Evidence map›Paper›PMID 41583223›Full record

ArticleCureus2025

Fatal Flaw in the Folate Pathway: Methotrexate-Bactrim Interaction, Misleading Levels, and a Cautionary Case.

Shaivya Pathak

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

1 author.

Shaivya PathakInternal Medicine, East Carolina University, Greenville, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methotrexate (MTX) is one of the most commonly prescribed medications for rheumatoid arthritis and other autoimmune disorders. While therapeutic drug monitoring (TDM) protocols are well-established for high-dose MTX (HD-MTX) in oncology, no such validated protocols exist for low-dose MTX (LD-MTX) therapy - the pharmacokinetics are highly variable, and serum concentrations correlate poorly with clinical toxicity. Among the most dangerous drug interactions is the combination of MTX with trimethoprim-sulfamethoxazole (TMP-SMX), which creates synergistic toxicity. This case details a rapid, fatal MTX toxicity event in a patient on stable LD therapy who received a short course of TMP-SMX for cellulitis. Severe pancytopenia and hemorrhagic oral mucositis developed despite a serum MTX concentration of 0.07 μmol/L - well below the commonly accepted toxic threshold. This case underscores that clinicians must prioritize prompt recognition of clinical symptoms over laboratory quantification when risk factors for drug interaction are present.

Indexed as

drug-drug interactionmethotrexate toxicitypancytopeniarheumatoid arthritistrimethoprim-sulfamethoxazole

Identifiers

PMID41583223
PMCPMC12828435

What Socratic holds

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LicenceCC BY
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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 Socratic graph.