Lecture 17 - alcohol dependance Flashcards

1
Q

describe the components of alcohol and its dependance in the body.

A

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

Blood Alcohol Concentration (BAC)= grams of alcohol in 100ml of blood. (80mg of alcohol in 100ml of blood is equiv to 0.08grams per 100ml) (0.08%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are figurative effects of BAC levels ?

A

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

more than 0.30% = loss of consciousness, anaesthesia,

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is used to measure alcohol in a person?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe the mechanism of action of alcohol

A

Agonist effect on GABA receptor- increased binding or influx of Cl- (a CNS depressant)
GABA synapses control activity of different neuronal systems- glutamate, dopamine, opioids
Many ‘neuropsychiatric effects’

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what does the sustained or chronic sue of alcohol lead to?

A

peripheral neuropathy and dementia caused by alcohol toxicity and vitamin B6 (thiamine) deficiency in specific midbrain.

alcohol prevents conversion of thiamine to TPP in the small intestine and interferes wits its liver storage.

it can cause sleep disturbance, depression or anxiety and overall malnourishment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how do the effects of alcohol occur in reference to aldehyde dehydrogenase?

A

genetic variation 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 causes nausea, vomiting, sweating and sever headaches

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

describe the metabolism of alcohol.

A

The metabolism of alcohol into acetylaldehyde and further into acetic acid depends on the availability of the coenzymes alcohol dehydrogenase and aldehyde dehydrogenase and coenzyme NAD.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

how does alcohol affect men and women differently?

A

females have less and metabolise 50% less than men.
Women have greater fat to muscle ratio- so less blood for proportional body weight (As fat has lower blood supply than muscle)- so have greater blood conc in women than men for equivalent doses of alcohol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are ways to manage the risk and from alcohol ?

A
  • Avoid talking about ‘safe levels’ of consumption instead reduce the risk of further harm – this depends on age, genes, concurrent medication, general / co morbidities
  • Risks include accidental injury, sexual misdemeanours, violence, CV disease, liver diseases, cancers.
  • Becomes a problem once dependent on alcohol for day to day functioning – AUDIT (alcohol use disorders identification test) or CAGE questions- considered Cutting down your alcohol consumption, got annoyed by people criticising your drinking, felt guilty about your drinking, had a drink 1st thing in the morning (eye opener)
  • Binge Drinking – twice the upper limit of the max daily drinking level (6 units for women, 8 units for men
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is the pharmacist intervention associated with alcohol consumption in a patient?

A
  • Establish drinking patterns- Ask about alcohol consumption at any relevant opportunity.
  • People with alcohol related probs may find it difficult to accept they have a problem and developed coping strategies to manage their drinking- Approach in a non judgemental and open manner.
  • IBA (Alcohol Identification and Brief Advice)-a process of identifying people who may be have alcohol issues via a structured conversation about alcohol consumption.
  • Consider concomitant health problems, cognitive functioning, readiness to change.
  • Ensure questioning is sensitive to culture and faith.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what brief intervention should be addressed?

A
  • Patient centred conversations- non judgemental
  • Signpost to services/resources (alcohol awareness)
  • Avoid sudden stop if severely dependent
    Use FRAMES – 3-5mins
  • Feedback- patients personal risk or impairment
  • Responsibility- emphasise personal responsibility for change
  • Advice- suggest how the patient can cut down or abstain
  • Menu- offer the patient alternative options for changing their drinking pattern
  • Empathetic - listen reflectively, explore with the patient reasons for change.
  • Self efficacy- enhance the patients belief in their ability to change
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is sued to assess the degree of dependant or harm of alcohol?

A

Subjective for the individual BUT various questionnaires used to assess the degree of dependence or harm.
e.g SADQ (severity of alcohol dependence questionnaire) is a 20 item questionnaire- centred on the drive to consume alcohol
Answers rated on a four-point scale: Almost never – 0, Sometimes 1, Often 2, Nearly always 3
> 31 or higher indicates “severe alcohol dependence”.
16 -30 indicates “moderate dependence”
< 16 usually indicates only a mild physical dependency.

Routine laboratory screening, including LFTs (aspartate aminotransferase (AST), alanine aminotransferase (ALT) the AST/ALT ratio is >1.5 OR gamma glutamyltransferase ↑GGT, complete blood count (high Mean Corpuscular Volume [MCV]) and reduced vitamin B12 and folate levels can be “red flags” .

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the alcohol withdrawal timeline?

A

1: anxiety, insomnia, nausea and abdominal pain
2: high blood pressure, increased body temperature…
3: hallucination, fever, seizures and agitation

Abrupt cessation can lead to withdrawal symptoms- Benzodiazepines given to manage these either by a ‘symptom triggered approach’
or a ‘fixed dose regimen’

Delirium Tremens is a serious withdrawal effect with high mortality- a type of agitated delirium approx. 72hrs after last drink.
Need adequate fluid and nutritional replacement (parenteral thiamine or Vit B with ascorbic acid Pabrinex® im high potency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what drugs are used in maintaining abstinence of alcohol withdrawal?

A

Reduce cravings to support abstinence:
acamprosate, disulfiram, naltrexone, nalmefene - BUT also high placebo effect if engaging with any health professional and joining support groups (AA).

Disulfiram has limited efficacy but thrice weekly supervised consumption may be superior to unsupervised daily acamprosate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is the treatment of alcohol withdrawal?

A

For alcohol withdrawal i.e management of autonomic over arousal, fits or delirium tremens (DTs)

Use BZs due to similarity in mechanism of action with alcohol (GABA mediated) BZs diminish the severity of the symptoms as neuronal systems begin to revert back to pre-alcohol states
Chlordiazepoxide (CDP) used- long acting, prescribed on a reducing dosage regime over 5-7 days.
Starting dose based on symptom severity i.e 60-100mg/day.
Diazepam most often used- reduce by 1/6 of total dose per week – Usually by specialist services (might have patient in general medicine ward/community detox).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

describe disulfirams mechanism of action and monitoring requirements, and when it should be used in treatment.

A

Irreversibly inhibits aldehyde dehydrogenase causing accumulation of acetaldehyde – sweating, nausea, facial flushing, tachycardia, hypotension.
Intensity to reaction is dose dependent (Loading dose of 400mg-800mg), followed by 100-200mg maintenance.
Start 24 hrs after last drink
Monitor every 2 weeks for 1st 2 months, monthly thereafter.
Liquid or tablets- supervised as 2 or 3 times a week (daily dose X 7 divided by 2) as enzyme inhibition is irreversible and clinical effect lasts 7-10 days

Recommended by NICE as 2nd line for moderate to severe alcohol dependence in patients who are not suitable for acamprosate or naltrexone to have specified preference for disulfiram and who aim to stay abstinent from alcohol.

17
Q

describe the properties of acamprosate as a drug used in maintaining alcohol abstinence.

A

Acamprosate: a GABA A agonist and glutamate (NMDA) antagonist – reduces reward and craving

  • 7 days to reach therapeutic levels so can start immediately after detox.
  • Daily dose is 1998mg (666mg tablet three times a day) for >60kgs
  • Usually >6 months treatment
  • Efficacy enhanced with psychosocial and behavioural therapies
  • Determine renal and hepatic function prior to use-

Side effects include- diarrhoea, abdominal pain, nausea, pruritis.

18
Q

describe nalmefene as an instance drug for alcohol treatment

A

Nalmefene- opioid antagonist (Mu and delta receptors AND a partial agonist at Kappa receptors)

As required use i.e 18mg tablet taken 1-2 hours before exposure to alcohol.
Side effects include-nausea, vomiting, sweating- need to be careful regarding surreptitious opioid use.

Scottish Medicines Consortium (2014): “Nalmefene should only be prescribed in conjunction with continuous psychosocial support focused on treatment adherence and reducing alcohol consumption. This drug should help otherwise responsible drinkers to limit their weekly intake of alcohol. Often people decide to just have one drink, which then leads to a binge. Nalmefene should hopefully stop most cases of this

19
Q

describe naltrexone as an instance drug for alcohol treatment

A

Naltrexone – non selective opioid antagonist.

Start at 50mg a day- usually for 6 months duration.
Side effects include nausea, headache, abdominal pain,
Baseline liver and renal function (hepatotoxicity at high dose)
Avoid opioid analgesia

20
Q

what are comorbid mental health disorders associated with alcohol dependance ?

A

Often present with other MH conditions- esp anxiety or depression

Depression can diminish after 3 -4 weeks of abstinence.
* Meta analysis show that antidepressants with mixed pharmacology (TCAs) perform better than SSRIs in reducing depressive symptoms but effect size is modest and risks of TCAs outweigh benefits- combination of antidepressant and naltrexone compared with each drug alone may give better outcome.

Bipolar Affective Disorder- phase dependent
* consider interaction with AED or Lithium (esp electrolyte imbalance if continue to drink)

Schizophrenia
* Optimise antipsychotic medication- naltrexone or acamprosate preferred.

21
Q

what is foetal school syndrome or other alcohol related neurodevelopemntal disorders?

A

Pregnant women exposes the foetus to same blood levels as herself as alcohol passes so readily through the placenta.
Alterations in GABA receptor expression/cell migration in the cortex, leading to cognitive and behavioural deficits in child.

Signs and symptoms of FAS
Low body weight.
Poor coordination.
Hyperactive behaviour.
Difficulty with attention.
Poor memory.
Difficulty in school (especially maths)
Learning disabilities.
Speech and language delay

minor east abnormalities, low nasal bridge, thin upper lip etc