Evidence map›Paper›PMID 41947805›Full record

ArticleTherapeutic advances in neurological disorders2026

A Delphi consensus on integrating novel therapies into the management of generalized myasthenia gravis.

John Vissing, Fritz Zimprich, Sari Atula, Andrew Chan, Henning Andersen, Raffi Topakian, Martijn R Tannemaat, Konrad P Weber, Hakan Cetin, Christoph Neuwirth and 2 more

Abstract read
In one paragraph

Article in Therapeutic advances in neurological disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

12 authors.

John VissingCopenhagen Neuromuscular Center, Rigshospitalet, University of Copenhagen, Copenhagen DK-1165, Denmark.ORCID https://orcid.org/0000-0001-6144-8544
Fritz ZimprichDepartment of Neurology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-6998-5480
Sari AtulaHUS Neurocenter, University of Helsinki, Helsinki, Finland.
Andrew ChanDepartment of Neurology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Henning AndersenDepartment of Neurology, Aarhus University, Aarhus, Denmark.
Raffi TopakianDepartment of Neurology, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.
Martijn R TannemaatDepartment of Neurology, Leiden University Medical Center, Leiden, Netherlands.ORCID https://orcid.org/0000-0003-2929-0390
Konrad P WeberDepartments of Neurology and Ophthalmology, University Hospital Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0003-2526-4582
Hakan CetinDepartment of Neurology, Medical University of Vienna, Vienna, Austria.
Christoph NeuwirthNeuromuscular Diseases Unit/ALS Clinic, HOCH, Cantonal Hospital St Gallen, St Gallen, Switzerland.
Hanna KuusistoNeurocenter, Tampere University Hospital, Tampere, Finland.ORCID https://orcid.org/0000-0002-3697-4961
Wolfgang N LoescherDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The treatment landscape for myasthenia gravis (MG) has evolved with the introduction of novel therapies. An international consensus on patient selection criteria and optimal time to initiate these therapies could improve clinical outcomes and reduce delays for likely beneficiaries. Objective: This Delphi consensus was undertaken by MG specialists from selected European countries to explore gaps in the application of national guidelines and elicit expert opinion in practice. Design: A mixed-method approach was used; qualitative and quantitative study phases were combined to explore key concepts and reach consensus. Methods: The qualitative first phase involved seven healthcare professionals (HCPs) and two patient advocacy group representatives who participated in idea generation. Findings from this phase supported the development of a Delphi survey, which was completed by 16 HCPs in two rounds. This constituted the quantitative second phase of the study. Consensus was defined as ⩾70% agreement or disagreement on a 6-point Likert scale. Results: In total, 65% of statements achieved consensus. Key findings include-HCPs highly regard international guidelines but find critical discrepancies between the "ideal" scenario and current clinical practices. Consensus was achieved on the importance of incorporating patient-related quality of life in decision-making, despite limited current methods. Consensus was obtained on steroid tapering and treatment-switch criteria based on steroid dose and duration. Consensus was also achieved on suitable patient profiles, including those with persistent symptoms, severe side effects, or needing rapid control. Conclusion: This study recognized that guidelines offer valuable direction but do not replace individualized treatment decisions. This study identified the areas of alignment and opportunities to refine patient selection criteria and treatment-switch categories, particularly to integrate novel therapy use in MG management, highlighting a path to a more patient-centric approach.

Indexed as

Delphi consensusEuropegeneralizedinnovative therapiesmyasthenia gravis

Identifiers

PMID41947805
PMCPMC13051163

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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.