Evidence map›Paper›PMID 42124385›Full record

ArticleSeminars in dialysis

Risk of Serious Adverse Events and Death With Low-Dose Methotrexate Versus Hydroxychloroquine in Adults Receiving Dialysis.

Flory T Muanda, Peter G Blake, Matthew A Weir, Fatemeh Ahmadi, Mohammad Ali Omrani, Sheikh S Abdullah, Eric McArthur, Jessica M Sontrop, Brad L Urquhart, Amit X Garg

Abstract readComparative Study
In one paragraph

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

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0citing papers in PubMed
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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

10 authors.

Flory T MuandaICES, Ontario, Canada.ORCID 0000-0003-4682-6564
Peter G BlakeDivision of Nephrology, Department of Medicine, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Matthew A WeirICES, Ontario, Canada.
Fatemeh AhmadiICES, Ontario, Canada.
Mohammad Ali OmraniDepartment of Physiology and Pharmacology, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.ORCID 0000-0001-6847-0699
Sheikh S AbdullahICES, Ontario, Canada.
Eric McArthurICES, Ontario, Canada.
Jessica M SontropDepartment of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Brad L UrquhartDepartment of Physiology and Pharmacology, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Amit X GargICES, Ontario, Canada.

Funding

Academic Medical Organization of Southwestern Ontario, the Schulich School of Medicine and Dentistry, Western UniversityCIHRLawson Health Research InstituteMinistry of Long-Term CareOntario Ministry of Health
6 · The paper itself

Abstract

backgroundSeveral case reports have linked low-dose methotrexate to serious adverse events, including death, in dialysis patients. We compared the risk of serious adverse events in dialysis patients initiating low-dose methotrexate versus hydroxychloroquine.

methodsUsing linked healthcare databases in Ontario, Canada (1997-2020), we identified 55 new users of low-dose methotrexate and 407 new users of hydroxychloroquine. The primary outcome was the 90-day risk of death or hospitalization with myelosuppression, sepsis, pneumotoxicity, or hepatotoxicity. Adjusting for age, sex, and a proxy for polypharmacy, a modified Poisson regression was used to estimate adjusted risk ratios (aRR), and a binomial regression was used to estimate adjusted risk differences (aRD).

resultsThe median prescribed dose was 10 mg/week (IQR, 10-17.5) for methotrexate and 300 mg/day (IQR, 200-400) for hydroxychloroquine. The primary outcome occurred in 16/55 low-dose methotrexate users (29.1%) and in 29/407 hydroxychloroquine users (7.1%); aRR: 3.14 (95% CI, 1.75 to 5.63); aRD: 19.5% (95% CI, 7.5% to 31.4%). Findings were consistent across sensitivity analyses.

conclusionLow-dose methotrexate should be avoided in dialysis patients whenever possible, and alternative DMARDs should be considered.

Indexed as

HydroxychloroquineKidney Failure, ChronicMethotrexateRenal DialysisAdultAgedAntirheumatic AgentsDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedOntarioRetrospective StudiesAntirheumatic AgentsHydroxychloroquineMethotrexatedialysisdosagehydroxychloroquinelow‐dose methotrexatetoxicity

Identifiers

PMID42124385
PMCPMC13511332

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