1.Bilateral idiopathic optic perineuritis in a young Malay woman: A case report
Ayesha Mohd Zain ; Umi Kalthum Md Noh ; Mushawiahti Mustapha ; Norshamsiah Md. Din ; Mae Lynn Catherine Bastion
Neurology Asia 2015;20(4):407-409
A 28-year-old Malay woman presented with severe loss of vision in both eyes associated with periocular
pain on eye movement. She was completely blind at presentation and examination showed optic discs
swelling. Optic nerve imaging showed ‘doughnut sign’, characteristic of optic perineuritis. Steroid was
given over six months. Visual function improved gradually and was maintained at one year follow-up.
This case highlights the importance of differentiation between optic neuritis and optic perineuritis as
visual recovery depends on prolonged management with corticosteroid in optic perineuritis.
Optic Neuritis
2.Possible Tuberculous Meningitis Complicated with Optic Neuritis.
Joonwon LEE ; Hyung Chan KIM ; Soo Young BAE ; Dongah LEE ; Kang Min PARK
Journal of the Korean Neurological Association 2016;34(3):253-255
No abstract available.
Optic Neuritis*
;
Tuberculosis, Meningeal*
3.Unilateral Optic Neuritis after Acute Hepatitis A.
Jeong Bin BONG ; Hyun Goo KANG ; Dae Soo SHIN ; Hyung Suk HAN
Korean Journal of Clinical Neurophysiology 2016;18(1):28-30
No abstract available.
Hepatitis A*
;
Hepatitis*
;
Optic Neuritis*
4.Sinusitis after optico retrobulbar neuritis
Journal of Vietnamese Medicine 2001;263(9):18-27
The study included 63 cases decreased vision caused by optico- retrobulbar neuritis (ORN) and subsequently treated sinustis in the Institute of ORL during 2 years 1991- 1992, leading to the conclusion: Further studies must be carried out to definite the relationship between sinusitis and decreased vision caused by ORN
Sinusitis
;
Optic Neuritis
5.Questioning the Diagnosis of Recurrent Optic Neuritis Associated with Neuro-Behçet's Disease.
Soo Young BAE ; Yong Wan KIM ; Kyong Jin SHIN
Journal of Clinical Neurology 2018;14(2):242-243
No abstract available.
Diagnosis*
;
Optic Neuritis*
6.Landmark studies in neuro-ophthalmology
Franz Marie Cruz ; Prem S. Subramanian
Philippine Journal of Ophthalmology 2019;44(1):3-8
High-quality clinical evidence, derived from well-designed and implemented clinical trials, serves to advance clinical
care and to allow physicians to provide the most effective treatments to their patients. The field of ophthalmology,
including the subspecialty of neuro-ophthalmology, abounds with such high-quality clinical trials that provide
Level 1 clinical evidence. This review article summarizes the research design, key findings, and clinical relevance
of select monumental clinical studies in neuro-ophthalmology with the primary goal of providing the readers with
the rationale for current standard of care of various neuro-ophthalmic diseases. This includes the Optic Neuritis
Treatment Trial, Ischemic Optic Neuropathy Decompression Trial, Idiopathic Intracranial Hypertension Treatment
Trial, Rescue of Hereditary Optic Disease Outpatient Study, and Controlled High-Risk Avonex® Multiple Sclerosis
Study
Optic Neuritis
;
Optic Neuropathy, Ischemic
;
Intracranial Hypertension
7.Estimations of the lethal and exposure doses for representative methanol symptoms in humans.
Annals of Occupational and Environmental Medicine 2017;29(1):44-
BACKGROUND: The aim of this review was to estimate the lethal and exposure doses of a representative symptom (blindness) of methanol exposure in humans by reviewing data from previous articles. METHODS: Available articles published from 1970 to 2016 that investigated the dose-response relationship for methanol exposure (i.e., the exposure concentration and the biological markers/clinical symptoms) were evaluated; the MEDLINE and RISS (Korean search engine) databases were searched. The available data from these articles were carefully selected to estimate the range and median of a lethal human dose. The regression equation and correlation coefficient (between the exposure level and urinary methanol concentration as a biological exposure marker) were assumed from the previous data. RESULTS: The lethal human dose of pure methanol was estimated at 15.8–474 g/person as a range and as 56.2 g/person as the median. The dose-response relationship between methanol vapor in ambient air and urinary methanol concentrations was thought to be correlated. An oral intake of 3.16–11.85 g/person of pure methanol could cause blindness. The lethal dose from respiratory intake was reported to be 4000–13,000 mg/l. The initial concentration of optic neuritis and blindness were shown to be 228.5 and 1103 mg/l, respectively, for a 12-h exposure. CONCLUSION: The concentration of biological exposure indices and clinical symptoms for methanol exposure might have a dose-response relationship according to previous articles. Even a low dose of pure methanol through oral or respiratory exposure might be lethal or result in blindness as a clinical symptom.
Blindness
;
Humans*
;
Methanol*
;
Optic Neuritis
8.Optic Neuritis in a Patient with Bickerstaff's Brainstem Encephalitis.
Jae Gun PARK ; Chang Hun BIN ; Min Su PARK
Journal of Clinical Neurology 2016;12(4):507-508
No abstract available.
Brain Stem*
;
Encephalitis*
;
Humans
;
Optic Neuritis*
9.Research Advances in Biomarkers for Demyelinating Optic Neuritis.
Xiang CHEN ; Shi-hui WEI ; Mao-nian ZHANG
Acta Academiae Medicinae Sinicae 2016;38(1):122-127
Optic neuritis refers to all inflammatory diseases in the optic nerve. The most common type is demyelinating optic neuritis. Biomarkers can indicate its pathophysiological process and thus are useful in disease diagnosis and treatment. This article reviews the known biomarkers for demyelinating optic neuritis.
Biomarkers
;
Demyelinating Diseases
;
Humans
;
Optic Neuritis
10.Efficacy of vitamin supplementation in preventing color vision abnormalities among patients undergoing DOTS for Tuberculosis
Jan Michael R. Reyes ; Anne Marfe L. Tan ; Melizza T. Ramirez ; Roland B. Bagnes ; Evelyn S. Morabe ; Emerson M. Cruz
Philippine Journal of Ophthalmology 2013;38(1):50-55
Objective:
To determine if vitamin supplementation can prevent the development of color vision abnormalities
in patients taking ethambutol as part of DOTS for tuberculosis (TB).
Methods:
A randomized, placebo-controlled, single-blind clinical trial was conducted among newly diagnosed
category-1 TB patients enrolled in DOTS health centers in the third district of Manila from June 2011 to August
2012. Before starting therapy, the participants underwent a complete eye evaluation including baseline color vision
tests using the Ishihara Color Vision Plates (Ishihara), Farnsworth Panel D-15 (FD 15), and Lanthony Desaturated
D-15. Only subjects who passed the three color vision tests were included in the study. They were divided into 2
groups: Group A received vitamin supplementation and Group B received a placebo. Follow-up color vision testing
was done monthly for 3 months.
Results:
There were 105 patients included in the study, 77 males and 28 females, age ranging from 16 to 68 years with a
mean of 37 years. Forty three (43) patients received vitamin supplementation (group A) and 62 received placebo (group
B). After one month of DOTS, 5 of 43 patients (11. 6%) in group A and 10 of 62 patients (16.1%) in group B developed
color vision abnormalities, detected only with the Lanthony Desaturated test. The absolute risk reduction (ARR) of
color vision abnormalities by vitamin supplementation was 4.5%, with the number needed to treat (NNT) of 23. After
the second month of therapy, ARR was 7.4% and NNT was 14. ARR was highest in the third month at 8.3%, with
a corresponding decreased NNT of 12. Among patients who developed color vision abnormalities, reversal of the
abnormalities was observed in 80% of 5 subjects in group A, and 40% of 10 patients in group B. By the third month of
treatment, all in group A already had normal color vision, while 40% in group B still showed abnormal color vision.
Conclusion
This study showed that vitamin supplementation was effective in reducing the risk of, and in reversing
cases of, color vision abnormalities among patients undergoing DOTS therapy for tuberculosis.
Tuberculosis
;
Ethambutol
;
Color Vision
;
Optic Neuritis