Early clinical and subclinical visual evoked potential and Humphrey's visual field defects in cryptococcal meningitis

Cryptococcal induced visual loss is a devastating complication in survivors of cryptococcal meningitis (CM). Early detection is paramount in prevention and treatment. Subclinical optic nerve dysfunction in CM has not hitherto been investigated by electrophysiological means. We undertook a prospectiv...

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Veröffentlicht in:PloS one 2012-12, Vol.7 (12), p.e52895-e52895
Hauptverfasser: Moodley, Anand, Rae, William, Bhigjee, Ahmed, Connolly, Cathy, Devparsad, Natasha, Michowicz, Andrew, Harrison, Thomas, Loyse, Angela
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Rae, William
Bhigjee, Ahmed
Connolly, Cathy
Devparsad, Natasha
Michowicz, Andrew
Harrison, Thomas
Loyse, Angela
description Cryptococcal induced visual loss is a devastating complication in survivors of cryptococcal meningitis (CM). Early detection is paramount in prevention and treatment. Subclinical optic nerve dysfunction in CM has not hitherto been investigated by electrophysiological means. We undertook a prospective study on 90 HIV sero-positive patients with culture confirmed CM. Seventy-four patients underwent visual evoked potential (VEP) testing and 47 patients underwent Humphrey's visual field (HVF) testing. Decreased best corrected visual acuity (BCVA) was detected in 46.5% of patients. VEP was abnormal in 51/74 (68.9%) right eyes and 50/74 (67.6%) left eyes. VEP P100 latency was the main abnormality with mean latency values of 118.9 (±16.5) ms and 119.8 (±15.7) ms for the right and left eyes respectively, mildly prolonged when compared to our laboratory references of 104 (±10) ms (p
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Early detection is paramount in prevention and treatment. Subclinical optic nerve dysfunction in CM has not hitherto been investigated by electrophysiological means. We undertook a prospective study on 90 HIV sero-positive patients with culture confirmed CM. Seventy-four patients underwent visual evoked potential (VEP) testing and 47 patients underwent Humphrey's visual field (HVF) testing. Decreased best corrected visual acuity (BCVA) was detected in 46.5% of patients. VEP was abnormal in 51/74 (68.9%) right eyes and 50/74 (67.6%) left eyes. VEP P100 latency was the main abnormality with mean latency values of 118.9 (±16.5) ms and 119.8 (±15.7) ms for the right and left eyes respectively, mildly prolonged when compared to our laboratory references of 104 (±10) ms (p&lt;0.001). Subclinical VEP abnormality was detected in 56.5% of normal eyes and constituted mostly latency abnormality. VEP amplitude was also significantly reduced in this cohort but minimally so in the visually unimpaired. HVF was abnormal in 36/47 (76.6%) right eyes and 32/45 (71.1%) left eyes. The predominant field defect was peripheral constriction with an enlarged blind spot suggesting the greater impact by raised intracranial pressure over that of optic neuritis. Whether this was due to papilloedema or a compartment syndrome is open to further investigation. Subclinical HVF abnormalities were minimal and therefore a poor screening test for early optic nerve dysfunction. 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Early detection is paramount in prevention and treatment. Subclinical optic nerve dysfunction in CM has not hitherto been investigated by electrophysiological means. We undertook a prospective study on 90 HIV sero-positive patients with culture confirmed CM. Seventy-four patients underwent visual evoked potential (VEP) testing and 47 patients underwent Humphrey's visual field (HVF) testing. Decreased best corrected visual acuity (BCVA) was detected in 46.5% of patients. VEP was abnormal in 51/74 (68.9%) right eyes and 50/74 (67.6%) left eyes. VEP P100 latency was the main abnormality with mean latency values of 118.9 (±16.5) ms and 119.8 (±15.7) ms for the right and left eyes respectively, mildly prolonged when compared to our laboratory references of 104 (±10) ms (p&lt;0.001). Subclinical VEP abnormality was detected in 56.5% of normal eyes and constituted mostly latency abnormality. VEP amplitude was also significantly reduced in this cohort but minimally so in the visually unimpaired. HVF was abnormal in 36/47 (76.6%) right eyes and 32/45 (71.1%) left eyes. The predominant field defect was peripheral constriction with an enlarged blind spot suggesting the greater impact by raised intracranial pressure over that of optic neuritis. Whether this was due to papilloedema or a compartment syndrome is open to further investigation. Subclinical HVF abnormalities were minimal and therefore a poor screening test for early optic nerve dysfunction. However, early optic nerve dysfunction can be detected by testing of VEP P100 latency, which may precede the onset of visual loss in CM.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23285220</pmid><doi>10.1371/journal.pone.0052895</doi><tpages>e52895</tpages><oa>free_for_read</oa></addata></record>
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subjects Abnormalities
Acquired immune deficiency syndrome
Acuity
Adolescent
Adult
AIDS
Asymptomatic Diseases - epidemiology
Automation
Care and treatment
Cohort Studies
Compartment syndrome
Cryptococcal meningitis
Cryptococcus neoformans
Defects
Early Diagnosis
Evoked Potentials, Visual - physiology
Eye (anatomy)
Feasibility studies
Female
Fungal infections
Health screening
HIV
Hospitals
Human immunodeficiency virus
Humans
Infections
Intracranial pressure
Latency
Male
Medical research
Medicine
Meningitis
Meningitis, Cryptococcal - complications
Meningitis, Cryptococcal - epidemiology
Meningitis, Cryptococcal - physiopathology
Middle Aged
Neuritis
Neurology
Optic nerve
Optic neuritis
Pathogenesis
Patients
Swelling
Vision Disorders - diagnosis
Vision Disorders - epidemiology
Vision Disorders - etiology
Vision Disorders - physiopathology
Visual acuity
Visual evoked potentials
Visual field
Visual Field Tests
Visual fields
Visual Fields - physiology
Young Adult
title Early clinical and subclinical visual evoked potential and Humphrey's visual field defects in cryptococcal meningitis
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