Evidence map›Paper›PMID 39981027›Full record

ArticleCase reports in nephrology and dialysis

Treatment of Pediatric Colchicine Poisoning with Single-Pass Albumin Dialysis: A Case Report.

Atessa Bahadori, Rishil Patel, Cal Robinson, Steve Balgobin, Michael Zappitelli, Nithiakishna Selvathesan

Abstract readCase Reports
In one paragraph

Article in Case reports in nephrology and dialysis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Atessa BahadoriDepartment of Paediatrics, Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Rishil PatelDepartment of Paediatrics, Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Cal RobinsonDepartment of Paediatrics, Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Steve BalgobinDepartment of Paediatrics, Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Michael ZappitelliDepartment of Paediatrics, Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Nithiakishna SelvathesanDepartment of Paediatrics, Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Colchicine has a narrow therapeutic index, and doses >0.5 mg/kg are considered toxic with a high mortality rate. Case Presentation: A previously healthy 15-year-old presents to the emergency department with abdominal pain and vomiting following intentional ingestion of colchicine (0.56 mg/kg) 12 h prior. By 24 h post-ingestion, they developed a multi-organ injury with hepatic dysfunction, coagulopathy, lactic acidemia, and pancytopenia, which prompted consideration of extracorporeal therapy (ECT). Considering the characteristics of colchicine, they were treated with continuous venovenous hemodiafiltration (CVVHDF) with single-pass albumin dialysis (SPAD) for 42 h. They were subsequently discharged from the intensive care unit 48 h after stopping CVVHDF with normal kidney function, resolved coagulopathy, and resolving pancytopenia and hepatic dysfunction. The rationale for CVVHDF with SPAD was based on the high protein binding, variably high volume of distribution, previous reports showing a sieving coefficient of 0.2 with CVVH, and the high mortality risk. We anticipated a high potential for rebound. Thus, continuous clearance would facilitate redistribution from the extravascular to intravascular space. SPAD was used to enhance the elimination of protein-bound fractions; the principle is that adding albumin to dialysate creates a protein-binding disequilibrium where the drug from the blood side may bind to albumin on the dialysate side. Conclusion: Colchicine ingestion of >0.5 mg/kg is highly toxic, and in addition to supportive management, continuous kidney replacement therapy with SPAD may be considered.

Indexed as

Albumin dialysisColchicineContinuous kidney replacement therapyPediatric dialysisPoisoning

Identifiers

PMID39981027
PMCPMC11735033

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.