Temporal macular thinning associated with X-linked Alport syndrome.

IMPORTANCE: Optical coherence tomography (OCT) findings of temporal macular thinning are important in the diagnosis and prognosis of X-linked Alport syndrome (XLAS). OBJECTIVES: To report OCT findings and severity of temporal macular thinning in a cohort with XLAS and to correlate these and other ocular findings with mutation genotype. DESIGN: Patients with XLAS underwent genotyping for COL4A5 mutations and complete eye examinations with retinal imaging using spectral domain OCT and fundus photography. Temporal macular thinning was calculated from OCT measurements by comparing the ratio of the retinal thickness of the temporal to the nasal subfields with a published normative database. SETTING: University departments of ophthalmology and nephrology. PARTICIPANTS: Thirty-two patients from 24 families. MAIN OUTCOME AND MEASURES: Temporal thinning index calculated from spectral domain OCT scans. RESULTS: All study patients had a mutation associated with the X-linked COL4A5 gene. Eleven different mutations were identified. Eleven of 32 patients (34%) expressed the L1649R mutation. Of a total of 63 eyes with available OCT scans, 44 (70%) had severe pathological temporal macular thinning. The L1649R mutation was associated with the least amount of severe temporal macular thinning and later onset of renal failure. CONCLUSIONS AND RELEVANCE: Temporal macular thinning is a prominent sign associated with XLAS, suggesting that OCT measurements are essential in the diagnosis and prognosis of the disease. The L1649R mutation in the COL4A5 gene causes a relatively mild form of XLAS characterized by late-onset renal failure and less frequent, severe temporal macular thinning relative to other COL4A5 mutations. The pathological basis for the retinal abnormalities of XLAS remains to be established.

The impact of short-term topical gatifloxacin and moxifloxacin on bacterial injection after hypodermic needle passage through human conjunctiva.

PURPOSE: To determine the bacterial contamination rate of a 27-gauge needle bore during conjunctival penetration in donor eye bank eyes and the effect of short-term use of topical 0.3% gatifloxacin and 0.5% moxifloxacin. METHODS: One hundred consecutive human donors had 10 conjunctival penetrations per 10 syringes per eye before antibiotic placement; this was repeated 15 min after antibiotic use. Samples were cultured by expressing 0.3 mL of saline through the needle. Positive cultures were speciated. RESULTS: There were 1,033 positive cultures (25.8% of all cultures); 568 (28.4%) pre-antibiotics, 249 (24.9%) after gatifloxacin (P=0.04, compared to the pre-antibiotic rate), and 216 (21.6%) after moxifloxacin (P<0.001). The most common organism was Staphylococcus epidermidis [334 positive cultures (8.4%)]. No antibiotic effect was seen on this or other organisms except S. aureus [4.6% pre-antibiotic, 2.8% after gatifloxacin (P=0.02), and 1.8% after moxifloxacin (P<0.001)] and other Staphylococcus species [5.3% pre-antibiotic, 3.6% after gatifloxacin (P=0.04), and 3.2% after moxifloxacin (P=0.01)]. CONCLUSIONS: Transconjunctival penetration often results in needle bore contamination; bacteria are included in an injected solution. Fifteen minutes of exposure to 2 topical antibiotics had a minimal effect on bacterial contamination and no significant effect on many common pathogens.

Cataract development associated with collagen copolymer posterior chamber phakic intraocular lenses: clinicopathological correlation.

PURPOSE: To assess the histopathology of anterior subcapsular cataract associated with a collagen copolymer posterior chamber phakic intraocular lens (pIOL) (Visian Implantable Collamer Lens) using light microscopy after pIOL explantation and cataract surgery. SETTING: John A. Moran Eye Center, University of Utah, Salt Lake City, Utah, USA. DESIGN: Laboratory investigation. METHODS: Pathology specimens related to explanted pIOLs were reviewed and preoperative and postoperative patient data collected. The anterior lens capsules and explanted pIOLs were examined. RESULTS: Four eyes (3 patients) had pIOL explantation for low vault and anterior subcapsular cataract. The explanted pIOLs were the shorter length models (3, 12.1 mm; 1, 12.6 mm). Anterior segment optical coherence tomography (AS-OCT) confirmed the low pIOL vault before explantation in 2 eyes. Histopathology of the anterior subcapsular cataract showed fibrous metaplasia with a variable number of lens epithelial cell (LEC) layers attached to the inner surface of the anterior capsulorhexis specimens. Light microscopy of the explanted pIOLs showed no pigment on 1 lens, mild pigment deposition on 1 haptic, and pigment deposition throughout the anterior surface of 2 pIOLs. CONCLUSIONS: Anterior subcapsular cataract associated with the pIOLs was caused by low vaulting (confirmed on AS-OCT) and consequent fibrous metaplasia of the anterior LECs. Surgeons should consider the possibility of anterior subcapsular cataract associated with shorter platforms when selecting a pIOL length for appropriate vault.

Intraocular pressure changes during injection of microincision and conventional intraocular lenses through incisions smaller than 3.0 mm.

PURPOSE: To compare intraocular pressure (IOP) during insertion of a new microincision intraocular lens (IOL) (Akreos AO MI60) and a conventional IOL (AcrySof Natural SN60AT) and to determine the minimum incision sizes for insertion in a cadaver eye model. SETTING: John A. Moran Eye Center, University of Utah, Salt Lake City, Utah, USA. METHODS: After phacoemulsification in phakic cadaver eyes, multiple IOL insertions were attempted through 1.8 mm to 2.5 mm wounds. The final incision size and insertion success were evaluated in each case. A pressure transducer placed in the vitreous cavity measured real-time IOP changes (100 readings per second), including the mean and peak IOP during IOL implantation. RESULTS: The minimum incision size for the microincision IOL insertion was 1.9 mm using a wound-assisted technique and 2.2 mm using a cartridge-insertion technique. The minimum incision size for wound-assisted implantation of the conventional IOL was 2.4 mm. During successful implantation, the mean and peak IOPs were similar between the 2 IOL types. The peak IOPs exceeded 60 mm Hg (retinal perfusion pressure). In unsuccessful attempts, the mean and peak IOPs were higher for the conventional IOL, reaching 306.05 mm Hg in 1 eye. CONCLUSIONS: Monitoring during implantation of both IOL types confirmed that IOP increases during insertion, including during microincision surgery using a wound-assisted technique. Further studies are necessary to evaluate the effect of pressure spikes on the optic nerve during IOL insertion.

Pigmentary dispersion syndrome with a secondary piggyback 3-piece hydrophobic acrylic lens. Case report with clinicopathological correlation.

We describe a case of pigmentary dispersion syndrome resulting from secondary piggyback implantation of a 3-piece hydrophobic acrylic squared-edged intraocular lens (IOL) in the ciliary sulcus. The intraocular pressure remained elevated despite pharmacological treatment, with a heavily pigmented trabecular meshwork. The piggyback IOL was subsequently explanted and replaced by a silicone IOL with smooth round edges. Examination of the explanted IOL under light and scanning electron microscopy showed clusters of pigment epithelial cells located around the periphery of the anterior optic surface.