Pain Flashcards

1
Q

CII

A
  1. DEA and Missouri BNDD needed for prescribe controlled substances, including discontinuation
  2. CII: no refill, no call into pharmacy or clarified over phone
    3 hydrocodone and hydrocodone containing products are CII
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2
Q

dysesthesia

A

impairment of sensitivity especially to touch

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3
Q

WHO weak vs strong opioids

A

Weak: Codeine, Dihydrocodeine, dextropropoxyphene, tramadol
Strong: morphine, methadone, fentanyl, hydromorphone, pethidine, oxycodone, buprenorphine, dextromoramide

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4
Q

Full agonists

A
  1. morphine
  2. fentanyl
  3. hydromorphone
  4. codeine
  5. methadone
  6. tramadol
  7. pethidine
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5
Q

partial agonist

A
  1. buprenorphine
  2. pentazocine
  3. butorphanol
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6
Q

agonists-antagonists

A
  1. nalbuphine

2. nalorphine

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7
Q

Full antagonists

A
  1. naloxone
  2. naltrexone
  3. methylnaltrexone
  4. alvimopan (ADL 8-2698)
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8
Q

codeine phosphate

A
  1. natural but w/o analgesic effect itself
  2. Metabolized in liver: glucuronidation, N- & O-demethylation (P450 2D6)
  3. codeine—->O-demethylation—>morphine (2-10%)–>analgesia
  4. 9% Caucasians w/o analgesia
  5. ultrarapid metabolizers: up to 29% some Middle Eastern & North African–>brestfeed–>toxicity; 0.5% some Asian
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9
Q

codeine phosphate (cont.)

A
  1. PO: 30-120 mg Q 4hrs —> duration of action 4-6 hrs
  2. If 60 mg PO: NNT of 12 for at least 50% pain relief
  3. Improving non-opioid analgesics
  4. major adverse: constipation
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10
Q

dextropropoxyphene

A
  1. synthetic: structurally related to methadone
  2. high but saturable 1st-pass
  3. In liver: demethylation–>norpropoxyphene–>analgesic
  4. PO: 50-100mg q6-8hrs
  5. confusion, hallucination, convulsion, prolonged QT–>torsades de points, cardiac arrest–>withdrawal or discouragement
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11
Q

dihydrocodeine

A
  1. semisynthetic
  2. analgesia: independent of metabolization to dihydromorphine
  3. analgesic efficacy similar to codeine, inferior to ibuprofen (200mg) or diclofenac (50 mg)
  4. advantage: slow-release preparation for q12 hrs
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12
Q

tramadol

A
  1. opioid agonist + monoaminergic
  2. PO: bioavailability 80-90%
  3. Effective, fewer side effects, efficacy on NP
  4. P450 2D6–>O-desmethyltramadol (M-1)–>opioid-like analgesia
  5. recommended dose limits: 600mg/day due to regulation, but unsupported by data
  6. MC side effects: N/V
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13
Q

morphine PO vs epidural vs i.t.

A

PO—>epidural: 2-5%

PO—>i.t. 0.5-1%

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