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. 2021 Apr 17;41(9):2951–2961. doi: 10.1007/s10792-021-01854-6

Table 1.

Characteristics of the patients in Group 1 and Group 2

Group 1
(n = 44)
Group 2
(n = 60)
p
Age, years
 Mean ± SD 71.0 ± 8.1 74.7 ± 8.0 0.024a
Gender, n (%) 0.853b
 Female 20 (45.5) 25 (41.7)
 Male 24 (54.5) 35 (58.3)
Follow-up time, months
 Median (IQR) 30.50 (47.25) 27.04 (41.00) 0.927c
BCVA at presentation, logMAR
 Median (IQR)
  Study eye 0.30 (0.54) 0.61 (1.08) 0.023c
  Fellow-eye 0.61 (1.75) 0.40 (1.25) 0.483c
BCVA at V0, logMAR
 Median (IQR)
  Study eye 0.40 (0.48) 0.52 (0.70) 0.031c
  Fellow-eye 0.61 (1.36) 0.52 (1.25) 0.597c
IVI count before V0, n
 Median (IQR) 10.0 (8.75) 10.0 (9.00) 0.974c
Planned extension period at V0, weeks
 Median (IQR) 8.57 (5.96) 10.0 (5.96) 0.604c
Any accompanying disorders, n (%) 0.095b
 Present 19 (43.2) 37 (61.7)
 Absent 25 (56.8) 23 (38.3)
Diabetes mellitus, n (%) 0.971b
 Present 10 (22.7) 15 (25.0)
 Absent 34 (77.3) 45 (75.0)
Hypertension, n (%) 0.044b
 Present 16 (36.4) 35 (58.3)
 Absent 28 (63.6) 25 (41.7)
Coronary artery disease, n (%) 0.696d
 Present 3 (6.8) 3 (5.0)
 Absent 41 (93.2) 57 (95.0)

Statistical significance is highlighted in bold

BCVA best-corrected visual acuity, IVI intravitreal injection, IQR interquartile range, logMAR logarithm of the minimum angle of resolution, SD standard deviation, V0 the last visit before the restriction period where the IVI at restriction period scheduled

aIndependent-samples t test

bPearson Chi-square test with continuity correction

c Mann–Whitney U test

d Fisher’s exact test