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Toxicity, Mushroom - Hallucinogens

Last Updated: November 9, 2006
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Synonyms and related keywords: Amanita gemmata, Amanita muscaria, fly agaric, Amanita pantherina, the panther, Amanita phalloides, Amanita verna, Amanita virosa, hallucinogenic fungi, psilocybin-containing mushrooms, Psilocybe caerulipes, Psilocybe cubensis, Gymnopilus spectabilis, Panaeolus species, Panaeolus foenisecii, Psathyrella foenisecii, ibotenic acid, muscimol, hallucinogenic mushroom, fungal hallucinogens, mushroom toxicity, hallucinogen toxicity, hallucinogen poisoning, hallucinogen exposure

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Author: C Crawford Mechem, MD, MS, FACEP, Associate Professor, Department of Emergency Medicine, University of Pennsylvania School of Medicine; Assistant Professor, Department of Pediatric Emergency Medicine, Children's Hospital, Philadelphia; EMS Director, Philadelphia Fire Department

Coauthor(s): Diane Giorgi, MD, Clinical Assistant Professor, Department of Emergency Medicine, Mount Sinai Medical Center

C Crawford Mechem, MD, MS, FACEP, is a member of the following medical societies: American College of Emergency Physicians, National Association of EMS Physicians, and Society for Academic Emergency Medicine

Editor(s): Miguel C Fernandez, MD, FACEP, FAAEM, FACMT, Associate Clinical Professor; Medical and Managing Director, South Texas Poison Center, Department of Surgery/Emergency Medicine and Toxicology, University of Texas Health Science Center at San Antonio; John T VanDeVoort, PharmD, Clinical Assistant Professor, College of Pharmacy, University of Minnesota; Michael Hodgman, MD, Assistant Clinical Professor of Medicine, Department of Emergency Medicine, Bassett Healthcare; John Halamka, MD, Chief Information Officer, CareGroup Healthcare System, Assistant Professor of Medicine, Department of Emergency Medicine, Beth Israel Deaconess Medical Center; Assistant Professor of Medicine, Harvard Medical School; and Asim Tarabar, MD, Assistant Clinical Professor of Emergency Medicine, Yale University School of Medicine; Consulting Staff, Department of Emergency Medicine, Yale-New Haven Hospital

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Background: Hallucinogenic fungi have been used in divinatory or religious contexts for at least 3000 years. However, not until the 1950s were the involved species of fungi identified and the chemical nature of active substances determined.

In general, 2 groups of mushrooms with significant psychoactive effects exist.

  • Mushrooms containing ibotenic acid and muscimol (isoxazoles), including Amanita gemmata, Amanita muscaria (fly agaric), and Amanita pantherina (the panther), comprise the first group. These are not to be confused with deadly Amanita phalloides, Amanita verna, and Amanita virosa. For centuries, A muscaria has been consumed in central Asia as a hallucinogen. Some Siberian tribes report that 3 fresh A muscaria mushrooms can be lethal, while others claim that eating as many as 21 of these mushrooms is safe.

  • Psilocybin-containing mushrooms, including Psilocybe caerulipes, Psilocybe cubensis, Gymnopilus spectabilis, Panaeolus species (eg, Panaeolus foenisecii), and Psathyrella foenisecii, comprise the second group of mushrooms with psychoactive effects.

Mushrooms containing ibotenic acid and muscimol and those containing psilocybin are New World fungal hallucinogens. Reports of toxicity associated with this group of mushrooms have increased because of their growing popularity as hallucinogens.

Pathophysiology: Ibotenic acid is an agonist at central glutamic acid receptors; its decarboxylated derivative is an agonist at gamma-amino butyric acid receptors. Central effects of these hallucinogenic mushrooms are thought to be caused by these actions. Although muscarinic acid originally was isolated from A muscaria, the clinical syndrome does not suggest marked significance; in fact, anticholinergic findings may be observed.

The psilocybin group contains the indoles psilocybin and psilocin. Psilocin and its phosphate ester, psilocybin, are similar in structure to lysergic acid diethylamide (LSD). They are structural analogues of serotonin (5-hydroxytryptamine); thus, hallucinogenic effects probably are mediated through effects on serotonergic receptors.

Frequency:

  • In the US: Estimating frequency of hallucinogenic mushroom use is difficult. Psilocybin-containing mushrooms are popular recreational drugs of abuse.

Mortality/Morbidity: Mortality from hallucinogenic mushrooms is very rare.

Age: While little data exist on the age of users of hallucinogenic mushrooms, college students are known to abuse psilocybin mushrooms.


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History: Hallucinogenic mushrooms usually are ingested for their psychoactive properties.

  • Mushrooms containing ibotenic acid and muscimol
    • Symptoms begin 30 minutes to 1 hour postingestion; however, symptom onset rarely may be delayed as long as 3 hours.
    • Hallucinations may be accompanied by dysarthria, dystaxia, and muscle cramps and may persist for as long as 8 hours. However, a recent case report describes an otherwise healthy 48-year-old man who accidentally ingested A muscaria mushrooms. He experienced a 5-day paranoid psychosis accompanied by visual and auditory hallucinations. By the sixth day, he had returned to baseline, with no long-term adverse effects reported (Brvar, 2006).
    • Central nervous system (CNS) effects range from agitation to coma.
    • Heavy intoxication may cause vomiting, diarrhea, and seizures.
    • Fatal A pantherina poisonings have been reported in the Pacific Northwest.
  • Psilocybin-containing mushrooms
    • Alterations in perception begin within 30 minutes and subside after 6 hours.
    • Widely varying CNS manifestations, including euphoria and visual and religious hallucinations, have been reported. Visual hallucinations may include perceived motion of stationary objects or surfaces.
    • Patients presenting in the ED may experience more unpleasant effects such as fear, agitation, confusion, delirium, psychosis, and schizophrenialike syndromes.
    • Symptoms may include nausea and sympathomimetic activity such as mydriasis and tachycardia.
    • Frequent use may cause transient elevation of hepatic enzymes.
    • Symptoms in children include hyperpyrexia and seizures.

Physical: Predominant findings in these intoxications are neurologic.

Fever, tachycardia, and hypotension may occur because of agitation.

  • Neurologic findings
    • Ataxia
    • Incoordination
    • Confusion
    • Delirium
    • Psychosis
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Abdominal Trauma, Blunt
Toxicity, Anticholinergic
Toxicity, Hallucinogen
Toxicity, Sympathomimetic


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Lab Studies:

  • Serum levels and urine tests for toxins such as muscarine, muscimol, and psilocybin are available but are rarely helpful or necessary in clinical practice. They are more applicable to forensic investigations.
  • Laboratory studies can be helpful in identifying complications of hallucinogenic mushroom abuse, which may include acute renal failure and rhabdomyolysis.

Procedures:

  • Prepare mushroom specimens, if available, for identification. However, an experienced mycologist rather than a physician should make definitive identification. With hallucinogenic mushrooms, definitive identification seldom is necessary.
    • Slice the mushroom stem from the cap very close to the gills and lay the cap on paper with gills down to make a spore print.
    • Make prints on black and white paper. These can be sent to the regional poison control center or its designee for analysis. Whole mushrooms can be sent.
    • Samples should include, if possible, the deeply rooted portion of fungus as well as cap and gills.
    • Do not package samples in plastic because they may decompose rapidly. Place samples in a paper bag with an absorbant, such as a piece of filter paper, to prevent condensation.
    • Exact mushroom identification is ascertained in less than 3% of cases.
    • The widespread availability of digital cameras now makes it possible to rapidly transmit images of mushroom samples to mycologists by means of the Internet. Although making a definitive identification by this method may not be possible, ruling out certain species may be possible.
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Prehospital Care: Prehospital care primarily is supportive with attention to ABCs.

Emergency Department Care: ED care primarily is supportive.

  • Consider gastric lavage if ingestion occurred within approximately 1 hour of presentation. However, no data exist to support efficacy in this setting.
  • Consider activated charcoal.
  • Provide agitated patients with a quiet nonthreatening environment.
  • Consider intravenous fluids if signs of volume depletion are present.
  • Do not treat fever with antipyretics; fever probably is caused by agitation and increased motor activity.
  • Benzodiazepines may be used for sedation and treatment of panic attacks, hallucinations, and seizures.

Consultations: Contact the regional poison center for consultation, referral, and, if necessary, assistance in mushroom identification.
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The goal of pharmacotherapy is to reduce morbidity, prevent complications, and neutralize the toxin.

Drug Category: GI decontaminants -- These agents are the preferred method when GI decontamination is desired. They are generally mixed and given with a cathartic (eg, 70% sorbitol), except in young pediatric patients in whom electrolyte disturbances may be of concern.
Drug Name
Activated charcoal (Liqui-Char) -- Most useful if administered within 2 h of ingestion. Limited outcome studies exist, especially when administration is >1 h after ingestion. Administration of charcoal by itself (in aqueous solution), as opposed to coadministration with a cathartic, is becoming the current practice standard because no studies have shown benefit from cathartics and, while most drugs and toxins are adsorbed within 30-90 min, laxatives take hours to work. Dangerous fluid and electrolyte shifts have occurred when cathartics are used in small children.
When ingested dose is known, charcoal may be given at 10 times ingested dose of agent over 1 or 2 doses. For maximum effect, administer within 30 min of ingesting poison.
Adult Dose1 g/kg PO/NG (50-75 g usual dose)
Pediatric Dose1 g/kg PO/NG (12.5-25 g usual dose)
<2 years: Cathartic administration not recommended
ContraindicationsDocumented hypersensitivity; poisoning or overdosage of mineral acids and alkalies; unprotected airway with absent gag reflex
Interactions May inactivate ipecac syrup if used concomitantly; effectiveness of other medications decreases with coadministration; do not mix with sherbet, milk, or ice cream (decreases adsorptive properties)
Pregnancy C - Safety for use during pregnancy has not been established.
PrecautionsProtect airway prior to administration in patients with absent gag reflex or depressed level of consciousness; when considering repeat dosing, monitor for active bowel sounds to minimize risk
Drug Category: Benzodiazepines -- These agents prevent seizure recurrence and terminate clinical and electrical seizure activity.
Drug Name
Diazepam (Valium) -- Depresses all levels of CNS (eg, limbic and reticular formation), possibly by increasing activity of GABA.
Individualize dosage and increase cautiously to avoid adverse effects.
Adult Dose5-10 mg IV q10-15min until symptoms resolve; not to exceed 30 mg
Pediatric Dose30 days to 5 years: 0.2-0.5 mg IV (slowly) q2-5min until symptoms resolve; not to exceed 5 mg
>5 years: 1 mg IV (slowly) q2-5min until symptoms resolve; not to exceed 10 mg
ContraindicationsDocumented hypersensitivity; hypotension; acute narrow-angle glaucoma
InteractionsIncreases toxicity of benzodiazepines in CNS with coadministration of phenothiazines, H1 blockers, barbiturates, alcohols, and MAOIs
Pregnancy D - Unsafe in pregnancy
PrecautionsCaution with other CNS depressants, low albumin levels, or hepatic disease (may increase toxicity)
Drug Name
Lorazepam (Ativan) -- DOC for treatment of status epilepticus (persists in CNS longer than diazepam). Rate of injection should not exceed 2 mg/min. May be administered IM if unable to obtain vascular access.
Adult Dose0.044 mg/kg (2-4 mg) IV, titrate to effect
Status epilepticus: 4 mg IV over 2-5 min; may repeat second dose in 10-15 min, if needed; not to exceed 8 mg
Pediatric DoseChildren: 0.05 mg/kg IV (range, 0.02-0.1 mg/kg)
Adolescents: Administer as in adults
Status epilepticus:
Neonates: 0.05 mg/kg over 2-5 min; may repeat in 10-15 min, if needed
Infants and children: 0.1 mg/kg over 2-5 min, with second dose of 0.05 mg/kg IV at 10-15 min, if needed; not to exceed 4 mg
Adolescents: 0.7 mg/kg; not to exceed 4 mg, given slowly over 2-5 min, with second dose in 10-15 min, if needed
ContraindicationsDocumented hypersensitivity; preexisting CNS depression; hypotension; narrow-angle glaucoma
InteractionsAlcohol, phenothiazines, barbiturates, and MAOIs increase CNS toxicity
Pregnancy D - Unsafe in pregnancy
PrecautionsMonitor for respiratory depression with high or repeated doses; contains benzyl alcohol, which may be toxic to infants in high doses; caution in renal or hepatic impairment, myasthenia gravis, organic brain syndrome, Parkinson disease, or patients who may have inhibition of benzodiazepine metabolism and clearance (eg, using nicotine, taking cimetidine)
Drug Name
Midazolam (Versed) -- Used as alternative in termination of refractory status epilepticus. Because water soluble, takes approximately 3 times longer than diazepam to peak EEG effects. Thus, clinician must wait 2-3 min to fully evaluate sedative effects before initiating procedure or repeating dose. Has twice the affinity for benzodiazepine receptors than diazepam. May be administered IM if unable to obtain vascular access.
Adult Dose0.01-0.05 mg/kg (usually 0.5-4 mg, not to exceed 10 mg) IV given slowly over several min; may repeat q10-15min until adequate response achieved
Pediatric Dose<32 weeks: 0.5 mcg/kg/min IV infusion
>32 weeks: 1 mcg/kg/min IV infusion
Children: 0.05-0.2 mg/kg IV over 2-3 min, followed by 1-2 mcg/kg/min continuous infusion
Status epilepticus (refractory to standard therapy), >2 months and children: 0.15 mg/kg followed by continuous infusion of 1 mcg/kg/min, titrating dose upward q5min until seizures controlled
ContraindicationsDocumented hypersensitivity; preexisting hypotension; narrow-angle glaucoma; sensitivity to propylene glycol (diluent)
InteractionsSedative effects may be antagonized by theophyllines; narcotics, cimetidine, ethanol, and erythromycin may accentuate sedative effects because of decreased clearance; reduce dose of thiopental by 15% when using together
Pregnancy D - Unsafe in pregnancy
PrecautionsCaution in congestive heart failure, pulmonary disease, renal impairment, hepatic failure, neuromuscular disease, hypotension, and patients >60 y; monitor for respiratory depression with high or repeated doses; consider lower dosages in patients with organic brain syndrome and those who may have inhibition of benzodiazepine metabolism and clearance (eg, using nicotine, taking cimetidine)
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Further Inpatient Care:

Complications:

Patient Education:

  BIBLIOGRAPHY Section 9 of 9   Click here to go to the previous section in this topic Click here to go to the top of this page
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