Our system is currently under heavy load due to increased usage. We're actively working on upgrades to improve performance. Thank you for your patience.
2003
DOI: 10.1001/archneur.60.10.1491-b
|View full text |Cite
|
Sign up to set email alerts
|

Development of Generalized Myasthenia Gravis in Patients With Ocular Myasthenia Gravis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
12
0
1

Year Published

2006
2006
2016
2016

Publication Types

Select...
5
3
1

Relationship

0
9

Authors

Journals

citations
Cited by 21 publications
(14 citation statements)
references
References 3 publications
1
12
0
1
Order By: Relevance
“…First of all, the prevalence of OMG was very similar to those reported in earlier studies with approximately 50% of our patients presenting with solely ocular disturbances [3,4]. In addition, the current study adds to the increasing body of evidence that shows a beneficial effect of early corticosteroid treatment on the risk of secondary generalization [4][5][6][7][8].…”
Section: Discussionsupporting
confidence: 88%
See 1 more Smart Citation
“…First of all, the prevalence of OMG was very similar to those reported in earlier studies with approximately 50% of our patients presenting with solely ocular disturbances [3,4]. In addition, the current study adds to the increasing body of evidence that shows a beneficial effect of early corticosteroid treatment on the risk of secondary generalization [4][5][6][7][8].…”
Section: Discussionsupporting
confidence: 88%
“…Previous studies have reported that ocular disturbances are the first and sole manifestation of MG in about 50% of patients and that between 50% and 60% of patients presenting with OMG subsequently progress to develop generalized disease, usually within the first 1 to 2 years [2,3]. Early immunosuppressive therapy, specifically corticosteroids and/or azathioprine, has been suggested to prevent or delay the secondary generalization [4][5][6][7][8], but the cost-to-benefit ratio of this treatment remains controversial with no randomized controlled study conducted thus far [9]. Only a few studies have addressed the prognostic factors for OMG [2,4], and several clinical and laboratory factors, such as older age at onset, presence of anti-acetylcholine receptor (AChR) antibody, high antibody titers, and the presence of thymoma, were claimed to be associated with an increased risk of secondary generalization.…”
mentioning
confidence: 99%
“…With this argument in mind several groups have retrospectively investigated the generalization rate of their patients with newly diagnosed ocular MG (OMG) when either being treated with corticosteroids or when receiving no immunosuppressive medication at all [4,[9][10][11][12][13][14][15][16]. Six of the available seven small retrospective studies have identified a reduced generalization rate under steroids when assessed within the first 2 years of treatment with relative risks in the range from 0.14 to 0.32, whereas the seventh study observed an increased risk with corticosteroids [4,[9][10][11][12][13][14][15][16].…”
Section: Introductionmentioning
confidence: 99%
“…Although this is based on retrospective analysis (Benatar andKaminski 2007, Bhanushali et al 2008). Dosing regimens vary but typically, 10-20 mg once a day is started and increased by 5-10 mg every 3 days until visual symptoms are improved significantly, which usually occurs in the first few weeks of therapy (Kupersmith et al 2003;Mee et al 2003;Papapetropoulos et al 2003). 60-80 mg per day is a maximum dose.…”
Section: Corticosteroid Treatmentmentioning
confidence: 99%