Management of Delirium Tremens
Benzodiazepines are the gold standard first-line treatment for delirium tremens, with intravenous diazepam or lorazepam administered in escalating doses until symptom control is achieved. 1, 2, 3
Immediate Pharmacological Management
Benzodiazepine Therapy (First-Line)
- Administer IV benzodiazepines as the cornerstone of treatment, with diazepam or lorazepam as preferred agents given in escalating doses until symptoms are controlled. 1, 2, 3
- Use lorazepam preferentially in elderly patients and those with advanced liver disease to minimize accumulation risk due to its shorter half-life and lack of active metabolites. 1
- Continue benzodiazepine therapy for several days with gradual tapering to prevent recurrence, as abrupt discontinuation after prolonged use can precipitate withdrawal symptoms. 4
- In benzodiazepine-refractory cases, consider phenobarbital, propofol, or dexmedetomidine as second-line agents. 3
Adjunctive Antipsychotic Therapy
- Add haloperidol (0.5-2 mg IV slow bolus) only for persistent psychotic symptoms such as hallucinations or severe agitation that do not respond to benzodiazepines alone. 1, 5
- Discontinue antipsychotics immediately once distressful symptoms resolve, as they do not shorten delirium duration or improve mortality and may increase seizure risk. 1, 5
- Avoid using antipsychotics as monotherapy or for routine delirium management. 1
Essential Supportive Care
Metabolic and Physiological Stabilization
- Correct dehydration, electrolyte disturbances (especially hypokalemia and hypomagnesemia), and glucose abnormalities immediately, as these metabolic derangements worsen delirium and increase mortality. 1, 5
- Monitor vital signs continuously for autonomic instability, including tachycardia, hypertension, hyperthermia, and tachypnea. 5
- Maximize oxygen delivery through supplemental oxygen, blood pressure support, and treatment of hypoxia. 5
Thiamine Supplementation
- Administer high-dose thiamine (vitamin B1) to prevent Wernicke-Korsakoff syndrome, using intravenous administration in patients with poor nutritional status or severe complications despite rare anaphylactic reaction risk. 6
- Give thiamine before or concurrent with glucose administration to avoid precipitating acute thiamine deficiency. 6
Non-Pharmacological Interventions
Environmental Modifications
- Create a therapeutic environment with a quiet room, adequate lighting, noise-reduction strategies, and minimal relocations. 4, 5
- Display easily visible calendars and clocks to promote orientation. 4, 5
- Maintain consistency of caregivers and encourage family/friends to stay at bedside with familiar objects from home. 4, 5
Communication and Reorientation
- Frequently reassure and reorient the patient using clear, simple language and careful explanation of all activities. 4, 5
- Clearly identify all caregivers and communicate one task at a time. 4, 5
Physical Care
- Minimize physical and chemical restraints, using them only when absolutely necessary for safety. 4, 5
- Increase supervised mobility as tolerated and regulate bowel/bladder function. 5
- Ensure adequate nutrition and provide sensory aids as appropriate. 5
Monitoring and Ongoing Assessment
Continuous Surveillance
- Reevaluate delirium screening regularly using validated tools like the Confusion Assessment Method (CAM), as mental status changes wax and wane. 5, 7
- Monitor for transition between hyperactive and hypoactive delirium subtypes. 5
- Track response to interventions and adjust management accordingly. 5
Identification of Underlying Causes
- Screen systematically for precipitating factors: infections (especially pneumonia and urinary tract infections), medications with anticholinergic properties, pain, sepsis, and organ dysfunction. 4, 5
- In dialysis patients, rule out aluminum neurotoxicity first as a potentially reversible cause. 7
Post-Acute Management
Relapse Prevention
- Consider relapse prevention medications such as acamprosate or naltrexone after the acute withdrawal phase resolves, though these are not useful during active withdrawal. 1
- Avoid disulfiram in patients with liver disease due to hepatotoxicity risk. 1
Comprehensive Follow-Up
- Ensure transition to comprehensive inpatient addiction treatment (CIAT) after emergency stabilization, as this results in better 6-month outcomes with fewer relapses compared to emergency treatment alone. 8
- Wait 2-4 weeks after complete delirium resolution before performing formal cognitive testing to avoid confounding dementia assessment. 5
Critical Pitfalls to Avoid
- Never use benzodiazepines as routine treatment for general delirium (non-alcohol withdrawal), as they are strongly deliriogenic and increase delirium risk. 4, 5
- Do not overlook hypoactive delirium, which may be mistaken for sedation or depression. 5
- Avoid using haloperidol or other antipsychotics as first-line monotherapy for delirium tremens, as benzodiazepines remain the evidence-based standard. 1, 3
- Do not assume cognitive impairment is solely baseline dementia without systematic delirium screening. 5
- Avoid excessive water-sodium intake in patients with heart disease due to pulmonary edema risk. 6