Management of Alcohol Withdrawal in Adults
Immediate Assessment and Thiamine Administration
Administer thiamine 100-500 mg intravenously immediately before any glucose-containing fluids to every patient with suspected alcohol withdrawal—this is mandatory to prevent precipitating acute Wernicke encephalopathy. 1, 2, 3
- Assess vital signs for autonomic instability: tachycardia (>100 bpm), hypertension (systolic >140 mmHg), fever (>38°C), and diaphoresis 2, 3
- Evaluate hand tremor intensity, hyperreflexia, agitation level, nausea, and vomiting—these typically begin 6-24 hours after the last drink 2, 4, 5
- Screen for dangerous complications: dehydration, electrolyte imbalances (especially magnesium and potassium), infection (pneumonia, spontaneous bacterial peritonitis), gastrointestinal bleeding, pancreatitis, hepatic encephalopathy, and renal failure 2, 3
Severity Assessment Using CIWA-Ar
- Use the Clinical Institute Withdrawal Assessment for Alcohol Scale, Revised (CIWA-Ar) to quantify withdrawal severity 2, 6
- CIWA-Ar scores ≥8 indicate need for pharmacological treatment with benzodiazepines 2
- Reassess CIWA-Ar every 1-2 hours during active withdrawal to guide symptom-triggered dosing 6
Inpatient vs. Outpatient Decision
Admit to hospital if any of the following are present: 1, 2, 3, 4
- History of withdrawal seizures or delirium tremens
- Significant current withdrawal symptoms (tremor with vomiting, CIWA-Ar ≥15)
- Chronic heavy drinking >80 g/day for ≥10 years
- Co-existing serious medical illness (liver disease, infection, cardiovascular disease, pancreatitis, gastrointestinal bleeding)
- Co-existing serious psychiatric illness or active suicide risk
- Inadequate social support or unstable housing
- Failure of prior outpatient treatment
- Malnourishment or suspected Wernicke encephalopathy
Outpatient management is appropriate only for: 4, 5
- Mild to moderate withdrawal (CIWA-Ar <15)
- No history of seizures or delirium tremens
- Adequate social support with reliable daily supervision
- No serious medical or psychiatric comorbidities
Benzodiazepine Regimen
First-Line: Long-Acting Benzodiazepines (Most Patients)
Long-acting benzodiazepines (diazepam or chlordiazepoxide) provide superior protection against seizures and delirium tremens and are the preferred choice for most patients. 1, 2, 7, 8
- Initial: 50-100 mg orally
- Maintenance: 25-100 mg every 4-6 hours as needed based on CIWA-Ar scores
- Maximum: 300 mg in first 24 hours
- Begin taper after 96 hours (day 4) by reducing daily dose by 25% every 2-3 days
- Complete discontinuation by day 10-14 maximum
- Initial: 10 mg orally or IV
- Maintenance: 5-10 mg every 3-4 hours as needed
- For severe withdrawal with altered consciousness: 10 mg IV initially, then 5-10 mg IV every 3-4 hours
Alternative: Short-Acting Benzodiazepines (Specific Populations)
Switch to lorazepam if the patient has: 2, 3, 7
- Hepatic dysfunction or cirrhosis
- Advanced age (>65 years)
- Obesity
- Respiratory compromise
- Recent head trauma
- 2-4 mg orally/IV/IM every 4-6 hours
- Total daily dose: 6-12 mg/day
- Taper by 10-25% every 2-4 days after symptom control
Critical Benzodiazepine Principles
- Benzodiazepines are the only proven treatment to prevent seizures and reduce mortality from delirium tremens 1, 2, 3, 9, 8
- Limit total duration to 10-14 days maximum to prevent iatrogenic dependence 2, 3
- Never discontinue abruptly—always taper gradually 2
- Dispense in small quantities or supervise each dose to reduce misuse risk 1, 3
- Over 70% of cirrhotic patients may not require benzodiazepines; use symptom-triggered dosing only when CIWA-Ar ≥8 2, 3
Thiamine Administration Protocol
- Prophylactic: 100-300 mg/day orally or IV for all patients
- High-risk patients (malnourished, severe withdrawal, suspected Wernicke encephalopathy): 100-500 mg/day IV
- Continue for 2-3 months after withdrawal resolution
- Always give thiamine before any glucose-containing IV fluids—giving glucose first can precipitate acute Wernicke encephalopathy 2, 3
Supportive Care and Monitoring
- Aggressive fluid replacement with attention to electrolyte correction, especially magnesium supplementation 2, 3, 8
- Continuous vital sign monitoring for autonomic instability 2, 3
- Monitor for withdrawal complications: seizures (peak 12-48 hours), hallucinations (12-24 hours), delirium tremens (peak 48-72 hours, up to day 5) 2, 4, 5
- Daily physician visits for 3-5 days after last drink in outpatient settings 2
- Regular monitoring can be stopped after 24 hours if no specific withdrawal signs appear in cirrhotic patients 2
Management of Complications
Withdrawal Seizures
- Do NOT use anticonvulsants (phenytoin, carbamazepine) to prevent further alcohol withdrawal seizures—they are ineffective and may worsen outcomes 1, 2, 3, 7
- Benzodiazepines are the only effective treatment for preventing and treating withdrawal seizures 1, 2, 3
- Ensure adequate benzodiazepine dosing if seizure occurs 8
Delirium Tremens (Severe Withdrawal Delirium)
- Escalate benzodiazepine dosing aggressively 8
- Antipsychotics (haloperidol 0.5-5 mg) may be added ONLY as adjuncts to adequate benzodiazepine doses for severe agitation or hallucinations—never use as monotherapy 1, 2, 3, 9
- Antipsychotics alone lower seizure threshold and worsen outcomes 3
- For benzodiazepine-refractory cases in ICU: consider phenobarbital or propofol as second-line agents 2, 8
Adjunctive Medications (Limited Role)
- Beta-blockers (propranolol IV): may be added for persistent tachycardia despite adequate benzodiazepines, but never as monotherapy—they do not prevent seizures or delirium tremens 2, 9, 5
- Dexmedetomidine: adjunctive therapy only for severe ICU cases refractory to benzodiazepines; does not prevent seizures 2
- Carbamazepine (200 mg every 6-8 hours): alternative only for mild-moderate withdrawal in patients with benzodiazepine contraindications or abuse history; contraindicated if CIWA-Ar ≥15 2, 7, 4, 5
Post-Withdrawal Relapse Prevention
Psychiatric consultation is mandatory after stabilization for evaluation of alcohol use disorder severity and long-term abstinence planning. 2, 3
Pharmacologic relapse prevention options: 1, 2, 3
- Acamprosate (≈2 g/day for patients ≥60 kg): safe in liver disease, reduces craving
- Naltrexone (25 mg for 1-3 days, then 50 mg daily): contraindicated in alcoholic liver disease due to hepatotoxicity risk
- Baclofen (up to 80 mg/day): the only medication with proven safety in cirrhotic patients
- Disulfiram (500 mg daily for 1-2 weeks, then 125-500 mg daily): contraindicated in severe alcoholic liver disease
- Topiramate: emerging evidence for both withdrawal and relapse prevention 7
Psychosocial interventions: 1, 3
- Encourage engagement with Alcoholics Anonymous or other mutual help groups
- Offer motivational interviewing and structured psychological interventions
- Involve family members when appropriate
Critical Pitfalls to Avoid
- Never administer glucose-containing IV fluids before thiamine—this precipitates Wernicke encephalopathy 2, 3
- Never use anticonvulsants alone for withdrawal seizure prevention—benzodiazepines are mandatory 1, 2, 3
- Never use antipsychotics as monotherapy—they worsen outcomes and lower seizure threshold 1, 2, 3
- Never extend benzodiazepines beyond 14 days—this creates iatrogenic dependence 2, 3
- Never discontinue benzodiazepines abruptly—always taper gradually 2
- Do not assume all cirrhotic patients need benzodiazepines—use symptom-triggered dosing only 2, 3
- Do not prescribe naltrexone in patients with alcoholic liver disease—hepatotoxicity risk 2, 3