Purpose: To evaluate the mid-term efficiency of laser peripheral iridotomy (LPI) in preventing intraocular pressure (IOP) increase and angle closure in the fellow eye after acute primary angle closure glaucoma.
Method: prospective, noncomparative, interventional case series--29 consecutive cases with acute primary angle closure glaucoma on presentation were enrolled in the study in 2001. Mean follow-up time: 14 months (12-18 months).
Presentation: assessment of IOP and gonioscopy of the fellow eye; LPI of the fellow eye within 24h of presentation. IOP assessment of the fellow eye thrice a day until discharge. Gonioscopy of the fellow eye at discharge. One month later: visual field; optic nerve head evaluation of the fellow eye after pupil dilation; IOP monitoring until pupil recovery. IOP assessment on a monthly basis.
Results: 2 patients presented with bilateral angle closure attack; 2 patients presented with angle closure attack of the second eye, which had not received adequate preventive treatment; 1 patient developed angle closure of the fellow eye immediately after the initial gonioscopy but was promptly managed with LPI; 7 patients had IOP > 21 mm Hg of the fellow eye on presentation, required medication after LPI but did not develop acute angle closure during the follow-up; 17 patients had normal IOP of the fellow eye, remained normal during the follow-up and did not require medication.
Conclusion: LPI is highly efficient in preventing acute angle closure in the fellow eye; in the eyes that were normal on presentation, LPI also prevents later IOP increase.
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J Neurosci
January 2025
Department of Ophthalmology, Harvard Medical School, Boston, MA, United States.
We employed high-resolution fMRI to distinguish the impacts of anisometropia and strabismus amblyopia on the evoked ocular dominance (OD) response. Sixteen amblyopic participants (8 females) plus 8 individuals with normal vision (1 female), participated in this study for whom, we measured the difference between the response to stimulation of the two eyes, across areas V1-V4.In controls, the evoked OD response formed the expected striped pattern within V1.
View Article and Find Full Text PDFOphthalmol Retina
January 2025
Byers Eye Institute, Stanford University, Palo Alto, CA,. Electronic address:
Purpose: We surveyed vitreoretinal (VR) fellowship program directors (PDs) to elucidate how they assess surgical competency among VR fellows. In addition, we also surveyed fellowship program graduates for the years 2022 and 2023 regarding assessment metrics and tools used during VR fellowship training.
Design: Web-based, cross-sectional descriptive study.
Retina
January 2025
Department of Ophthalmology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Purpose: To investigate the effect of Henle fiber layer hemorrhage (HFLh) on retinal sensitivity (RS) before and after displacement of the submacular hemorrhage (SMH) caused by retinal arterial macroaneurysm (RAM) rupture.
Methods: This retrospective study included 31 eyes undergoing vitrectomy for SMH. Eyes were grouped based on the presence or absence of HFLh (HFLh [+/-] group).
Retin Cases Brief Rep
January 2025
School of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Purpose: This study examines the multimodal imaging (MMI) findings in two cases of unilateral Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis (SNIFR), including detailed findings from the unaffected fellow eye.
Methods: Macular spectral domain optical coherence tomography (OCT) and 3x3 mm optical coherence tomography angiography (OCTA), microperimetry, full-field electroretinography (ff-ERG) for both the affected and the fellow eye were reviewed.
Results: The MMI findings were consistent across the two cases (71-year-old female and 60-year-old female).
Semin Ophthalmol
January 2025
Wills Eye Hospital Mid Atlantic Retina, Thomas Jefferson University, Philadelphia, PA, USA.
Introduction And Primary Objective: Pediatric rhegmatogenous retinal detachment (RRD) presents unique challenges in diagnosis and management. A thorough evaluation of family, medical, and ocular history is helpful, as systemic and genetic conditions can predispose children to RRD. Trauma, high myopia, and history of prematurity are also common risk factors.
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