Myasthenic ophthalmoparesis: Time To resolution after initiating immune therapies

被引:28
作者
Europa, Tarin A. [1 ]
Nel, Melissa [1 ]
Heckmann, Jeannine M. [1 ]
机构
[1] Univ Cape Town, Neurol Res Grp, Div Neurol, Dept Med, Cape Town, South Africa
基金
新加坡国家研究基金会;
关键词
extraocular muscle; myasthenia gravis; ophthalmoplegia; prednisone; steroid; OCULAR MYASTHENIA; SOUTH-AFRICANS; GRAVIS; STANDARDS; TRIAL;
D O I
10.1002/mus.26172
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Although immunotherapies such as prednisone are effective in treating myasthenic muscle weakness, their effect on resolution of myasthenic-induced persistent ophthalmoparesis is unknown. Methods: We observed patients with myasthenia gravis during their first year of immunotherapy, documenting ophthalmoplegia scores and drug doses. Results: Seventy-six of 87 cases had persistent ophthalmoparesis. With immunotherapy, the median time to resolution of ophthalmoparesis was 7 months, and 37% of cases resolved within 3 months. Patients starting therapy within 12 months of symptom onset were twice as likely to have resolution in the first year (P=0.028). Resolution of ophthalmoparesis within 3 months, compared with later resolution, was associated with higher initial prednisone doses (mean 0.5 vs. 0.3mg/kg/day; P=0.014). However, 25% of the higher dose group also received intravenous immunoglobulin/plasma exchange; after their exclusion, the finding was not significant. Discussion: One-third of cases with myasthenic ophthalmoparesis resolved within 3 months of immunotherapy, particularly in response to more aggressive immunotherapy. Muscle Nerve58: 542-549, 2018
引用
收藏
页码:542 / 549
页数:8
相关论文
共 28 条
[1]  
[Anonymous], COCHRANE DATABASE SY
[2]   The effects of prednisone and steroid-sparing agents on decay accelerating factor (CD55) expression: Implications in myasthenia gravis [J].
Auret, Jennifer ;
Abrahams, Amaal ;
Prince, Sharon ;
Heckmann, Jeannine M. .
NEUROMUSCULAR DISORDERS, 2014, 24 (06) :499-508
[3]  
Bateman KJ, 2007, SAMJ S AFR MED J, V97, P959
[4]   Evidence report: The medical treatment of ocular myasthenia (an evidence-based review) - Report of the Quality Standards Subcommittee of the American Academy of Neurology [J].
Benatar, Michael ;
Kaminski, Henry J. .
NEUROLOGY, 2007, 68 (24) :2144-2149
[5]   EFFICACY OF PREDNISONE FOR THE TREATMENT OF OCULAR MYASTHENIA (EPITOME): A RANDOMIZED, CONTROLLED TRIAL [J].
Benatar, Michael ;
McDermott, Michael P. ;
Sanders, Donald B. ;
Wolfe, Gil I. ;
Barohn, Richard J. ;
Nowak, Richard J. ;
Hehir, Michael ;
Juel, Vern ;
Katzberg, Hans ;
Tawil, Rabi .
MUSCLE & NERVE, 2016, 53 (03) :363-369
[6]   Treatment of ocular symptoms in myasthenia gravis [J].
Bhanushali, Minal J. ;
Wuu, Joanne ;
Benatar, Michael .
NEUROLOGY, 2008, 71 (17) :1335-1341
[7]   A systematic review of population based epidemiological studies in Myasthenia Gravis [J].
Carr, Aisling S. ;
Cardwell, Chris R. ;
McCarron, Peter O. ;
McConville, John .
BMC NEUROLOGY, 2010, 10
[8]   The Pattern of Extra-Ocular Muscle Involvement in Ocular Myasthenia [J].
Cleary, Marie ;
Williams, Graeme John ;
Metcalfe, Richard Andrew .
STRABISMUS, 2008, 16 (01) :11-18
[9]   MEDICAL PROGRESS - MYASTHENIA-GRAVIS [J].
DRACHMAN, DB .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (25) :1797-1810
[10]   THE NATURAL COURSE OF MYASTHENIA-GRAVIS AND EFFECT OF THERAPEUTIC MEASURES [J].
GROB, D ;
BRUNNER, NG ;
NAMBA, T .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1981, 377 (DEC) :652-669