Evidence map›Paper›PMID 40225232›Full record

ArticleRheumatology advances in practice2025

Urine toxicology screening reduces misdiagnosis of cocaine-induced ANCA-positive disease as idiopathic granulomatosis with polyangiitis.

James Bateman, Mir Nadeem, James Barraclough, Tochukwu Adizie, Mark Pucci, Tom Sheeran

Abstract read
In one paragraph

Article in Rheumatology advances in practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

James BatemanInstitute of Clinical Sciences, College of Medicine and Health, University of Birmingham, Birmingham, UK.ORCID https://orcid.org/0000-0003-1952-2821
Mir NadeemDepartment of Rheumatology, Royal Wolverhampton NHS Trust, Wolverhampton, UK.
James BarracloughDepartment of Rheumatology, Royal Wolverhampton NHS Trust, Wolverhampton, UK.
Tochukwu AdizieDepartment of Rheumatology, Royal Wolverhampton NHS Trust, Wolverhampton, UK.
Mark PucciWest Midlands Poisons Unit, Sandwell and West Birmingham NHS Trust, Birmingham, UK.
Tom SheeranDepartment of Rheumatology, Royal Wolverhampton NHS Trust, Wolverhampton, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Study aims were to assess the impact of urine cocaine screening in distinguishing cocaine-induced midline destruction lesions (CIMDLs) from idiopathic ANCA-associated systemic vasculitis (AASV), to evaluate the adoption and effectiveness of screening and to explore its clinical implications. Methods: We conducted a retrospective single-centre case series, reviewing rheumatology patients with suspected new or relapsing AASV, ages 18-55 years, from April 2021 to July 2024. Patients were in two groups: an active screening group offering urinary cocaine testing for all patients and a standard care group, with ad hoc testing based on clinical suspicion. Demographics, clinical presentations and diagnostic pathways were analysed. Results: Of 11 cases in the active screening group, all denied cocaine use, 7 were diagnosed with CIMDL from urine screening and 4 patients were treated for vasculitis. In the standard care group of 15 patients, 2 patients had CIMDLs (admitted cocaine use), no patients had urine screening and 13 were treated for AASV. In total, there were nine CIMDL cases [mean age 38.2 years (interquartile range 11; six females), most [7/9 (78%)] were from active screening. CIMDL presentations were heterogeneous, including vocal cord palsy, lymphadenopathy and cutaneous vasculitis. CIMDL cases were positive for perinuclear ANCA (6/9) and PR3 (7/9), with no MPO positivity, and 5/9 (71%) failed to provide an adequate initial urine sample. There were no formal complaints or concerns from screening. Conclusion: These data support the effectiveness and acceptability of systematic screening for cocaine to improve the identification of CIMDLs, reducing misdiagnosis and unnecessary treatment. A protocol for systematic screening is proposed to improve the care for these patients.

Indexed as

ANCA-associated vasculitiscocainecocaine-induced midline destruction lesiondrug screeningurine screening

Identifiers

PMID40225232
PMCPMC11993301

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