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. 2020 Feb 7;9(3):3. doi: 10.1167/tvst.9.3.3

Table 2.

Comparison of Visual Function and Patient-Reported Outcomes

Control Post-PRP PDR Follow-up Minus Baselinea
Assessments Baseline Follow-up P value Baseline Follow-up P value Control Post-PRP PDR P value
Visual acuity (logMAR) –0.07 ± 0.09 –0.03 ± 0.10 0.866 0.18 ± 0.21 0.20 ± 0.28 0.580 0.04 ± 0.07 0.02 ± 0.18 0.866
Pelli-Robson contrast sensitivity (log) 1.76 ± 0.14 1.64 ± 0.09 0.070 1.44 ± 0.17 1.31 ± 0.21 0.012 –0.12 ± 0.18 –0.14 ± 0.22 0.853
Reading acuity (logMAR) –0.04 ± 0.05 0.19 ± 0.20 < 0.001 0.23 ± 0.32 0.41 ± 0.22 < 0.001 0.23 ± 0.19 0.18 ± 0.20 0.515
FDP 24-2 (dB)
 MD 0.73 ± 2.76 0.91 ± 1.84 0.820 –7.20 ± 5.12 –8.48 ± 6.23 0.371 0.18 ± 2.53 –0.98 ± 4.76 0.459
 PSD 2.53 ± 0.32 2.97 ± 0.75 0.019 5.74 ± 1.89 6.42 ± 1.78 0.020 0.44 ± 0.53 –0.49 ± 5.72 0.317
 FS 29.55 ± 5.72 30.00 ± 4.63 0.541 22.41 ± 1.89 23.86 ± 5.33 0.272 0.45 ± 4.78 1.07 ± 5.67 0.925
HFA 10-2 (dB)
 MD –0.04 ± 0.80 –1.18 ± 1.50 0.009 –4.08 ± 2.94 –5.00 ± 3.19 0.170 –1.14 ± 1.09 –0.92 ± 3.07 0.370
 PSD 1.25 ± 0.58 1.20 ± 0.24 0.750 3.02 ± 2.20 3.19 ± 2.88 0.728 –0.05 ± 0.48 0.17 ± 2.96 0.852
 FS 36.50 ± 2.64 34.60 ± 2.41 0.012 30.38 ± 6.05 28.62 ± 5.38 0.039 –1.90 ± 1.91 –1.76 ± 6.76 0.950
HFA 60-4 total threshold (dB) 1149 ± 117 1042 ± 173 0.027 230 ± 203 201 ± 209 0.572 –97.92 ± 133.61 –17.43 ± 112.43 0.108
Dark adaptation (min) 8.85 ± 1.69 9.01 ± 4.51 0.706 13.54 ± 5.75 15.14 ± 8.83 0.619 0.71 ± 0.71 1.59 ± 6.48 0.977
LLQ composite score 97.5 ± 2.4 93.7 ± 5.9 0.102 62.7 ± 22.1 62.0 ± 20.9 0.819 –3.77 ± 6.96 –0.63 ± 12.47 0.447
NEI-VFQ composite score 97.8 ± 1.4 94.7 ± 5.0 0.067 77.7 ± 15.5 76.6 ± 18.5 0.618 –3.06 ± 4.94 –1.14 ± 10.32 0.567

FS, foveal sensitivity; MD, mean deviation; PSD, pattern standard deviation.

After 5 years, diabetic patients treated with PRP had age-related decreases in vision, which were comparable with those seen in the control participants. These patients also had stable quality of life despite poor vision.

a

Compared the extent of vision loss and change in patient-reported outcomes over time between the control and diabetic patients.