Posterior vitreous detachment

Background

Separation of posterior vitreous from the retina, as a result of vitreous degeneration

and shrinkage

Age-related event (prevalence):
- 50-59 yrs = 24%
- 80-90 yrs = 87
Risk factors
- myopia
- trauma
- intraocular inflammation
in the majority of cases PVD is benign
in acute phase, concern is for causing retinal tear, which can lead to retinal detachment
Prompt diagnosis and surgical treatment of retinal detachment can prevent impending

vision loss or can restore vision

Clinical Assessment	Disposition
Floaters and/or flashes with “red flag” sign of acute Retinal Detachment Monocular visual field loss (“curtain of darkness”)	Same-day (immediate) referral to retinal surgeon (minutes may matter) High risk of Retinal Detachment
New-onset floaters and/or flashes with high-risk features: Subjective or objective visual reduction examination Vitreous hemorrhage or vitreous pigment on slitlamp examination	Same-day referral to ophthalmologist or retinal surgeon
New-onset floaters and/or flashes without high-risk features	Referral to ophthalmologist within 1 to 2 weeks Counsel patient regarding high-risk features
Recently diagnosed uncomplicated posterior vitreous detachment with New shower of floaters New subjective visual reduction	Rereferral to ophthalmologist to rule out new retinal tear or detachment Contact ophtho to help determine urgency
Stable symptoms of floaters and/or flashes for several weeks to months, not particularly bothersome to the patient and without high-risk features	Elective referral to ophthalmologist Counsel patient regarding high-risk features that should prompt urgent reassessment

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