This Neurology\/Psychiatry Exam focuses on Pain and Addiction, assessing knowledge of pain pathways, chronic pain types, and medication effects like gabapentin and pregabalin. It evaluates understanding of pain scale applications and tricyclic antidepressants' efficacy in pain management.
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CIWA-Ar
COWS
McGill
NIH Consensus Scale
None of the above
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False
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False
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False
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False
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Maximum doses dependent on indication
Requires renal adjustment
Should be used in caution in patients at risk of cardiovascular disease due to potential peripheral edema
Starting dose - 500mg/day; Titration-Within 1 week
All of the above are True
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False
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Short-acting benzodiazepines create a smoother withdrawal course as they can be doses for symptoms on an as needed basis
Because benzodiazepine are metabolized via CYP3A4, liver impairment is a contraindication
Symptom-triggered treatment with benzodiazepines shows less time on BZD and shorter length of stay (than fixed dose treatment), but requires more monitoring
Lorazepam and Diazepam can be given PO, IM, or IV but Chlordiazepoxide and Oxazepam are limited to PO and IM use
All of the above are False
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False
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False
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WE stems from thiamine deficiency due to alcohol abuse
Characterized by neurologic complications such as confusion, opthalmoplegia (affected eye movement), and gait ataxia
Treatment should begin immediately with suspected WE (even before possible test results)
While there are no specific guidelines, IV therapy as a 2000mg continuous infusion (over 60mins) is preferred
Complications of WE include deterioration to Korsakoff’s Syndrome
All of the above are True
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Chronic back pain is observe only in the case of morphologic changes
Diabetic neuropathy is the result of vasoconstriction of microvasculature
Postherpetic neuralgia may last for years
“Tingling” sensation is the result of neurons that are hypersensitized due to change in sodium receptor concentrations and demyelinated axons.
All of the above are correct
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False
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FDA approved for treatment of opioid withdrawal
As an alpha-2 adrenergic receptor agonist, it suppresses the sympathetic CNS system
Dosing based on COWS assessment
Given in combination with other medication
All of the above are True
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True
False
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False
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Common ADE- Dizziness, somnolence
Onset of action = 2-3 weeks, Trial requires = 3-8 weeks
Requires renal adjustment
Titration- Day 1- 300mg at bedtime; Day 2- 300mg BiD; Day 3- 300mg TiD
All of the above are True
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False
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Controlled release formulation can be mixed into small (
Less histamine release than morphine at initiation
Requires no change in initial dose in renal dysfunction
Titration - dose is increased every 1-2 weeks as tolerated
All of the above are False
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Dose tapering depends on opiate of abuse from which patient is withdrawing
Indicated for both treatment of opiate withdrawal and opiate maintenance treatment
Mechanism of action - Full mu receptor agonist weak NMDA antagonist
Monitor for QT prolongation via EKG
All of the above are True
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Acute toxicity stems from down regulation of alcohol dehydrogenase
Alcohol binds to the benzodiazepine site on the GABA receptor
Chronic consumption of alcohol leads to hypersensitivity to glutamate
Eventual effect is extended periods of open chloride ion channels
All of the above are True
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Cannot be used in patients with hepatic dysfunction
Initiation doses: IR - 5mg q4hr, SR/CR - 15 mg q8-12hr, ER - 30 mg qd
Metabolized to an active metabolite; avoid in renal dysfunction
Risk of allergic reaction
Titrated every 2 days until no longer tolerated
All of the above are True
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Epileptogenic risk
Non-controlled substance
Reduced risk of respiratory depression
Titrate up as tolerated
All of the above are True
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Titration: Daily dose should be increased by 25% at time
Short acting doses should be 10% of the daily dose given
Administration of short-acting doses should be PO q4-6 hrs
Discontinuation: Daily dose taper 10% each week as tolerated (withdrawal)
All of the above are True
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Buprenorphine is a partial mu receptor agonist and weak kappa receptor agonist
Buprenorphine is highly protein bound
Buprenorphine yields an active metabolite via CYP3A4 metabolism
Dosing of Suboxone is based on most recent opioid dose
Time to peak effect of Suboxone is 30-60mins.
All of the above statements are True
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False
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Dosed at 30-60 mg, requiring no titration
Requires renally adjusted dose if CrCl < 30mL/min
Has a relatively short trial time at 2-3 weeks
Specific precaution for use in hypertensive patients
All of the above are True
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