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Published on: October 25, 2018
Pediatric Ocular Myasthenia Gravis
1Department of Ophthalmology, Texas Children's Hospital, Baylor College of Medicine, 6701 Fannin Street- 5th floor Suite 610.25, Houston, TX, 77478, USA.
Insights
Pediatric ocular myasthenia gravis (OMG) treatments include pyridostigmine and prednisone, with steroid-sparing agents and thymectomy for refractory cases. Research gaps exist, especially in pediatric randomized trials for these advanced OMG therapies.
Area of Science:
- Neurology
- Ophthalmology
- Pediatrics
Background:
- Pediatric ocular myasthenia gravis (OMG) presents unique challenges in diagnosis and management.
- Current literature often focuses on adult or generalized juvenile forms of myasthenia gravis (MG).
Purpose of the Study:
- To review current treatment strategies for pediatric ocular myasthenia gravis (OMG).
- To critically appraise available literature on pediatric OMG treatments and outcomes.
- To identify research gaps and future directions in pediatric OMG therapy.
Main Methods:
- Literature review and critical appraisal of studies on pediatric ocular myasthenia gravis (OMG).
- Analysis of treatment options, including pyridostigmine, prednisone, steroid-sparing agents, and thymectomy.
- Evaluation of reported outcomes and generalization rates in pediatric OMG.
Main Results:
- Pyridostigmine and prednisone are primary treatments for pediatric OMG, achieving stabilization in many patients.
- Steroid-sparing agents (azathioprine, cyclosporine, mycophenolate mofetil, tacrolimus) and thymectomy show promise for refractory pediatric OMG.
- Rates of generalization range from 15-35%, with about 25% achieving remission; however, no pediatric randomized controlled trials exist for advanced therapies.
Conclusions:
- While initial treatments are effective for many, refractory pediatric OMG may benefit from steroid-sparing agents and thymectomy.
- Significant gaps remain in the evidence base, particularly the lack of pediatric randomized controlled trials for advanced OMG treatments.
- Further research is crucial to optimize therapeutic strategies and improve outcomes for pediatric ocular myasthenia gravis.
Purpose Of Review:
We present a review of current strategies in the treatment of pediatric ocular myasthenia gravis (OMG). A critical appraisal was performed of the current literature available on OMG and the treatment options available for all age populations. From this data, we present the evidence surrounding therapeutic options for pediatric OMG and discuss treatment outcomes in the pediatric population. We also present gaps in the literature with regard to pediatric OMG and possibilities for future research.
Recent Findings:
While there is data on the use of steroid-sparing immunosuppressive agents for myasthenia gravis (MG), as a whole it is more specific for the use in generalized juvenile myasthenia gravis (JMG) and more focused toward the adult population. In the currently available literature, there have been reports published on the use of steroid-sparing agents including azathioprine, cyclosporine, and mycophenolate mofetil. A recent open-label trial has provided evidence for the use of tacrolimus to improve symptoms of JMG including OMG that were refractory to prednisone. In addition to this, there has been evidence that thymectomy is effective in controlling pediatric OMG and shows a pattern toward preventing generalization of MG, reducing prednisone dosing, and increasing resolution of disease. There are other treatments used in the pediatric population of MG, including intravenous immunoglobulin (IVIG), plasmapheresis, and rituximab, but currently there are no reports on use in OMG. In the population of patients with pediatric OMG, a high percentage of patients are able to obtain stabilization of symptoms using only pyridostigmine or pyridostigmine in combination with oral prednisone. Rates of generalization of OMG range from 15 to 35%, with higher rates in the adolescent population, but approximately 25% of pediatric patients with OMG can have complete remission. For pediatric OMG patients with ophthalmologic manifestations that are refractory to pyridostigmine and prednisone, the use of steroid-sparing agents has been practiced more recently. In addition to this, thymectomy has been utilized in this population. In both of these instances, no pediatric randomized control trials have been performed to date.
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