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Current fatality rate of suspected cyclopeptide mushroom poisoning in the United States.

AbstractOBJECTIVE:
This study was designed to determine the fatality rate of suspected cyclopeptide-containing mushroom ingestions reported to the National Poison Data System (NPDS).
BACKGROUND:
Although silibinin reportedly improves survival in suspected cyclopeptide-containing mushroom ingestions, the greater than 20% untreated fatality rate that is often cited is based on decades-old data. An ongoing open-label silibinin trial will likely use historical cases as comparators. A recent single poison control center (PCC) study showed a fatality rate of 8.3%. This study was designed to validate those findings in the NPDS.
METHODS:
This study was an 11-year (1/1/2008-12/31/2018) retrospective review of suspected cyclopeptide-containing mushroom ingestions reported to NPDS. Inclusion and exclusion criteria were the same as the ongoing silibinin trial: Age >2-years-old; history of eating foraged mushrooms; gastrointestinal symptoms within 48 h of mushroom ingestion; and aminotransferases above the upper limit of normal within 48 h after ingestion. Each original participating PCC confirmed eligibility, diagnosis, treatment, and outcome on included cases.
RESULTS:
During the study period, 8,953 mushroom exposures were reported to NPDS, of which 296 met inclusion criteria. The PCC survey response rate was 60% (28/47 PCCs), and the individual case response rate was 59% (174/296). Twenty-six cases were subsequently excluded leaving 148 included cases. The overall mortality rate was 8.8% (13/148). Mortality in silibinin/silymarin-treated vs untreated cases was 9.5% (4/42), vs 8.5% (9/106), respectively. A mycologist identified mushrooms in 16.9% of cases (25/148), of which 80% (20/25) were cyclopeptide-containing. Among these confirmed cases, the mortality rate was 10% (1/10) in both silibinin/silymarin-treated and untreated cases.
CONCLUSIONS:
The contemporary mortality rate of patients with presumed cyclopeptide-mushroom poisoning is only 8.8%. This likely represents improved supportive care for patients with acute liver injury and should be considered the current standard for historical controls in the United States.
AuthorsJonathan De Olano, Josh J Wang, Eric Villeneuve, Sophie Gosselin, Rana Biary, Mark K Su, Robert S Hoffman
JournalClinical toxicology (Philadelphia, Pa.) (Clin Toxicol (Phila)) Vol. 59 Issue 1 Pg. 24-27 (Jan 2021) ISSN: 1556-9519 [Electronic] England
PMID32237919 (Publication Type: Journal Article)
Chemical References
  • Antidotes
  • Peptides, Cyclic
  • Silymarin
  • Silybin
Topics
  • Antidotes (therapeutic use)
  • Cause of Death
  • Chemical and Drug Induced Liver Injury (diagnosis, drug therapy, etiology, mortality)
  • Databases, Factual
  • Humans
  • Mortality
  • Mushroom Poisoning (diagnosis, drug therapy, mortality)
  • Peptides, Cyclic (poisoning)
  • Poison Control Centers
  • Prognosis
  • Retrospective Studies
  • Risk Assessment
  • Risk Factors
  • Silybin (therapeutic use)
  • Silymarin (therapeutic use)
  • Time Factors
  • United States

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