Aims: To characterize photopsia in posterior vitreous detachment (PVD), retinal tears (RT) and rhegmatogenous retinal detachment (RRD).
Methods: Seventy seven patients presenting to an eye emergency department and vitreoretinal clinic with photopsia had documentation of their symptoms.
Results: A total of 27 patients had PVD alone, 7 had RTs and 25 RRD. In patients with isolated PVD, photopsia were temporal (94%), lasting seconds (81%) and vertically orientated (59%) flashes. Patients with photopsia located in quadrants other than temporal were more likely to have RRD (p = 0.0003). Patients with an oblique or horizontal orientation of their photopsia were likely to have RRD or RT (p = 0.001, specificity 96%, sensitivity 40%).
Conclusions: Most patients with PVD have a typical presentation of photopsia, with temporal, vertically orientated, momentary flashes. Patients with RTs or RRD may describe subtle differences in their photopsia which may raise the index of suspicion for the presence of a complication from PVD.
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http://dx.doi.org/10.1111/j.1475-1313.2009.00685.x | DOI Listing |
Sci Rep
November 2024
Department of Hepatopancreatobiliary Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, No.420, Fuma Road, Fuzhou, Fujian, China.
Avatrombopag is a next-generation thrombopoietin receptor agonist approved for the treatment of thrombocytopenia in patients with chronic liver disease scheduled to undergo surgery and thrombocytopenia in patients with chronic immune thrombocytopenia. However, realistic data on its post-marketing long-term safety and tolerability in large sample populations are incomplete. The adverse event (AE) reports of avatrombopag were analyzed based on the FAERS database.
View Article and Find Full Text PDFCureus
October 2024
Ophthalmology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Dr. D.Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Autoimmune retinopathy (AIR) is a rare retinal disorder that causes a gradual loss of vision due to autoantibodies targeting retinal antigens, leading to photoreceptor degeneration. Early diagnosis and timely intervention are critical for preserving visual function in affected patients. Over the course of a year, a 30-year-old woman had bilateral, abrupt, painless, progressive diminution of vision, nyctalopia, photopsia, and a restricted peripheral field of vision.
View Article and Find Full Text PDFOphthalmol Retina
October 2023
Beijing Tongren Eye Center, Beijing Key Laboratory of Intraocular Tumor Diagnosis and Treatment, Beijing Ophthalmology & Visual Sciences Key Lab, Medical Artificial Intelligence Research and Verification Key Laboratory of the Ministry of Industry and Information Technology, Beijing Tongren Hospital, Capital Medical University, Beijing, China. Electronic address:
Ocul Immunol Inflamm
December 2024
Ophthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Purpose: To present a presumed case of non-paraneoplastic autoimmune retinopathy (nPAIR) following COVID-19 in a healthy woman.
Methods: A single case was evaluated and followed for 32 months.
Results: A healthy 32-year-old woman presented with photopsia and paracentral scotoma (OU) after a recent COVID-19 infection.
J Vitreoretin Dis
June 2024
Mississauga Retina Institute, Toronto, ON, Canada.
To describe the multimodal imaging findings associated with benign yellow dot maculopathy. A case report was analyzed. A healthy 42-year-old White man was evaluated after several weeks of photopsias and an inferior retinal tear in the right eye.
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