ALCOHOL DEPENDENCE Flashcards

1
Q

what is alcohol

A

a by-product of the fermentation of various fruits and grains - drinking alcohol is a common widely accepted activity in most countries and cultures

fat and water soluble, readily diffuses across all cell membranes, peak blood levels are within 30-60min

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2
Q

blood alcohol concentration (BAC)

A

grams of alcohol in 100ml of blood

> 0.15% = significant impairment of balance, slurred speech, nausea, vomiting

> 0.30% = loss of consciousness, anaesthesia

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3
Q

easiest way to measure alcohol

A

measure alcohol through expired through respiration - breathalyzer (estimates BAC by analysing a sample of the breath which contains alcohol passed from bloodstream into the lungs)

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4
Q

alcohol’s moa

A

agonist effect on GABA receptor - increasing binding or influx of Cl- (CNS depressant)

GABA synapses control activity of different neuronal systems - glutamate, dopamine, opioids

many ‘neuropsychiatric effects’

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5
Q

chronic consequences of alcohol

A
  • peripheral neuropathy and dementia caused by alcohol toxicity and vit B6 (thiamine) deficiency
  • sleep disturbance, depression or anxiety
  • overall malnourishment
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6
Q

alcohol effect on thiamine

A
  • alcohol prevents conversion of thiamine to TPP in small intestine and interferes with its storage in the liver
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7
Q

how genetic variation impacts alcohol

A

(far east population) have an inactive form of aldehyde dehydrogenase - acetaldehyde is not further converted into acetic acid - so small amounts of alcohol result in toxic levels of acetaldehyde which cause nausea, vomiting, sweating and severe headache

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8
Q

how gender impacts alcohol metabolism

A

females have less alcohol dehydrogenase and metabolise 50% less than men

women have greater fat-to-muscle ratio - so less blood for proportional body weight, so have greater blood concentration in women then men

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9
Q

risks from alcohol

A

accidental injury
sexual misdemeanours
violence
CV disease
liver diseases
cancers

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10
Q

when is drinking alcohol considered a ‘problem’

A

once dependent on alcohol for day-to-day functioning - AUDIT (alcohol use disorder identification test) or CAGE questions

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11
Q

IBA (alcohol identification and brief advice)

A

a process of identifying people who maybe have alcohol issues via a structured conversation about alcohol consumption

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12
Q

brief intervention (not appropriate for dependency) - FRAMES

A

Feedback > patients personal risk or impairment
Responsibility > emphasise personal responsibility for change
Advice > suggest how to cut down/abstain
Menu > offer alternative options
Empathetic > listen reflectively, explore reasons for change
Self efficacy > enhance the pts belief in their ability to change

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13
Q

SADQ (severity of alcohol dependence questionnaire) is a 20 item questionnaire - scoring system

A

answers rated on a 4-point scale: never (0), sometimes (1), often (2), nearly always (4)

> 31 indicates severe alcohol dependence

16-30 indicates moderate dependence

<16 only a mild physical dependence

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14
Q

tests required for alcohol dependence

A

complete blood count (reduced vitamin B12 and folate levels can be red flags)

LFTs (AST/ALT >1.5)

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15
Q

management of alcohol withdrawal

A
  • abrupt cessation can lead to withdrawal symptoms - BZs given to manage either by ‘symptom triggered approach’ or ‘fixed-dose regimen’
  • delirium tremens is a serious withdrawal effect with high mortality - a type of agitated delirium approx. 72 hours after last drink
  • need adequate fluid and nutritional replacement (parenteral thiamine or vit B with ascorbic acid Pabrinex IM)
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16
Q

CDP in treating alcohol withdrawal

A

chlordiazepoxide used long-acting, prescribed on a reducing dosage regimen over 5-7 days

starting dose based on symptom severity

16
Q

treatment of alcohol withdrawal

A
  • use BZs due to similarity in moa with alcohol (GABA mediated)
  • BZs diminish the severity of the symptoms as neuronal systems begin to revert back to pre-alcohol states
  • diazepam most common
16
Q

drugs that reduce cravings to support abstinence

A

acamprosate
disulfiram
naltrexone
nalmefene

BUT also high placebo effect if engaging with any health professional and joining support groups (AA)

17
Q

disulfiram moa

A
  • irreversibly inhibits aldehyde dehydrogenase causing accumulation of acetaldehyde - sweating, nausea, facial flushing, tachycardia, hypotension
18
Q

disulfiram monitoring and dose

A
  • intensity to reaction is dose-dependent (loading dose of 400-800mg) followed by 100-200mg maintenance
  • start 24 hours after last drink
  • monitor every 2 weeks for 1st 2 months, then monthly
  • liquid or tablets - supervised 2 or 3 times weekly as enzyme inhibition is irreversible and clinical effect lasts 7-10 days
19
Q

acamprosate moa

A
  • GABA A agonist and glutamate (NMDA) antagonist - reduces craving
  • 7 days to reach therapeutic levels so can start immediately after detox
  • side effects: diarrhoea, abdominal pain, nausea, pruritis
20
Q

acamprosate dose and monitoring

A
  • daily dose is 1998mg (666mg tds) for >60kgs
  • usually over 6 months treatment
  • determine renal and hepatic function prior to use
21
Q

nalmefene moa

A

opioid antagonist (mu and delta receptors AND a partial agonist at kappa receptors)

side effects: nausea, vomiting, sweating

22
Q

nalmefene dose

A

as required use i.e. 18mg tablet taken 1-2 hours before exposure to alcohol

23
Q

naltrexone moa

A

non-selective opioid antagonist

side effects: nausea, headache, abdominal pain

24
Q

naltrexone dose

A

start at 50mg daily - usually for 6 months duration

hepatoxicity at high dose

avoid opioid analgesia

25
Q

drug of choice when co-morbid with schizophrenia

A

naltrexone or acamprosate preferred

26
Q

signs and symptoms of FAS

A
  • low body weight
  • poor coordination
  • hyperactive behaviour
  • difficulty with attention
  • poor memory
  • difficulty in school (esp. maths)
  • learning disabilities
  • speech and language delays