Traumatic optic neuropathy management: a systematic review.
Blanch Richard J, Joseph Iric John, Cockerham Kimberly
AI Summary
This review found no evidence that medical treatments, including IVMP (which showed harm), or optic canal decompression benefit traumatic optic neuropathy, except for orbital compartment syndrome requiring urgent intervention.
Abstract
Background
Traumatic optic neuropathy is classically described in up to 8% of patients with traumatic brain injury (TBI), but subclinical or undiagnosed optic nerve damage is much more common. When more sensitive testing is performed, at least half of patients with moderate to severe TBI demonstrate visual field defects or optic atrophy on examination with optical coherence tomography. Acute optic nerve compression and ischaemia in orbital compartment syndrome require urgent surgical and medical intervention to lower the intraocular pressure and diminish the risk of permanent optic nerve dysfunction. Other manifestations of traumatic optic neuropathy have more variable treatments in international practice.
Methods
We conducted a systematic review of traumatic optic neuropathy treatments in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) statement.
Results
We included three randomised controlled trials of intravenous methylprednisolone (IVMP), erythropoietin, and levodopa-carbidopa combination, with no evidence of benefit for any treatment. In addition, large studies in TBI have found strong evidence of increased mortality in patients treated with megadose IVMP.
Conclusions
There is therefore no evidence of benefit for any medical treatment and strong evidence of harm from IVMP. There is also no evidence of benefit for optic canal decompression for traumatic optic neuropathy. Orbital compartment syndrome is a separate entity that requires both medical and surgical interventions to prevent visual loss.
MeSH Terms
Shields Classification
Key Concepts6
A systematic review of traumatic optic neuropathy treatments, including three randomised controlled trials, found no evidence of benefit for intravenous methylprednisolone (IVMP), erythropoietin, and levodopa-carbidopa combination.
Large studies in traumatic brain injury (TBI) have found strong evidence of increased mortality in patients treated with megadose intravenous methylprednisolone (IVMP).
There is no evidence of benefit for optic canal decompression for traumatic optic neuropathy.
Orbital compartment syndrome is a separate entity that requires both medical and surgical interventions to prevent visual loss.
Traumatic optic neuropathy is classically described in up to 8% of patients with traumatic brain injury (TBI).
At least half of patients with moderate to severe traumatic brain injury (TBI) demonstrate visual field defects or optic atrophy on examination with optical coherence tomography when more sensitive testing is performed.
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