Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis

Myasthenia gravis (MG) is a disorder of the neuromuscular junction that can deteriorate into myasthenic crisis, involving weakness of bulbar and respiratory muscles. In this study, we describe the clinical manifestations of myasthenic crisis, identify risk factors, and examine treatments and outcome...

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Main Authors: Selen Ozyurt Kose, Ezgi Nazli, Kemal Tutkavul, Nils Erik Gilhus
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-07-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2023.1201451/full
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author Selen Ozyurt Kose
Ezgi Nazli
Kemal Tutkavul
Nils Erik Gilhus
Nils Erik Gilhus
author_facet Selen Ozyurt Kose
Ezgi Nazli
Kemal Tutkavul
Nils Erik Gilhus
Nils Erik Gilhus
author_sort Selen Ozyurt Kose
collection DOAJ
description Myasthenia gravis (MG) is a disorder of the neuromuscular junction that can deteriorate into myasthenic crisis, involving weakness of bulbar and respiratory muscles. In this study, we describe the clinical manifestations of myasthenic crisis, identify risk factors, and examine treatments and outcomes. All 95 patients with generalized MG treated at our center during the last 10 years were included in this retrospective study. We collected data from the patients' records, including clinical follow-ups, muscle antibodies, thymic status, and treatments. The characteristics of patients who did and did not experience myasthenic crisis were compared. Features of all myasthenic crises were also assessed. Twelve patients (13%) developed myasthenic crisis during the observation period. Men were more often affected at older ages. Seven patients experienced multiple myasthenic crises. Thymoma increased the risk of a crisis, whereas thymic hyperplasia decreased the risk. Myasthenic crises were more common in the summer months. No patients died during a myasthenic crisis. Risk factors for myasthenic crisis were thymoma, older age, MuSK antibodies, and previous crises. Individualized and active immunosuppressive treatment and optimal intensive care during crises provide a good outcome for patients with generalized MG.
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spelling doaj.art-c70041f17ce94be3a9d88fe601029fc22023-07-14T02:11:20ZengFrontiers Media S.A.Frontiers in Neurology1664-22952023-07-011410.3389/fneur.2023.12014511201451Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravisSelen Ozyurt Kose0Ezgi Nazli1Kemal Tutkavul2Nils Erik Gilhus3Nils Erik Gilhus4Department of Clinical Neurophysiology, Marmara University Pendik Teaching and Research Hospital, Istanbul, TurkeyDepartment of Neurology, Health Sciences University Haydarpasa Numune Teaching and Research Hospital, Istanbul, TurkeyDepartment of Neurology, Health Sciences University Haydarpasa Numune Teaching and Research Hospital, Istanbul, TurkeyDepartment of Neurology, Haukeland University Hospital, Bergen, NorwayDepartment of Clinical Medicine, University of Bergen, Bergen, NorwayMyasthenia gravis (MG) is a disorder of the neuromuscular junction that can deteriorate into myasthenic crisis, involving weakness of bulbar and respiratory muscles. In this study, we describe the clinical manifestations of myasthenic crisis, identify risk factors, and examine treatments and outcomes. All 95 patients with generalized MG treated at our center during the last 10 years were included in this retrospective study. We collected data from the patients' records, including clinical follow-ups, muscle antibodies, thymic status, and treatments. The characteristics of patients who did and did not experience myasthenic crisis were compared. Features of all myasthenic crises were also assessed. Twelve patients (13%) developed myasthenic crisis during the observation period. Men were more often affected at older ages. Seven patients experienced multiple myasthenic crises. Thymoma increased the risk of a crisis, whereas thymic hyperplasia decreased the risk. Myasthenic crises were more common in the summer months. No patients died during a myasthenic crisis. Risk factors for myasthenic crisis were thymoma, older age, MuSK antibodies, and previous crises. Individualized and active immunosuppressive treatment and optimal intensive care during crises provide a good outcome for patients with generalized MG.https://www.frontiersin.org/articles/10.3389/fneur.2023.1201451/fullmyasthenia gravismyasthenic crisisventilation supportprognosistreatment
spellingShingle Selen Ozyurt Kose
Ezgi Nazli
Kemal Tutkavul
Nils Erik Gilhus
Nils Erik Gilhus
Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis
Frontiers in Neurology
myasthenia gravis
myasthenic crisis
ventilation support
prognosis
treatment
title Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis
title_full Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis
title_fullStr Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis
title_full_unstemmed Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis
title_short Occurrence and severity of myasthenic crisis in an unselected Turkish cohort of patients with myasthenia gravis
title_sort occurrence and severity of myasthenic crisis in an unselected turkish cohort of patients with myasthenia gravis
topic myasthenia gravis
myasthenic crisis
ventilation support
prognosis
treatment
url https://www.frontiersin.org/articles/10.3389/fneur.2023.1201451/full
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