Peter Heydon

ORCID: 0000-0001-7029-4188
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About
Contact & Profiles
Research Areas
  • Ocular Diseases and Behçet’s Syndrome
  • Ocular Oncology and Treatments
  • Retinal Diseases and Treatments
  • Retinal and Optic Conditions
  • Ophthalmology and Eye Disorders
  • Pharmaceutical Practices and Patient Outcomes
  • Web Data Mining and Analysis
  • Glaucoma and retinal disorders
  • Mosquito-borne diseases and control
  • CAR-T cell therapy research
  • Retinal and Macular Surgery
  • Ocular Infections and Treatments
  • Virus-based gene therapy research
  • CNS Lymphoma Diagnosis and Treatment
  • Intraocular Surgery and Lenses
  • Malaria Research and Control
  • Ophthalmology and Visual Health Research
  • Blood Pressure and Hypertension Studies
  • Cytomegalovirus and herpesvirus research
  • Sinusitis and nasal conditions
  • Text and Document Classification Technologies
  • Nasolacrimal Duct Obstruction Treatments
  • Advanced Text Analysis Techniques
  • Acute Myeloid Leukemia Research
  • Retinal Imaging and Analysis

Liverpool Hospital
2019-2024

Royal Prince Alfred Hospital
2017-2022

The University of Sydney
2022

Moorfields Eye Hospital
2019-2020

University College London
2019-2020

Concord Repatriation General Hospital
2017

Sydney Hospital
2014-2016

Background/aims Human grading of digital images from diabetic retinopathy (DR) screening programmes represents a significant challenge, due to the increasing prevalence diabetes. We evaluate performance an automated artificial intelligence (AI) algorithm triage retinal English Diabetic Eye Screening Programme (DESP) into test-positive/technical failure versus test-negative, using human following standard national protocol as reference standard. Methods Retinal 30 405 consecutive episodes...

10.1136/bjophthalmol-2020-316594 article EN cc-by-nc British Journal of Ophthalmology 2020-06-30

Invasive fungal sinusitis causes painful orbital apex syndrome with ophthalmoplegia and visual loss; the mechanism is unclear. We report an immunocompromised patient invasive in whom loss was due to posterior ischaemic optic neuropathy, shown on diffusion-weighted MRI, presumably from invasion of small meningeal-based arteries at apex. After intensive antifungal drugs, exenteration immune reconstitution, survived, but we were uncertain if helped. suggest that evidence acute neuropathy should...

10.1080/01658107.2017.1392581 article EN Neuro-Ophthalmology 2017-11-07

10.5694/mja16.00563 article The Medical Journal of Australia 2017-03-29

To present the first reported case of presumptive intraocular recurrence lymphoma following Chimeric Antigen Receptor (CAR) T-cell therapy despite systemic control by CD19-CAR T cells.Observational report.A 59-year-old man with diffuse, large, B-cell subsequently developed secondary central nervous system disease chemotherapy. He underwent stem cell transplantation but relapsed again and was scheduled to receive CAR therapy. vitritis several weeks before treatment, vitreous biopsy showing...

10.1097/icb.0000000000001246 article EN Retinal Cases & Brief Reports 2022-02-07

We present a rare case of 39-year-old female with extramedullary relapse acute myeloid leukaemia (AML) isolated to the left eye 2 months post allogeneic haematopoietic stem cell transplant. She initially presented painless erythema, swelling, and visual impairment. Initial ophthalmology review revealed conjunctival chemosis, raised intraocular pressure, serous retinal detachments. was treated for suspected orbital cellulitis intravenous antibiotic antifungal therapy but clinically progressed...

10.1155/2024/2235819 article EN cc-by Case Reports in Ophthalmological Medicine 2024-02-21

Combined hamartoma of the retina and retinal pigment epithelium (CHR‐RPE) is a rare, benign, unilateral generally sporadic condition that typically manifests in childhood with reduced visual ac...

10.1111/cxo.12387 article EN Clinical and Experimental Optometry 2016-03-09

<h3>Introduction</h3> Intracranial germinoma is a rare but important differential in the work of up central nervous system (CNS) lesions. <h3>Case</h3> An 18-year-old male presented with 3-month history intermittent visual blurring and headaches. He had absent upward gaze. Fundoscopy showed focal optic disc oedema phlebitis right eye. MRI brain revealed bilateral enhancing thalamic lesions minor cystic change left thalamus. Cerebrospinal fluid (CSF) normal biochemistry, 27 white cells (96%...

10.1136/bmjno-2022-anzan.178 article EN Abstracts 2022-08-01
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