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. 2021 Jul 24;10(3):82–90. doi: 10.1007/s13670-021-00359-5

Table 2.

Medications for the Maintenance Treatment of Alcohol Use Disorder (AUD)

Medication Acamprosate Disulfiram Naltrexone Gabapentin Topiramate
FDA Approval for AUD? Yes Yes Yes No No
Indications and clinical pearls

For maintenance of abstinence from alcohol for patients who have completed detoxification and are abstinent from alcohol before beginning acamprosate

Preferred in patients with hepatic impairment

For highly motivated patients who have completed detoxification

Cravings are not reduced with disulfiram

Reduces alcohol cravings; can reduce the number of drinks that a daily drinker consumes

Monthly injectable formulation may be helpful for compliance

Off label use: Moderate to severe alcohol use disorder

May be helpful in mild alcohol withdrawal syndrome or patients with neuropathic pain

Off label use: Alcohol use disorder
Mechanism of action Promotes balance between the excitatory and inhibitory neurotransmitters, glutamate and GABA Disrupts the metabolism of alcohol by inhibiting enzyme aldehyde dehydrogenase causing an unpleasant physical reaction when combined with alcohol Blocks opiate receptors that are involved in the rewarding effects of drinking and craving for alcohol Calcium channel blocker and y-aminobutyric acid (GABA) modulator Antagonizes excitatory neurotransmitters (glutamate) and decreases dopamine release in reward pathway

Dosing

Note: For older patients, recommended to start low and go slow with dosing, but can titrate based on response and tolerability

666 mg PO TID

333 mg PO TID (for patients with renal impairment)

Start 125 mg PO daily (must be abstinent from alcohol >12 h), increase to 250 mg daily after several days

Maintenance usually 250–500 mg daily

50 mg PO daily

OR

380 mg IM (gluteal) q4 weeks

Do not initiate therapy until patient is opioid-free for at least 7–10 days (by urinalysis).

Start 300 mg PO daily and increase dose in increments of 300 mg every 1–2 days up to a target dose of 600 mg three times a day

Start 25 mg PO daily and increase dose by 25 mg weekly

Poor tolerability seen in patients on doses greater than 100 mg/day

Common side effects Diarrhea (dose related, transient), weakness, peripheral edema, insomnia, anxiety Skin eruptions (e.g., acne, allergic dermatitis), drowsiness, fatigue, impotence, headache, metallic taste Headache, nausea, somnolence, vomiting Drowsiness, fatigue, dizziness, stomach upset, dry mouth

Dose-related sedative effects (dizziness, drowsiness, fatigue)

Stomach upset, decreased appetite, anorexia, weight reduction, increased anxiety, paresthesias

Contraindications and older adult considerations Because of elevated risk of diminished renal function in people aged >65, baseline and frequent renal function tests (q3–6 months) are important in this population

Contraindicated in severe myocardial disease or coronary occlusion, psychoses, and in those with high levels of impulsivity, suicidality, and hypersensitivity to disulfiram or to other thiuram derivatives

Risk of hepatic toxicity in otherwise healthy adults

Counsel patient that any alcohol ingestion can result in reaction (e.g., cough syrups, mouthwash)

Can precipitate opioid withdrawal

Do not use in patients with hepatitis or other liver dysfunction

Do not use in chronic kidney disease

May cause respiratory depression in older adults

Increased risk of falls due to somnolence

Can exacerbate myasthenia gravis

Extended-release formulation contraindicated with recent alcohol use (6 h prior or after dose) and patients with metabolic acidosis with concomitant metformin use

Risk of weight loss and short and long-term cognitive impairment (even at low doses, i.e., ≤100 mg/day) makes it not a first line treatment for AUD in older adults