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Burns, Ted M.

A5033438287 | I4210134211

Mayo Clinic

University of Virginia Medical Center

Citations 8

Thymectomy may not be associated with clinical improvement in MuSK myasthenia gravis

Muscle & Nerve | December 21, 2018 | Volume: 59 | Issue: 4 | Pages: 404-410

10.1002/mus.26404 | PMID 30575980

ABSTRACT Introduction : A randomized trial demonstrated benefit from thymectomy in nonthymomatous acetylcholine receptor (AChR)‐antibody positive myasthenia gravis (MG). Uncontrolled observational and histologic studies suggest thymectomy may not be efficacious in anti–muscle‐specific kinase (MuSK)‐MG. Methods : The therapeutic impact of thymectomy was evaluated from data collected for a multicenter, retrospective blinded review of rituximab in MuSK‐MG. Results : Baseline characteristics were similar between thymectomy ( n = 26) and nonthymectomy ( n = 29) groups, including treatment with rituximab (42% vs. 45%). At last visit, 35% of thymectomy subjects reached the primary endpoint, a Myasthenia Gravis Foundation of America (MGFA) post‐intervention status (PIS) score of minimal manifestations (MM) or better, compared with 55% of controls ( P = 0.17). After controlling for age at onset of MG, rituximab, prednisone, and intravenous immunoglobulin/plasma exchange treatment, thymectomy was not associated with greater likelihood of favorable clinical outcome (odds ratio = 0.43, 95% confidence interval 0.12–1.53, P = 0.19). Discussion : Thymectomy was not associated with additional clinical improvement in this multicenter cohort of MuSK‐MG patients. Muscle Nerve 59:404–410, 2019
Rituximab as treatment for anti-MuSK myasthenia gravis

Neurology | August 11, 2017 | Volume: 89 | Issue: 10 | Pages: 1069-1077

10.1212/wnl.0000000000004341 | PMID 28801338

Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine

Muscle & Nerve | December 13, 2015 | Volume: 53 | Issue: 2 | Pages: 165-168

10.1002/mus.25009 | PMID 26662952

Can mycophenolate mofetil be tapered safely in myasthenia gravis? A retrospective, multicenter analysis

Muscle & Nerve | April 23, 2015 | Volume: 52 | Issue: 2 | Pages: 211-215

10.1002/mus.24694 | PMID 25906756

ABSTRACTIntroduction: Mycophenolate mofetil (MMF) is frequently used to treat myasthenia gravis, but there is little information to guide clinicians on the safety of reducing the dose in well‐controlled patients. Methods: This retrospective chart review at 3 institutions identified 92 patients who had undergone MMF taper after achieving either pharmacologic remission or minimal manifestations status. Statistical analysis was performed to assess differences in patient characteristics between patients who had successfully tapered MMF and those who relapsed. Results: Of 92 patients undergoing a taper, 30 relapsed. The relapses were mild, transient, and usually responded to increased MMF dose. MG crisis did not occur. The mean dose at time of relapse was 888 mg/day. Patients with relapses were tapered more quickly (8.4 vs. 62.4 months). Conclusions: Tapering MMF appears safe after years of disease stability. Reducing the dose at a dose of only 500 mg/day every 12 months is recommended. Muscle Nerve 52: 211–215, 2015
Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter

Neurology | May 13, 2012 | Volume: 61 | Issue: 9 | Pages: 1291-1293

10.1212/01.wnl.0000092016.98256.21 | PMID 14610143

The Evaluation of Polyneuropathies

Neurology | February 15, 2011 | Volume: 76 | Issue: 7_supplement_2 | Pages: No page available

10.1212/wnl.0b013e31820c3622 | PMID 21321354

Pearls and Oy-sters: Evaluation of peripheral neuropathies

Neurology | February 9, 2009 | Volume: 72 | Issue: 6 | Pages: No page available

10.1212/01.wnl.0000342135.27500.df | PMID 19204254

Neurology ® podcasts

Neurology | September 4, 2007 | Volume: 69 | Issue: 10 | Pages: 948-948

10.1212/01.wnl.0000281541.78240.9e