Evidence map›Paper›PMID 41524776›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2026

Pharmacological and speech-language pathology management of dysphagia in patients with myasthenia gravis.

F Ferrara, F De Berardinis

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In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 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

2 authors.

F FerraraPharmaceutical Department, ASL Napoli 3 Sud, Naples, Italy. f.ferrara@aslnapoli3sud.it.
F De BerardinisDepartment of Mental Health, ASL Roma 3, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG) is a rare, complex autoimmune neuromuscular disorder characterized by fluctuating muscle weakness. Bulbar involvement, particularly dysphagia (difficulty swallowing), is a common and debilitating symptom that significantly increases the risk of aspiration pneumonia, malnutrition, and dehydration, profoundly impacting quality of life. The management of myasthenic dysphagia requires a sophisticated, interdisciplinary approach. This review aims to provide a comprehensive overview of the current and emerging pharmacological treatments for myasthenia gravis and to detail the specific assessment and management strategies employed by speech-language pathologists (SLPs) for associated dysphagia. A narrative review of the literature was conducted, focusing on the pathophysiology, classification, and treatment of MG, with a specific emphasis on bulbar dysfunction. The review synthesizes evidence for traditional immunosuppressants, novel targeted biologics (complement inhibitors and FcRn antagonists), and evidence-based speech-language pathology interventions. Pharmacological management has evolved from symptomatic treatment (anticholinesterases) and broad immunosuppression (corticosteroids, azathioprine) to highly specific, targeted therapies. Complement inhibitors (e.g., eculizumab, ravulizumab) and neonatal Fc receptor (FcRn) antagonists (e.g., efgartigimod, rozanolixizumab) have demonstrated significant and rapid efficacy in reducing autoantibody load and improving clinical scores (MG-ADL, QMG) in generalized MG, including for patients with refractory disease. Concurrently, SLP management is critical for functional safety and efficacy. This includes precise assessment using clinical (e.g., EAT-10, bedside swallowing evaluations) and instrumental methods (VFSS, FEES) to characterize the pathophysiology of weakness and fatigability. Management is individualized, focusing on compensatory strategies (e.g., postural adjustments, diet modification standardized by the IDDSI framework) and behavioral techniques, all timed to coincide with peak medication efficacy. The treatment landscape for MG has been revolutionized by targeted biologics, offering profound improvements for many patients. Effective management of dysphagia, however, relies on the synergy between optimal medical therapy and specialized SLP intervention. This integrated approach is essential to ensure swallowing safety, nutritional adequacy, and improved quality of life for individuals living with myasthenia gravis.

Indexed as

Deglutition DisordersMyasthenia GravisSpeech-Language PathologyCholinesterase InhibitorsHumansImmunosuppressive AgentsCholinesterase InhibitorsImmunosuppressive AgentsAcetylcholine receptor (AChR)Complement inhibitorsDysphagiaFcRn antagonistsMuSKMyasthenia gravis (MG)Neuromuscular junctionPharmacotherapySpeech-language pathology

Identifiers

What OpenQuestion holds

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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.