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Purpose: To describe the refractive and visual outcomes after surgery for congenital or developmental cataract in the Ukraine., Methods: Cataract surgery was performed in 65 children aged 3-15 years. The cataracts were bilateral in 44 children and unilateral in 21. Examinations, including visual acuity (VA) and objective refraction using retinoscopy, were performed preoperatively and at 1 day, 6 months and 2 years postoperatively. Neither occlusion therapy nor spectacles were prescribed., Results: Almost all children (96%) gained in VA. In all, 40% of the bilateral cases achieved a corrected Snellen VA > or = 0.5 and 44% of the unilateral cases obtained a corrected VA > or = 0.2. The difference between VA (logMAR) preoperatively and 2 years postoperatively was statistically significant (p < 0.05). The bilateral cases showed a postoperative reduction in mean astigmatism from 3.9 D (1 day postoperatively) to 0.6 D (2 years postoperatively) (p < 0.001), while the unilateral cases showed a reduction from 4.2 D (1 day postoperatively) to 0.4 D (2 years postoperatively) (p < 0.001)., Conclusion: Good postoperative VA was achieved in the group with bilateral cataract. Surprisingly, even in the group with unilateral cataract, an increase in VA was obtained, despite the lack of postoperative correction with glasses or occlusion therapy.

Purpose: To evaluate long-term functional outcome after treatment of dense congenital bilateral cataract., Methods: The records of 22 consecutive children operated on before the age of 12 months at St. Erik's Eye Hospital over a 5-year period (1991-96) were reviewed retrospectively. Linear Snellen visual acuity (VA) at last check, presence of stereoacuity, nystagmus, strabismus and other complications are accounted for. Subject age at last check ranged from 4 to 9 years., Results: Visual acuity could be estimated in 19 children: the median VA of the better eye was 0.4 (range: counting fingers - 0.8) and of the fellow eye 0.15 (range: amaurosis - 0.8). In nine otherwise healthy children who were operated on early (by 1 month of age), VA varied from 0.4 to 0.8 in the better eye. Four of these children achieved stereopsis. Pupillary block glaucoma developed in five eyes (in three children). Chronic glaucoma developed in eight eyes (in five children). Glaucoma occurred predominantly in children who underwent cataract extraction during the first week of life. Two of the latter had marked microphthalmos., Conclusion: Good postoperative VA was achieved in most healthy children with dense bilateral congenital cataract when surgery was performed early (before 6-8 weeks of age). Chronic glaucoma developed predominantly when cataract extraction was performed during the first week of life.

Purpose: To evaluate long-term functional outcome after treatment of congenital unilateral cataract., Methods: The records of 30 consecutive children operated on before the age of 12 months at St. Erik's Eye Hospital over a 5-year period (1991-96) were reviewed retrospectively. The patients were followed until 4-9.5 years of age. Linear Snellen visual acuity (VA), occlusion therapy compliance, and the presence of nystagmus, strabismus and other complications are reported., Results: Six children achieved VA of 0.1 or better. They were all operated on before 3 months of age. Of the 12 infants operated on before 6 weeks of age, four have VA between 0.3 and 0.4 and eight have VA of finger counting or less. Four developed severe secondary glaucoma within 6 months of cataract extraction. Two of these had persistent fetal vasculature. Three eyes developing glaucoma became amaurotic. Occlusion therapy was abandoned before the age of 2.5 years in 21 children., Conclusion: Good levels of VA were achieved only in children who underwent cataract surgery before 3 months of age and who adhered to the occlusion therapy schedule. Severe secondary glaucoma developed in four out of 12 children operated on within 6 weeks. Full compliance with the occlusion therapy programme was uncommon.

Purpose: To examine after-cataract and eye growth in lensectomized newborn rabbits implanted with capsule tension rings of different sizes., Setting: S:t Eriks Eye Hospital, Karolinska Institute, Stockholm, Sweden., Methods: Two groups of 24-day-old rabbits were used. In Group 1 (n = 9), lensectomy was performed in both eyes. In one randomly selected eye, an open poly(methyl methacrylate) (PMMA) capsule tension ring with a 7.0 mm diameter and 0.13 mm thickness was implanted in the capsular bag. The other eye was left aphakic. In Group 2 (n = 10), an open PMMA capsule tension ring with a 10.0 mm diameter and 0.13 mm thickness was implanted in one randomly selected eye, and the other eye was left aphakic. Axial length, corneal diameter, corneal thickness, and intraocular pressure (IOP) were measured in all eyes preoperatively and 1, 2, and 3 months after surgery. The wet mass of the after-cataract was measured at 3 months. Three Group 1 eyes and four Group 2 eyes developed secondary glaucoma and were excluded from the study., Results: Axial growth did not differ significantly between the eyes implanted with the 7.0 mm ring and the aphakic eyes (mean difference 0.01 mm; F3;15 = 0.02; P > .25). Corneal diameter also did not differ (two-way analysis of variance [ANOVA]). Axial length growth was less in the eyes implanted with the 10.0 mm ring than in the aphakic eyes (mean difference 1.05 mm; F3;15 = 2.06; P < .25). The average decrease in corneal diameter growth was 1.0 mm in the implanted eyes. Growth in the eyes with the 10.0 mm ring was significantly less than in the eyes with the 7.0 mm ring (P = .05, Wilcoxon rank-sum test). Corneal thickness and IOP did not differ significantly between eyes (F3;15 = 0.6; P > .25; two-way ANOVA). Amount of after-cataract did not differ significantly between the aphakic eyes and the eyes implanted with the 7.0 mm ring. It was significantly less in the eyes with the 10.0 mm ring than in those with the 7.0 mm ring (Wilcoxon signed-rank test) and in the aphakic eyes (P < .025, Wilcoxon rank-sum test)., Conclusion: In the young rabbit eye, a 10.0 mm capsule ring reduced the eye growth compared with both the aphakic eye and the eye implanted with a 7.0 mm ring. The 10.0 mm ring also inhibited the production of after-cataract compared with the production in the aphakic eye and the eye implanted with the 7.0 mm ring.

Cataract surgery was performed in 21 eyes in 14 children (one to 12 years, 5.6 +/- 4.0 [mean +/- SD]). Cataract surgery was standardized and included capsulorhexis of the anterior capsule, irrigation/aspiration of the nucleus and cortex, puncture of the posterior capsule, injection of sodium hyaluronate (Healon GV, 14 mg/ml) between the posterior capsule and the vitreous, and capsulorhexis of the posterior capsule. At the end of the procedure, a heparin-surface-modified (HSM) poly-(methyl methacrylate) intraocular lens (IOL) was implanted in the capsular bag. Follow-up ranged from four to 16 months. No complications such as the appearance of vitreous in the anterior chamber occurred during surgery. A mild postoperative inflammation was seen in all cases. Opacification of the visual axis was seen in one eye ten months after surgery. Posterior synechial formation was seen in one eye. Our results suggest that capsulorhexis of the anterior and posterior capsules with implantation of an HSM IOL in the capsular bag is a safe procedure in children and produces good postoperative results.

Several studies have indicated that operation during the first months of life in children with dense congenital cataract improves the final visual acuity. In the current study seven otherwise healthy children operated on before the age of fifty-six days are compared with seven children operated on after the age of three months. The patients were followed by a team consisting of a paediatric ophthalmologist, a contact lens optician and an orthoptist. They were treated with contact lenses, spectacles with near addition and occlusion therapy when needed. Visual acuity was initially tested with preferential looking technique and later with Snellen optotypes. In the early treated group the visual development was almost normal with a final visual acuity of 20/20, while in the late treated group no patient obtained better visual acuity than 20/100. The findings indicate that dense congenital cataract should be treated before the age of three months.