Table 4.
Indications, clinical outcome, and type of implanted IOL in the study participants
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Patient | Age/Sex | Possible Causes | Pre-op UCVA | Pre-op BCVA | Post-op UCVA | Post-op BCVA | Targeted SE | Pre-op SE | Post- op SE | Diff SE (Post-op & Targeted) | IOL Type/power |
1 | 6 Mo M | Incorrect keratometry | – | – | – | +3.00 | +14.00 | +2.00 | +1.00 | 3-piece/ +21.00 | |
2 | 4 Y F | Known case of PHPV pseudophakic myopic shift | 20/800 | 3/10 | 2/10 | 3/10 | 0.00 | -9.50 | 0.00 | 0.00 | 1-piece/ –10.00 |
3 | 41 Y F | Biometric error due to chorioretinal coloboma | 20/600 | 5/10 | 5/10 | 5/10 | 0.00 | +10.0 | 0.00 | 0.00 | 3-piece/ +15.50 |
4 | 71 Y M | Keratometric error due to corneal nebule | 2/10 | 8/10 | 8/10 | 8/10 | 0.00 | +5.00 | 0.00 | 0.00 | 3-piece/ +7.50 |
5 | 65 Y F | Keratometric error due to KCN | 1/10 | 7/10 | 7/10 | 7/10 | 0.00 | +6.50 | –0.50 | 0.00 | 3-piece/ +10.0 |
6 | 70 Y M | Biometric error due to SO | 20/400 | 2/10 | 2/10 | 2/10 | 0.00 | +7.00 | +0.50 | + 0.50 | 3-piece/ +10.00 |
7 | 47 Y M | (known case of RP) Acceptable RE | 3/10 | 4/10 | 5/10 | 4/10 | 0.00 | +2.00 | 0.00 | 0.00 | 3-piece/ +3.00 |
8 | 15 Mo M | Known case of PHPV myopic shift | – | – | – | – | +4.00 | –500 | +3.50 | –0.50 | 1-piece/ –9.00 |
9 | 57 Y M | Wrong IOL power, Human error | 20/400 | 4/10 | 5/10 | 4/10 | 0.00 | +3.50 | 0.00 | 0.00 | 3-piece/ +5.00 |
10 | 11 Y M | Hx of congenital cataract sx, Myopic shift | 20/800 | 2/10 | 2/10 | 2/10 | 0.00 | –9.00 | 0.00 | 0.00 | Sulcuflex/ –10.00 |
11 | 64 Y M | Keratometric error due to PMD | 1/10 | 4/10 | 4/10 | 4/10 | 0.00 | –7.75 | –1.00 | –1.00 | Sulcoflex/ –8.00 |
BCVA, best-corrected visual acuity; UCVA, uncorrected visual acuity; SE, spherical error; PHPV, persistent hyperplastic primary vitreous; RP, retinitis pigmentosa; SO, silicon oil; RE, refractive error; sx, surgery; KCN, keratoconus; PMD, pellucid marginal degeneration; IOL, intraocular lens; op, operative; Diff, difference; M, male; F, female; Hx, history of; Mo, month; Y, year |