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. Author manuscript; available in PMC: 2020 Mar 1.
Published in final edited form as: Lancet Neurol. 2019 Jan 25;18(3):259–268. doi: 10.1016/S1474-4422(18)30392-2

Table 1.

Demographic and clinical characteristics

Prednisone Alone
(N=33)
Thymectomy plus Prednisone
(N=35)
Gender
Women 24 (73) 27 (77)
Men 9 (27) 8 (23)
Median age in years at enrollment (range) 35.4 (18.0–63.0) 34.3 (18.0–63.0)
Median disease duration in years at enrollment (range) 1.49 (0.24–3.97) 1.22 (0.15–2.95)
Ethnicity
Asian 3 (9) 5 (14)
Black, African American 3 (9) 2 (6)
Hispanic 15 (45) 12 (34)
White, not Hispanic origin 10 (30) 13 (37)
Other (Mixed, Native American, or Alaskan) 2 (6) 3 (9)
MG Foundation of America Class at enrollment
Class IIa 12 (36) 12 (34)
Class IIb 8 (24) 9 (26)
Class III 12 (36) 12 (34)
Class IV 1 (3) 2 (6)
Therapy at enrollment
Pyridostigmine 32 (97) 33 (94)
Corticosteroids 24 (73) 26 (74)
Prior intravenous immunoglobulin 7 (21) 2 (6)
Prior plasma exchange 4 (12) 5 (14)
Enrollment measures
Quantitative MG score 13.00 ± 4.68 12.34 ± 5.05
Alternate day prednisone dosage, mg 48.5 ± 30.7 46.3 ± 32.7
MG Activity of Daily Living score 5.48 ± 2.99 5.37 ± 3.46

Data are n (%) or mean (SD)

Myasthenia Gravis Foundation of America Class (II mild weakness, III moderate weakness, IV severe weakness, (“a” denotes predominantly limb and axial, “b” denotes predominantly bulbar).