Back to research feed

Clinical toxicology (Philadelphia, Pa.)

May 6, 2026 · via Europe PMC

A large pediatric cohort of colchicine intoxication: prognostic factors and experience with rapid sequence apheresis.

Kesici S, Saritas Nakip O, Korgal N, Bayrakci B.

Observational StudyAbstract only — full text under license

AI summary — for doctors, generated from the abstract only

Pediatric colchicine poisoning can cause cardiovascular toxicity at lower doses than traditionally reported, and diarrhea signals risk.

What was studied

Retrospective PICU cohort of 84 children (2011-2025), with 17 given rapid sequence apheresis.

Key findings

  • Cardiovascular involvement rose with dose (20.6%, 50%, 71.4%)
  • Diarrhea raised odds of cardiovascular complications (OR 3.24)
  • Thresholds above 0.39 mg/kg or 24 mg total predicted cardiovascular toxicity; five patients died

Clinical relevance

Informs risk stratification and observation.

Who should care

Emergency Medicine

Limitations

Retrospective, single PICU, apheresis benefit not established.

Treat colchicine ingestions seriously even at modest doses and watch for diarrhea.

This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.

Abstract

Introduction

Severe colchicine intoxication often leads to multi-organ failure and death. With no specific antidote and ineffective conventional elimination methods, we hypothesized that rapid sequence apheresis could reduce the intravascular colchicine reservoir. This study describes pediatric colchicine poisoning, focusing on dose-related outcomes and the clinical role of rapid sequence apheresis.

Methods

This retrospective observational analysis included children admitted to a tertiary pediatric intensive care unit for colchicine poisoning (2011-2025). Clinical data, ingested dose, organ involvement, and patient characteristics were evaluated. Logistic regression and ROC analyses were used to identify variables associated with disease severity and poor outcomes, including those treated with rapid sequence apheresis.

Results

Eighty-four patients were included (median dose: 0.3 mg/kg). Across dose groups (0.8 mg/kg), higher doses correlated with increased frequency of diarrhea (20.6%, 57.1%, and 57.1%, respectively, P = 0.071) and cardiovascular involvement (20.6%, 50%, and 71.4%, respectively; P = 0.004). Logistic regression showed that diarrhea significantly increased the likelihood of cardiovascular complications (OR: 3.24, P = 0.006). The ROC analysis identified thresholds of >0.39 mg/kg and >24 mg total dose as predictors of cardiovascular toxicity. Seventeen patients (20.2%) underwent rapid sequence apheresis. Despite advanced supportive care, five patients died, including two who ingested <0.5 mg/kg and received rapid sequence apheresis.

Discussion

Our findings suggest that higher ingested doses and early gastrointestinal manifestations such as diarrhea may serve as indicators of increased risk for cardiovascular complications in pediatric colchicine intoxication. In addition, clinically significant toxicity may occur at doses lower than traditionally reported thresholds.

Conclusion

Pediatric colchicine intoxication may lead to significant cardiovascular complications even at relatively lower doses. Early recognition of high-risk clinical indicators, including gastrointestinal symptoms, leukocytosis, and ingested dose, may facilitate clinical risk stratification and early identification of patients at increased risk of adverse outcomes. Rapid sequence apheresis was used in selected severe cases in our cohort; however, its therapeutic role requires further investigation.

DOI

10.1080/15563650.2026.2657988

PMID

42089449

Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.

Want more like this?

Browse more from the feed. A free account unlocks the full feed, saving and communities.

Back to the research feed

Create a free account · Sign in