Treatment of Binge Drinking
For patients with binge drinking episodes, the primary treatment approach is psychosocial intervention (motivational interviewing, brief interventions, cognitive-behavioral therapy) combined with early detection and screening, while pharmacotherapy with acamprosate or naltrexone should be reserved for those who meet criteria for alcohol dependence or have failed psychosocial interventions. 1, 2, 3
Initial Assessment and Screening
Screening Tools
- Use the AUDIT-C (Alcohol Use Disorders Identification Test - Consumption) as the initial screening tool, with scores >4 in men or >3 in women indicating positive screening requiring further evaluation 1
- Question 3 of AUDIT-C specifically addresses binge drinking: "How often do you have 5 or more drinks on one occasion?" 1
- The NIAAA Single Alcohol Screening Question (SASQ) can also be used: "How many times in the past year have you had 4 (women) or 5 (men) or more drinks in a day?" with any positive response warranting follow-up 1
Defining Binge Drinking
- Binge drinking is defined as consumption of 4-5 standard drinks (56-70g alcohol) within approximately 2 hours, bringing blood alcohol concentration to 0.08% or higher 1
- Weekly binge drinking carries a hazard ratio of 3.45 for decompensated liver disease independent of average daily alcohol intake, and this risk increases to 6.82 in women 4
- Daily alcohol consumption carries higher cirrhosis risk (RR 3.65) compared to episodic drinking, but episodic drinking still poses significant health risks 1
Psychiatric Co-morbidity Assessment
Depression and Anxiety Screening
- Screen all patients with binge drinking for psychiatric co-morbidity, as alcoholics have high prevalence of anxiety disorders, affective disorders, and schizophrenia 1
- Distinguish between independent psychiatric disorders (requiring specific treatment) versus concurrent disorders (which may resolve with alcohol cessation) 1
- Depressive symptoms are associated with increases in heavy episodic drinking over time, consistent with self-medication behavior, while anxiety symptoms may be protective against future binge drinking 5
- Do not initiate antidepressants until after at least 2 weeks of complete alcohol abstinence to determine if psychiatric symptoms are independent or alcohol-induced 2
Coordination of Care
- Psychiatric consultation is mandatory for evaluation, ongoing treatment planning, and long-term abstinence strategies 6, 2
- Coordinate care between hepatologists and addiction specialists (psychiatrists, psychologists, social workers) to reduce the gap between signs of alcohol dependence appearing and referral 1
Treatment Approach Based on Severity
For Hazardous/Harmful Use (Binge Drinking Without Dependence)
Psychosocial interventions are first-line treatment:
- Motivational interviewing to help patients evaluate their situations 7
- Brief interventions to facilitate more healthy behaviors 7
- Cognitive-behavioral therapies to avoid relapses 7
- These interventions are recommended as first-line for adults with hazardous or harmful use of alcohol 3
Pharmacotherapy considerations:
- Pharmacological treatment is NOT routinely recommended for hazardous/harmful use in adults 3
- Only naltrexone has been investigated in hazardous/harmful use, but evidence is limited and use remains off-label 3
- In adolescents with hazardous/harmful use, there is severe lack of data regarding efficacy and safety of approved medications, raising important safety and ethical concerns 3
For Alcohol Dependence With Binge Drinking Pattern
Pharmacotherapy is indicated:
- Acamprosate or naltrexone should be first-line pharmacotherapy for relapse prevention 2
- Acamprosate (333 mg tablets, dosed as 666 mg three times daily) has proven efficacy in 24 randomized controlled trials and is safe in liver disease 2, 8
- Acamprosate is a glutamatergic modulator that helps maintain abstinence when used as part of a comprehensive treatment program including counseling and support 8
- Naltrexone 50 mg once daily is effective for reducing heavy drinking but is contraindicated in patients with liver disease due to hepatotoxicity risk 2, 9
- Disulfiram is effective but should be avoided in severe alcoholic liver disease due to hepatotoxicity 2
Management of Liver Complications
Assessment
- Calculate average weekly alcohol consumption: >14 standard drinks/week for females or >21 standard drinks/week for males increases cirrhosis risk 1
- Weekly binge drinking combined with metabolic syndrome produces supra-additive increases in risk of decompensated liver disease (HR 4.29) 4
- Assess for impaired liver function through clinical examination and laboratory testing (complete metabolic panel, liver function tests) 6
Medication Adjustments
- If hepatic dysfunction is present, acamprosate requires dose adjustment for moderate renal impairment and is contraindicated in severe renal impairment (creatinine clearance ≤30 mL/min) 8
- Avoid naltrexone entirely in patients with alcoholic liver disease due to hepatotoxicity 2, 9
Alcohol Withdrawal Management (If Present)
Recognition
- Alcohol withdrawal symptoms typically begin 6-24 hours after last drink, peak at 3-5 days, and resolve within one week 6, 10
- Symptoms include tremors, anxiety, nausea, vomiting, autonomic instability, and in severe cases (3-5% of patients), delirium tremens occurring approximately 72 hours after cessation 10
Treatment
- Benzodiazepines are the gold standard for alcohol withdrawal syndrome and should not be prescribed beyond 7-14 days to prevent iatrogenic dependence 2
- Long-acting benzodiazepines (diazepam, chlordiazepoxide) provide superior protection against seizures and delirium tremens 6, 2
- Administer thiamine 100-500 mg IV immediately before any glucose administration to prevent Wernicke encephalopathy 6
- Continue thiamine 100-300 mg/day for 2-3 months following resolution of withdrawal symptoms 6
Critical Distinction
- Acamprosate does NOT eliminate or diminish withdrawal symptoms and should only be started after detoxification is complete 8
- Patients must be abstinent from alcohol on the day of randomization before starting acamprosate 8
Common Pitfalls to Avoid
- Do not use anticonvulsants for alcohol withdrawal seizures, as these are rebound phenomena with lowered seizure threshold, not genuine seizures requiring anticonvulsant therapy 6
- Do not administer glucose-containing IV fluids before thiamine, as this can precipitate acute Wernicke encephalopathy 6
- Do not continue benzodiazepines beyond 10-14 days due to abuse potential 6
- Do not prescribe naltrexone to patients with liver disease due to hepatotoxicity risk 2, 9
- Do not assume psychiatric symptoms are independent disorders until after 2 weeks of complete abstinence 2
- Do not use pharmacotherapy as monotherapy; it must be combined with counseling and psychosocial support 8, 7
Monitoring and Follow-up
- Monitor for emergence of depressive symptoms or suicidality in patients treated with acamprosate, and report such symptoms immediately 8
- Advise patients to continue medication even in the event of relapse and discuss any renewed drinking with their physicians 8
- Address nicotine dependence, as alcoholics tend to be heavier smokers and cigarette smoking is synergistic with alcohol in causing cardiovascular disease and cancer 1
- Regular follow-up to assess treatment adherence, as compliance-enhancing techniques should be implemented for all components of the treatment program 9