Pharmacology: Narcotics Flashcards

1
Q

nociceptive pain can be divided into ___ or __ pain

A

somatic or visceral pain.

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2
Q

visceral pain

A

contant, aching squeezing, harder to localize, can be referred

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3
Q

somatic pain/parietal pain

A

constant or intermitten, gnawing, aching, usually well localized. Sharper.

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4
Q

neuropathic pain can be ___ or ___

A

dysesthetic or neuralgic.
overall, neuropathic pain is due to damage to nervous system and causes the sharp nerve pains. due to destruction, infiltration, compression of nerve tissue.

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5
Q

neuralgic pain

A

lancinating, sharp shooting pain.

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6
Q

dysesthetic pain

A

burning, contant allodyniec pain.

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7
Q

acronym for assessing pain

A

WWQQAAAT: Where, when, quality (peritonitic or diffuse), quantity (1-10), aggravating, alleviating, associated symptoms, timeline/disease progression

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8
Q

T/f neuropathic pain is harder to treat

A

true. it’s resistant to treatment and there are limited surgical interventions.

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9
Q

opiates vs opioids

A

opiates= naturally present in opium– morphine, codeine, thebaine

opioids= manufacture- semisynthetic are derived from an opiate (heroin from morphine)

  • some opioids are 100% man made like fentanyl and methadone.
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10
Q

what factors affect pharcokinetics vs pharmacodynamic

A

kinetics: absorption, distribution, metabolism, excretion
dynamics: receptor binding, signal messaging, physiological effects.

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11
Q

why is the effect of a given dose less after oral rather than parenteral administration

A

due to significant first pass metabolism

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12
Q

bioavailability =

A

fraction of the administered dose of a drug that reaches the systemic circulation in an active form

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13
Q

specificity of a test

A

probability that the test will be negative for someone who doesn’t have the disease

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14
Q

sensitivity of a test

A

the ability of a test to correctly identify those with the disease (true positive rate),

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15
Q

ppv

A

positive predictive value; the is the probability that subjects with a positive screening test truly have the disease.

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16
Q

morphine gets conjugated with ___ acid to form a pharmacologically inactive metabolite, ____

A

conjugates with glucoronic acid to form 3-glucuronide. forms the principal metabolite. (6- glucuronide form is more active than morphine)
 has a longer half life
 Systemically it is about 2X as potent as morphine
 Intrathecally, it is about 100X more potent than morphine

17
Q

primary method of morhphine excretion

A

morphine is excreted by the kidney in the form of 3-glucuronide.

18
Q

morphine causes PEAR:

A
P = physical dependence
E= euphoria
A= analgesia
R= respiratory depression
19
Q

examples of full agonists, partial agonists, antagonists to Mu receptor

A

full agonist: morphine, hydromorphone, oxycodone, fentanyl

partial agonist: buprenorphien

antagonist: naloxone or naltrexone.

20
Q

T/F you should use a long acting formulation for opioid naive patients

A

false. to avoid dependence, opioid naive patients should receive short-acting formulations

21
Q

T/F opioids should be given IM

A

no. never!

preferred route is oral. When unable to swallow, IV or transdermal.

22
Q

what is breakthrough analgesia

A

done usually in chronic pain patients when schedule dosing (ex/ every 4 hours) is required, then as per needed (PRN) dosing for episodes of increasing pain.

23
Q

by how much should you titrate the opioid dose if the original dose is not giving pain control?

A

increase the dose by 25-50% if the patient is not achieving adequate pain control.

24
Q

neurotoxicity of opioids

A

anxiety, agitation, restlessness, delirium. Not reversible with naloxone.

25
Q

T/F narcosis is reversible with nalozone

A

true. narcosis is deep sedation, hypotension and decreased ventilation which can be reversed.

26
Q

T/F neurotoxicity is reversible with naloxone

A

false. the anxiety and agitation and delirium opioids can cause are not reversible with naloxone.