Table 2. Medication-assisted Therapy for AUD in ALD.
Medication | Dosing | Mechanism | Treatment considerations for AUD in ALD |
---|---|---|---|
Naltrexone | 50–150 mg QD; 380 mg IM monthly | Opioid receptor antagonist | FDA approved for AUD; a large number of studies show efficacy; no RCTs in ALD patients. It is heavily metabolized by liver and while hepatotoxicity risk is rare it may occur at high doses |
Acamprosate | 333–666 mg TID | NMDA receptor antagonist | FDA approved for AUD, a large number of studies show efficacy; no RCTs in ALD patients. No hepatic metabolism but it is contraindicated in severe renal insufficiency |
Topiramate | 100–400 mg BID | GABA and glutamate modulator | RCTs with a dose escalation design showed efficacy; no RCTs in ALD patients |
Ondansetron | 1–16 microg/kg BID | 5-HT3 receptor antagonist | One RCT showed reduced drinking in the more severe AUD type 2; no RCTs in ALD patients. Hepatic metabolism but no reports of toxicity |
Gabapentin | 600–1,800 mg TID | GABA modulator | RCTs with comorbid anxiety disorders and insomnia showed efficacy; no RCTs in ALD patients. Minimal hepatic metabolism and no reports of hepatotoxicity. Dose adjustments for ESRD |
Baclofen | 10–60 mg TID | GABAB receptor agonist | One RCT evidence for efficacy in advanced ALD Minimal hepatic metabolism and no reports of toxicity |
ALD, alcohol-related liver disease; AUD, alcohol use disorder; QD, once a day; NMDA, N-methyl-D-aspartate; IM, intramuscular; RCT, randomized controlled trial.