Evidence map›Paper›PMID 31243203›Full record

ArticleInternal medicine (Tokyo, Japan)2019

Anti-proteinase 3-positive Eosinophilic Granulomatosis with Polyangiitis Revealed by Cardiac Tamponade.

Yuji Yamamoto, Yasushi Otani, Fukuko Okabe, Midori Yoneda, Osamu Morimura, Kinya Abe

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2019. 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
0.3field-weighted citation impact, top 34% 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, 3 citations in OpenAlex.

  1. Review
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

6 authors at 1 institution in 1 country.

Yuji YamamotoDepartment of Internal Medicine, Toyonaka Municipal Hospital, Japan.
Yasushi OtaniDepartment of Internal Medicine, Toyonaka Municipal Hospital, Japan.
Fukuko OkabeDepartment of Internal Medicine, Toyonaka Municipal Hospital, Japan.
Midori YonedaDepartment of Internal Medicine, Toyonaka Municipal Hospital, Japan.
Osamu MorimuraDepartment of Internal Medicine, Toyonaka Municipal Hospital, Japan.
Kinya AbeDepartment of Internal Medicine, Toyonaka Municipal Hospital, Japan.
Toyonaka Municipal Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis characterized by asthma, eosinophilia, and diffuse eosinophilic infiltration. Although cardiovascular involvement is common and a leading cause of EGPA-related mortality, severe pericarditis-led cardiac tamponade occurs rarely. We herein report a 72-year-old man with anti-proteinase 3 (anti-PR3) anti-neutrophil cytoplasmic antibody (ANCA)-positive EGPA diagnosed by the presence of cardiac tamponade, which responded quickly to pericardiocentesis and a single administration of prednisolone. This is the first case of anti-PR3 ANCA-positive EGPA with cardiac tamponade; the patient displayed clinical features of both ANCA-positive and ANCA-negative cases.

Indexed as

AgedAntibodies, Antineutrophil CytoplasmicCardiac TamponadeDiagnosis, DifferentialEchocardiographyEosinophiliaGranulomatosis with PolyangiitisHumansMaleMyeloblastinTomography, X-Ray ComputedAntibodies, Antineutrophil CytoplasmicMyeloblastinanti-proteinase 3 anti-neutrophil cytoplasmic antibodiescardiac tamponadeChurg-Strauss syndromeeosinophilic granulomatosis with polyangiitispericarditis

Identifiers

PMID31243203
PMCPMC6859378
OpenAlexW2955926245

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.