02. Alcohol Use Disorder

Background

Epidemiology

  • In 2018, 14.4 million adults ages 18 and older had an AUD, including 9.2 million men and 5.3 million women.

Neurobiology

  • People who are chronically exposed to alcohol experience changes in neural circuits involved with arousal, reward, and stress responses, utilizing dopamine, GABA, glutamate, and serotonin, leading to changes in sensitivity to alcohol’s long term effects.

Diagnosis

Screening:

  • Single question screener: “how many times in the past year have you had 5 (for men) or 4 (for women) or more drinks in a day?”
  • ≥ 1 binge-drinking day in past year -> sensitivity 82-87%, specificity 61-79%.
  • AUDIT-C: 1st 3 questions of AUDIT, score 0-12.
  • ≥ 4 -> sensitivity 74-76%, specificity 80-83%.
  • ≥ 3 -> sensitivity 74-88%, specificity 64-83%.
  • AUDIT: 10-item self-report instrument, score 0-40.
  • ≥ 4 -> sensitivity 84-85%, specificity 77-84%.

Assessment for AUD via DSM 5: AUD is a problematic pattern of alcohol use leading to clinically significant impairment or distress, as manifested by at least 2 of the following occurring within a 12-month period:

  • 6Cs (lost control, unable to cut back, cravings, health consequences, physical consequences, relationship consequences).
  • Spent a lot of time drinking or recovering.
  • Interfered with home/school/work role.
  • Give up other important activities.
  • Increased tolerance.
  • Withdrawal symptoms.
  • 2-3=mild, 4-5=moderate, and 6 or more severe AUD

Treatment

For those with moderate to severe AUD.

  • Assess if pregnant: no AUD medication for pregnant patients, use psychosocial treatment.
  • 1st line: naltrexone, NNT 12 for reduced use, 20 for stopping.
  • Extended-release naltrexone.
  • 2nd line: acamprosate (only for patient interested in maintaining sobriety, if not, see 3rd line).
  • 3rd line: gabapentin.
  • Can be used as adjuvant to naltrexone.
  • 4th line: topiramate and others.
  • Psychosocial treatment (groups such as AA, SMART Recovery, individual therapy, intensive outpatient, and residential treatment).

 

Medication

Dosage

Mechanism

Adverse Effect

Contra-indications

Use in liver or renal disease

Considerations

Disulfiram

250-500 mg daily

Aldehyde dehydrogenase inhibitor à negative physical effects of EtOH intake

Drowsiness, diarrhea, headache, dermatitis, hepatitis (rare)

LFT > 5x ULN

Alcohol use in past 24 hours

Severe CV disease

Liver: no

Renal: yes

Good for highly motivated patients or patients already on methadone DOT

Naltrexone

25 mg on day 1, followed by 50 mg daily; available as long acting injection

µ-opioid antagonist à reduces cravings, blocks pleasurable effect of EtOH, reduces binges

GI upset, transaminitis, somnolence, insomnia, dizziness

LFT > 5x ULN

Decompensated cirrhosis

Short-acting opioids in past 24 hours

Long-acting opioids in past 7 days

Liver: no

Renal: yes

Can’t be used with opioids

Acamprosate

666 mg TID (6 pills!)

Modulates glutamate hyperactivity à improves dysphoria, promotes abstinence

Diarrhea, fatigue

Dose reduce in CKD

Liver: yes

Renal: reduce in CKD to 333 mg TID

Only useful in maintaining sobriety. If patient wants to cut down but not stop drinking, try another option

 

 

Gabapentin (not FDA approved)

Day 1-3: 300 mg TID, followed by 600 mg TID

Facilitates GABA à improves anxiety, sleep, dysphoria

Somnolence, dizziness

Dose reduce in CKD

Liver: yes

Renal: dose reduce

Can use with naltrexone

Topiramate (not FDA approved)

Week 1: 25 mg qHS, week 2: 25 mg BID, increase dose by 25 mg BID per week to reach 150 mg BID

Facilitates GABA, decreases glutamate à improves dysphoria, cravings, impulsivity

Cognitive slowing, paresthesia, somnolence, metabolic acidosis (rare), kidney stones, glaucoma

Dose reduce in CKD

Hx of kidney stones

Hx of narrow-angle glaucoma

Pregnancy planning

Using OCP

Liver: yes

Renal: dose reduce

Not for use in pregnancy

 

Kranzler H R, Soyka M. Diagnosis and Pharmacotherapy of Alcohol Use Disorder

Addiction Care Team (ACT) AUD power point slides