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. Author manuscript; available in PMC: 2016 Nov 1.
Published in final edited form as: Am J Ophthalmol. 2015 Jul 29;160(5):944–952.e1. doi: 10.1016/j.ajo.2015.07.036

Table 1.

Demographic and Clinical Characteristics of Children with Optic Pathway Gliomas Experiencing New Onset Vision Loss or Stable Vision.

New Vision Loss
(N= 10)
Stable Vision
(N = 45)
Age, yrs (mean/median) 6.9/5.8 6.5/5.5
 Range (1.1 – 17.8) (1.2 – 17.1)
Female sex, n (%) 5 (50) 30 (67)
Race, n (%)
 White/Caucasian 9 (90) 34 (76)
 Black/African American 1 (10) 6 (13)
 Multiracial 0 5 (11)
Ethnicity, n (%)
 Non-Hispanic 10 (100) 42 (93)
 Hispanic 0 (0) 3 (7)
Diagnosis, n (%)
 NF1 – Optic Pathway Glioma 2 (20) 29 (64)
 Sporadic – Optic Pathway Glioma 8 (80) 16 (36)
Treatment of Optic Pathway Glioma, n (%)
 Never 1 (10) 18 (40)
 During Study 9 (90) 17 (38)
 Past 0 (0) 10 (22)
Total Visits, n (mean/median) 67 (6.2/5) 183 (4.0/4)
 Range (3 – 12) (3 – 9)
Duration of Enrollment, months (mean/median) 16.5/15.6 13.4/13.4
 Range (6.1 – 34.1) (5.7 – 23.7)
Abnormal Vision Prior to Study Entry, n (%) 5 (50) 13 (29)
Vision Loss Events During Studya
Time to Event, months (mean/median) 6.3/4.7
 Range (3.0 – 14.1)
 Visual acuity, n (%) 7 (39)
 Visual field, n (%) 8 (44)
 Both visual acuity/field, n (%) 3 (17)
a

18 events of vision loss experienced during the study.

NF1 = Neurofibromatosis type 1.