Cyclopeptide mushroom poisoning: A retrospective series of 204 patients

Author:

Lecot Jérémy1ORCID,Cellier Morgane1,Courtois Arnaud2,Vodovar Dominique345,Le Roux Gaël16,Landreau Anne78,Labadie Magali2,Bruneau Chloé1,Descatha Alexis169

Affiliation:

1. Poison Control Center Angers University Hospital (CHU Angers) Angers France

2. Poison Control Center Bordeaux University Hospital (CHU Bordeaux) Bordeaux France

3. Poison Control Center, Fernand‐Widal‐Lariboisiere Hospital, APHP Federation of Toxicology APHP Paris France

4. UFR medicine Paris University Paris 75010 France

5. Faculty of Pharmacy INSERM UMRS 1144 Paris France

6. University of Angers, CHU Angers, University of Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) ‐ UMR_S1085 Angers France

7. Faculty of Health Angers University Angers France

8. Univ Angers, Univ Brest, IRF, SFR ICAT Angers France

9. Department of Occupational Medicine, Epidemiology and Prevention Donald and Barbara Zucker School of Medicine, Hofstra/Northwell Hempstead New York USA

Abstract

AbstractCyclopeptide mushroom poisoning is responsible for 90%–95% of deaths from macrofungi ingestion. The main objectives of this study are to describe cases of cyclopeptide mushroom poisoning and to determine risk factors that may influence the severity/mortality of poisoned patients. We included all cases of amatoxin toxicity reported to two French Poison Centers from 2013 through 2019. We compared the severity with the Poison Severity Score (PSS) and the outcomes of patients using simple logistic regression and multinomial logistic regression. We included 204 cases of amatoxin toxicity. More than three‐quarters developed an increase in AST and/or ALT (78.1%), and over half developed a decrease in prothrombin ratio (<70%: 53%) and/or Factor V (<70%: 54%). One‐third developed an acute renal injury (AKI). Twelve patients (5.9%) developed post‐poisoning sequelae (persistent kidney injury more than 1 month after ingestion and liver transplant). Five patients (2.5%) received a liver transplant, and nine died (4.4%). The mean time to onset of digestive disorders was shorter in PSS2 and PSS3–4 patients (10.9 ± 3.9/11.3 ± 6.3 h) than in PSS1 patients (14 ± 6.5 h; p < 0.05). Patients who died or developed post‐poisoning sequelae had more frequent cardiovascular comorbidities compared with recovered patients (60.0% versus 29.5%; p < 0.01).

Publisher

Wiley

Subject

Pharmacology,Toxicology,General Medicine

Reference33 articles.

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5. Toxins of Amanita phalloides

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