Evidence map›Paper›PMID 40766205›Full record

ReviewTherapeutic advances in neurological disorders2025

National guidelines for diagnosis, treatment, and management of myasthenia gravis in Israel.

Shahar Shelly, Marc Gotkine, Adi Wilf Yarkoni, Itay Lotan, Alon Abraham, Amir Dori, Gil I Wolfe, Keren Regev, Adi Vaknin, Tamir Ben-Hur

Abstract readReview
In one paragraph

Review in Therapeutic advances in neurological disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
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

10 authors.

Shahar ShellyRuth and Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 3525408, Israel.ORCID https://orcid.org/0000-0002-3585-1687
Marc GotkineDepartment of Neurology, Hadassah, Hebrew University Medical Center and Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Adi Wilf YarkoniDepartment of Neurology, Rabin Medical Center, Petach Tikva, Israel.
Itay LotanDepartment of Neurology, Rabin Medical Center, Petach Tikva, Israel.
Alon AbrahamDepartment of Neurology, Tel Aviv Sourasky Medical Center, and the Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Amir DoriDepartment of Neurology, Sheba Medical Center, Tel Aviv Sourasky Medical Center, and the Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Gil I WolfeDepartment of Neurology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo/SUNY, Buffalo, NY, USA.
Keren RegevDepartment of Neurology, Tel Aviv Sourasky Medical Center, and the Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Adi VakninDepartment of Neurology, Hadassah, Hebrew University Medical Center and Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Tamir Ben-HurDepartment of Neurology, Hadassah, Hebrew University Medical Center and Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG) is a chronic autoimmune neuromuscular disorder characterized primarily by fluctuating skeletal muscle weakness affecting ocular, bulbar, truncal, limb, and respiratory muscles. The disease is typically mediated by anti-acetylcholine receptor (AChR) antibodies, and less commonly by anti-muscle-specific kinase) or anti-low-density lipoprotein receptor-related protein 4 antibodies. Despite significant advancements in diagnostics and immunotherapy, disparities in treatment access and practice variability remain prevalent in Israel. To address these gaps, updated national guidelines have been developed, integrating the latest international evidence and adapting it to the local healthcare landscape, regulation, and population diversity. This national guideline emphasizes precise diagnostic evaluation through comprehensive clinical assessment, standardized antibody testing, neurophysiological studies, and mediastinal imaging for thymic pathology assessment. Utilizing standardized scales, including MG activities of daily living, quantitative MG score, and MG Foundation of America post-intervention status, is crucial for disease staging and therapeutic decision-making. Therapeutic goals prioritize achieving full remission or a state of minimal manifestations of disease with negligible treatment-related side effects. Guidelines for treatment strategies are based on antibody status, disease severity, patient age, and comorbidities. Thymectomy is recommended for patients with generalized AChR antibody-positive MG, ideally within 2 years of disease onset. Pregnant women, older adults, children, and patients with cancer need specific immunotherapy approaches. Multidisciplinary care, structured patient education, and psychosocial support are integral to managing MG effectively. These national guidelines aim to standardize clinical practices, enhance patient outcomes, and reduce healthcare disparities in the management of MG across Israel.

Indexed as

AChR antibodiesautoimmuneIsraelLRP4 antibodiesMuSK antibodiesmyasthenia gravisneuromuscular junctiontreatment guidelines

Identifiers

PMID40766205
PMCPMC12322348

What OpenQuestion holds

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LicenceCC BY-NC
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.