Early Aggressive Treatment Strategy against Myasthenia Gravis

2011 ◽  
Vol 65 (1) ◽  
pp. 16-22 ◽  
Author(s):  
Yuriko Nagane ◽  
Shigeaki Suzuki ◽  
Norihiro Suzuki ◽  
Kimiaki Utsugisawa
2017 ◽  
Vol 381 ◽  
pp. 1082-1083 ◽  
Author(s):  
K. Utsugisawa ◽  
Y. Nagane ◽  
T. Akaishi ◽  
Y. Suzuki ◽  
T. Imai ◽  
...  

2021 ◽  
pp. jrheum.211126
Author(s):  
Gang Wang ◽  
Ning Zhuo ◽  
Jingyang Li

We read the recent article by Sehgal et al with great interest.1 The authors described a 37-year-old patient with eosinophilic fasciitis (EF) who showed no improvement after an initial aggressive treatment strategy (intravenous [IV] methylprednisolone, prednisone, methotrexate, mycophenolate mofetil, and IVIG). Subsequently, the use of the Janus kinase ( JAK) 1/2 inhibitor baricitinib resulted in considerable improvement in the patient's symptoms and skin appearance. However, there are some details that need further clarification.


2017 ◽  
Vol 55 (6) ◽  
pp. 794-801 ◽  
Author(s):  
Kimiaki Utsugisawa ◽  
Yuriko Nagane ◽  
Tetsuya Akaishi ◽  
Yasushi Suzuki ◽  
Tomihiro Imai ◽  
...  

Author(s):  
Alon Abraham ◽  
Leif E. Lovblom ◽  
Vera Bril

ABSTRACT:To explore whether higher degrees of electrophysiological abnormalities are associated with a more frequent exposure to a more aggressive treatment regimen, we performed a retrospective chart review of patients attending the neuromuscular clinic from June 2012 to December 2015 and included 87 patients. We compared treatment regimens during the follow-up period between patients with high and low jitter and decrement. Myasthenia gravis patients with high jitter or decrement at baseline were more frequently treated with intravenous immunoglobulins (IVIG) and/or plasma exchange (PLEX) during the follow-up period. In patients with mild disease, IVIG or PLEX treatment was associated with high decrement.


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