Evidence map›Paper›PMID 38152089›Full record

ReviewTherapeutic advances in neurological disorders2023

Guideline for the management of myasthenic syndromes.

Heinz Wiendl, Angela Abicht, Andrew Chan, Adela Della Marina, Tim Hagenacker, Khosro Hekmat, Sarah Hoffmann, Hans-Stefan Hoffmann, Sebastian Jander, Christian Keller and 14 more

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Therapeutic advances in neurological disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 114 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 5 pooled it
26.1field-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.

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

114 citing papers in PubMed, 5 syntheses or guidelines pooled it, 127 citations in OpenAlex.

  1. Pooled it
  2. Guideline
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  6. Trial
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  13. Disease severity as the dominant clinic-available marker of myasthenic crisis occurrence: a single-centre retrospective study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  14. Article
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  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 15 institutions in 3 countries.

Heinz WiendlDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, Münster 48149, Germany.ORCID https://orcid.org/0000-0003-4310-3432
Angela AbichtFriedrich-Baur-Institut an der Neurologischen Klinik und Poliklinik, LMU Munich, Munich, Germany.
Andrew ChanUniversitätsklinik für Neurologie, Inselspital Bern, Bern, Switzerland.
Adela Della MarinaKlinik für Kinderheilkunde I, Universitätsklinikum Essen, Essen, Germany.
Tim HagenackerKlinik für Neurologie, Universitätsklinikum Essen, Essen, Germany.ORCID https://orcid.org/0000-0002-3631-3450
Khosro HekmatHerzzentrum, Uniklinik Cologne, Cologne, Germany.
Sarah HoffmannCharité - Universitätsmedizin Berlin, Klinik für Neurologie mit Experimenteller Neurologie, Berlin, Germany.
Hans-Stefan HoffmannKlinik für Thoraxchirurgie, Krankenhaus Barmherzige Brüder, Regensburg, Germany.
Sebastian JanderKlinik für Neurologie, Marien Hospital Düsseldorf, Düsseldorf, Germany.
Christian KellerDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Alexander MarxPathologisches Institut, Universitätsklinikum Mannheim, Mannheim, Germany.
Arthur MelmsFacharztpraxis für Neurologie und Psychiatrie, Stuttgart, Germany.
Nico MelzerKlinik für Neurologie, Universitätsklinikum Düsseldorf, Düsseldorf, Germany.
Wolfgang Müller-FelberKinderklinik und Kinderpoliklinik im Dr. von Haunerschen Kinderspital, LMU Munich, Munich, Germany.
Marc PawlitzkiKlinik für Neurologie, Universitätsklinikum Düsseldorf, Düsseldorf, Germany.ORCID https://orcid.org/0000-0003-3080-2277
Jens-Carsten RückertChirurgische Klinik, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Christiane Schneider-GoldNeurologie, Katholisches Klinikum Bochum, Bochum, Germany.ORCID https://orcid.org/0000-0002-9232-201X
Benedikt SchoserFriedrich-Baur-Institut an der Neurologischen Klinik und Poliklinik, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-2757-8131
Bettina SchreinerKlinik für Neurologie, Universitätsspital Zürich, Zürich, Switzerland.
Michael SchroeterKlinik und Poliklinik für Neurologie, Uniklinik Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0001-8441-4793
Bettina SchubertDeutsche Myasthenie Gesellschaft e.V., Bremen, Germany.
Jörn-Peter SiebHelios Hanseklinikum Stralsund, Stralsund, Germany.
Fritz ZimprichUniversitätsklinik für Neurologie, AKH-Wien, Wien, Austria.
Andreas MeiselCharité - Universitätsmedizin Berlin, Klinik für Neurologie mit Experimenteller Neurologie, Berlin, Germany.ORCID https://orcid.org/0000-0001-7233-5342
Charité - Universitätsmedizin Berlin · DEEssen University Hospital · DELudwig-Maximilians-Universität München · DEDüsseldorf University Hospital · DEUniversity Hospital Münster · DEHeidelberg University · DEKatholisches Klinikum Bochum · DEKlinik und Poliklinik für Neurologie · DEKlinik und Poliklinik für Psychiatrie und Psychotherapie · DEKrankenhaus Barmherzige Brüder · DEMarien Hospital Düsseldorf · DEMedical University of Vienna · ATUniversity Hospital of Bern · CHUniversity Hospital of Zurich · CHUniversity of Applied Sciences Stralsund · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG), Lambert-Eaton myasthenic syndrome (LEMS), and congenital myasthenic syndromes (CMS) represent an etiologically heterogeneous group of (very) rare chronic diseases. MG and LEMS have an autoimmune-mediated etiology, while CMS are genetic disorders. A (strain dependent) muscle weakness due to neuromuscular transmission disorder is a common feature. Generalized MG requires increasingly differentiated therapeutic strategies that consider the enormous therapeutic developments of recent years. To include the newest therapy recommendations, a comprehensive update of the available German-language guideline 'Diagnostics and therapy of myasthenic syndromes' has been published by the German Neurological society with the aid of an interdisciplinary expert panel. This paper is an adapted translation of the updated and partly newly developed treatment guideline. It defines the rapid achievement of complete disease control in myasthenic patients as a central treatment goal. The use of standard therapies, as well as modern immunotherapeutics, is subject to a staged regimen that takes into account autoantibody status and disease activity. With the advent of modern, fast-acting immunomodulators, disease activity assessment has become pivotal and requires evaluation of the clinical course, including severity and required therapies. Applying MG-specific scores and classifications such as Myasthenia Gravis Activities of Daily Living, Quantitative Myasthenia Gravis, and Myasthenia Gravis Foundation of America allows differentiation between mild/moderate and (highly) active (including refractory) disease. Therapy decisions must consider age, thymic pathology, antibody status, and disease activity. Glucocorticosteroids and the classical immunosuppressants (primarily azathioprine) are the basic immunotherapeutics to treat mild/moderate to (highly) active generalized MG/young MG and ocular MG. Thymectomy is indicated as a treatment for thymoma-associated MG and generalized MG with acetylcholine receptor antibody (AChR-Ab)-positive status. In (highly) active generalized MG, complement inhibitors (currently eculizumab and ravulizumab) or neonatal Fc receptor modulators (currently efgartigimod) are recommended for AChR-Ab-positive status and rituximab for muscle-specific receptor tyrosine kinase (MuSK)-Ab-positive status. Specific treatment for myasthenic crises requires plasmapheresis, immunoadsorption, or IVIG. Specific aspects of ocular, juvenile, and congenital myasthenia are highlighted. The guideline will be further developed based on new study results for other immunomodulators and biomarkers that aid the accurate measurement of disease activity.

Indexed as

congenital myasthenic syndromesdisease-modifying treatmentLambert-Eaton myasthenic syndromemyasthenia gravismyasthenic syndromestreatment guideline

Identifiers

PMID38152089
PMCPMC10752078
OpenAlexW4390231663

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.