Evidence map›Paper›PMID 38321574›Full record

ReviewEuropean journal of neurology2024

Generalized myasthenia gravis with acetylcholine receptor antibodies: A guidance for treatment.

Nils Erik Gilhus, Henning Andersen, Linda Kahr Andersen, Marion Boldingh, Sini Laakso, Margret Oddny Leopoldsdottir, Sidsel Madsen, Fredrik Piehl, Trine Haug Popperud, Anna Rostedt Punga and 2 more

Abstract readReview
In one paragraph

Review in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 4 pooled it
–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

44 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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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.

Nils Erik GilhusDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0001-6522-5102
Henning AndersenDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0002-9082-2694
Linda Kahr AndersenCopenhagen Neuromuscular Center, Department of Neurology, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0002-4780-7739
Marion BoldinghDepartment of Neurology, Oslo University Hospital, Oslo, Norway.ORCID 0009-0002-4370-9012
Sini LaaksoDepartment of Neurology, Brain Center, Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-0104-2849
Margret Oddny LeopoldsdottirMG Felag Islands, Reykjavik, Iceland.
Sidsel MadsenThe National Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark.
Fredrik PiehlDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-8329-5219
Trine Haug PopperudDepartment of Neurology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-1036-5949
Anna Rostedt PungaDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-2178-9413
Liselotte SchirakowMG Group, The Danish Muscular Dystrophy Organization, Aarhus, Denmark.
John VissingCopenhagen Neuromuscular Center, Department of Neurology, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0001-6144-8544

Funding

Danish Muscular Dystrophy Organization
6 · The paper itself

Abstract

backgroundGeneralized myasthenia gravis (MG) with antibodies against the acetylcholine receptor is a chronic disease causing muscle weakness. Access to novel treatments warrants authoritative treatment recommendations. The Nordic countries have similar, comprehensive health systems, mandatory health registers, and extensive MG research.

methodsMG experts and patient representatives from the five Nordic countries formed a working group to prepare treatment guidance for MG based on a systematic literature search and consensus meetings.

resultsPyridostigmine represents the first-line symptomatic treatment, while ambenonium and beta adrenergic agonists are second-line options. Early thymectomy should be undertaken if a thymoma, and in non-thymoma patients up to the age of 50-65 years if not obtaining remission on symptomatic treatment. Most patients need immunosuppressive drug treatment. Combining corticosteroids at the lowest possible dose with azathioprine is recommended, rituximab being an alternative first-line option. Mycophenolate, methotrexate, and tacrolimus represent second-line immunosuppression. Plasma exchange and intravenous immunoglobulin are used for myasthenic crises and acute exacerbations. Novel complement inhibitors and FcRn blockers are effective and fast-acting treatments with promising safety profiles. Their use depends on local availability, refunding policies, and cost-benefit analyses. Adapted physical training is recommended. Planning of pregnancies with optimal treatment, information, and awareness of neonatal MG is necessary. Social support and adaptation of work and daily life activities are recommended.

conclusionsSuccessful treatment of MG rests on timely combination of different interventions. Due to spontaneous disease fluctuations, comorbidities, and changes in life conditions, regular long-term specialized follow-up is needed. Most patients do reasonably well but there is room for further improvement. Novel treatments are promising, though subject to restricted access due to costs.

Indexed as

Myasthenia GravisReceptors, CholinergicAutoantibodiesHumansImmunosuppressive AgentsPractice Guidelines as TopicAutoantibodiesImmunosuppressive AgentsReceptors, Cholinergicacetylcholine receptor antibodiesimmunosuppressionmyasthenia gravisthymustreatment

Identifiers

PMID38321574
PMCPMC11236053

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Registered trials

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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.