Ocular myasthenia gravis: treatment successes and failures in patients with long-term follow-up.

Abstract

We previously reported that prednisone reduced the frequency of generalized myasthenia (GMG) and controlled diplopia without major adverse effects at 2 years in patients with ocular myasthenia gravis (OMG). Questions remain as to whether study subjects had long-standing disease, biasing results towards a steroid benefit, and if prednisone merely delayed GMG onset. Here, we performed a record review of a referral neuro-ophthalmology service OMG database for patients who were followed-up for > or =4 years or until GMG developed. We studied the effect of prednisone on GMG incidence and control of ocular symptoms. Generally, patients with diplopia were recommended for prednisone therapy. Most remained on daily 2.5-10 mg for diplopia control. We compared the results for prednisone-treated and "untreated" (pyridostigmine only) patients. Of 87 patients, 55 were in the prednisone-treated and 32 were in the untreated groups. GMG developed in 7 (13%) of the prednisone-treated (OR 0.41; 95% CI 0.22-0.76) and in 16 (50%) of the untreated (OR 2.78; 95% CI 1.68-4.60) patients. After OMG onset, GMG developed at a mean 5.8 and 0.22 years in prednisone and untreated groups. Diplopia was present at the last exam in 27% of the prednisone-treated (mean 7.2 years) and in 57% of the untreated (mean 4.6 years) OMG patients. For 48 prednisone-treated patients who did not develop GMG, OMG treatment failure occurred in 13. Thus, prednisone delays the onset of GMG and has sustained benefit in reducing the incidence of GMG and controlling diplopia. Without prednisone, GMG develops in 50% of OMG patients, typically within 1 year.

• Authors: Mark J Kupersmith
• Journal: Journal of neurology (J Neurol) Vol. 256 Issue 8 Pg. 1314-20 (Aug 2009) ISSN: 1432-1459 [Electronic] Germany
• PMID: 19377863 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Inflammatory Agents
• Immunosuppressive Agents
• Prednisone

Topics

• Adolescent
• Adult
• Age of Onset
• Aged
• Aged, 80 and over
• Anti-Inflammatory Agents (administration & dosage)
• Child
• Child, Preschool
• Diplopia (drug therapy, etiology, physiopathology)
• Disease Progression
• Female
• Follow-Up Studies
• Humans
• Immunosuppressive Agents (administration & dosage)
• Male
• Middle Aged
• Myasthenia Gravis (complications, drug therapy, physiopathology)
• Oculomotor Muscles (drug effects, physiopathology)
• Prednisone (administration & dosage)
• Retrospective Studies
• Time
• Time Factors
• Treatment Outcome
• Young Adult