
        | What are the Pharmakokinetics of opioids? |  | Definition 
 
        | - Conjugated in liver - Excreted via kidney (90-95%) - First-order kinetics - Cmax after 1 hours, 30 minutes, or 6 minutes depending on dosage form - Half-life at steady state is 3-4 hours - steady state after 4-5 half-lives or 24 hours - Duration of effect 3-5 hours with immediate release formulas - If renal problems decreasing dose or interval (urine problems indicative of this) Bolus effect: drowsiness 30-60 min. after admin., pain before next dose due, must change up release formula. - When changing from oral to invasive form, use roughly 1/3 of dose (sig. first pass effect)   |  | 
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        | Term 
 
        | What are the general rules for figuring out doses when switching up opioids and dosage forms? |  | Definition 
 
        | - If going from Morphine to Dilaudid divide dose by 4 - If Morphine PO to more invasive form divide by 3 - If Dilaudid PO to more invasive divide by 5   - Could be cross tolerance, so start with 50-75% of equianalgesic dose - For methadone, start with 10-25% of published equianalgesic dose - For immediate/intermediate release, tapering is the same as stated before - For extended release, never chew, may put down feeding tubes, dose q8, 12, or 24h and reassess every 2-4 days when SS is reached - Methadone adjustment is variable, could be q6-8h, adjust every 4-7 days |  | 
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        | Term 
 
        | What should you use for opioid breakthrough pain doses? |  | Definition 
 
        | - Increase breakthrough dose as ATC dose is increased  - For PO it is 10-20% of total daily dose q1h - Parenteral = 50-100% of hourly rate q15 (minutes or hours?) |  | 
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        | Term 
 
        | What are  the cross-sensitivity likelihoods for the different opioid classes, and what KIND of opioid are they? |  | Definition 
 
        |   •Phenanthrenes  –Morphine – N M –Codeine – N M –Hydromorphone – SS * M –Levorphanol - SS * M –Oxycodone - SS * M –Oxymorphone – SS * M –Buprenorphine - SS * M –Nalbuphine – SS M –Butorphanol – S * M  
•Benzomorphans  –Pentazocine – S M •Phenylpiperidines  –Meperidine – S D –Fentanyl – S M –Alfentanyl – S M –Sufentanyl – S D •Diphenylheptanes  –Methadone – S U –Propoxyphene – S M   Likelihood of X-sensitivity 
•Phenanthrenes – probable •Benzomorphans – possible •Phenylpiperidines – low risk •Diphenylheptanes – low risk |  | 
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        | Term 
 
        | What are the starting doses for PO Morphine, Oxycodone, and Hydromorphone in a patient with severe pain?  How would you titrate this therapy? |  | Definition 
 
        | Morphine - 10-15mg   Oxycodone - 5-10mg   Hydromorphone (Dilaudid) - 2-4mg   *If titrated properly, there is no ceiling dose for these opioids   Repeat dose or titrate upwards by 50-100% q1-2 hours until adequate analgesia is met ( >50% reduction in pain) or side effects are encountered |  | 
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        | Term 
 
        | What are the sustained release oral opioids available, their starting doses, and how would we titrate using these therapies? |  | Definition 
 
        | Available:  Morphine in the form of MS Contin, Oramorph SR, Kadian - starting dose 20-30mg po q12h   Oxycodone in the form of Oxycontin - starting dose 20mg q12h   Steady state reached by 24 hours   Can be titrated every 24 hours for unrelieved pain.  For moderate increase by 25-50% q24h, for severe do 50-100% q24h |  | 
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        | Term 
 
        | What is significant regarding the Fentanyl patch? |  | Definition 
 
        | - No analgesic effect for 12-24h - Steady state only after 72 hours - therefore replace or increment q72 hours - Do NOT use for initial dose titration - Fentanyl levels decay w/ half-life of 17 hours after removal of patch - Need "breakthrough" medication - One 25 microgram/hr patch = 60mg of morphine a day |  | 
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        | Term 
 
        | What exactly is "breakthrough" pain? |  | Definition 
 
        | - Idiopathic/Spontaneous - Disease progression - Incident - End-of-dose failure |  | 
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        | Term 
 
        | Drug Profile:  Hydrocodone |  | Definition 
 
        | - Mild to moderate pain - Only available in combo - Onset of actoin 10-20 minutes - Duration = 3-6 hours - Dose is 1-2 q4-6h - Dose is limited by APAP - Better accepted than codeine |  | 
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        | Term 
 | Definition 
 
        | - Mild to moderate pain - Metabolized into morphine by the body - Often combined with APAP - 60 mg of Codeine = 600mg of aspirin - Usualy dose = 15-60mg q4-6h - APAP limits overall dose - ADR's include drowsiness and constipation - Smoking DECREASES effectiveness |  | 
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        | Term 
 
        | Drug Profile: Propoxyphene |  | Definition 
 
        | - Mild to moderate pain - Often combined with APAP or ASA - Dose is 100mg q4h - MDD = 600mg - Active metabolite is Norpropoxyphene, causes pulmonary edema and cardiotoxicity |  | 
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        | Term 
 | Definition 
 
        | - Oral, rectal, parental formulations - LA and immediate release - Onset = 15-60 minutes - Duration is 4-6h or 8-12h - Two main metabolites, M3G and M6G (active) - Caution in renal impairment |  | 
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        | Term 
 | Definition 
 
        | - In combo with APAP or ASA for mild-moderate pain - Long and short acting oral formulations - Onset = 10-15 minutes - Duration = 4-6h |  | 
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        | Term 
 | Definition 
 
        | - Oral, parenteral, and transdermal formulations - Transdermal patch for stable, chronic pain - Opioid naive should start with 25mcg/hr - Can use multiple patches at once - Need to rotate sites - Make take about 16 hours for analgesia to set in - Difficult to adjust dose/convert from another opioid - Absorption increases with heat |  | 
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        | Term 
 
        | Drug Profile:  Hydromorphone |  | Definition 
 
        | - Oral, parenteral, rectal formulations - No LA formula - Oral - Onset = 15-30 minutes - Duration = 4-6 hours - More potent than morphine |  | 
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        | Term 
 | Definition 
 
        | - Oral, rectal, parenteral dosage forms - Onset = 30-60 minutes - Duration = 4-6h (for acute) / >8h for chronic - Half-life is long and variable (12 to 190 hours) - Low abuse potential - Stigma - Multiple conversion methods |  | 
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        | Term 
 
        | What is good about combining therapies? |  | Definition 
 
        | AMDA (American Medical Directors Association) and AGS (American Geriatric Society) have stated that combining low doses of different analgesics may produce pain relief with a lower incidence of side effects (synergistic effect)   |  | 
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        | Term 
 
        | There are many adjuvants available for different kinds of pain, what adjuvants are available for peripheral neuropathies? |  | Definition 
 
        | - Burning, pins and needles type pain - Use Tricyclics:  Amitriptyline, Nortriptyline, Imipramine, Desipramine, Doxepin, or Venlafaxine |  | 
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        | Term 
 
        | There are many adjuvants available for different kinds of pain, what adjuvants are available for refractory pain? |  | Definition 
 
        | - Antiarrhythmics - Use Lidocaine, Mexilitine |  | 
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        | Term 
 
        | There are many adjuvants available for different kinds of pain, what adjuvants are available for lancinating, shooting, stabbing, burning? |  | Definition 
 
        | - Use anticonvulsants, antihypertensives, or topicals Drugs:  Gabapentin, Carbamazepine, Valproate, Clonidine, Capsaicin |  | 
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        | Term 
 
        | There are many adjuvants available for different kinds of pain, what adjuvants are available for Bone Pain? |  | Definition 
 
        | - Dull and aching feeling - Use:  NSAIDS, Bisphosphonates, Steroids, Calcitonin |  | 
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        | Term 
 
        | There are many adjuvants available for different kinds of pain, what adjuvants are available for muscle spasms? |  | Definition 
 
        | For Muscle Spasms use:   - Baclofen - Carisoprodol - Methocarbamol - Orphenadrine |  | 
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        | Term 
 
        | How would you best manage opioid-related side effects? |  | Definition 
 
        | - ATC opioids call for ATC laxatives (stimulants preferred) - Patients do not develop tolerance for this - For N/V eat and drink slowly, avoid irritating/fatty foods, sit upright, oral hygiene freq., treat with phenothiazines, metoclopramide, haloperidol, dexamethasone, lorazepam - For diarrhea, perform good personal hygiene, avoid high reside foods like raisin bran, avoid food temp. extremes, avoid caffeine and replenish fluids. - For sedation, use stimulants, reduce dose, patients not in pain sleep longer (FYI) - Anaphylactic rxns common - Urticaria and Pruritus due to mass cell destabilization, treat with 2nd gen. antihistamines |  | 
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