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Evaluation of Alcohol Use

Elie Massaad Med III Student


Psychiatry Clerkship
Pathophysiology of Alcohol tolerance
GABA is the major inhibitory neurotransmitter in the brain
Chronic ethanol use induces an insensitivity to GABA more inhibitor
is required to maintain a constant inhibitory tone

Ethanol inhibits glutamate induced excitation Increase glutamate

receptors Cessation of alcohol results in unregulated excess

excitation Symptoms of alcohol withdrawal


Alcohol Use Disorders Identification Test
(AUDIT)
Developed by the World Health Organization
10 items that assess alcohol consumption
internally consistent and valid in a variety of
populations
Score of 8 or more suggest hazardous or
harmful alcohol use
Positive scores suggest the need for more
assessment
Management : 1- Rule out other diagnoses
1-Alcohol withdrawal remains a clinical diagnosis
2- In patients presenting with altered mental status and fever
Extensive testing Lumbar puncture & Cranial CT

Meningitis Hepatic Failure

Mimics Alcohol Symptoms

Intracranial GI Bleeding
Hemorrhage
2-Symptom control and supportive care
Benzodiazepines are used to control psychomotor agitation and prevent
progression to more severe withdrawal.
Supportive care :
1. IV fluids
2. Nutritional supplementation
3. IV dextrose should be given for hypoglycemia Prevent alcoholic
ketoacidosis
4. Thiamine supplementation prevent Wernicke-Korsakoff syndrome
5. Electrolytes should also be evaluated and replaced as necessary ( Keep
in mind Magnesium = NMDA antagonist Repair Hypomagnesemia
6. Frequent clinical reassessment including vital signs
Initial treatment of severe AWS in the ED begins with IV loading of
benzodiazepines.
Achieve appropriate and rapid sedation with normalization of vital signs.
Improvement in vital signs In sympathetic tone & stabilization of
the autonomic system.
Appropriate sedation with abnormal vital signs should prompt an
evaluation for other illnesses or injuries in addition to or instead of
alcohol withdrawal
The front-loading therapy method :
Loading doses of benzodiazepines should be 5 to 20 mg of diazepam every
5 to 10 minutes
or
1 to 4 mg of lorazepam every 10 to 15 minutes
Kindling effect
Repeated episodes of withdrawal become
increasingly resistant to to treatment with
benzodiazepines

After administration of a dose of 40 mg


lorazepam or 200 mg diazepam in a patient
who still does not appear calm or sedated

Switch to another type of medications


Barbiturates can directly open the Cl ion channel at appropriate doses
and both enhance the binding of GABA to the GABAA receptor and increase
the duration of Cl ion channel opening.
The advantage of barbiturates is that they work in the absence of any native
GABA.
In addition, the combination of phenobarbital with any benzodiazepine
actually promotes the binding of the benzodiazepine to the GABAA
receptor, possibly increasing the efficacy of the benzodiazepine action.

The downside of adding phenobarbital is that respiratory and cardiac


depressive effects occur more frequently than with benzodiazepines alone
The appropriate dose is 65 to 260 mg every 15 to 30 minutes until
symptom control has been achieved
Propofol
Small case studies have documented the effectiveness of propofol in
resistant AWS
This medication is believed to work on the GABA receptor by :
Slowing channel closing time and therefore potentiating the effect of GABA
Works on the NMDA receptor as an antagonist, leading to less NMDA activity
Can be given in bolus or by continuous infusion
Short acting, discontinuing it allows almost immediate evaluation of the patient's
mental status

The main disadvantage of propofol is that most patients will need


mechanical ventilation for respiratory support.
Management Summary
Continued pharmacologic sedative treatment
(scheduled vs symptomatic treatment)
Multiple studies, starting with a definitive study by Saitz et al, have
demonstrated superiority of symptomatic over scheduled dosing for
continued treatment of AWS
Symptomatic treatment results in a significantly lower duration of
therapy and lower total medication doses
Inpatient providers frequently use the Clinical Institute Withdrawal
Assessment (CIWA) scale to guide additional medication doses
CIWA Scale

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