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Table 3 List of the eye-related pathologies experienced by the 14 patients from the safety population not reaching monocular CDVA equal or better than 0.3 logMAR

From: Clinical safety and efficacy of a hydrophilic acrylic intraocular lens in a real-world population: a 1-year follow-up retro-prospective study

Case number

CDVA (logMAR)

Factors contributing to CDVA > 0.3 logMAR

Preop.

12 months

1

0.4

0.6

Diabetic macular oedema; diabetic proliferative retinopathy; clinically significant PCO requiring Nd:YAG

2

1.0

0.92

Amblyopia

3

0.4

0.4

No distinct ocular disorders despite diabetes; clinically significant PCO requiring Nd:YAG

4

2.3

0.7

Cornea guttata; macular atrophy; early stage band keratopathy

5

1.3

1.3

Retinal scar (geographic atrophy); amblyopia

6

0.4

0.5

Dry macular degeneration; geographic atrophy

7

0.6

0.6

Amblyopia; macular traction; retinoschisis

8

0.4

0.5

Dry macular degeneration; adult vitelliform maculopathy

9

0.4

1.0

Cornea guttata; ocular hypertension requesting surgical intervention (trabeculectomy) and leading to hyperaemia and hyphema

10

0.4

0.4

Glaucoma; dry macular degeneration; drusen macula; glaucomatous papilla; amblyopia

11

0.52

0.34

Epiretinal membrane

12

0.3

0.4

No distinct ocular disorders despite diabetes mellitus; clinically significant PCO requiring Nd:YAG

13

0.6

0.32

Age-related macular degeneration; transition from drusen age-related macular degeneration to neovascular wet age-related macular degeneration; corneal erosion; clinically significant PCO

14

0.7

0.38

Slight age-related macular degeneration with drusen; vitreous detachment; clinically significant PCO requiring Nd:YAG