5 research outputs found
Retinal thickness study with optical coherence tomography in patients with diabetes
To quantitatively assess retinal thickness by optical coherence
tomography (OCT) in normal subjects and patients with diabetes. This study was
intended to determine which retinal thickness value measured with OCT best
discriminates between diabetic eyes, with and without macular edema. METHODS: OCT
retinal thickness was measured by a manual technique in a total of 26 healthy
volunteers (44 control eyes) and 85 patients with diabetes (148 eyes) with the
clinical diagnosis of no diabetic retinopathy (45 eyes), nonproliferative
diabetic retinopathy without clinically significant macular edema (CSME; 54
eyes), proliferative diabetic retinopathy without CSME (21 eyes), and 28 eyes
with diabetic retinopathy with CSME. Independent predictors of the presence of
CSME were quantified by using univariate and multivariate logistic regression
analyses. Receiver operating characteristic (ROC) curves were generated to
evaluate and compare the predictor variables. The correlation of retinal
thickness measurements and visual acuity was calculated. RESULTS: There were
statistically significant differences in foveal thickness between control eyes
and all the other eye groups (P = 0.001). Diabetic eyes with CSME had a
statistically significant greater thickness in each of the areas compared with
the other groups. In a multivariate logistic regression model, foveal thickness
was a strong and independent predictor of CSME (odds ratio [OR], 1.037; 95%
confidence interval [CI] 1.02-1.05). The area under the ROC curve of this
predictor variable was 0.94 (P = 0.001). For a cutoff point of 180 microm, the
sensitivity was 93%, and specificity was 75%. Foveal thickness correlated with
visual acuity in a log minimum angle of resolution (logMAR) scale (Spearman's rho
= 0.9, P = 0.001). CONCLUSIONS: These results suggest that foveal thickening over
180 microm measured by OCT may be useful for the early detection of macular
thickening and may be an indicator for a closer follow-up of the patient with
diabetes
Termoterapia transpupilar en neovascularización subretiniana oculta secundaria a degeneración macular asociada a la edad. Primeros resultados
To determine the efficacy of transpupillary thermotherapy (TTT) to treat choroidal neovascularization (CNV) in patients with age-related macular degeneration (ARMD).
Patients and Methods: Eight patients (ten eyes) with occult CNV were treated by TTT. A 810 nm diode laser was used to perform TTT. The diode laser was delivered through a panfunduscopic contact lens.
Results: Three eyes showed a visual acuity improvement and a decrease in exudation on fluorescein angiography. Four eyes remained stable. Nevertheless, lesions worsened after treatment in three cases. One of these cases suffered an overtreatment.
Conclusions: TTT may be a useful therapy in some cases of CNV in patients with age-related macular degeneration. Randomized and multicentric studies are necessary to stablish precise indications of this therap
PRPH2-Related Retinal Diseases: Broadening the Clinical Spectrum and Describing a New Mutation
Over 175 pathogenic mutations in the Peripherin-2 (PRPH2) gene are linked to various retinal diseases. We report the phenotype and genotype of eight families (24 patients) with retinal diseases associated with seven distinct PRPH2 gene mutations. We identified a new mutation, c.824_828+3delinsCATTTGGGCTCCTCATTTGG, in a patient with adult-onset vitelliform macular dystrophy (AVMD). One family with the p.Arg46Ter mutation presented with the already described AVMD phenotype, but another family presented with the same mutation and two heterozygous pathogenic mutations (p.Leu2027Phe and p.Gly1977Ser) in the ATP Binding Cassette Subfamily A Member 4 (ABCA4) gene that cause extensive chorioretinal atrophy (ECA), which could be a blended phenotype. The p.Lys154del PRPH2 gene mutation associated with the p.Arg2030Glu mutation in the ABCA4 gene was found in a patient with multifocal pattern dystrophy simulating fundus flavimaculatus (PDsFF), for whom we considered ABCA4 as a possible modifying gene. The mutation p.Gly167Ser was already known to cause pattern dystrophy, but we also found ECA, PDsFF, and autosomal-dominant retinitis pigmentosa (ADRP) as possible phenotypes. Finally, we identified the mutation p.Arg195Leu in a large family with common ancestry, which previously was described to cause central areolar choroidal dystrophy (CACD), but we also found ADRP and observed that it caused ECA more frequently than CACD in this family
Tarsal switch using an anterior approach to correct severe ptosis
Background To present the outcomes of the tarsal switch procedure using an anterior approach to correct severe ptosis with poor levator muscle function (<4 mm) with absent or poor Bell’s phenomenon. Methods This retrospective case series included 11 patients with severe neurogenic or acquired myogenic palpebral ptosis. All patients underwent the tarsal switch procedure through an anterior approach from 2012 to 2015. Margin reflex distance (MRD1 and MRD2) and the palpebral fissure were evaluated preoperatively and postoperatively. Data were compared using the Wilcoxon signed-rank test. P-values <0.05 were considered to indicate statistical significance. Results Surgery was performed on 18 eyelids (11 patients). The median age at surgery was 57 years (range, 29-86 years). Four patients had unilateral ptosis and seven had bilateral ptosis. Nine patients had myogenic ptosis and two had neurogenic ptosis. Postoperatively, the chin-up position improved in all patients. The MRD1 increased statistically significantly, from 0 mm preoperatively to 1.0 mm postoperatively (P=0.001). The MRD2 decreased statistically significantly, from 4.5 mm preoperatively to 3.0 mm postoperatively (P=0.001). The palpebral fissure did not change (4.0 mm preoperatively to 4.0 mm postoperatively) (P=0.13). Conclusions The tarsal switch procedure through an anterior approach is an effective alternative for correcting severe ptosis, especially neurogenic or acquired myogenic ptosis. This procedure can be performed with minimal risk of ocular surface exposure and provides stable outcomes