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Biomedical subjects

G D Barrett

Publications and source records attributed to G D Barrett.

At least 19 recordsLinked to original sources

Coexistent adenoviral keratoconjunctivitis and Acanthamoeba keratitis.

A 17-year-old youth presented with bilateral follicular conjunctivitis and nummular subepithelial corneal infiltrates. Failure of this to settle in an outpatient setting led to corneal scraping with microscopy and culturing for bacteria, fungi, Herpes simplex, adenovirus and Acanthamoeba as an inpatient. Polymerase chain reaction analysis of corneal cells was positive for adenovirus, and culture on live Escherichia coli-coated agar plates was positive for Acanthamoeba by phase contrast microscopy on day two. We conclude that Acanthomoeba infection can complicate adenoviral keratoconjunctivitis. This observation is in keeping with previously reported modes of infection by Acanthamoeba, whereby any epithelial breach seems to allow inoculation of the eye by this opportunistic organism.

Acanthamoeba↗

In vitro bacterial adherence to hydrogel and poly(methyl methacrylate) intraocular lenses.

PURPOSE: To compare the in vitro adherence of Staphylococcus epidermidis to poly-(hydroxyethyl methacrylate) (polyHEMA) or hydrogel intraocular lenses (IOLs) and poly(methyl methacrylate) (PMMA) IOLs. SETTING: Lions Eye Institute, Perth, Western Australia. METHODS: One-piece hydrogel lenses and one-piece PMMA lenses were suspended for 60 minutes in standardized suspensions of a well-characterized strain of S. epidermidis and then sonicated in a known quantity of balanced salt solution to remove the adherent bacteria. Quantitative cultures of the sonicates were performed and the results analyzed statistically. RESULTS: The mean bacterial adherence of S. epidermidis to the PMMA IOLs (58,400 CFU) was more than 20 times greater than that to the hydrogel IOLs (1953 CFU). The difference was statistically significant (P < .001). CONCLUSIONS: Adherence of S. epidermidis to hydrogel IOLs is significantly lower than to PMMA IOLs. This suggests that the risk of postoperative endophthalmitis after cataract extraction and IOL implantation may be lower with the use of hydrogel IOLs.

Bacterial Adhesion↗

A new hydrogel intraocular lens design.

A new hydrogel intraocular lens was designed to improve fixation and support. The lens, IOGEL model 2000S, has a 6.00 mm optic that merges via a crescentic flange into a terminal loop for an overall diameter of 12.00 mm. The haptics are more flexible than existing loops and the design of the lens is based on a concept of minimum loop rigidity; that is, a haptic that is rigid enough to support the weight of a lens in aqueous within the capsular bag is considered adequate for modern cataract surgery. I evaluated the lens design's safety and efficacy. Excluding patients with pre-existing macular degeneration, the corrected acuity of all patients at last follow-up was 20/40 or better in 100%, 20/30 or better in 95%, 20/25 to 20/20 or better in 85%, and 20/15 or better in 15%. The new haptic can accommodate compression of the capsular bag and allows early, reliable fixation. The centration of the lens was excellent early in the postoperative period and later after capsular fibrosis developed.

Aged↗

Combined small incision phacoemulsification and trabeculectomy.

A method of combined cataract extraction and trabeculectomy is described in which phacoemulsification is performed through a 3.5 mm incision with insertion of a foldable hydrogel lens. This procedure is suitable for most cases in which glaucoma and cataract are coincident. In an initial series of ten patients followed for nine months, all those without additional pathology achieved a corrected visual acuity of 20/40 or better. The maximum induced astigmatism was 0.5 diopters (D), with no change or a reduction in astigmatism in seven patients (70%). Astigmatic shift between week 1 and three months was minimal (average = 0.075 D), with little change thereafter. Intraocular pressures were controlled (< or = 21 mm Hg) without adjunctive medication in all but one of the patients at nine months. This combined procedure preserves the principal advantages of small incision phacoemulsification: low induced astigmatism, early refractive stabilization, and rapid visual rehabilitation. In addition, reducing the extent of tissue dissection may reduce the stimulus to wound healing and early filtration failure.

Aged↗

An improved universal theoretical formula for intraocular lens power prediction.

Although available empirically derived and theoretical formulas perform adequately for eyes of average axial length, both have been shown to be deficient for eyes that have unusually short and long axial lengths. I developed a formula based on a theoretical model eye in which anterior chamber depth is related to axial length and keratometry. A relationship between the A-constant and a "lens factor" is also used to determine anterior chamber depth. The location of the intraocular lens' principle planes of refraction is retained as a relevant variable in the formula, and the user need not know the material and construction of the lens and or its constant. I compared the new formula with the SRK II, Holladay, and SRK/T formulas in a group of 100 unselected patients and in selected subgroups of patients with average, short, and long axial lengths. The new formula was significantly more accurate than the other third-generation formulas and maintained its accuracy in the subgroups. The formula can be described as universal because it can be used for different lens styles and for eyes with short, medium, and long axial lengths.

Anterior Chamber↗

Pterygium excision with conjunctival autografting: an effective and safe technique.

The optimum mode of treatment for symptomatic pterygia would combine efficacy (a low recurrence rate) with safety (freedom from sight threatening complications), and would not affect visual acuity adversely. The efficacy of pterygium excision with conjunctival autografting in a sun exposed population in which pterygia are prevalent has previously been questioned. A cross sectional review of 93 eyes of 85 patients was carried out by slit-lamp examination a minimum of 6 months (range 6-76 months) after pterygium excision and free conjunctival autografting. Case notes were reviewed to obtain details of complications and visual acuity changes related to surgery. Of six recurrences (6.5%) four of these were asymptomatic with minor recurrences. Two patterns of recurrence were identified: cross graft recurrence (three cases) and outflanking (three cases). Complications (wound dehiscence, three cases; Tenon's granuloma one case; conjunctival cyst, one case) were all corrected by minor surgical revision without sequelae. Unaided acuities were unchanged or improved 3 months after surgery in 86 cases, with a minor diminution (1 Snellen line) in seven cases. This study demonstrates a low recurrence rate for a safe technique in an area in which ongoing ultraviolet light exposure levels are high and pterygia are prevalent.

Adult↗

Cytotoxic effects of residual chemicals from polymeric biomaterials for artificial soft intraocular lenses.

Development of improved hydrogels for soft intraocular lenses, based on 2-hydroxyethyl methacrylate monomer, requires the use of various other monomers and polymerization additives which have potential ocular toxicity. Three monomers, 2-hydroxyethyl methacrylate, methyl methacrylate, and 2-ethoxyethyl methacrylate, as well as two common inhibitors, hydroquinone and 4-methoxyphenol, were subjected to in vitro cytotoxicity assays as aqueous solutions at different concentrations. A new polymerization initiator, 2,2'-azo-bis-(2,4-dimethyl valeronitrile), was thermally decomposed in water at different concentrations and the products were also assayed for cytotoxicity. Assays were based on incubation with human choroidal fibroblasts. Cell death was evaluated by trypan blue dye exclusion, DNA synthesis inhibition, and lactate dehydrogenase tests. While methyl methacrylate and 2-ethoxyethyl methacrylate were found nontoxic, the other chemicals displayed high cytotoxicity. However, when extracts of synthesized poly(2-hydroxyethyl methacrylate) specimens, differentially treated after polymerization, were subjected to the same assays it was found that toxicity from residual 2-hydroxyethyl methacrylate monomer was lost during steam sterilization and storage in water because of the removal of the monomer through aqueous washing. The lack of toxicity in these specimens suggests that residual contents of inhibitor and initiator are too low to cause toxic effects on choroidal fibroblasts. It is concluded that hydrogels have low cytotoxic effects in vitro.

Anisoles↗

Further studies on ultraviolet-absorbing hydrogels for intraocular lenses: relationship between concentration of a polymerizable benzophenone, absorption, and extractability.

A tendency to reduce the use of benzophenone absorbers is currently evident in the manufacture of the UV-absorbing IOLs, mainly because the cutoff wavelengths are inferior to those provided by benzotriazoles. In principle, by incorporating large amounts of benzophenones it may be possible to achieve high cutoff wavelengths. A covalently bondable benzophenone UV absorber, Cyasorb UV-2098, was incorporated in poly(2-hydroxyethyl methacrylate) (PHEMA) in increasing concentrations, and certain associated phenomena were investigated. At 4% w/w absorber content, the nonhydrated polymers turned partially opaque. In water-swollen hydrogels, opacification occurred at a lower absorber content (2% w/w). By using extraction techniques and gas chromatography, we also found that up to 8% w/w of the absorber remained unpolymerized and could leach out from any material containing less than 5% w/w absorber. In samples with higher initial content of absorber, the amount of unreacted, leachable absorber was significantly higher (25% to 30%). Based on this study model (hydrogel/Cyasorb UV-2098), we concluded that benzophenone absorbers cannot provide cutoff wavelengths higher than those provided by benzotriazoles.

Acrylates↗

Laser-induced damage to transparent polymers: chemical effect of short-pulsed (Q-switched) Nd:YAG laser radiation on ophthalmic acrylic biomaterials. I. A review.

The use of short-pulsed lasers in ophthalmic surgery inspired and called for research on the damage inflicted by the laser radiation upon the acrylic polymers from which artificial intraocular lenses are made. The possible release of toxic monomers by laser-induced depolymerization is of great concern but past investigations of this phenomenon have been very limited. The present knowledge of various types of laser-induced damage to transparent polymers is reviewed with particular emphasis on the acrylic materials and intraocular lenses.

Lasers↗

Laser-induced damage to transparent polymers: chemical effect of short-pulsed (Q-switched) Nd:YAG laser radiation on ophthalmic acrylic biomaterials. II. Study of monomer release from artificial intraocular lenses.

Commercial intraocular lenses and polymer specimens, both poly(methyl methacrylate) (PMMA) and poly(2-hydroxyethyl methacrylate) p(HEMA), were subjected to various levels of irradiation from a Q-switched Nd:YAG laser, and then to extraction and sample-enrichment techniques. The extracts were analysed by capillary gas chromatography. In PMMA samples, residual contents of 0.05-0.89% (wt) MMA were found and it appeared that the laser radiation did not cause a detectable increase of the monomer content. No residual HEMA could be found in p(HEMA) samples before or after laser bombardment. It is concluded that the accidental exposure of lenses to Nd:YAG laser cannot produce a significant release of monomers. Depolymerization induced by laser is a process unlikely to occur at the energy levels used in ophthalmic surgery.

Gas Chromatography-Mass Spectrometry↗

Results of the intercapsular technique with the IOGEL lens.

Standard biconvex 12 mm diameter IOGEL PC-1 hydrogel intraocular lenses were inserted into the eyes of 55 patients using intercapsular in-the-bag placement and extracapsular ciliary sulcus placement. All patients had senile cataracts. Endothelial specular microscopic assessment was performed preoperatively and postoperatively at six and 12 months. Viscoelastic agents were not used in any of the cases and upper haptic positioning was achieved with dialing and irrigation and iris retraction in each group, respectively. Major complications in both groups were iridocapsular synechias. This resulted in dislocation of a single haptic into the anterior chamber angle in one ciliary-sulcus-placed lens and in an updrawn pupil in one of the intercapsular cases. Pigment dispersion syndrome occurred in one case with a ciliary-sulcus-placed lens. In one case in each group a Nd:YAG laser posterior capsulotomy was performed. Whereas the visual results in each group were similar, the percentage cell loss was significantly greater in the group with lenses in the ciliary sulcus at six months postoperatively. The lower cell loss in the intercapsular group was attributed to the protective effect of the anterior capsule on the endothelium during the major intraocular manipulations.

Aged↗

Intraocular lens calculation formulas for new intraocular lens implants.

Several different formulas are available for preoperative calculation of the required implant power for a desired postoperative refraction. However, the application of both theoretical and statistically derived regression formulas to the new generation of soft intraocular lens implants poses several difficulties. In this paper the calculation of an A constant for a specific intraocular hydrogel lens implant, as well as the derivation of a universal theoretical formula, is described. The theoretical formula can be applied to other implant styles with various optical configurations and composed of different biomaterials. The SRK and theoretical formulas have been applied retrospectively to a series of patients receiving an intraocular hydrogel lens implant. A comparison shows that both perform satisfactorily in predicting the desired postoperative refraction.

Computer Simulation↗

Multicenter trial of an intraocular hydrogel lens implant.

Several features suggest that hydrogels may have potential advantages as an intraocular lens material. The IOGEL lens is a single piece hydrogel composed of 38% poly HEMA. Clinical experience with the IOGEL lens in Australia has been published, and the safety and efficacy of the lens is currently being investigated in a multicenter trial in Europe, the U.S.A., Canada, Australia, and Japan. This is the first large-scale study of a hydrogel implant. The IOGEL lens clinical study was initiated in May 1986 in Europe, in September 1986 in the U.S.A., and in November 1986 in Canada and Australia. The enrollment progress in May 1987 showed that 501 cases had been implanted in Europe, Canada, and Australia and 100 cases in the U.S.A. The visual acuity outcome is equivalent to that reported in the literature. Patients in the multinational trial achieved 20/40 or better in 86% of cases and in 96% of cases excluding unrelated pathologies. Although hydrogels have only had limited use in the clinical situation, the results of this study suggest that the IOGEL lens is a viable alternative to polymethylmethacrylate lens implants.

Clinical Trials as Topic↗

Clinical results of hydrogel lens implantation.

Polymethylmethacrylate has proven to be a useful intraocular lens (IOL) implant material and remains the most widely used material for the fabrication of IOLs. Complications, however, from IOL implantation still occur. A hydrogel lens has been designed for posterior chamber placement. A clinical study from August 1983 to June 1985 was undertaken to determine the safety and efficacy of this new lens manufactured from 38% poly HEMA. The noninflammatory postoperative complications were limited to lens decentration and opacification of the lens capsule. Three cases of posterior capsule opacification required YAG laser capsulotomy. Laser capsulotomy is feasible and the lens appeared to be more resistant to damage from the YAG laser than polymethylmethacrylate lenses. In general, the material appeared to be well tolerated and there have been no cases of persistent iritis or clinically detectable cystoid macular edema. If the visual acuity outcome by age decade for all patients irrespective of follow-up time is considered, 92% of patients achieved 20/40 or better corrected visual acuity.

Aged↗