Evidence map›Paper›PMID 35236714›Full record

SynthesisClinical journal of the American Society of Nephrology : CJASN2022

Extracorporeal Treatment for Methotrexate Poisoning: Systematic Review and Recommendations from the EXTRIP Workgroup.

Marc Ghannoum, Darren M Roberts, David S Goldfarb, Jesper Heldrup, Kurt Anseeuw, Tais F Galvao, Thomas D Nolin, Robert S Hoffman, Valery Lavergne, Paul Meyers and 5 more

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Clinical journal of the American Society of Nephrology : CJASN, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

17 citing papers in PubMed, 11 citations in OpenAlex.

  1. Toxidromes.Nature reviews. Disease primers · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Beyond the budget impact model: A case study for glucarpidase and the real cost of managing curable toxicities.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2025
    Article
  7. Article
  8. Review
  9. Review
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  12. Article
  13. Review
  14. Article
  15. Article
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  17. Article
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

15 authors at 9 institutions in 6 countries.

Marc GhannoumResearch Center, CIUSSS du Nord-de-l'île-de-Montréal, University of Montreal, Montreal, Quebec, Canada.ORCID 0000-0002-4794-4127
Darren M RobertsDepartment of Clinical Pharmacology and Toxicology, St Vincent's Hospital, Sydney, New South Wales, Australia; and St Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia; and Drug Health Services, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.ORCID 0000-0001-9101-7577
David S GoldfarbNephrology Division, NYU Langone Health and NYU Grossman School of Medicine, New York, New York.
Jesper HeldrupChildhood Cancer and Research Unit, University Children's Hospital, Lund, Sweden.ORCID 0000-0002-6211-1967
Kurt AnseeuwDepartment of Emergency Medicine, ZNA Stuivenberg, Antwerp, Belgium.
Tais F GalvaoSchool of Pharmaceutical Sciences, University of Campinas, Campinas, Sao Paulo, Brazil.
Thomas D NolinDepartment of Pharmacy and Therapeutics, and Department of Medicine Renal-Electrolyte Division, University of Pittsburgh Schools of Pharmacy and Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0003-4339-1382
Robert S HoffmanDivision of Medical Toxicology, Ronald O. Perelman Department of Emergency Medicine, NYU Grossman School of Medicine, New York, New York.
Valery LavergneResearch Center, CIUSSS du Nord-de-l'île-de-Montréal, University of Montreal, Montreal, Quebec, Canada.
Paul MeyersDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
Sophie GosselinCentre Intégré de Santé et de Services Sociaux (CISSS) de la Montérégie-Centre Emergency Department, Hôpital Charles-Lemoyne, Greenfield Park, Quebec, McGill University Emergency Department, Montreal, Quebec and Centre Antipoison du Québec, Quebec, Canada.
Tudor BotnaruEmergency Department, Lakeshore General Hospital, CIUSSS de l'Ouest-de-l'lle-de-Montreal, McGill University, Montreal, Quebec, Canada.
Karine MardiniPharmacy Department, Verdun Hospital, CIUSSS du Sud-Ouest-de-l'ïle-de-Montréal, University of Montreal, Montreal, Quebec, Canada.
David M WoodClinical Toxicology, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, United Kingdom.ORCID 0000-0002-7826-7237
EXTRIP workgroup
New York University · USUniversité de Montréal · CACentre Intégré Universitaire de Santé et de Services Sociaux du Centre-Sud-de-l'Île-de-Montréal · CAGuy's and St Thomas' NHS Foundation Trust · GBMcGill University · CAMemorial Sloan Kettering Cancer Center · USUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Pittsburgh · USZiekenhuisnetwerk Antwerpen Stuivenberg · BE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Methotrexate is used in the treatment of many malignancies, rheumatological diseases, and inflammatory bowel disease. Toxicity from use is associated with severe morbidity and mortality. Rescue treatments include intravenous hydration, folinic acid, and, in some centers, glucarpidase. We conducted systematic reviews of the literature following published EXtracorporeal TReatments In Poisoning (EXTRIP) methods to determine the utility of extracorporeal treatments in the management of methotrexate toxicity. The quality of the evidence and the strength of recommendations (either "strong" or "weak/conditional") were graded according to the GRADE approach. A formal voting process using a modified Delphi method assessed the level of agreement between panelists on the final recommendations. A total of 92 articles met inclusion criteria. Toxicokinetic data were available on 90 patients (89 with impaired kidney function). Methotrexate was considered to be moderately dialyzable by intermittent hemodialysis. Data were available for clinical analysis on 109 patients (high-dose methotrexate [>0.5 g/m

Indexed as

Drug OverdoseDrug-Related Side Effects and Adverse ReactionsPoisoningHumansLeucovorinMethotrexateObservational Studies as TopicRenal DialysisLeucovorinMethotrexateextracorporeal treatmentEXTRIPglucarpidasehemodialysismethotrexatenephrotoxicitytoxicity

Identifiers

PMID35236714
PMCPMC8993465
OpenAlexW4214911320

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.