Mushroom toxicity: Difference between revisions
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##Diaphoresis, muscle fasciculations, miosis, bradycardia, bronchorrhea | ##Diaphoresis, muscle fasciculations, miosis, bradycardia, bronchorrhea | ||
##Resolves in 4-12hr | ##Resolves in 4-12hr | ||
#Disulfiram-like effect | |||
## Usually when drinking alcohol | |||
## Flushing, tachycardia, diaphoresis, hypotension | |||
===Treatment=== | ===Treatment=== | ||
Revision as of 20:42, 21 May 2014
Background
- Two categories:
- Early-Onset Poisoning
- Toxicity begins within 2hr of ingestion; clinical course is usually benign
- Late-Onset Poisoning
- Toxicity begins 6hr after ingestion; clinical course is often serious/ possibly fatal
- Early-Onset Poisoning
Early-Onset Poisoning
- Comprises majority of mushroom-induced intoxications
Clinical Features
- Depends on the type of mushroom ingested
- GI
- Nausea/vomiting/diarrhea
- Resolves within 24hr
- CNS
- Euphoria, hallucinations
- Lasts 4-6hr
- Muscarinic
- SLUDGE symptoms
- Diaphoresis, muscle fasciculations, miosis, bradycardia, bronchorrhea
- Resolves in 4-12hr
- Disulfiram-like effect
- Usually when drinking alcohol
- Flushing, tachycardia, diaphoresis, hypotension
Treatment
- GI predominant symptoms:
- Activated charcoal 0.5-1gm/kg
- Do not give antidiarrheal meds
- CNS predominant symptoms:
- Place in dark, quiet room
- Benzos may be given to pts who are agitated
- Muscarinic predominant symptoms:
- Consider atropine for severe symptoms; 0.5-1mg IV for adults; 0.01mg/kg IV for peds
Disposition
- Discharge once symptoms have subsided
Delayed-Onset Poisoning
- Amanita species causes 95% of deaths
- Toxin inhibits formation of mRNA and is heat stable
Amanita phalloides
Clinical Findings
- Stage 1 (GI)
- Occurs 6-24hr after ingestion and lasts 12-24hr
- The later the onset of symptoms the better the outcome
- GI predominant symptoms:
- Abd pain, vomiting and diarrhea (which may become bloody)
- Stage 2 (convalescent)
- Occurs 48hr after ingestion and lasts 12-24hr
- Symptoms subside and pt appears better
- Liver deteriorates silently and precipitously (LFTs begin to rise)
- Stage 3 (failure)
- Occurs 2-4d after ingestion
- Fulminant liver failure
- Hyperbilirubinemia, coagulopathy, hepatic encephalopathy, hepatorenal syndrome
Treatment
- Immediate therapy
- Activated charcoal
- Some advocate repeated doses during the first 24hr
- Amatoxin undergoes enterohepatic circulation
- Some advocate repeated doses during the first 24hr
- Penicillin
- High doses 1 mil units/kg/d effective in animal studies (inhibits amatoxin uptake)
- Silibinin (milk thistle)
- Free radical scavenger used successfully in Europe; 25-50mg/kg/d
- Activated charcoal
- Ongoing therapy
- Glucose monitoring
- Hypoglycemia is one of the most common causes of death in early mushroom toxicity
- Liver/renal failure monitoring
- Serial LFTs, chem, coags
- Prepare for liver transplant
- Progressive coagulopathy, encephalopathy, renal failure are indications for transplant
- Glucose monitoring
Disposition
- Admit all pts suspected of ingesting amatoxin containing mushrooms for at least 48hr
Gyromitra mushrooms
- also known as "brain fungi"
- inhibits formation of Vitamin B6 and BAGA
Clinical findings
- GI upset, fatigue, muscle cramps
- Can present with refractory seizures
Treatment
- Supportive care
- High dose pyridoxine for refractory seizures (5g IV initially)
Crotinarius mushrooms
- contain toxin Orellanine
Clinical findings
- Headache, chills, malaise, nausea and vomiting over days
- Can see delayed renal failure 1-3 weeks after exposure
Treatment
- Supportive
- If renal failure from mushroom exposure, recovery can take several weeks. May need temporary hemodialysis.
Source
Tintinalli
