eMedicine Specialties > Psychiatry > Addiction

Amphetamine-Related Psychiatric Disorders: Treatment & Medication

Author: Michael Larson, DO, Clinical Instructor, Department of Child and Adolescent Psychiatry, Harvard University
Contributor Information and Disclosures

Updated: Jan 29, 2008

Treatment

Medical Care

Initial treatment should include medically stabilizing the patient's condition by assessing his or her respiratory, circulatory, and neurologic systems. The offending substance may be eliminated by means of gastric lavage and acidification of the urine. Psychotropic medication can be used to stabilize an agitated patient with psychosis. Because most cases of amphetamine-related psychiatric disorders are self-limiting, removal of the amphetamines should suffice.

  • Induced emesis, lavage, or charcoal may be helpful in the event of overdose.
  • The excretion of amphetamines can be accelerated by the use of ammonium chloride, given either IV or orally (PO).
    • Amphetamine intoxication can be treated with ammonium chloride, often found in OTC expectorants, such as ammonium chloride (Quelidrine), baby cough syrup, Romilar, and P-V-Tussin.
    • The recommended dose to acidify the urine is ammonium chloride 500 mg every 2-3 hours.
    • The ingredients in OTC cough syrups vary, and the clinician should become familiar with 1 or 2 stock items for use in the emergency department.
    • Ammonium chloride (Quelidrine), an OTC expectorant, can be used in the absence of liver or kidney failure.
  • Administer IV fluids to provide adequate hydration.
  • If the patient is psychotic or if he or she is in danger of harming him or herself or others, a high-potency antipsychotic, such as haloperidol (Haldol), can be used. Exercise caution because of the potential for extrapyramidal symptoms, such as acute dystonic reactions, and neuroleptic malignant syndrome.
  • Agitation also can be treated cautiously with benzodiazepines PO, IV, or intramuscularly (IM). Lorazepam (Ativan) and chlordiazepoxide (Librium) are commonly used.
  • Administer naloxone (Narcan) in the event of concurrent opiate toxicity. Use caution to avoid precipitation of acute opioid withdrawal in a patient who has used high doses of opioid on a long-term basis.
  • Beta-blockers, such as propranolol (Inderal), can be used in the event of elevated blood pressure and pulse. They also may be helpful with anxiety or panic.
  • Psychiatric hospitalization may be necessary when psychosis, aggression, and suicidality cannot be controlled in a less restrictive environment.

Consultations

  • Neurologist
  • Internal medicine specialist
  • Psychiatrist: Consult for inpatient substance abuse treatment or further psychiatric stabilization.
  • Social services: Social services coordinate outpatient services, such as Alcoholics Anonymous and Narcotics Anonymous meetings and sober houses, and provide appointments. Some large metropolitan areas have groups that specifically focus on crystal methamphetamine abuse in the gay population.

Activity

Patients intoxicated with amphetamines are dangerous, and their activity should be limited (eg, no driving) until their symptoms have resolved.

Medication

Several psychiatric conditions can be associated with amphetamine intoxication and withdrawal, all of which may require different management strategies. However, amphetamine-related psychiatric disorders are typically self-limited and usually remit on their own.

Amphetamine-related psychiatric disorders occur most often during intoxication; therefore, treatment should focus on controlling medical and psychiatric symptoms while eliminating the offending substance. Medical therapy involves stabilizing agitation and minimizing psychosis. Gastric lavage directly removes the amphetamines before they have an opportunity to be absorbed. Medication and charcoal eliminate amphetamines from the gastrointestinal and circulatory systems.

If the induced disorders persist and interfere with the patient's social and occupational functioning, treatment should be related to the remaining psychiatric symptoms. Antidepressants, such as sertraline (Zoloft), fluoxetine (Prozac), paroxetine (Paxil), and citalopram (Celexa), can be used to treat depression. Antimanic agents, such as valproic acid (Depakote), carbamazepine (Tegretol), and lithium carbonate, can be used to treat mania. Anxiety can be treated with nonbenzodiazepine drugs, such as beta-blockers and antimanic agents.

Data from recent studies suggest typical antipsychotics (haloperidol thioridazine, Thorazine, etc) may increase amphetamine and cocaine cravings in patients with dual diagnoses of amphetamine and cocaine abuse. Typical antipsychotics should be used for acute stabilization with the intention of switching to an atypical antipsychotic drug (eg, risperidone, quetiapine, olanzapine, aripiprazole, and ziprasidone) for long-term use.

For the purposes of this discussion, specific treatment of amphetamine toxicity is reviewed. For further information, please refer to the articles on Depression, Substance-Induced Mood Disorder, Depressed Type, Bipolar Affective Disorder, Schizophrenia, Anxiety Disorders, and Sleeping Disorders.

Antipsychotics

Clinicians should select a high-potency antipsychotic that is available in tablet, liquid, and IM forms for administration in emergency situations. Antipsychotics help control psychotic symptoms and provide rapid tranquilization of the agitated and psychotic patient.


Haloperidol (Haldol)

Provides rapid sedation of agitated anxious patient; available PO and IM, allowing for flexible, emergency administration.

Adult

2-5 mg PO/IV/IM

Pediatric

0.5-2 mg PO/IV/IM

May increase TCA serum concentrations and hypotensive action of antihypertensive agents; phenobarbital or carbamazepine may decrease effects; coadministration with anticholinergics may increase intraocular pressure; encephalopathy-like syndrome associated with concurrent administration of lithium

Documented hypersensitivity; narrow-angle glaucoma; bone-marrow suppression; severe cardiac or liver disease; severe hypotension; subcortical brain damage

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in severe cardiovascular disease and in patients receiving anticonvulsants, anticoagulants, or rifampin; may increase prolactin levels; may cause extrapyramidal symptoms of muscle rigidity, inability to walk or talk, akathisia, and dystonia (opisthotonos and oculogyric crisis); extrapyramidal symptoms readily treated with benztropine mesylate (Cogentin), diphenhydramine (Benadryl) PO/IV/IM, or trihexyphenidyl (Artane)


Thiothixene (Navane)

Blocks postsynaptic blockade of CNS dopamine receptors, inhibiting dopamine-mediated effects. PO and IM forms allow for rapid tranquilization.

Adult

5-20 mg PO/IM single dose or divided throughout day

Pediatric

2.5-10 mg PO/IM single dose or divided throughout day

Decreases effects of guanethidine; increases toxicity of CNS depressants, anticholinergics, and alcohol

Documented hypersensitivity; lactation; circulatory collapse; comatose; CNS depression by any cause; blood dyscrasias

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Increases prolactin levels; increases photosensitivity; caution in cardiovascular disease and history of convulsions or state of alcohol withdrawal (may precipitate seizures); may cause extrapyramidal symptoms of muscle rigidity, inability to walk or talk, akathisia, and dystonia (opisthotonos and oculogyric crisis); extrapyramidal symptoms readily treated with benztropine mesylate (Cogentin), diphenhydramine (Benadryl) PO/IV/IM, or trihexyphenidyl (Artane)

Benzodiazepines

These drugs are primarily used to sedate agitated patients. Availability in PO, IV, and IM forms allowing the drug to be used in emergency situations. Caution must be used in the violent, aggressive patient because benzodiazepines may cause disinhibition.


Lorazepam (Ativan)

Provides rapid onset and efficacy in sedating aggressive patient; flexible administration in emergency situation.

Adult

5-10 mg PO/IV/IM single dose or divided over 24 h

Pediatric

1-5 mg PO/IV/IM single dose or divided throughout day

Toxicity of benzodiazepines in CNS increases with concurrent alcohol, phenothiazines, barbiturates, or MAOIs

Documented hypersensitivity; preexisting CNS depression; hypotension; narrow-angle glaucoma

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Because of concern of sedation in elderly and debilitated patients, initial doses should be 2 mg; caution in renal or liver failure; paradoxical excitement can occur, resulting in rage behavior; should be used with caution in patients who are depressed and at risk of suicide


Chlordiazepoxide (Librium, Libritabs, Mitran)

Depresses all levels of CNS, including limbic and reticular formation, possibly by increasing activity of gamma-aminobutyric acid (GABA) activity, major inhibitory neurotransmitter.

Adult

25-50 mg PO and repeat in 2-4 h if necessary

Pediatric

Not established

Coadministration with alcohols, phenothiazines, barbiturates, and MAOIs increases CNS toxicity; cisapride can significantly increase levels

Documented hypersensitivity; narrow-angle glaucoma

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in patients receiving other CNS depressants or with low albumin levels or hepatic failure

Opiate antagonists

These drugs inhibit the action of opiates.


Naloxone (Narcan)

Used to treat concurrent opiate toxicity. Consider in patients with altered mental status due to opiate overdose. Poorly absorbed PO route and should be administered IM or IV. Available in IV, IM, and SC forms. Use caution to avoid precipitating acute opioid withdrawal in patient using opioids long term.

Adult

0.4-2 mg IV/IM/SC/ET

Pediatric

Not established

Decreases analgesic effects of narcotics

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in cardiovascular disease; naloxone may precipitate withdrawal symptoms in patients addicted to opiates

Beta-blockers

Propranolol (Inderal) is useful in patients who are agitated, anxious, and hyperarousable because of amphetamines. They are temporarily used until the amphetamine is eliminated from the patient's system. For some patients, anxiety can be prolonged, and nonaddictive beta-blockers may be helpful.


Propranolol (Inderal)

Antihypertensive agent useful in psychiatry to treat anxiety and impulse control. Often well tolerated with minimal effect on hemodynamics of blood pressure and pulse.

Adult

Immediate control of anxiety: 40 mg PO 1 dose
Persistent anxiety: 10 mg PO hs to 40 mg bid as initial dose, reaching maintenance dose not to exceed 120-240 mg qd

Pediatric

Acute anxiety: 0.5 mg/kg PO 1 dose
Persistent anxiety: 1 mg/kg PO per dosage schedule (0.5 mg/kg bid)

Coadministration with aluminum salts, barbiturates, NSAIDs, penicillins, calcium salts, cholestyramine, and rifampin may decrease effects; calcium channel blockers, cimetidine, loop diuretics, and MAOIs may increase toxicity; may increase toxicity of hydralazine, haloperidol, benzodiazepines, and phenothiazines

Toxicity of benzodiazepines in CNS increases with concurrent alcohol, phenothiazines, barbiturates, or MAOIs; cardiogenic shock; sinus bradycardia; bronchial asthma; heart failure

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Not indicated for hypertensive emergencies; use with caution in impaired renal or liver function; may reduce intraocular pressure and should be used with caution in glaucoma because withdrawal can cause rebound increase in intraocular pressure

Expectorants

Expectorants are used to acidify the urine and increase amphetamine excretion when intoxication from amphetamines has resulted in psychiatric and medical complications. These agents are available in PO form, and the patient must be able to swallow or receive a nasogastric tube.


Ammonium chloride (Quelidrine)

Commonly used as OTC expectorant; acidifies urine at high doses. Safe and easy to use.

Adult

Acidification of urine: 500 mg PO/IV q2-4h
As expectorant: 300 mg PO/IV q2-4h

Pediatric

Not established

May reduce aspirin, chlorpropamide, ephedrine, methadone, pseudoephedrine, spirolactone, and para aminosalicylic acid

Documented hypersensitivity; severe hepatic and renal dysfunction; primary respiratory acidosis

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in hepatic and renal impairment

Adsorbents

These agents, given through a nasogastric tube into the stomach, absorb intentionally and accidentally ingested substances to prevent their further absorption into the systemic circulation.


Activated charcoal suspension (Actidose-aqua, Inst-Aqua, Liquid-Char)

Bottles and tubes. Use long after amphetamine ingestion can reduce systemic levels by adsorbing amphetamines recirculating through gastric mucosa.

Adult

Bottle: 25-50 mg PO; dose depends on size of patient
Tube: 15-50 mg PO; dose depends on size of patient

Pediatric

Bottle: 25-50 mg PO; dose depends on size of patient; should begin with 15 mg in children and increase to 50 mg in adolescents; safe and well tolerated
Tube: 15-50 mg; dose depends on size of patient; should begin with 15 mg in children and increase to 50 mg in adolescents; safe and well tolerated

May inactivate ipecac syrup if used concomitantly; effectiveness of other medications decreases with coadministration; do not mix charcoal with sherbet, milk, or ice cream (decreases adsorptive properties)

Documented hypersensitivity; poisoning or overdosage of mineral acids and alkalies

Pregnancy

A - Fetal risk not revealed in controlled studies in humans

Precautions

Not effective in ethanol, methanol, or iron-salt poisoning; induce emesis before administration; after emesis with ipecac syrup, patient may not tolerate for 1-2 h; can administer in early stages of gastric lavage; without sorbitol, gastric lavage returns black

More on Amphetamine-Related Psychiatric Disorders

Overview: Amphetamine-Related Psychiatric Disorders
Differential Diagnoses & Workup: Amphetamine-Related Psychiatric Disorders
Treatment & Medication: Amphetamine-Related Psychiatric Disorders
Follow-up: Amphetamine-Related Psychiatric Disorders
References

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Further Reading

Keywords

amphetamine-induced psychotic disorders, amphetamine-induced psychosis, amphetamine, amphetamine derivatives, methamphetamine, dextroamphetamine, 3, 4-methylenedioxymethamphetamine, MDMA, cathinone, methcathinone, ecstasy, XTC, methamphetamine, crystal meth, crystal methamphetamine, ice, khat, Catha edulis Forsk, Qat tree, psychosis, delusions, hallucinations, depression, bipolar affective disorder, schizophrenia, sleep disorders, delirium, para -methoxyamphetamine, PMA, 2, 5-dimethoxy-4-bromo-amphetamine, DOB, 3, 4-methylenedioxyamphetamine, MDA

Contributor Information and Disclosures

Author

Michael Larson, DO, Clinical Instructor, Department of Child and Adolescent Psychiatry, Harvard University
Michael Larson, DO is a member of the following medical societies: American Academy of Addiction Psychiatry, American Academy of Child and Adolescent Psychiatry, American Medical Association, and Massachusetts Medical Society
Disclosure: Nothing to disclose.

Medical Editor

Denis F Darko, MD, Director, Central Nervous System Clinical Research, Clinical Science, Green Hospital
Denis F Darko, MD is a member of the following medical societies: American Academy of Sleep Medicine, American College of Physicians, American Medical Association, American Psychiatric Association, American Psychosomatic Society, and Endocrine Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Eduardo Dunayevich, MD, Adjunct Assistant Professor, Department of Psychiatry, University of Cincinnati; Clinical Research Physician, Neuroscience, Lilly Research Laboratories
Eduardo Dunayevich, MD is a member of the following medical societies: American Psychiatric Association
Disclosure: Nothing to disclose.

CME Editor

Harold H Harsch, MD, Program Director of Geropsychiatry, Department of Geriatrics/Gerontology, Associate Professor, Department of Psychiatry and Department of Medicine, Froedtert Hospital, Medical College of Wisconsin
Harold H Harsch, MD is a member of the following medical societies: American Psychiatric Association
Disclosure: lilly Honoraria Speaking and teaching; BMS Honoraria Speaking and teaching; Forest Labs Honoraria Speaking and teaching; AstraZeneca Honoraria Speaking and teaching; Pfizer Grant/research funds Other; Northstar Grant/research funds Other; Novartis  Other

Chief Editor

Stephen Soreff, MD, President of Education Initiatives, Nottingham, NH; Faculty, Metropolitan College of Boston University, Boston, MA
Stephen Soreff, MD is a member of the following medical societies: American College of Mental Health Administration and American Psychosomatic Society
Disclosure: Nothing to disclose.

 
 
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