Literature DB >> 32145521

Initial deterioration and intravenous methylprednisolone therapy in patients with myasthenia gravis.

Takamichi Sugimoto1, Kazuhide Ochi2, Ruoyi Ishikawa3, Taku Tazuma3, Masahiro Hayashi3, Naoko Mine3, Hiroyuki Naito3, Eiichi Nomura3, Tatsuo Kohriyama4, Takemori Yamawaki3.   

Abstract

INTRODUCTION: In myasthenia gravis (MG) patients on intravenous methylprednisolone (IVMP) therapy, initial deterioration should be carefully monitored because it may cause myasthenic crisis. The aim of this study was to investigate the onset, duration and related factors of initial deterioration from the first IVMP in MG patients.
METHODS: A total dose of IVMP in the first cycle of 750 mg or less, over 750 to 1500 mg, and over 1500 to 3000 mg was used in the analysis. Initial deterioration was evaluated in qualitative and quantitative evaluation and was defined as an increase of 2 or more points on the The Myasthenia Gravis Activities of Daily Living (MG-ADL) scale after the start of IVMP therapy in the quantitative evaluation.
RESULTS: We enrolled 51 mainly mild MG patients. The mode of onset of initial deterioration from the first IVMP treatment was day 4 in the qualitative and quantitative evaluation. In addition, the mode of duration was 3 days. In multiple logistic regression analysis, factors related to initial deterioration were MGFA classification with overall disease duration up to just before IVMP and thymectomy before IVMP in both the qualitative and the quantitative evaluation (p < .001). One to four cycles of IVMP improved the MG-ADL score at hospital discharge from that at the start of IVMP (p < .001).
CONCLUSION: Disease severity and thymectomy before IVMP are related to initial deterioration in MG patients. IVMP can be repeated after initial deterioration weekly in most patients.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Disease severity; Initial deterioration; Methylprednisolone; Muscle fatigue; Myasthenia gravis; Thymectomy

Mesh:

Substances:

Year:  2020        PMID: 32145521     DOI: 10.1016/j.jns.2020.116740

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  5 in total

Review 1.  Exacerbation of myasthenia gravis following corticosteroid treatment: what is the evidence? A systematic review.

Authors:  Itay Lotan; Mark A Hellmann; Adi Wilf-Yarkoni; Israel Steiner
Journal:  J Neurol       Date:  2020-10-16       Impact factor: 6.682

Review 2.  Pharmacotherapy of Generalized Myasthenia Gravis with Special Emphasis on Newer Biologicals.

Authors:  Deepak Menon; Vera Bril
Journal:  Drugs       Date:  2022-05-31       Impact factor: 11.431

Review 3.  Utilization of MG-ADL in myasthenia gravis clinical research and care.

Authors:  Srikanth Muppidi; Nicholas J Silvestri; Robin Tan; Kimberly Riggs; Trevor Leighton; Glenn A Phillips
Journal:  Muscle Nerve       Date:  2022-01-06       Impact factor: 3.852

4.  Clinical characteristics and outcome predictors of a Chinese childhood-onset myasthenia gravis cohort.

Authors:  Lifen Yang; Yulin Tang; Fang He; Ciliu Zhang; Miriam Kessi; Jing Peng; Fei Yin
Journal:  Front Pediatr       Date:  2022-09-29       Impact factor: 3.569

5.  Local use of dexamethasone in the treatment of ocular myasthenia gravis.

Authors:  Minghua Shi; Yingjia Ye; Junping Zhou; Aijiao Qin; Jing Cheng; Hongxing Ren
Journal:  BMC Ophthalmol       Date:  2020-10-28       Impact factor: 2.209

  5 in total

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