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1.
Doc Ophthalmol ; 135(1): 43-52, 2017 08.
Artigo em Inglês | MEDLINE | ID: mdl-28451988

RESUMO

PURPOSE: To describe the clinical characteristics, macular structure and function, and to document sequential changes over 5 years in a 10-year-old boy with bilateral primary foveomacular retinitis. METHODS: A 10-year-old boy presented with sudden onset scotoma in both eyes, experienced after getting up from bed on a non-eclipse day. He persistently denied direct sun-gazing. He neither had any significant systemic illness, nor was using any medications. In addition to a detailed examination at presentation that included fundus fluorescein angiogram (FFA), electroretinogram (ERG), pattern ERG and electrooculogram (EOG), he was examined periodically for 5 years with Humphrey visual field (HVF), spectral domain optical coherence tomogram (SDOCT), Amsler grid charting and multifocal ERG. The macular structure and functions were analyzed over the years and correlated with the symptoms. RESULTS: All findings were bilaterally symmetrical at each visit. At presentation, his corrected visual acuity was 20/25 with subfoveal yellow dot similar to solar retinopathy, central scotoma with reduced foveal threshold in HVF 24-2, micropsia in Amsler grid, missing of two plates on Ishihara color vision chart, transfoveal full thickness hyper-reflective band on SD OCT, unremarkable FFA and normal foveal peak in mfERG. The flash ERG and EOG were unremarkable. A month later, his VA improved to 20/20, he had relative scotoma in Amsler grid, no scotoma in HVF (10-2), restoration of the inner segment of the photoreceptors with sharp defect involving ellipsoid and photoreceptor interdigitation zone in SDOCT and blunting of foveal peaks in mfERG. Three months later, his corrected VA was 20/20 with relative scotoma in Amsler grid, normal color vision, no scotoma in HVF 10-2 and unchanged SDOCT findings. In subsequent examinations at 6, 9, 14, 29, 39 and 60 months, he was symptomless with VA 20/20, unremarkable fundus, normal Amsler grid and HVF (normal foveal threshold), unchanged SDOCT findings and the reduced foveal peaks on mfERG in both eyes got normalized only at 60 months. CONCLUSION: Presented here is a case of bilaterally symmetrical idiopathic foveomacular retinitis that had a clinical appearance similar to solar retinopathy. The fundus changes persisted for 4 weeks, the symptoms and changes in Amsler grid lasted for 3 months, and the foveal threshold in visual fields normalized within 3 months. Maximum change in the SDOCT defect occurred within a month, and the extrafoveal defect in the ellipsoid and photoreceptor interdigitation line persisted despite resolution of symptoms and resolution of the visual field defect and normal distance vision. Probably, the foveal lesion detected on SDOCT was too small to cause a reduction in the distance visual acuity or show up in the visual field and mfERG later.


Assuntos
Fóvea Central/fisiopatologia , Retinite/fisiopatologia , Escotoma/fisiopatologia , Criança , Eletroculografia , Eletrorretinografia , Angiofluoresceinografia , Seguimentos , Humanos , Masculino , Retinite/diagnóstico , Escotoma/diagnóstico , Estatística como Assunto , Tomografia de Coerência Óptica , Acuidade Visual/fisiologia , Testes de Campo Visual , Campos Visuais/fisiologia
2.
Med J Armed Forces India ; 73(2): 129-133, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28924312

RESUMO

BACKGROUND: Infantile esotropia is a convergent strabismus presenting before 6 months of age and is the most common strabismus disorder presenting in the ophthalmology OPD. The dilemma of whether to go for early surgery and how early has been a matter of research for the last 50 years. We describe our results of surgery in infantile esotropia at variable age groups, as well as with different reoperation rates and compare with the results in western literature. METHODS: A prospective study was carried out through a review of 113 cases operated for infantile esotropia between February 2013 and August 2014. The variables studied were: age at surgery, type of fixation, refractive error, associated nystagmus, inferior oblique overaction or dissociated vertical deviation (DVD), type of surgery performed and pre- and postoperative deviation angles. RESULTS: There were 67 male and 46 female cases of infantile esotropia. The age group of patients varied from 6 months to 12 years. Latent nystagmus was seen in 22 cases, inferior oblique overaction in 49 cases and DVD (mild) in 14 cases. Bimedial rectus recession was done in 78 cases and recession-resection in non-dominant eye in remaining 35 cases. The postoperative residual deviation was <10 PD in 102 cases, between 10 and 16 PD in 5 cases and more than 16 PD in 6 cases. Only 6 cases (5.3%) required reoperation for correction of residual deviation. CONCLUSION: The authors recommend surgery before 12 months in all cases of infantile esotropia. The reoperation rates in the current study were considerably low.

4.
J Cataract Refract Surg ; 47(11): e24-e28, 2021 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-33278233

RESUMO

The Argentinian flag sign is a known complication in intumescent white cataracts, which arises instantly after an initial prick with a sharp hypodermic needle on a stretched out anterior capsule. Increased intralenticular pressure is believed to be responsible for propagation of the initial prick into a radial capsular tear. However, it is the linear cut configuration of the initial prick, created by the hypodermic needle on the tense anterior capsule, which spontaneously opens up and propagates toward the periphery along its margins. To overcome this, a new instrument was devised, sewing needle microcapsulotome, to puncture the capsule and create a single or multiple round openings with smooth margins, allowing the bag to decompress satisfactorily without yielding to disruptive intralenticular forces. This technique of sewing needle microcapsulotomy, to prevent the Argentinian flag sign, was found to be highly effective and safe in a series of surgeries on intumescent cataracts.


Assuntos
Extração de Catarata , Catarata , Capsulorrexe , Humanos , Agulhas , Punções
5.
Med J Armed Forces India ; 71(Suppl 2): S549-51, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26858493
6.
Indian J Ophthalmol ; 67(6): 824-827, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-31124495

RESUMO

Purpose: To analyze the causes for late presentation in a series of patients with advanced retinopathy of prematurity (ROP) in a tertiary eye care institute in Eastern India. Methods: We analyzed our medical records and ROP database retrospectively from 2007 to 2015 and prospectively thereafter till 2017 to identify the factors for late presentation in babies with advanced ROP (stages 4 and 5). Results: A total of 71 eligible subjects were analyzed. The mean chronological age was 15.1 months (2 months to 14 years). The three important barriers were: (1) the system and neonatal care policy failure (n = 45; 63.3%), (2) parental negligence and ignorance (n = 19; 26.7%), and (3) ophthalmologist's misdiagnosis or unavailability (n = 7; 10%). Majority of the babies (63.3%) were admitted in the neonatal care unit when they were due for ROP screening with an average duration of stay of 35.5 days. Conclusion: The main barriers to early screening for ROP were related to availability of trained human resources, ignorance of "parents and health care personnel," and distance from the point of care. This calls for training of ophthalmologists, advocacy with neonatologists and parents, and create systems for better coordination and compliance of the care providers.


Assuntos
Atenção à Saúde/organização & administração , Triagem Neonatal/métodos , Tempo para o Tratamento/estatística & dados numéricos , Seleção Visual/métodos , Adolescente , Criança , Pré-Escolar , Feminino , Seguimentos , Idade Gestacional , Humanos , Incidência , Índia/epidemiologia , Recém-Nascido , Masculino , Prognóstico , Retinopatia da Prematuridade/diagnóstico , Retinopatia da Prematuridade/epidemiologia , Estudos Retrospectivos , Fatores de Risco
7.
Indian J Ophthalmol ; 65(12): 1415-1418, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29208824

RESUMO

We describe an efficient technique, "Terminal Chop," for full thickness nuclear segmentation in mature hard cataracts. Terminal chop utilizes the principle of secondary rock breakage system with stress concentration to break these hard nuclei. In this technique consonant to drag picks, a specially designed chopper "Terminator" is used to initiate a unique dispersive mechanical force to create a full thickness nuclear crack (crack formation) at the weakest soft and thin equator, which automatically traverses through the center and to the equator on the other side. Lateral separation of both the instruments placed at the equator, propagates the initial full thickness nuclear crack (crack propagation), breaking the entire nucleus into two complete pieces including the posterior plate. The direction of splitting follows the cleavage plane in a more direct manner, thus requiring least fracture force, least manipulation and stress, much lower than compressive stress, causing minimal trauma, and highly satisfactory postoperative results.


Assuntos
Catarata/diagnóstico , Núcleo do Cristalino/cirurgia , Facoemulsificação/instrumentação , Desenho de Equipamento , Humanos , Núcleo do Cristalino/patologia , Índice de Gravidade de Doença
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