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Independent risk factors for myasthenic crisis and disease exacerbation in a retrospective cohort of myasthenia gravis patients.
Nelke, Christopher; Stascheit, Frauke; Eckert, Carmen; Pawlitzki, Marc; Schroeter, Christina B; Huntemann, Niklas; Mergenthaler, Philipp; Arat, Ercan; Öztürk, Menekse; Foell, Dirk; Schreiber, Stefanie; Vielhaber, Stefan; Gassa, Asmae; Stetefeld, Henning; Schroeter, Michael; Berger, Benjamin; Totzeck, Andreas; Hagenacker, Tim; Meuth, Sven G; Meisel, Andreas; Wiendl, Heinz; Ruck, Tobias.
  • Nelke C; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstraße 5, 40225, Duesseldorf, Germany.
  • Stascheit F; Department of Neurology with Institute of Translational Neurology, University and University Hospital Münster, Munster, Germany.
  • Eckert C; Charité, Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Department of Neurology With Experimental Neurology, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Pawlitzki M; Charité, Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, NeuroCure Clinical Research Center, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Schroeter CB; Department of Neurology with Institute of Translational Neurology, University and University Hospital Münster, Munster, Germany.
  • Huntemann N; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstraße 5, 40225, Duesseldorf, Germany.
  • Mergenthaler P; Department of Child and Adolescent Psychiatry and Psychotherapy, University Hospital Münster, Munster, Germany.
  • Arat E; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstraße 5, 40225, Duesseldorf, Germany.
  • Öztürk M; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstraße 5, 40225, Duesseldorf, Germany.
  • Foell D; Charité, Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Department of Neurology With Experimental Neurology, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Schreiber S; Charité, Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, NeuroCure Clinical Research Center, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Vielhaber S; Department of Neurology and Center for Translational Neuro- and Behavioral Sciences (C-TNBS), University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Gassa A; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstraße 5, 40225, Duesseldorf, Germany.
  • Stetefeld H; Department of Neurology, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstraße 5, 40225, Duesseldorf, Germany.
  • Schroeter M; Department for Pediatric Rheumatology and Immunology, University of Münster, Munster, Germany.
  • Berger B; Department of Neurology, University of Magdeburg, Magdeburg, Germany.
  • Totzeck A; German Center for Neurodegenerative Diseases, Bonn, Germany.
  • Hagenacker T; Center for Behavioral Brain Sciences, Magdeburg, Germany.
  • Meuth SG; Department of Neurology, University of Magdeburg, Magdeburg, Germany.
  • Meisel A; German Center for Neurodegenerative Diseases, Bonn, Germany.
  • Wiendl H; Center for Behavioral Brain Sciences, Magdeburg, Germany.
  • Ruck T; Department of Cardiothoracic Surgery, University of Cologne and University Hospital Cologne, Cologne, Germany.
J Neuroinflammation ; 19(1): 89, 2022 Apr 12.
Article en En | MEDLINE | ID: mdl-35413850
ABSTRACT

BACKGROUND:

Myasthenic crisis (MC) and disease exacerbation in myasthenia gravis (MG) are associated with significant lethality and continue to impose a high disease burden on affected patients. Therefore, we sought to determine potential predictors for MC and exacerbation as well as to identify factors affecting outcome.

METHODS:

We examined a retrospective, observational cohort study of patients diagnosed with MG between 2000 and 2021 with a mean follow-up of 62.6 months after diagnosis from eight tertiary hospitals in Germany. A multivariate Cox regression model with follow-up duration as the time variable was used to determine independent risk factors for MC and disease exacerbation.

RESULTS:

815 patients diagnosed with MG according to national guidelines were included. Disease severity at diagnosis (quantitative MG score or Myasthenia Gravis Foundation of America class), the presence of thymoma and anti-muscle specific tyrosine kinase-antibodies were independent predictors of MC or disease exacerbation. Patients with minimal manifestation status 12 months after diagnosis had a lower risk of MC and disease exacerbation than those without. The timespan between diagnosis and the start of immunosuppressive therapy did not affect risk. Patients with a worse outcome of MC were older, had higher MGFA class before MC and at admission, and had lower vital capacity before and at admission. The number of comorbidities, requirement for intubation, prolonged mechanical ventilation, and MC triggered by infection were associated with worse outcome. No differences between outcomes were observed comparing treatments with IVIG (intravenous immunoglobulin) vs. plasma exchange vs. IVIG together with plasma exchange.

CONCLUSIONS:

MC and disease exacerbations inflict a substantial burden of disease on MG patients. Disease severity at diagnosis and antibody status predicted the occurrence of MC and disease exacerbation. Intensified monitoring with emphasis on the prevention of infectious complications could be of value to prevent uncontrolled disease in MG patients.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunoglobulinas Intravenosas / Miastenia Gravis Tipo de estudio: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunoglobulinas Intravenosas / Miastenia Gravis Tipo de estudio: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article