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Biomedical subjects

P M Keech

Publications and source records attributed to P M Keech.

3 recordsLinked to original sources

A prospective study of contact lens complications in a managed care setting.

BACKGROUND: Understanding the rate of contact lensrelated complications and the factors that affect their occurrence can facilitate better prescribing decisions. METHODS: In a managed care setting, 1496 patient visits were evaluated using a common protocol by 11 optometrists to determine the prevalence of all contact lens-related complications. RESULTS: Over one-half (61%) of the visits were normal, with the remainder showing some type of complication. The more prevalent complications included superficial punctate staining (17.3%) and neovascularization (11.4%). Total complications were less prevalent with rigid gas permeable (RGP) and disposable lens types. Planned replacement soft lenses, used on a daily wear schedule, had the lowest prevalence of more serious complications when compared to conventional soft and disposable lenses. Patients on an extended wear schedule greater than 3 days were more likely to experience complications. The use of nonapproved care systems showed more complications, with serious complications reduced when a one-step care system was used. CONCLUSION: Choice of lens type, wearing schedule, and care system does affect the prevalence of complications, which underlines the importance of the recommendations of the prescriber.

Adolescent↗

The effect of cycloplegia on the determination of refractive error by the Ophthalmetron.

The Ophthalmetron was used to measure the refractive error of 10 male optometry students. Although there was a high incidence of invalid readings, more repeatable results were obtained with use of a cycloplegic. Measurements made under cycloplegia revealed 0.41 D more hyperopia but no differences in astigmatism as compared to the noncycloplegic refraction. Instrument myopia was shown not to be a factor.

Accommodation, Ocular↗

Case report: familial cone dysfunction.

Four generations of a family with hereditary retinal degeneration underwent extensive optometric evaluation, including electrodiagnostic testing. The compiled data indicate a partial cone dysfunction transmitted as an autosomal dominant trait. The optometrist's role in the diagnosis of such conditions is discussed as well as his role in family counseling. The cone dysfunction under discussion is differentiated from other tapetoretinal degenerations.

Aged↗