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Biomedical subjects

M Rolando

Publications and source records attributed to M Rolando.

At least 19 recordsLinked to original sources

Optic disc surface smoothness and visual field indices.

BACKGROUND: In order to ascertain whether the optic disc surface smoothness (ODSS) could be used to predict the amount of visual field damage in glaucomatous eyes, the correlations between ODSS and visual field indices were evaluated. METHODS: One eye was randomly chosen from each of 40 normals and 50 patients with glaucoma. The morphology of the optic disc surface was analyzed using the Topcon IMAGEnet X Rev-3.51b. In order to define the level of "smoothness" of the optic disc surface, the differences of the relative position of each surface point was studied by measuring the standard deviation (SD) from the average height of the points (number of points ranged from 623 to 1883 depending on the size of the disc area) that identify the optic disc surface. All the subjects were also examined with the Humphrey perimeter (Program 30-2) and the results were analyzed by Mann-Whitney U-test and Spearman rank correlation coefficient. RESULTS: The difference in ODSS between the glaucomatous and the normal eyes was statistically significant. No significant correlation was found between age and ODSS. A significant correlation was found between ODSS and mean deviation (MD) and between ODSS and corrected pattern standard deviation (CPSD). In the glaucoma group there were significant correlations between ODSS and the perimetric indices MD and CPSD; no correlations were found in the normal group. CONCLUSION: The ability of ODSS to reflect the level of visual field change in glaucomatous eyes appears to be rather limited, even if statistically significant. This fact does not limit the clinical usefulness of ODSS as a diagnostic parameter in consequence of its strong correlations with the other morphometric parameters and its high sensitivity and specificity in separating normal from glaucomatous eyes.

Female

Forecasting of hydrophilic contact lens tolerance by means of tear ferning test.

BACKGROUND: The ability of the tear ferning test to predict future hydrophilic contact lens tolerance was studied. METHODS: The tear ferning test (TFT) was performed on one randomly chosen eye of each of the 116 subjects who came to our contact lens clinic for hydrophilic contact lens application. The TFT was performed at the time of enrollment (TO) and then 1 month (T1), 3 months (T2) and 6 months (T3) after contact lens fitting. The specificity and the sensitivity of the TFT in identifying future contact lens tolerance was then studied. The statistical significance of the differences in behavior through the study period among the subjects with different pre-fitting TFT results was evaluated by means of survival curves. RESULTS: When only type I ferning was considered as a marker of good tear film conditions, the ability of the TFT to forecast contact lens tolerance had 78.95% sensitivity, 78.35% specificity and 78.45% diagnostic precision. The TFT showed sensitivity of 100%, specificity of 86.6% and diagnostic precision of 97.4% when performed after 1 month of contact lens wearing (T1). Survival curve analysis showed a statistically significant difference in behavior between the group of subjects with pre-fitting ferning type I and the other three groups (P < 0.001). CONCLUSION: The TFT appears to have good sensitivity and specific for prediction of contact lens tolerance in a clinical setting.

Contact Lenses, Hydrophilic

A comparative study of computerised visual field testing and optic disc morphometric parameters in the follow-up of primary open angle glaucoma.

PURPOSE: To evaluate the correlation between computerised visual field testing and optic disc morphometric parameters (rim area, rim/disc area ratio, cup/disc area ratio and optic disc surface smoothness (ODSS)) in the follow-up of a group of patients affected by primary open angle glaucoma (POAG). METHODS: Reliable automated perimetry (Humphrey 640 VFA, central 30-2 threshold program) was performed at T0 (the enrollment time), T1 (after 6 +/- 1 months; range 5-7 months), T2 (12 +/- 1 months), T3 (18 +/- 1 months), and T4 (the end of the follow-up period: 24 +/- 2 months) in one eye randomly chosen from each of 30 POAG patients. Computerised optic disc analysis (IMAGEnet X Rev-3-51b, Topcon Europe, The Netherlands) was performed at T0 and T4. To evaluate the correlation between morphometric parameters and computerised visual field testing, the stability or worsening of visual field test was evaluated by means of 'Mean Deviation linear regression analysis' (STATPAC 2 software); that of morphometric parameters was studied using their coefficients of variation. A rank of '0' was assigned to stability and a rank of '1' to worsening. The Spearman rank correlation coefficient was used to evaluate statistically the correlations between visual field analysis and morphometric parameters. Furthermore kappa statistic was used to evaluate the agreement of morphometric parameter changes with visual field progression analysis. RESULTS: According to the MD slope regression analysis, in 18 patients the visual fields were stable while in 12 they were worsening during the follow-up period. In 86.65% of patients (n = 26) the morphometric parameter ODSS and visual field analysis were concordant (p < 0.0001). In 80% of patients (n = 24) the cup/disc area ratio and visual field analysis were concordant (p < 0.001). The other morphometric parameters (rim area, rim/dics area ratio) were less correlated with visual field analysis than ODSS (p < 0.05). The agreement of visual field analysis with all the morphometric parameters was good (kappa = 0.690, 95% confidence interval (CI) of kappa = 0.589-0.790). The agreement of visual field analysis with ODSS and cup/disc area (kappa = 0.688; 95% CI = 0.511-0.864) was better than the agreement of visual field analysis with rim area and rim/disc area ratio (kappa = 0.438; 95% CI = 0.260-0.655). CONCLUSION: Analysis of the progression of visual field damage and optic nerve head morphometric parameters should both be taken into account in glaucoma follow-up. Among the morphometric parameters evaluated by means of Topcon IMAGEnet, ODSS and (to a lesser extent) the cup/disc ratio should have the greatest weight.

Aged

Effect of betaxolol on primary open-angle glaucoma and normal-tension glaucoma patients.

This study is aimed at establishing the efficacy of the therapeutic agent, betaxolol, in diurnal control of IOP (intraocular pressure). Therapy was performed on 32 eyes affected by POAG (primary open-angle glaucoma) and 16 eyes affected by NTG (normal-tension glaucoma). Two preparations of betaxolol were utilized: betaxolol hydrochloride 0.50% (Betoptic) was administered to 15 POAG and 7 NTG eyes; betaxolol hydrochloride 0.25% ophthalmic suspension (Betoptic S) was administered to 17 POAG and 9 NTG eyes. IOP measurements were taken every two hours from 8 a.m. to 8 p.m. IOP was measured before therapy and at 12 hours, 30 days, and 3 months of therapy. Betaxolol hydrochloride 0.50% was more effective at lowering IOP during the day. Diurnal pressure peaks, which are a risk factor concerning the maintenance of visual field in glaucoma patients, were also reduced using 0.50% betaxolol hydrochloride.

Adrenergic beta-Antagonists

Bacterial load and protein deposits on 15-day versus 1-day disposable hydrophilic contact lenses.

PURPOSE: This study quantified the bacterial load and protein deposits on 1- and 15-day disposable contact lenses after use in normal wearers. METHODS: Sixteen patients were randomly assigned to a 1-day contact lens (1-Day Acuvue) in one eye and to a 15-day contact lens (Acuvue) in the contralateral eye. Only one specified solution was allowed for the care of 15-day lenses. All patients were evaluated every month for 6 months (at times T1, T2, T3, T4, T5, T6). At times T1, T3, and T5, the lenses were removed in a sterile fashion and sent for laboratory quantification of Staphylococcus aureus and Pseudomonas aeruginosa. At T2, T4, and T6, quantification of protein deposits was determined, and at T0 and T6, impression cytology of the conjunctiva was performed. RESULTS: P. aeruginosa was not identified on any lens. At T1, T3, and T5, S. aureus was significantly greater on the 1-day versus 15-day lenses (p < 0.001). In contrast, protein deposits were significantly greater on the 15-day lenses at all time points (T2, T6: p < 0.01; T4: p < 0.05). Impression cytology of the 15-day lens eyes revealed a worsening trend compared to the 1-day lens; however, no statistically significant differences were found between the two groups (p = 0.29). CONCLUSION: Results of this study suggest that the use of cleaning and preservative solutions can alter the ocular surface bacterial environment of the contact lens wearer and that these changes are not a direct consequence of contact lens wear. The bactericidal activity of these solutions could, with time, also affect ocular surface cells, leading to contact lens intolerance and ocular surface disease.

Adult

Low spatial-contrast sensitivity in dry eyes.

PURPOSE: Blurred vision in keratoconjunctivitis sicca eyes could be the result of the loss of the glossy surface of the tear film because of changes in composition or thickness irregularities. Spatial-contrast sensitivity in keratoconjunctivitis sicca and normal control eyes was tested before and after a tear substitute. METHODS: Three different groups of subjects were enrolled: one group of dry eyes with nonsignificant signs of epithelial disease (n = 12), the second group of dry eye positive with 1% Bengal rose staining of the cornea and of the conjunctiva (n = 18), and a third of normal eyes as control group (n = 15). In all the 45 eyes, spatial-contrast sensitivity was tested under the best correction by means of the Vistech Multivision Contrast Tester 8000 (Vistech Consultants, Dayton, OH, U.S.A.) before and 15 min after the instillation of a 0.4% Na-hyaluronate tear substitute without preservatives. RESULTS: A significant decrease of spatial-contrast sensitivity ranging from 35 to 70% was present in keratoconjunctivitis sicca eyes compared with a third group of age-matched normal eyes used as control. The spatial-contrast sensitivity was significantly lower also in the presence of preserved corneal surface. The addition of a tear substitute improved spatial contrast-sensitivity thresholds in all groups. CONCLUSION: Tear-film disease can affect the transfer function of modulation of the ocular surface.

Adult

RA/DA cumulative curve analysis of local and diffuse neuroretinal rim area damage in glaucoma patients.

AIM: To evaluate the validity of cumulative rim/disc area (RA/DA) curve analysis as a clinical tool for the identification of glaucoma induced optic disc pathology. METHODS: 71 normal and 83 glaucomatous eyes were evaluated from a series of 154 subjects recruited for this study. For each eye, the cumulative distribution of RA/DA was calculated from 36 equally spaced rim sectors of each optic disc obtained by the automatic evaluation of simultaneous videographics (Image-net X Rev.3/51b). To increase the sensitivity of this analysis in early glaucoma and in normal eyes, these cumulative curves were subsequently divided into two equal segments and the slopes of their respective regression lines compared. RESULTS: The median RA/DA value obtained from the 36 sectors was significantly different in glaucomatous eyes compared with normals (p < 0.001). Nevertheless, the curves (5th-95th percentile of the cumulative curves distribution) of early glaucomatous eyes fell within the normal range. When the cumulative curve of these marginal cases was then divided into two equal segments, the comparison of the slopes of the regression lines showed a significant difference (p < 0.05) in 100% of early glaucomatous eyes. Furthermore, normal eyes were shown to be true negatives in 93% of the cases in which no significant difference between the two slopes was observed. CONCLUSION: Analysis of the RA/DA cumulative curve from 36 sectors of the optic disc was a valid method for the identification of glaucomatous disc pathology; however, a further calculation of the slopes of the two RA/DA regression lines was needed to identify early glaucomatous damage.

Female

Fluctuations of intraocular pressure during the day in open-angle glaucoma, normal-tension glaucoma and normal subjects.

PURPOSE: The aim of the present paper is to describe the variations in intraocular pressure (IOP) during the day in normals, in patients with primary open-angle glaucoma (POAG) and in patients with normal-tension glaucoma (NTG). IOP represents one of the most important risk factors for glaucoma. However the IOP value is not constant during the day and IOP fluctuation could influence the diagnostic and prognostic evaluation of the glaucomatous disease. METHODS: For this purpose IOP was evaluated every 2 h from 8 a.m. to 8 p.m. in one randomized eye of 33 normal subjects, 95 POAG and 50 NTG patients. RESULTS: The results show that the highest IOP values were detectable in the morning in all three groups. The lowest values were found in the early afternoon hours. These variations were most evident in POAG patients. The daily IOP fluctuations were directly proportional to IOP level. CONCLUSION: The study evidents that a single tonometric evaluation, especially if done in the first hours of the afternoon, is not sufficient to correctly evaluate the IOP-related risk in glaucoma patients. If the pressure peaks are important in determining the extent of glaucomatous damage in NTG patients IOP should not have an important role in optic nerve head damage. The use of diurnal curves seems to be mandatory for the assessment of IOP-related risk and of efficiency of the therapeutic approach.

Aged

Efficacy and safety of 0.3% carbomer gel compared to placebo in patients with moderate-to-severe dry eye syndrome.

PURPOSE: Carbomer gel is a water-soluble polymeric resin that has been reported to maintain the tear film in contact with the eye for an extended period. The efficacy and safety of this new artificial tear were assessed. METHODS: A multicenter, single-masked, randomized, placebo-controlled study was carried out on 123 patients with moderate-to-severe dry eyes. The placebo was a mannitol solution with benzalkonium chloride 0.008% as preservative. Patients were observed over an 8-week period, and subjective and objective changes analyzed, compared to a baseline of no therapy, after 1 to 7 days washout period from previous medication. RESULTS: All primary subjective symptoms decreased significantly in the carbomer gel-treated group compared to the placebo group (i.e., dryness, discomfort, and foreign body sensation). The carbomer gel also significantly improved the rose bengal staining score relative to placebo. When data for the primary subjective efficacy variables were stratified for disease severity, there was a statistically significant improvement from baseline by day 10 for severely affected patients and from day 42 for patients with moderate disease. Secondary subjective symptoms that improved significantly in the tear gel group compared to placebo were photophobia, erythema, tear breakup time, blurry-filmy, dry-sandy sensation, and physician impression. However, no significant improvements in the secondary subjective symptoms of tearing, itching, scaling, conjuctival discharge, palpebral conjunctival redness, bulbar conjuctival redness, conjunctival luster, relief of discomfort, ease of use, and overall acceptability were found in either group over the baseline score. In addition, neither carbomer gel nor placebo improved the baseline fluorescein staining score or the Schirmer test score. Two patients suffered local allergic reactions to the carbomer gel or its preservative, which settled on withdrawal of the medication. CONCLUSIONS: Carbomer gel was more efficacious than was placebo in improving a number of subjective and objective symptoms of moderate-to-severe dry eye syndrome. The results of this study indicate that carbomer gel was a safe as was the placebo.

Acrylic Resins

Intraimage reproducibility of measurements in the macular area using a computerized system.

An accurate analysis of the morphological changes which take place during pathological processes of the posterior pole is important for a correct diagnosis and therapeutic approach. The purpose of the study was to determine the intraobserver and interobserver reproducibility of the Image-net system 100 (Topcon, Japan) to take measurements on the retina. The program 'Linear/Areal Measurement functions' of Image-net system 100 which is an image digitalization technique, was tested. Twelve patients were consecutively selected from the patients of the Retina Center of the Department of Ophthalmology, University of Genoa. Three images of each eye were taken from each subject and only the best image was used in this study. The intraobserver and interobserver reproducibility of both the distance between two pre-set points (linear measurement), and the perimeter and area of preselected retinal zones were calculated. The repeatability (or intraobserver reproducibility) of the linear sizes was measured by the coefficient of variation and ranged from 0.32% to 7.38%, while the interobserver reproducibility ranged from 0.46% to 5.22%. The repeatability and reproducibility of the perimeters ranged from 0.72% to 9.63% and from 0.6% to 5.7%, respectively, while the repeatability and reproducibility of the areas ranged from 0.72% to 9.63% and from 0.6% to 5.7%, respectively. Although the results were quite good, the quality of the image of the fundus and the number of observers influenced the coefficient of variation; furthermore, the anatomy of the areas to be measured and the computer 'mouse' could increase the value of the coefficient of variation.

Angiography, Digital Subtraction

Study of the correlation between average values of optic disc parameters and their measurement variability using stereovideographic digital analysis.

Purpose of our study was to find whether there is a correlation between average values of optic nerve head parameters and their coefficient of variation for repeated measurements. Disc stereo video images were taken with Topcon Imagenet (IS100) and analyzed with the Optic Disc Analysis program. Eleven normal and 9 glaucomatous eyes were selected. A significant correlation was found for horizontal cup/disc ratio (r = -0.037, p = 0.037) and disc area (r = 0.776, p = 0.027) in intra-observer intra-image repeated measurements. Vertical, horizontal and average cup/disc ratios (r = -0.81, r = -0.74, r = -0.78 p < 0.05) showed a significant correlation for intra-observer inter-image repeated measurements. For inter-observer intra-image measurements, a significant correlation was present for average cup/disc ratio (r = -0.64, p = 0.043). Our data show that bidimensional semiquantitative parameters in use for optic nerve head assessment, analyzed by computerized stereovideography, have an intrinsic measurement variability. The variability is significantly related to the value of the measured parameter only when their reference points are determined manually by the operator.

Adult

Effect of the synthetic retinoid fenretinide on dark adaptation and the ocular surface.

BACKGROUND: Fenretinide, a synthetic derivative of retinoic acid, is under study in clinical trials for the prevention of breast, skin basal cell, bladder, and oral cancer in patients at risk. Although fenretinide is well tolerated even after prolonged use, it does lower plasma retinol levels and thus may affect night vision. PURPOSE: The purpose of this study was to measure changes in dark adaptation resulting from fenretinide administration, to compare the measured results with the patient's subjective perception, to define the association with plasma retinol levels, to assess the reversibility of alterations in night vision, and to assess the effects of fenretinide on the surface of the eye. METHODS: The study involved 65 women who had been operated on for stage I breast cancer. Of the study group, 34 received 200 mg daily of fenretinide for a median of 32 months, while 31 control subjects did not. Dark adaptation was studied with the Goldmann-Weekers adaptometer and with a subjective questionnaire. Plasma retinol levels were measured at each test of dark adaptation. Effects of fenretinide on the ocular surface were evaluated through conjunctival impression cytology. RESULTS: Of the patients on fenretinide, eight (23.5%) showed mild and nine (26.5%) showed moderate alterations of measured dark adaptability, compared with just two controls (6.5%) with mild alterations (cumulative odds ratio = 15.4; P = .0008). A significant inverse correlation exists between the final sensitivity threshold of dark-adaptometry and plasma retinol levels, with mild alterations arising below 16 micrograms/dL and moderate alterations below 10 micrograms/dL. Abnormal rod function improved significantly after 7 days and normalized 1 month after use of fenretinide was stopped or vitamin A supplementation was begun, while the conventional 3-day drug suspension, or drug half dose, did not allow sufficient recovery. Alterations of conjunctival cytology were slightly higher in patients receiving fenretinide, but no clinical disorders of the ocular surface were observed. CONCLUSIONS: The women treated with 200 mg fenretinide daily showed a relatively high incidence of mild-to-moderate alterations of dark-adaptometry as measured with the Goldmann-Weekers adaptometer. However, the real-life implication of the measurements is an open question, for the questionnaire shows that 50% of the patients with altered dark adaptometry were asymptomatic.

Breast Neoplasms

Measurement variability in digital analysis of optic discs.

The optic disc of nine patients with typical glaucomatous disc damage and ten normal controls has been studied by means of the Optic Disc Analysis program of the Topcon Image-net System. Vertical, horizontal and average cup/disc ratio (VC/D, HC/D, AC/D), disc, cup, rim area (DA, CA, RA), cup volume (CV) have been evaluated and the coefficient of variation (COV) of multiple measurements was calculated. For intra-observer intra-image variability assessment, sterovideographs of each disc were taken once and analyzed 10 times (COV range: 1.39-12.08%). Intra-observer interimage variability was evaluated on eight stereovideographs of each disc taken at one minute intervals (COV range: 1.63-96%). Inter-observer intra-image measurements were taken on each disc by 5 different observer (COV range: 1.28-27.08%).

Adult