Literature DB >> 9541821

Visual field defects in optic neuritis and anterior ischemic optic neuropathy: distinctive features.

J Gerling1, J H Meyer, G Kommerell.   

Abstract

BACKGROUND: We analyzed the value of visual-field defects in the differential diagnosis of optic neuritis (ON) and non-arteritic anterior ischemic optic neuropathy (AION).
METHODS: Ninety-nine consecutive patients with acute-onset optic neuropathy formed the basis for this study. Compressive and vasculitic neuropathies were excluded. Eighty-six patients fulfilled the criteria for either ON (50 patients): < or = 35 years, normal disk, recovery of visual function, or AION (36 patients): > or = 60 years, swelling of the disk, no recovery of visual function. Without knowledge of other clinical data, visual fields obtained by Gold-mann perimetry were classified into five types of defects (forced choice). With the correct diagnosis at hand, fields were reviewed for characteristic features.
RESULTS: Forced-choice classification into defect types [%]: Central scotoma ON 68, AION 18; superior altitudinal defect ON 13 AION 7; inferior altitudinal defect ON 8, AION 52; peripheral defect ON 1, AION 5; diffuse defect ON 10, AION 18. Search for pathognomonic defects: a scotoma centered on the fixation point with a sloping border occurred exclusively in ON (25 of 50 patients). An inferior altitudinal defect with a sharp border along the horizontal meridian, particularly in the nasal periphery, occurred only in AION (10 of 36 patients). A steep centrocecal scotoma occurred in 3 of the 36 AION cases and not at all in the ON cases. Scotomas in the center breaking through to the periphery, superior altitudinal defects (with a sloping border along the horizontal meridian) and diffuse depressions verging on blindness occurred in both ON and AION.
CONCLUSION: A sctoma centered on the fixation point with a sloping border is highly characteristic of ON, while an inferior altitudinal defect with a sharp border along the horizontal meridian, particularly in the nasal periphery, is highly characteristic of AION. To identify these diagnostic criteria, it can be necessary to examine full fields. With restriction of perimetry to 30 degrees a large central scotoma can be mistaken for a diffuse defect and the border in the nasal periphery can be missed.

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Mesh:

Year:  1998        PMID: 9541821     DOI: 10.1007/s004170050062

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  18 in total

1.  Variation of visual evoked potential delay to stimulation of central, nasal, and temporal regions of the macula in optic neuritis.

Authors:  S Rinalduzzi; A Brusa; S J Jones
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-01       Impact factor: 10.154

Review 2.  Isolated, relapsing and progressive demyelinating diseases of the central nervous system.

Authors:  Axel Petzold
Journal:  J Neurol       Date:  2008-12       Impact factor: 4.849

3.  Diameter of the optic nerve in idiopathic optic neuritis and in anterior ischemic optic neuropathy.

Authors:  J Gerling; P Janknecht; L L Hansen; G Kommerell
Journal:  Int Ophthalmol       Date:  1997       Impact factor: 2.031

Review 4.  [Optic disc swelling : A compilation of relevant differential diagnoses].

Authors:  V Prokosch; D C Dragnea; S Pitz
Journal:  Ophthalmologe       Date:  2016-11       Impact factor: 1.059

5.  Visual field profile of optic neuritis: a final follow-up report from the optic neuritis treatment trial from baseline through 15 years.

Authors:  John L Keltner; Chris A Johnson; Kimberly E Cello; Mariya Dontchev; Robin L Gal; Roy W Beck
Journal:  Arch Ophthalmol       Date:  2010-03

6.  Comparison of optic nerve head topography findings in eyes with non-arteritic anterior ischemic optic neuropathy and eyes with glaucoma.

Authors:  Josepha Horowitz; Tagil Fishelzon-Arev; Eitan Z Rath; Eitan Segev; Orna Geyer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-03-06       Impact factor: 3.117

7.  Photopic negative response of full-field and focal macular electroretinograms in patients with optic nerve atrophy.

Authors:  Kunifusa Tamada; Shigeki Machida; Daisuke Yokoyama; Daijiro Kurosaka
Journal:  Jpn J Ophthalmol       Date:  2009-12-18       Impact factor: 2.447

8.  Visual field defects of optic neuritis in neuromyelitis optica compared with multiple sclerosis.

Authors:  Hideto Nakajima; Takafumi Hosokawa; Masakazu Sugino; Fumiharu Kimura; Jun Sugasawa; Toshiaki Hanafusa; Toshiyuki Takahashi
Journal:  BMC Neurol       Date:  2010-06-18       Impact factor: 2.474

9.  Visual field defects in acute optic neuritis--distribution of different types of defect pattern, assessed with threshold-related supraliminal perimetry, ensuring high spatial resolution.

Authors:  J Nevalainen; E Krapp; J Paetzold; I Mildenberger; D Besch; R Vonthein; J L Keltner; C A Johnson; U Schiefer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2008-02-01       Impact factor: 3.117

Review 10.  The investigation of acute optic neuritis: a review and proposed protocol.

Authors:  Axel Petzold; Mike P Wattjes; Fiona Costello; Jose Flores-Rivera; Clare L Fraser; Kazuo Fujihara; Jacqueline Leavitt; Romain Marignier; Friedemann Paul; Sven Schippling; Christian Sindic; Pablo Villoslada; Brian Weinshenker; Gordon T Plant
Journal:  Nat Rev Neurol       Date:  2014-07-08       Impact factor: 42.937

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