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ArticleThe European journal of health economics : HEPAC : health economics in prevention and care2026

Economic burden of myasthenia gravis in France: A nationwide claims database study (STAMINA).

Gérard De Pouvourville, Pascal Laforet, Emmanuelle Salort-Campana, Anne Crochard, Grégory Chollet, Camille Nevoret, Stéphane Bouée, Céline Tard

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Article in The European journal of health economics : HEPAC : health economics in prevention and care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

8 authors.

Gérard De PouvourvilleESSEC Business School, Paris, France.
Pascal LaforetNeurology Department, Raymond-Poincaré Hospital, Nord/Est/Ile de France Neuromuscular Center, Assistance Publique Hôpitaux de Paris, Garches, France.
Emmanuelle Salort-CampanaCentre de Référence Des Maladies Neuromusculaires PACA Réunion Rhône Alpes, APHM, Service du Pr Attarian, Marseille, France.
Anne CrochardUCB Pharma SA, Immeuble Défense Ouest 420, Rue d'Estienne d'Orves, 92700, Colombes, France. Anne.Crochard@ucb.com.ORCID http://orcid.org/0000-0003-3856-7275
Grégory CholletUCB Pharma SA, Immeuble Défense Ouest 420, Rue d'Estienne d'Orves, 92700, Colombes, France.
Camille NevoretCEMKA, Bourg-La-Reine, France.
Stéphane BouéeCEMKA, Bourg-La-Reine, France.
Céline TardCentre de Référence Des Maladies Neuromusculaires Nord/Est/Ile-de-France, U1172, CHU de Lille, Service de Neurologie, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG) is a chronic autoimmune disease with symptoms of muscle weakness and fatigability. The aim of this study was to estimate MG-related healthcare resource use (HCRU), associated direct costs and their determinants in France. Data were extracted from the French national claims database (SNDS) for the period 1/1/2008-31/12/2019. Adult patients with MG were identified using an algorithm based primarily on the G70 ICD-10 code. The incident and prevalent MG populations were compared with matched non-MG controls and direct costs were estimated. An exploratory indirect cost analysis restricted to sick leave and disability was also performed and a multivariable model used to identify patients' characteristics associated with higher direct MG costs. In 2019, the mean annual direct cost per patient with MG was €8,506 compared with €3,670 in controls, leading to an MG-excess cost of €4,836 per patient. Patients with MG had significantly (p < 0.0001) higher HCRU than controls in all items of inpatient and outpatient care. MG-excess costs were high, especially in the first year after disease identification and were mainly driven by hospitalizationsfor crises and exacerbations. They remained relatively stable thereafter. Patients with MG were on sick leave more often and for longer periods and were 2-3 times more likely to receive disability or living allowance than controls. The highest costs were concentrated during the first year after MG identification due to exacerbations and crises requiring hospitalization with costly medications and procedures. Novel innovative treatments are expected to change these main drivers of medical costs.

Indexed as

CostFranceMyasthenia gravisReal World Data

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