Article
Non-arteritic anterior ischaemic optic neuropathy in Malaysia: a 5 years review.
Department of Ophthalmology, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia.
International journal of ophthalmology
01/2011;
4(3):272-4.
DOI:10.3980/j.issn.2222-3959.2011.03.12
Source: PubMed
- Citations (7)
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Cited In (0)
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Article: Pathogenesis of nonarteritic anterior ischemic optic neuropathy.
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ABSTRACT: Based on histopathology, electron microscopic corrosion cast studies, optic nerve blood flow studies, and clinical data, the pathogenesis of idiopathic nonarteritic ischemic optic neuropathy includes the following features: (1) structurally crowded optic discs are predisposed; (2) laminar and retrolaminar regions are the most common locations for infarction; (3) there is flow impairment in the prelaminar optic disc during the acute phase; (4) lack of consistent choroidal flow impairment and the retrolaminar location of infarcts suggest vasculopathy within or distal to the paraoptic branches of the posterior choroidal arteries; (5) diabetes is the most consistently identified vasculopathic risk factor; (6) impaired autoregulation of the disc circulation by atherosclerosis, with a possible contribution from serotonin and endothelin-mediated vasospasm, may play a role; and (7) progression may be caused by secondary cell death after the initial ischemic insult or compression from cavernous degeneration and mechanical axonal distortion.Journal of Neuro-Ophthalmology 07/2003; 23(2):157-63. · 1.45 Impact Factor -
Article: Nonarteritic ischemic optic neuropathy.
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ABSTRACT: To describe the systemic and visual characteristics and prognosis in patients with nonarteritic ischemicoptic neuropathy (NAION) undergoing different treatments. Retrospective chart review was performed in Kaohsiung Veterans General Hospital patients from 1995-2005 with a clinical diagnosis of NAION, including nonarteritic anterior ischemic optic neuropathy and posterior ischemic optic neuropathy (PION). There were 14 PION patients out of a total of 103 cases. The average age at disease attack was 61 years old, and the ratio of males to females was 1.24:1. Comorbid systemic diseases and visual function were recorded at both initial presentation and the later follow-up period. The final results were recorded and compared by the different treatments they received in 4 groups. In all, NAION usually affected people > 50 years old, without any difference between sexes. Presenting visual acuity, age, and different treatment modes had no direct influence on the final visual outcome. The most significant associated factor was hypertension. NAION is a serious illness; the visual deficit persists even with aggressive treatment.Journal of the Chinese Medical Association 03/2007; 70(2):61-4. · 0.79 Impact Factor -
Article: Anterior ischemic optic neuropathy in children: case reports and review of the literature.
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ABSTRACT: Anterior ischemic optic neuropathy, infarction of the optic nerve head owing to inadequate perfusion through the posterior ciliary arteries, is a common cause of visual loss in adults but is rarely reported in children, in part because the diagnosis is overlooked. We report two cases of young children undergoing chronic peritoneal dialysis, who suffered bilateral visual loss from anterior ischemic optic neuropathy. Predisposing local anatomic and multiple systemic factors included a small optic nerve head with little cupping, possible intraocular hypertension, and systemic hypotension, hypovolemia, and anemia. The literature on anterior ischemic optic neuropathy is reviewed.Pediatric Neurology 06/2002; 26(5):358-64. · 1.52 Impact Factor
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Keywords
18 consecutive patients
acute loss
acute poor vision
cases
clinical presentations
common fundoscopic findings
diabetes mellitus
elderly individuals
gradual onset
Hospital Universiti Sains Malaysia
hyperemic disc
ischaemic heart disease
main risk factors
NAION
non-arteritic anterior ischaemic optic neuropathy
patients
permanent visual loss
sectorial swollen optic disc
systemic diseases