Evidence map›Paper›PMID 37161084›Full record

GuidelineNature reviews. Rheumatology2023

Evidence-Based Guideline for the diagnosis and management of eosinophilic granulomatosis with polyangiitis.

Giacomo Emmi, Alessandra Bettiol, Elena Gelain, Ingeborg M Bajema, Alvise Berti, Stella Burns, Maria C Cid, Jan W Cohen Tervaert, Vincent Cottin, Eugenia Durante and 20 more

Registry-linked trialOpen access · greenAbstract readPractice GuidelineReview
PubMed Publisher
In one paragraph

Guideline in Nature reviews. Rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07591753 (Assessing The Long-Term Effectiveness and Safety of Mepolizumab 300mg/Month in the European Real-Life Setting), which is not on this map. Cited by 191 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
191citing papers in PubMed, 4 pooled it
68.0field-weighted citation impact, top 1% 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.

NCT07591753 completednot on this mapstarted 2025, after this paper: background citation

Assessing The Long-Term Effectiveness and Safety of Mepolizumab 300mg/Month in the European Real-Life Setting (Mepo Long-term Study)

TypeobservationalSponsorEuropean EGPA Study GroupRan2025 to 2026Enrolled591ConditionsEosinophilic Granulomatosis With Polyangiitis (Churg-Strauss) (EGPA)ArmsMepolizumab 300 mg
3 · Its place in the literature

Who cites it

191 citing papers in PubMed, 4 syntheses or guidelines pooled it, 264 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Guideline
  5. Trial
  6. Article
  7. Eosinophilia and the Heart: Evolving Concepts.Current cardiology reports · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

131 more citing papers are in PubMed but not listed here.

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

30 authors at 19 institutions in 11 countries.

Giacomo EmmiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.ORCID 0000-0001-9575-8321
Alessandra BettiolDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Elena GelainNephrology and Dialysis Unit, Meyer Children's Hospital IRCCS, Florence, Italy.
Ingeborg M BajemaDepartment of Pathology, Groningen University Medical Center, Groningen, the Netherlands.
Alvise BertiRheumatology, Santa Chiara Regional Hospital, APSS Trento, Trento, Italy.ORCID 0000-0002-7831-921X
Stella BurnsVasculitis and Lupus Clinic, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Maria C CidDepartment of Autoimmune Diseases, Hospital Clinic de Barcelona, Barcelona, Spain.ORCID 0000-0002-4730-0938
Jan W Cohen TervaertDivision of Rheumatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Vincent CottinNational Reference Center for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, Claude Bernard University Lyon 1, University of Lyon, IVPC, INRAE, ERN-LUNG, Lyon, France.ORCID 0000-0002-5591-0955
Eugenia DuranteAPACS, Associazione Pazienti con Sindrome di Churg Strauss, Arosio, Italy.
Julia U HolleRheumazentrum Schleswig-Holstein Mitte, Neumünster/Kiel, Germany.
Alfred D MahrDepartment of Rheumatology, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Marcos Martinez Del PeroVasculitis and Lupus Clinic, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Chiara MarvisiRheumatology Unit, Università di Modena e Reggio Emilia, Modena, Italy.
John MillsVasculitis UK, Winster, UK.
Sergey MoiseevTareev Clinic of Internal Disease, Sechenov First Moscow State Medical University, Moscow, Russia.
Frank MoosigRheumazentrum Schleswig-Holstein Mitte, Neumünster/Kiel, Germany.
Chetan MukhtyarVasculitis Service, Rheumatology Department, Norfolk and Norwich University Hospital NHS Trust, Norwich, UK.
Thomas NeumannDepartment of Rheumatology, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Iacopo OlivottoMeyer Children Hospital and Careggi University Hospital, University of Florence, Florence, Italy.
Carlo SalvaraniUnit of Rheumatology, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Benjamin SeeligerDepartment of Respiratory Medicine and German Centre of Lung Research, Hannover Medical School, Hannover, Germany.ORCID 0000-0001-7373-752X
Renato A SinicoDepartment of Medicine and Surgery, University of Milano Bicocca, Milan, Italy.
Camille TailléReference center for rare respiratory diseases, Bichat Hospital, AP-HP-Nord, University Paris Cité, Paris, France.
Benjamin TerrierService de Médecine Interne, Hôpital Cochin, Université de Paris, Paris, France.
Nils VenhoffClinic for Rheumatology and Clinical Immunology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0001-7729-2759
George BertsiasRheumatology, Clinical Immunology and Allergy, University of Crete School of Medicine, Iraklio, Crete, Greece.ORCID 0000-0001-5299-1406
Loïc GuillevinNational Referral Center for Rare Systemic Autoimmune Diseases, Internal Medicine, Cochin Hospital, AP-HP, University of Paris, Paris, France.
David R W JayneUniversity of Cambridge, Box 118, Addenbrooke's Hospital, Cambridge, UK.ORCID 0000-0002-1712-0637
Augusto VaglioNephrology and Dialysis Unit, Meyer Children's Hospital IRCCS, Florence, Italy. augusto.vaglio@unifi.it.ORCID 0000-0002-3814-9172
Meyer Children's Hospital · ITUniversité Paris Cité · FRCambridge University Hospitals NHS Foundation Trust · GBUniversity of Modena and Reggio Emilia · ITUniversity of St.Gallen · CHHospital Clínic de Barcelona · ESMedizinische Hochschule Hannover · DEMonash Medical Centre · AUNorfolk and Norwich University Hospital · GBSechenov University · RUUniversité Claude Bernard Lyon 1 · FRUniversity Medical Center Groningen · NLUniversity of Alberta · CAUniversity of Cambridge · GBUniversity of Crete · GRUniversity of Florence · ITUniversity of Freiburg · DEUniversity of Milano-Bicocca · ITUniversity of Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, characterized by asthma, eosinophilia and granulomatous or vasculitic involvement of several organs. The diagnosis and management of EGPA are often challenging and require an integrated, multidisciplinary approach. Current practice relies on recommendations and guidelines addressing the management of ANCA-associated vasculitis and not specifically developed for EGPA. Here, we present evidence-based, cross-discipline guidelines for the diagnosis and management of EGPA that reflect the substantial advances that have been made in the past few years in understanding the pathogenesis, clinical subphenotypes and differential diagnosis of the disease, as well as the availability of new treatment options. Developed by a panel of European experts on the basis of literature reviews and, where appropriate, expert opinion, the 16 statements and five overarching principles cover the diagnosis and staging, treatment, outcome and follow-up of EGPA. These recommendations are primarily intended to be used by healthcare professionals, pharmaceutical industries and drug regulatory authorities, to guide clinical practice and decision-making in EGPA. These guidelines are not intended to limit access to medications by healthcare agencies, nor to impose a fixed order on medication use.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisChurg-Strauss SyndromeGranulomatosis with PolyangiitisAntibodies, Antineutrophil CytoplasmicDiagnosis, DifferentialHumansAntibodies, Antineutrophil Cytoplasmic

Identifiers

PMID37161084
OpenAlexW4376114466

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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.