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Table 1 Comparison of salient patients’ characteristicsa between the Ranibizumab and Aflibercept group at baseline, after completing the loading dose phase and after 1 year

From: Comparison of Eylea® with Lucentis® as first-line therapy in patients with treatment-naïve neovascular age-related macular degeneration in real-life clinical practice: retrospective case-series analysis

 

Ranibizumab (16 eyes)

Aflibercept (11 eyes)

Difference

Confidence interval

p-value

Baseline

 Age (mean ± SD) [years]

77.6 ± 9.20

75 ± 6.74

2.63

−4.08 to 9.33

0.428

 Female gender n (%)

11 (68.8 %)

8 (72.7 %)

  

0.586

 Right eye n (%)

7 (43.8 %)

6 (54.5 %)

  

0.436

 Cataract n (%)

9 (56.3 %)

9 (81.8 %)

  

0.167

 Serous PED n (%)

3 (18.8 %)

2 (18.2 %)

  

0.684

 Classic CNV n (%)

7 (43.8 %)

3 (27.3 %)

  

0.324

Loading phase

 Letters before treatment (mean ± SD)

52.25 ± 23.38

62.55 ± 22.20

−10.30

−28.78 to 8.19

0.262

 CFT before treatment (mean ± SD) [μm]

492.80 ± 165.60

352.50 ± 168.51

140.36

5.83 to 274.88

0.042

 Letters after loading dose (mean ± SD)

66.06 ± 10.49

68.91 ± 8.51

−2.85

−10.71 to 5.01

0.463

 CFT after loading dose (mean ± SD) [μm]

323.75 ± 93.00

267.73 ± 65.18

56.02

−10.93 to 122.98

0.097

1 year

 Letters after 1 year (mean ± SD)

67.25 ± 12.69

68.18 ± 13.06

−0.93

−11.29 to 9.43

0.856

 CFT after 1 year (mean ± SD) [μm]

337.31 ± 110.14

274.00 ± 77.76

63.31

−16.13 to 142.75

0.113

 Number of injections/year

8.28 ± 2.07

8.49 ± 1.97

−0.22

−1.85 to 1.42

0.787

  1. aDescriptives were based on eyes