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Mergenthaler, Philipp ; Stetefeld, Henning R. ; Dohmen, Christian ; Kohler, Siegfried ; Schönenberger, Silvia ; Bösel, Julian ; Gerner, Stefan T. ; Huttner, Hagen B. ; Schneider, Hauke ; Reichmann, Heinz ; Fuhrer, Hannah ; Berger, Benjamin ; Zinke, Jan ; Alberty, Anke ; Kleiter, Ingo ; Schneider-Gold, Christiane ; Roth, Christian ; Dunkel, Juliane ; Steinbrecher, Andreas ; Thieme, Andrea ; Lee, De-Hyung ; Linker, Ralf A. ; Angstwurm, Klemens ; Meisel, Andreas ; Neumann, Bernhard

Seronegative myasthenic crisis: a multicenter analysis

Mergenthaler, Philipp, Stetefeld, Henning R., Dohmen, Christian, Kohler, Siegfried, Schönenberger, Silvia, Bösel, Julian, Gerner, Stefan T., Huttner, Hagen B., Schneider, Hauke , Reichmann, Heinz, Fuhrer, Hannah, Berger, Benjamin , Zinke, Jan, Alberty, Anke, Kleiter, Ingo , Schneider-Gold, Christiane, Roth, Christian, Dunkel, Juliane, Steinbrecher, Andreas, Thieme, Andrea, Lee, De-Hyung, Linker, Ralf A., Angstwurm, Klemens, Meisel, Andreas und Neumann, Bernhard (2022) Seronegative myasthenic crisis: a multicenter analysis. Journal of Neurology 269 (7), S. 3904-3911.

Veröffentlichungsdatum dieses Volltextes: 12 Apr 2022 04:31
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.52141


Zusammenfassung

Myasthenic crisis (MC) is a life-threatening condition for patients with myasthenia gravis (MG). Seronegative patients represent around 10-15% of MG, but data on outcome of seronegative MCs are lacking. We performed a subgroup analysis of patients who presented with MC with either acetylcholine-receptor-antibody-positive MG (AChR-MG) or seronegative MG between 2006 and 2015 in a retrospective ...

Myasthenic crisis (MC) is a life-threatening condition for patients with myasthenia gravis (MG). Seronegative patients represent around 10-15% of MG, but data on outcome of seronegative MCs are lacking. We performed a subgroup analysis of patients who presented with MC with either acetylcholine-receptor-antibody-positive MG (AChR-MG) or seronegative MG between 2006 and 2015 in a retrospective German multicenter study. We identified 15 seronegative MG patients with 17 MCs and 142 AChR-MG with 159 MCs. Seronegative MCs were younger (54.3 +/- 14.5 vs 66.5 +/- 16.3 years; p = 0.0037), had a higher rate of thymus hyperplasia (29.4% vs 3.1%; p = 0.0009), and were more likely to be female (58.8% vs 37.7%; p = 0.12) compared to AChR-MCs. Time between diagnosis of MG and MC was significantly longer in seronegative patients (8.2 +/- 7.6 vs 3.1 +/- 4.4 years; p < 0.0001). We found no differences in duration of mechanical ventilation (16.2 +/- 15.8 vs 16.5 +/- 15.9 days; p = 0.94) and length of stay at intensive care unit (17.6 +/- 15.2 vs 17.8 +/- 15.4 days; p = 0.96), or in-hospital mortality (11.8% vs. 10.1%; p = 0.69). We conclude that MC in seronegative MG affects younger patients after a longer period of disease, but that crisis treatment efficacy and outcome do not differ compared to AChR-MCs.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftJournal of Neurology
Verlag:SPRINGER HEIDELBERG
Ort der Veröffentlichung:HEIDELBERG
Band:269
Nummer des Zeitschriftenheftes oder des Kapitels:7
Seitenbereich:S. 3904-3911
Datum7 April 2022
InstitutionenMedizin > Lehrstuhl für Neurologie
Identifikationsnummer
WertTyp
10.1007/s00415-022-11023-zDOI
Stichwörter / KeywordsGRAVIS; MORTALITY; ANTIBODY; Myasthenia gravis; Myasthenic crisis; Antibody status; Seronegative; Outcome
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenZum Teil
URN der UB Regensburgurn:nbn:de:bvb:355-epub-521411
Dokumenten-ID52141

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