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2.
Tomography ; 10(4): 480-492, 2024 Mar 29.
Article in English | MEDLINE | ID: mdl-38668395

ABSTRACT

The aim of this paper is to investigate whether a multifractal analysis can be applied to study choroidal blood vessels and help ophthalmologists in the early diagnosis of retinitis pigmentosa (RP). In a case study, we used spectral domain optical coherence tomography (SDOCT), which is a noninvasive and highly sensitive imaging technique of the retina and choroid. The image of a choroidal branching pattern can be regarded as a multifractal. Therefore, we calculated the generalized Renyi point-centered dimensions, which are considered a measure of the inhomogeneity of data, to prove that it increases in patients with RP as compared to those in the control group.


Subject(s)
Choroid , Retinitis Pigmentosa , Tomography, Optical Coherence , Adult , Female , Humans , Male , Middle Aged , Choroid/diagnostic imaging , Choroid/pathology , Fractals , Retinitis Pigmentosa/diagnostic imaging , Retinitis Pigmentosa/pathology , Tomography, Optical Coherence/methods
3.
Sci Rep ; 14(1): 4688, 2024 02 26.
Article in English | MEDLINE | ID: mdl-38409198

ABSTRACT

As retinitis pigmentosa (RP) is chronic and progressive, the chronological sequence of microvascular changes is important for understanding its pathophysiology. We aimed to investigate retinal and choroidal microvascular changes according to the RP stages. The stages of RP were classified into three stages according to the integrity and width of the inner segment ellipsoid zone: early, ≥ 2500 µm; moderate, < 2500 µm; advanced, absence. Using optical coherence tomography angiography, quantitative microvascular parameters were analyzed. In total, 91 eyes from 49 patients were included. For the superficial capillary plexus (SCP) and deep capillary plexus (DCP), perfusion densities (PDs) in the early stage (SCP: 37.32 ± 8.11%; DCP: 21.19 ± 9.15%) were greater than those in moderate (SCP: 34.16 ± 6.65%, P = 0.011; DCP: 15.67 ± 8.85%, P = 0.031) and advanced stages (SCP: 33.71 ± 9.02%, P = 0.030; DCP: 12.83 ± 6.29%, P < 0.001). The choroidal vascularity index in the early stage (0.58 ± 0.03) was greater than those in the moderate (0.57 ± 0.02, P = 0.017) and advanced stage (0.56 ± 0.02, P = 0.033). The area and perimeter of foveal avascular zone (FAZ) in advanced stage (0.44 ± 0.26 mm2, 2.96 ± 0.86 mm, respectively) were larger than those in early (0.26 ± 0.11 mm2, P = 0.020; 2.19 ± 0.53 mm, P = 0.006, respectively) and moderate stage (0.28 ± 0.13 mm2, P = 0.043; 2.24 ± 0.67 mm, P = 0.013, respectively). During RP disease progression, retinal and choroidal microvascular vessel density decreases in the early stage, followed by FAZ enlargement in the advanced stage.


Subject(s)
Retinal Vessels , Retinitis Pigmentosa , Humans , Retinal Vessels/diagnostic imaging , Fluorescein Angiography/methods , Tomography, Optical Coherence/methods , Visual Acuity , Retinitis Pigmentosa/diagnostic imaging
4.
PLoS One ; 19(1): e0296493, 2024.
Article in English | MEDLINE | ID: mdl-38166083

ABSTRACT

OBJECTIVE: Cystoid macular edema (CME) in retinitis pigmentosa (RP) is an important complication causing visual dysfunction. We investigated the effect of CME on photoreceptors in RP patients with previous or current CME, using an adaptive optics (AO) fundus camera. METHODS: We retrospectively observed the CME and ellipsoid zone (EZ) length (average of horizontal and vertical sections) by optical coherence tomography. The density and regularity of the arrangement of photoreceptor cells (Voronoi analysis) were examined at four points around 1.5° from superior to inferior and temporal to nasal. We also performed a multivariate analysis using CME duration, central macular thickness and transversal length of CME. RESULTS: We evaluated 18 patients with previous or current CME (18 eyes; age, 48.7 ± 15.6 years) and 24 patients without previous or current CME (24 eyes; age, 46.0 ± 14.5 years). There were no significant differences in age, logMAR visual acuity, or EZ length. In groups with and without CME, cell density was 11967 ± 3148 and 16239 ± 2935 cells/mm2, and sequence regularity was 85.5 ± 3.4% and 88.5 ± 2.8%, respectively; both parameters were significantly different. The correlation between photoreceptor density and age was more negative in group with CME. The CME group tended toward greater reductions in duration of CME. CONCLUSION: Complications of CME in RP patients may lead to a decrease in photoreceptor density and regularity. Additionally, a longer duration of CME may result in a greater reduction in photoreceptor density.


Subject(s)
Macular Edema , Retinitis Pigmentosa , Humans , Adult , Middle Aged , Macular Edema/complications , Retrospective Studies , Retinitis Pigmentosa/complications , Retinitis Pigmentosa/diagnostic imaging , Fovea Centralis , Tomography, Optical Coherence/methods , Photoreceptor Cells
5.
Arch. Soc. Esp. Oftalmol ; 99(1): 3-8, enero 2024. ilus, graf
Article in Spanish | IBECS | ID: ibc-229546

ABSTRACT

Antecedentes y objetivo: El espacio supracoroideo (SCS) es una estructura teórica que se sitúa entre el borde interno de la esclera y el límite externo del coroides. El SCS está siendo estudiado por sus posibles usos como vía para la administración de medicamentos y por técnicas quirúrgicas innovadoras para el tratamiento de muchas enfermedades retinianas. La retinitis pigmentosa (RP) es un grupo de trastornos hereditarios y progresivos caracterizados por el detrimento gradual de fotorreceptores que conduce a una discapacidad visual que se manifiesta típicamente como hemeralopía y pérdida progresiva del campo visual. El objetivo del estudio fue definir la morfología de los márgenes coroideos externos mediante el uso de tomografía de coherencia óptica de barrido (SS-OCT) en la RP.Materiales y métodosEstudio observacional retrospectivo diseñado para evaluar la presencia del ESC en la RP. Realizamos SS-OCT en un grupo de 55 pacientes afectados por RP (26 hombres y 29 mujeres, 110 ojos) con una edad media de 51,8±13,7 años. En el grupo de control incluimos a 28 sujetos sanos (6 hombres y 22 mujeres, 56 ojos) con una edad media de 48,8±16,6 años.ResultadosLas imágenes OCT permitieron delinear de manera precisa el margen coroideo externo y el margen escleral interno en los 110 ojos. En el grupo RP se detectó el ESC en 47 de los 110 ojos (42,7%), en el grupo de control se detectó el ESC en 11 ojos (19,6%).Los sujetos del grupo RP con SCS visibles presentaron un menor grosor retiniano (168,4 micrones) en comparación con aquellos con SCS visibles (211,2 micrones, p=0,007). (AU)


Background and objective: The suprachoroidal space (SCS) is a theoretical structure which can be demonstrated between the inner border of the sclera and the outer boundary of the choroid. SCS is being studied for its potential uses as a route for drug delivery and innovative surgical techniques for the treatment of many retinal diseases. Retinitis pigmentosa (RP) is a group of inherited eye disorders characterized by a gradual loss of photoreceptors, resulting in vision impairment, which typically presents as night blindness and progressive visual field loss. The purpose of the study is to define the morphology of outer choroidal margins by means of SS-OCT in RP.Material and methodThis is a retrospective observational study designed to evaluate the presence of SCS in RP. We performed swept source optical coherence tomography (SS-OCT) in a group of 55 patients affected by RP (26 males and 29 females, 110 eyes) with a mean age of 51.8±13.7 years. In the control group, we included 28 healthy subjects (6 males and 22 females, 56 eyes) with a mean age of 48.8±16.6 years.ResultsOCT scans allowed the outer choroidal margin and inner scleral margin to be delineated with certainty in all 110 eyes. In the RP group SCS was detected in 47 of 110 eyes (42.7%), in the control group SCS was detected in 11 eyes (19.6%).Subjects with SCS visible (RP group) had reduced retinal thickness (168.4μm) compared to those with not visible SCS (211.2μm, p=0.007). (AU)


Subject(s)
Humans , Choroid/anatomy & histology , Choroid/diagnostic imaging , Retina , Retinal Diseases , Retinitis Pigmentosa/diagnostic imaging , Retrospective Studies , Vision Disorders
6.
Arch. Soc. Esp. Oftalmol ; 98(5): 270-275, mayo 2023. graf, tab
Article in Spanish | IBECS | ID: ibc-219935

ABSTRACT

Propósito Evaluar cambios en la densidad vascular (VD) mediante la angiografía por tomografía de coherencia óptica (OCTA) en los diferentes sectores maculares de pacientes con retinitis pigmentosa (RP) y controles. Métodos Estudio observacional de 22 casos y 21 controles. Se reclutan 22 pacientes con RP y 21 controles. Se obtienen imágenes de tamaño 6×6 del área macular mediante Angio-OCT SS-DRI-Triton 1.22 (Topcon, Japón), desechando las imágenes con mala calidad. Se recoge agudeza visual, biomicroscopía, campo visual y tomografía de coherencia óptica (OCT) estructural. El área macular se divide en 4 sectores (nasal, superior, inferior y temporal), y se comparan los valores de VD entre ambos grupos en los plexos superficial (SVP) y profundo (DVP). Se estudia también la correlación entre la VD y el grosor macular. Resultados Diez pacientes con RP se desecharon por mala calidad de imagen. Se analizan 12 pacientes con RP y 21 controles sanos. El índice de campo visual (VFI) medio en el grupo RP fue del 26,11% (±17,29). La VD fue significativamente inferior en el grupo RP comparado con los controles en todos los sectores maculares del DVP (Superior 43,48±3,79 vs. 48,86±2,62; p<0,0001; Nasal 40,52±4,30 vs. 46,01±3,23; p=0,0002; Inferior 42,76±5,26 vs. 50,10±3,36; p<0,0001; Temporal 40,42±4,46 vs. 46,09±2,91; p=0,0001) y en todos menos en el sector nasal en el SVP (Superior 39,86±4,46 vs. 46,47±2,61; p<0,0001; Nasal 40,35±4,56 vs. 44,09±2,87; p=0,0067; Inferior 40,74±4,61 vs. 46,58±3,26; p=0,0002; Temporal 39,98±5,07 vs. 44,78±3,28; p=0,0024). La correlación entre la VD y el grosor macular se mostró positiva y significativa (RP: r=0,59; p=0,043; controles r=0,51; p=0,018). Conclusiones Los pacientes con formas avanzadas de RP muestran menor VD en el área macular que los controles sanos. Estas diferencias están presentes en todos los cuadrantes del DVP y en 3 de ellos en el SVP (AU)


Aims To describe the changes in vessel density (VD) using optical coherence tomography angiography (OCTA) of the different sectors in the macular area between retinitis pigmentosa (RP) patients and controls. Methods Observational case-control study. We initially included 22 patients with RP and 21 controls. We obtained 6x6 OCTA images of the macular area using Angio-OCT SS-DRI-Triton 1.22 (Topcon, Japan), together with visual acuity, biomicroscopy, visual field and optical coherence tomography examination. We compared the VD values in both groups for both superficial (SVP) and deep vascular plexus (DVP). Correlation between VD and macular thickness was also calculated. Results The mean visual field index (VFI) in the RP group was 26.11% (±17.29). VD was significantly lower in the RP group compared with healthy controls in all sectors of the DVP (Superior 43.48±3.79 vs 48.86±2.62, P<.0001; Nasal 40,52±4.30 vs 46,01±3.23, P=.0002; Inferior 42.76±5.26 vs 50.10±3.36, P<.0001; Temporal 40.42±4.46 vs 46.09±2.91, P=.0001) and in all but nasal sector in the SVP (Superior 39.86±4.46 vs 46.47±2.61, P<.0001; Nasal 40.35±4.56 vs 44.09±2.87, P=.0067; Inferior 40.74±4.61 vs 46.58±3.26, P=.0002; Temporal 39.98±5.07 vs 44.78±3.28, P=.0024). Correlation between VD and macular thickness was positive and significant (RP: r=.59, P=.043; controls r=.51, P=.018). Conclusions Patients with advanced forms of RP have less vessel density in the macular area than healthy subjects. These differences are present in all four quadrants in the DVP and three in the SVP (AU)


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Retinitis Pigmentosa/diagnostic imaging , Tomography, Optical Coherence , Case-Control Studies , Angiography
7.
Ann Afr Med ; 22(4): 451-455, 2023.
Article in English | MEDLINE | ID: mdl-38358145

ABSTRACT

Background: Optical coherence tomography (OCT) is a noninvasive, frequently used imaging technology that enables detailed viewing of retina anatomy. It is used to monitor disease progression in retinitis pigmentosa (RP) eyes, including detecting changes in retinal thickness. Purpose: The purpose of the study is to determine the clinical presentation and macular morphology in RP eyes using OCT imaging. Methods: A retrospective review of case records and OCT scans in eyes diagnosed with RP in two ophthalmic clinics in Nigeria. Biodata, Snellen best-corrected visual acuity (BCVA), intraocular pressure (IOP), vertical cup-to-disc ratio (VCDR), and presence of maculopathy were determined. Data were analyzed using IBM SPSS version 22.0 (IBM Corp. Armonk, NY, USA). Results: Fifty-five eyes of 28 patients (18 males and 10 females), with a mean age of 47.16 ± 15.56 years (22-77 years), were studied. 40-49 years was the most frequent age group, 28.6%. Severe visual impairment occurred in 22% of eyes and myopia in 32%. Twenty-nine percent had undergone cataract surgery or had a significant cataract. The mean IOP was 11 mmHg, and the mean VCDR was 0.46. On OCT examination, macular atrophy was the most common finding in 74.5% of eyes, epiretinal membrane in 16.3%, cystoid macular edema in 7.3%, vitreomacular adhesion in 5.4%, and vitreomacular traction in 1.8%. There was no association between macular morphology, macular thickness, and BCVA (P = 0.155, P = 0.424). Conclusion: OCT provides information on macula structure in RP eyes. About 14.5% of eyes had a normal macula, while 85.5% had a maculopathy, confirming that RP eyes have a higher rate of maculopathy than non RP eyes. OCT evaluation of an RP eye should be a standard workup for the early detection of such maculopathy and monitoring for disease progression.


Résumé Contexte: La tomographie par cohérence optique (OCT) est une technologie d'imagerie non invasive fréquemment utilisée qui permet une visualisation détaillée de l'anatomie de la rétine. Elle est utilisée pour surveiller la progression de la maladie dans les yeux de la rétinite pigmentaire (RP), y compris la détection des changements dans l'épaisseur de la rétine. Objectif: Le but de l'étude était de déterminer la présentation clinique et la morphologie maculaire des yeux présentant une RP à l'aide de l'imagerie OCT. Méthodes: Une revue rétrospective des dossiers de cas et des scans OCT dans les yeux diagnostiqués de RP a été réalisée dans deux cliniques ophtalmologiques au Nigeria. Les données biographiques, la meilleure acuité visuelle corrigée de Snellen (MAVC), la pression intraoculaire (PIO), le rapport cup-sur-disc vertical (RCDV) et la présence de maculopathie ont été déterminés. Les données ont été analysées à l'aide d'IBM SPSS version 22.0 (IBM Corp. Armonk, NY, USA). Résultats: Cinquante-cinq yeux de 28 patients (18 hommes et 10 femmes), âgés en moyenne de 47,16 ± 15,56 ans (22­77 ans) ont été étudiés. Les 40 à 49 ans étaient la tranche d'âge la plus fréquente à 28,6 %. Une déficience visuelle sévère est survenue dans 22 % des yeux et une myopie dans 32 %. Vingt-neuf pour cent avaient subi une chirurgie de la cataracte ou avaient une cataracte importante. La PIO moyenne était de 11 mmHg et le RCDV moyen était de 0,46. À l'examen OCT, on retrouvait l'atrophie maculaire prédominante dans 74,5 % des yeux, la membrane épirétinienne (16,3 %), l'œdème maculaire cystoïde (7,3 %), l'adhérence vitréomaculaire (5,4 %) et la traction vitréomaculaire (1,8 %). Il n'y avait aucune association entre la morphologie maculaire, l'épaisseur maculaire et la MAVC (P = 0,155, P = 0,424). Conclusion: l'OCT fournit des informations sur la structure de la macula dans la RP. Environ 14,5% des yeux avaient une macula normale contre 85,5% avec maculopathie, confirmant ainsi que les yeux avec RP ont un taux de maculopathie plus élevé que les yeux sans RP. L'évaluation OCT d'un œil avec RP devrait être un bilan standard pour la détection précoce de maculopathie et la surveillance de la progression de la maladie. Mots-clés: Membrane épirétinienne, dystrophie rétinienne héréditaire, atrophie maculaire, œdème maculaire, tomographie par cohérence optique, rétinite pigmentaire.


Subject(s)
Cataract , Macula Lutea , Macular Degeneration , Retinal Diseases , Retinitis Pigmentosa , Male , Female , Humans , Adult , Middle Aged , Retinitis Pigmentosa/diagnosis , Retinitis Pigmentosa/diagnostic imaging , Macula Lutea/diagnostic imaging , Tomography, Optical Coherence/methods , Disease Progression , Retrospective Studies
8.
Arq. bras. oftalmol ; 83(5): 410-416, Sept.-Oct. 2020. tab, graf
Article in English | LILACS | ID: biblio-1131638

ABSTRACT

ABSTRACT Purpose: To evaluate the inner retinal and choroidal thicknesses in patients with early retinitis pigmentosa. Methods: We analyzed spectral-domain optical coherence tomography images of 35 retinitis pigmentosa patients and 40 healthy individuals. We measured macular and ganglion cell complex thicknesses. We took choroidal thickness measurements in the subfoveal region and 500, 1,000, and 1,500 mm from the foveal center. Results: Patients with retinitis pigmentosa had significantly thinner macular thicknesses and choroidal thicknesses in all measurements, and their individual ganglion cell complex thickness measurements were lower than those in healthy individuals. The mean ganglion cell complex thickness was significantly lower in patients with retinitis pigmentosa than that in controls. The mean macular thickness was significantly correlated with the mean choroidal and mean ganglion cell complex thicknesses. (We found no correlation between the mean choroidal thickness and the mean ganglion cell complex thickness). Conclusions: The choroid was mildly affected in our patients with early retinitis pigmentosa. The tendency toward significance in the inner retina was possibly caused by a good visual acuity.


RESUMO Objetivo: Avaliar as espessuras internas da retina e da coroide em pacientes com retinite pigmentosa precoce. Métodos: Foram analisadas imagens de tomografia de coerência óptica de domínio espectral de 35 pacientes com retinite pigmentosa e 40 indivíduos saudáveis. Medimos a espessura do complexo de células maculares e ganglionares. Realizamos medições da espessura da coroide na região subfoveal e a 500 mm, 1000 mm e 1500 mm do centro da fóvea. Resultados: Pacientes com retinite pigmentosa apresentaram espessuras maculares e da coroide significativamente mais finas em todas as medições e suas medidas individuais da espessura do complexo de células ganglionares foram inferiores às de indivíduos saudáveis. A espessura média do complexo de células ganglionares foi significativamente menor nos pacientes com retinite pigmentosa do que nos controles. A espessura macular média foi significativamente correlacionada com as espessuras médias do complexo das células de coroide e das células ganglionares médias. Não encontramos correlação entre a espessura media da coroide e a espessura media do complexo de células ganglionares. Conclusões: A coroide foi levemente afetada em nossos pacientes com retinite pigmentosa precoce. A tendência à significância na retina interna foi possivelmente causada por uma boa acuidade visual.


Subject(s)
Humans , Retinitis Pigmentosa , Choroid/diagnostic imaging , Tomography, Optical Coherence , Retina/diagnostic imaging , Visual Acuity , Retinitis Pigmentosa/diagnostic imaging
12.
Arq. bras. oftalmol ; 82(6): 507-510, Nov.-Dec. 2019. tab
Article in English | LILACS | ID: biblio-1038689

ABSTRACT

ABSTRACT Purpose: The aim of this study was to evaluate anterior segment parameters and corneal aberrations in patients with retinitis pigmentosa using Scheimpflug imaging and to compare the findings with those for healthy controls. Methods: This single-center, case-control study included patients diagnosed with retinitis pigmentosa who were followed up at the Department of Ophthalmology of Kayseri Training and Research Hospital between February and June 2018. Age- and sex-matched healthy individuals with no known ophthalmologic disease formed the control group. Both patients with retinitis pigmentosa and controls underwent comprehensive ophthalmic assessments, including the measurement of the best-corrected visual acuity calculation of the spherical equivalent, slit-lamp examination, stereoscopic fundus examination, computerized visual field test, and electroretinography. Topographic and aberrometric values were measured using Scheimpflug-based tomography. Results: This study was performed on 52 eyes of 26 patients with retinitis pigmentosa (14 men) and 52 eyes of 26 healthy controls (11 men). The average keratometry (K avg) values for the patient and control groups were similar (43.87 ± 2.23 versus 43.61 ± 1.68; p=0.546), but the maximum keratometry (K max) value was significantly higher in the patient group (45.85 ± 2.35 and 44.69 ± 1.86; p=0.015). Patients with retinitis pigmentosa had a significantly lower central corneal thickness (518.5 ± 42.3 versus 534.1 ± 24.5, respectively; p=0.042) and maximal corneal thickness (509.1 ± 50.5 versus 530.5 ± 24.1, respectively; p=0.015). Additionally, the iridocorneal angle for the patients was significantly lower (31.6 ± 9.2 versus 35.9 ± 7.7, p=0.025). The aberrometric findings indicated that patients with retinitis pigmentosa had significantly more higher-order aberrations than those in the healthy controls (0.794 ± 51 and 0.398 ± 08, respectively; p<0.001). Conclusions: The results of the present study demonstrated that patients with retinitis pigmentosa have different anterior segment parameters and corneal aberrations compared to healthy controls. These results should be supported by further studies.


RESUMO Objetivo: Este estudo visou avaliar parâmetros do segmento anterior e aberrações corneanas em pacientes com retinite pigmentosa através de imagens de Scheimpflug e comparar os achados com os de controles saudáveis. Métodos: Este foi um estudo caso-controle unicêntrico que incluiu pacientes com o diagnóstico de retinite pigmentosa em acompanhamento no Departamento de Oftalmologia do Hospital de Treinamento e Pesquisa de Kayseri, entre fevereiro e junho de 2018. Indivíduos saudáveis pareados por idade e sexo, sem nenhum conhecimento da doença oftalmológica formou o grupo controle. Ambos os pacientes com retinite pigmentosa quanto os controles foram submetidos a avaliações oftalmológicas abrangentes, incluindo a medição do cálculo da acuidade visual melhor corrigida, o cálculo do equivalente esférico, biomicroscopia, fundoscopia estereoscópica, campimetria computadorizada e eletrorretinografia. Os valores topográficos e de aberrometria foram medidos através de tomografia baseada no sistema Scheimpflug. Resultados: O estudo incluiu 52 olhos de 26 pacientes com retinite pigmentosa (14 homens) e 52 olhos de 26 controles saudáveis (11 homens). Os valores médios da ceratometria (K avg) para grupos dos pacientes e controle foram semelhantes (43,87 ± 2,23 versus 43,61 ± 1,68, p=0,546), mas o valor máximo da ceratometria (K max) foi significativamente maior no grupo de pacientes (45,85 ± 2,35 e 44,69 ± 1,86; p=0,015). Pacientes com retinite pigmentosa apresentaram uma espessura corneana central significativamente menor (518,5 ± 42,3 versus 534,1 ± 24,5, respectivamente; p=0,042) e espessura corneana máxima (509,1 ± 50,5 verus 530,5 ± 24,1, respectivamente; p=0,015). Além disso, o ângulo iridocorneano para os pacientes foi significativamente menor (31,6 ± 9,2 versus 35,9 ± 7,7; p=0,025). Os achados da aberrometria indicaram que os pacientes com retinite pigmentosa apresentaram significativamente mais aberrações de ordem superior em comparação com os controles saudáveis (respectivamente 0,794 ± 51 e 0,398 ± 08, respectivamente; p<0,001). Conclusões: Os resultados do presente estudo demonstraram que pacientes com retinite pigmentosa têm diferentes parâmetros do segmento anterior e aberrações corneanas em comparação com controles saudáveis. Estes resultados precisam ser confirmados por novos estudos.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Retinitis Pigmentosa/pathology , Cornea/pathology , Anterior Chamber/pathology , Reference Values , Case-Control Studies , Retinitis Pigmentosa/diagnostic imaging , Statistics, Nonparametric , Cornea/abnormalities , Cornea/diagnostic imaging , Corneal Topography/methods , Aberrometry/methods , Corneal Pachymetry/methods , Anterior Chamber/diagnostic imaging
13.
Arch. Soc. Esp. Oftalmol ; 94(9): 465-468, sept. 2019. ilus, graf
Article in Spanish | IBECS | ID: ibc-186228

ABSTRACT

Mujer de 67 años con diabetes mellitus tipo 2 sin otros antecedentes de interés que consultó por disminución de agudeza visual de su ojo izquierdo de 4 meses de evolución. El examen de fondo de ojo reveló datos de retinopatía diabética no proliferativa moderada en el ojo derecho y lesiones pigmentadas en forma de espículas óseas y atrofia del epitelio pigmentario retiniano en la media periferia y en el área macular en el ojo izquierdo. El electrorretinograma de campo completo se mostró plano, con una insinuación leve de la onda b en adaptación a la luz con destello único de 3,0cd en el ojo izquierdo. En la tomografía de coherencia óptica se vio la retina atrófica en todas sus capas, quistes intrarretinianos y un desprendimiento neurosensorial seroso de la retina macular con una lesión subretiniana de alta reflectividad en el ojo izquierdo. Fueron descartadas causas infecciosas e inflamatorias. Se administraron 3 inyecciones de ranibizumab intravítreo con periodicidad mensual. La presencia de membrana neovascular coroidea asociada con retinitis pigmentosa unilateral no ha sido publicada previamente. El presente caso respondió a ranibizumab intravítreo


A 67 year-old woman with diabetes mellitus type 2 no medical background of interest was attended in hospital due to visual loss of left eye of 4 months of onset. The fundus examination revealed findings corresponding to moderate non-proliferative diabetic retinopathy in the right eye and pigmented lesions similar to bone spicules and atrophy of the retinal pigment epithelium in the middle periphery and in the macular area in the left eye. The full-field electroretinogram was flat, with a slight insinuation of the b-wave in the light adaptation with a single flash of 3.0cd in the left eye. The optical coherence tomography showed the atrophic retina in all its layers, as well as intraretinal cysts and a serous neurosensory detachment of the macular retina with a lesion of high reflectivity in the left eye. Infectious and inflammatory diseases were ruled out. Three doses of intravitreal ranibizumab were administered monthly. The presence of choroidal neovascular membrane associated with unilateral retinitis pigmentosa has not been previously reported. The patient improved with intravitreal ranibizumab


Subject(s)
Humans , Female , Aged , Choroidal Neovascularization/etiology , Retinitis Pigmentosa/complications , Angiogenesis Inhibitors/administration & dosage , Angiogenesis Inhibitors/therapeutic use , Atrophy/pathology , Choroidal Neovascularization/diagnostic imaging , Choroidal Neovascularization/drug therapy , Diabetic Retinopathy/complications , Diabetic Retinopathy/diagnostic imaging , Electroretinography , Fluorescein Angiography , Intravitreal Injections , Ranibizumab/administration & dosage , Ranibizumab/therapeutic use , Retinal Pigment Epithelium/pathology , Retinitis Pigmentosa/diagnostic imaging , Tomography, Optical Coherence
14.
Arq. bras. oftalmol ; 79(5): 315-318, Sept.-Oct. 2016. tab, graf
Article in English | LILACS | ID: biblio-827960

ABSTRACT

ABSTRACT Purpose: The aim of the present study was to use enhanced depth imaging optical coherence tomography (EDI-OCT) to investigate choroidal changes in patients with cone dystrophy (CD) and to correlate these findings with clinical and electroretinography (ERG) findings. Methods: This case-control study included 40 eyes of 20 patients with CD and 40 eyes of 40 age- and refraction-matched healthy individuals. Choroidal thickness (CT) measurements were obtained under the foveal center and at 500 and 1,500 μm from the nasal and temporal regions to the center of the fovea, respectively. EDI-OCT and ERG data were analyzed, and the correlations of CT with the best-corrected visual acuity (BCVA) and the central foveal thickness (CFT) were evaluated. Results: The mean subfoveal CTs in the CD and control groups were 240.70 ± 70.78 and 356.18 ± 48.55 μm, respectively. The subfoveal CT was significantly thinner in patients with CD than in the controls (p<0.001). The patients with CD also had significantly thinner choroids than the controls at each measurement location relative to the fovea (p<0.001). The subfoveal CT in the CD group correlated with CFT (p=0.012), but no significant correlation was found between the subfoveal CT and BCVA or photopic ERG responses. Conclusions: The present study demonstrated a significant thinning of the choroid in patients with CD. EDI-OCT is a useful technique for describing the choroidal changes occurring in CD. Future studies investigating the association between choroidal changes and outer retinal destruction or the disease stage may provide a better understanding of the pathophysiology of CD.


RESUMO Objetivo: O objetivo deste estudo foi a utilização de imagens de tomografia de coerência óptica com profundidade aprimorada (EDI-OCT) para investigar alterações da coroide em pacientes com distrofia de cones (CD) e correlacionar esses achados com os achados clínicos e de eletrorretinografia (ERG). Métodos: Este estudo de caso-controle incluiu 40 olhos de 20 pacientes com CD e 40 olhos de 40 indivíduos saudáveis com idades e refração pareados. As medidas da espessura da coroide (CT) foram obtidas sob o centro foveal e a 500 μm e 1.500 μm de distância do centro da fóvea, nas regiões nasais e temporais. Dados de EDI-OCT e ERG foram analisados e as correlações do CT com a acuidade visual melhor corrigida (BCVA) e da espessura foveal central (CFT) foram realizadas. Resultados: As CTs subfoveais médias nos grupos CD e controle foram 240,70 ± 70,78 μm e 356,18 ± 48,55 μm, respectivamente. A CT subfoveal foi significativamente mais fina em pacientes com CD do que nos controles (p<0,001). Os com CD pacientes apresentaram também coroides significativamente mais finas do que os controles, em cada local de medição em relação à fóvea (p<0,001). A CT subfoveal no grupo CD se correlacionou com o CFT (p=0,012), mas nenhuma correlação significativa foi encontrada entre a CT subfoveal e a acuidade visual ou respostas fotópicas da ERG. Conclusões: O presente estudo demonstrou um afinamento significativo da coroide em pacientes com CD. A EDI-OCT é uma técnica útil para descrever as mudanças que ocorrem na coroide de pacientes com CD. Futuros estudos investigando a associação entre as alterações da coroide e a destruição da retina externa ou estágio da doença irão proporcionar uma melhor compreensão da fisiopatologia da CD.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Young Adult , Retina/pathology , Retinitis Pigmentosa/pathology , Choroid/pathology , Organ Size , Reference Values , Retina/diagnostic imaging , Visual Acuity , Case-Control Studies , Retinitis Pigmentosa/diagnostic imaging , Choroid/diagnostic imaging , Statistics, Nonparametric , Tomography, Optical Coherence/methods , Electroretinography/methods
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