98%
921
2 minutes
20
Background: Diagnosis and management of Acute Retinal Necrosis (ARN) in children that does not respond to systemic acyclovir treatment can be challenging. We report two cases of ARN secondary to herpes simplex virus (HSV) type 2 that was resistant to acyclovir but was treated successfully with intravenous foscarnet.
Case Report: Two children diagnosed with ARN failed to show clinical response to systemic acyclovir treatment. Both cases had histories of previous HSV infections and vitreous taps positive for HSV-2. Both were converted to systemic foscarnet treatment with successful control of the retinitis and satisfactory visual outcomes.
Conclusions: Systemic foscarnet can be effective in the management of pediatric acute retinal necrosis caused by HSV-2 when there is an atypical response to conventional acyclovir treatment.
Download full-text PDF |
Source |
---|
Adv Emerg Nurs J
September 2025
Author Affiliations: School of Nursing, San Diego State University, San Diego, California (Dr Colio); Advanced Emergency Nursing Journal, Wolters Kluwer Health, Philadelphia, Pennsylvania (Dr Colio); American Academy of Nurse Practitioners Certification Board, Austin, Texas (Dr Colio); Imperial Card
Sudden visual disturbances are of significant concern and often among the most challenging scenarios for emergency providers in underserved communities without on-call ophthalmology services. Vulnerable areas in emergency training vary among nurse practitioners, physician assistants, and even physicians. Urgent and non-urgent ophthalmology disorders are commonly cited in the literature as one of the most challenging areas for emergency providers.
View Article and Find Full Text PDFJ Neurosci
September 2025
Department of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH 43210, USA
The purpose of this study was to investigate how Sphingosine-1-phosphate (S1P) signaling regulates glial phenotype, neuroprotection, and reprogramming of Müller glia (MG) into neurogenic MG-derived progenitor cells (MGPCs) in the adult male and female mouse retina. We found that S1P-related genes were dynamically regulated following retinal damage. (S1P receptor 1) and (sphingosine kinase 1) are expressed at low levels by resting MG and are rapidly upregulated following acute damage.
View Article and Find Full Text PDFJ Vitreoretin Dis
September 2025
Retina Group of Washington, Reston, VA, USA.
To present the first real-world safety data describing the clinical experience of geographic atrophy (GA) treatment with avacincaptad pegol in a large cohort. A retrospective, observational cohort study was conducted within the PRISM Vision Group by filtering for J codes for avacincaptad pegol from August 3, 2023, to October 10, 2024. The study included 461 eyes of 335 patients with GA who were treated with intravitreal avacincaptad pegol 2 mg (0.
View Article and Find Full Text PDFOcul Immunol Inflamm
September 2025
Manchester Royal Eye Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
Purpose: To report a rare case of bilateral necrotising retinitis caused by a potentially novel human adenovirus D (HAdV-D) in a post-bone marrow transplant patient and to highlight the diagnostic challenges and therapeutic role of intravenous cidofovir, alongside a review of previously reported cases of human adenovirus (HAdV) retinitis.
Methods: Retrospective case report.
Results: A 60-year-old man with a history of acute myeloid leukaemia, in remission post-bone marrow transplant, presented with bilateral hypertensive granulomatous panuveitis and necrotising retinitis.
Front Ophthalmol (Lausanne)
August 2025
Department of Ophthalmology, Tokushima University Graduate School, Tokushima, Japan.
Background: Central retinal artery occlusion (CRAO) is a vision-threatening emergency with no established effective treatment. Prostaglandin E (PGE), known for its vasodilatory and cytoprotective properties, may offer therapeutic benefits for retinal ischemia.
Methods: In this retrospective study, we compared visual outcomes between CRAO patients who received intravenous PGE within 24 hours of symptom onset (followed by oral administration) and those who received conventional therapy.