What is the recommended use and dosage of Acamprosate (Campral) for treating alcohol dependence?

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Acamprosate for Treating Alcohol Dependence

Acamprosate (Campral) is strongly recommended at a standard dose of 666 mg (two 333 mg tablets) taken three times daily for maintaining abstinence in alcohol-dependent patients who have already achieved abstinence at treatment initiation. 1

Indication and Efficacy

Acamprosate is specifically indicated for:

  • Maintenance of abstinence from alcohol in patients with alcohol dependence
  • Patients who are already abstinent at treatment initiation
  • Use as part of a comprehensive management program that includes psychosocial support 1

The evidence strongly supports acamprosate's efficacy:

  • It is the only intervention with moderate certainty evidence for increasing probability of abstinence (38% vs 25% with placebo) 2
  • Acamprosate demonstrates reduced dropout rates (42% vs 50% with placebo) 2
  • It is effective for maintaining abstinence for up to 12 months after detoxification 2, 3

Dosing Protocol

Standard Dosing

  • Standard dose: 666 mg (two 333 mg tablets) three times daily 1
  • Treatment should be initiated as soon as possible after alcohol withdrawal when abstinence is achieved 1
  • Continue treatment even if patient relapses 1
  • May be taken with or without food, though taking with meals was used in clinical trials 1

Renal Adjustment

  • Moderate renal impairment (CrCl 30-50 mL/min): 333 mg three times daily 1
  • Severe renal impairment (CrCl ≤30 mL/min): Contraindicated 1

Treatment Duration and Monitoring

  • Treatment should be maintained for at least 6-12 months 3
  • Regular monitoring of liver function and overall health is essential 3
  • Continue treatment even if patient relapses during therapy 1

Contraindications

Acamprosate is contraindicated in:

  • Patients with hypersensitivity to acamprosate or any components 1
  • Patients with severe renal impairment (CrCl ≤30 mL/min) 1

Pharmacokinetics and Drug Interactions

  • Peak plasma concentrations occur at 3-8 hours post-dose 1
  • Terminal half-life ranges from 20-33 hours 1
  • Primarily excreted unchanged in urine 1
  • No significant drug interactions with alcohol, disulfiram, or diazepam 1
  • When co-administered with naltrexone, acamprosate levels may increase by 25-33%, but no dosage adjustment is needed 1

Clinical Pearls and Pitfalls

Important Considerations

  • Acamprosate does not help with acute alcohol withdrawal symptoms 1
  • Efficacy has not been demonstrated in patients who have not undergone detoxification 1
  • Efficacy has not been adequately assessed in polysubstance abusers 1
  • Contains sodium sulfite, which may cause allergic reactions in susceptible individuals 1

Advantages over Other Medications

  • No hepatotoxicity risk, making it suitable for patients with liver disease 3
  • Can be used in patients who continue drinking alcohol (unlike disulfiram) 4
  • Not metabolized by the liver, making it safe for patients with hepatitis or liver disease 4

Comprehensive Treatment Approach

For optimal outcomes, acamprosate should be used within a comprehensive treatment program:

  • Complete alcohol abstinence should be the primary treatment goal 3
  • Combine with psychosocial interventions such as cognitive behavioral therapy or support groups 3, 1
  • Consider thiamine supplementation (100-300 mg/day) to prevent Wernicke encephalopathy 3

Acamprosate has demonstrated superior long-term outcomes compared to placebo, with studies showing 18.3% of acamprosate-treated patients remaining continuously abstinent at the end of treatment versus 7.1% with placebo 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Alcohol Use Disorder

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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