Evidence map›Paper›PMID 33972296›Full record

ArticleBMJ case reports2021

Hypocomplementemic urticarial vasculitis syndrome presenting with bilateral scleritis.

Ella Claire Berry, Jane Wells, Adrienne Morey, Anthea Anantharajah

Open access · greenAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in BMJ case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

4 authors at 4 institutions in 1 country.

Ella Claire BerryCanberra Health Services Library, ACT Government, Garren, Australian Capital Territory, Australia ella.c.berry@gmail.com.ORCID http://orcid.org/0000-0001-6128-683X
Jane WellsOphthalmology Unit, Canberra Health Services, Garran, Australian Capital Territory, Australia.
Adrienne MoreyACT Pathology, Canberra Health Services, Garran, Australian Capital Territory, Australia.
Anthea AnantharajahDepartment of Immunology, Canberra Health Services, Garran, Australian Capital Territory, Australia.
Act Health · AUAustralian Government · AUAustralian National University · AUFlinders University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare autoimmune disorder characterised by recurrent urticarial lesions and acquired hypocomplementemia with systemic manifestations. The authors present the case of a 70-year-old man who presented to the ophthalmology clinic with bilateral scleritis and ocular hypertension. He was diagnosed with HUVS after a 6-month period of bilateral scleritis, vestibulitis, significant weight loss, mononeuritis multiplex and recurrent urticarial vasculitis with pronounced persistent hypocomplementemia and the presence of anti-C1q antibodies. Disease control was eventually obtained with mycophenolate and prednisolone.

Indexed as

Autoimmune DiseasesScleritisUrticariaVasculitisAgedComplement System ProteinsHumansImmunosuppressive AgentsMaleComplement System ProteinsImmunosuppressive Agentsdermatologyimmunologyophthalmologyvasculitis

Identifiers

PMID33972296
PMCPMC8112411
OpenAlexW3160901325

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.