Evidence map›Paper›PMID 39494501›Full record

Observational studyEuropean journal of neurology2025

Tracking myasthenia gravis severity over time: Insights from the French health insurance claims database.

Shahram Attarian, Jean-Philippe Camdessanché, Andoni Echaniz-Laguna, Mariana Ciumas, Cécile Blein, Benjamin Grenier, Guilhem Solé

Abstract readObservational Study
In one paragraph

Observational study in European journal of neurology, 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. Article
  2. Article
  3. Article
  4. Observational
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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

7 authors.

Shahram AttarianReference Centre for Neuromuscular Disease and ALS, Timone University Hospital, Aix-Marseille University, CHU Timone, Filnemus, Euro-NMD, Marseille, France.ORCID 0000-0002-7211-4694
Jean-Philippe CamdessanchéDepartment of Neurology, Neuromuscular Disease Reference Centre, Hôpital Nord, University Hospital of Saint-Étienne, Saint-Étienne, France.ORCID 0000-0002-5282-6707
Andoni Echaniz-LagunaDepartment of Neurology, APHP, CHU de Bicêtre, INSERM U1195, Paris-Saclay University, Paris, France.ORCID 0000-0003-1012-9783
Mariana CiumasArgenx France, Paris, France.
Cécile BleinArgenx France, Paris, France.
Benjamin GrenierHEVA, Lyon, France.
Guilhem SoléNeurology and Neuromuscular Diseases Department, Neuromuscular Reference Centre AOC, Pellegrin Hospital, Bordeaux University Hospitals, Bordeaux, France.ORCID 0000-0001-9599-6573

Funding

Argenx
6 · The paper itself

Abstract

background and purposeFew data are available on the course of myasthenia gravis (MG) regarding disease severity and stability over time in real-world settings. This study used the French National Health Insurance Database (SNDS) to assess markers of disease severity in patients with MG longitudinally.

methodsAll patients with MG-related claims in the SNDS between 2013 and 2020 were identified. Patients were followed for up to 8 years after the first claim. Intensive care unit (ICU) stays, treatment with intravenous immunoglobulin (IVIg) or plasma exchange (PE), and death were documented throughout the follow-up period. Standardized mortality rates were estimated, and mortality-related variables were identified using a Cox model.

resultsIn all, 14,459 individuals constituted the full study population, including 6354 incident patients. In the incident population, 2199 (34.6%) were admitted to ICUs at least once, principally during the first year after the index date (N = 1477; 23.3%). This proportion decreased progressively to reach 3.0% in the seventh year. A total of 2817 patients received IVIg and 432 PE, again principally in the first year. In the full study population, the standardized mortality rate was 1.08 (95% confidence interval [CI] 1.03-1.13), being lower in men (0.95, 95% CI 0.89-1.02) than in women (1.15, 95% CI 1.07-1.23) and in patients aged >65 years (1.06, 95% CI 1.01-1.11) than in younger patients (1.50, 95% CI 1.24-1.76). Male gender, older age and higher comorbidity were independently associated with mortality.

conclusionsA subgroup of patients with MG require ICU admission and rescue therapy with IVIg or PE, indicative of poor disease control. New therapies are needed to improve disease control and reduce disease burden.

Indexed as

HospitalizationInsurance, HealthMyasthenia GravisPatient AcuityTime FactorsAdolescentAdultAgedAge FactorsComorbidityDatabases, FactualFemaleFranceHumansImmunoglobulins, IntravenousIntensive Care UnitsImmunoglobulins, Intravenousclinical coursedisease controldisease severityFrench National Health Insurance Database (SNDS)intensive caremyasthenia gravistreatment

Identifiers

PMID39494501
PMCPMC11622507

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.