Posterior vitreous detachment
most common cause of acute onset of flashes and floaters
- 66% of patients over 70 year
- Caused by
- age-related change in which the vitreous degenerates
- shrinks and separates from the retina.
- During separation, the vitreous may tug
- cause mechanical stimulation of the retina, resulting in flashes
Differential Diagnosis
Causes of Photopsia other than posterior vitreous detachment include the following:
- A retinal tear or retinal detachment
- Migraine with aura (classic)
- Migraine headache without aura
- Posterior uveitis (multiple evanescent white dot syndrome, acute idiopathic blind spot enlargement syndrome, acute posterior multifocal placoid pigment epitheliopathy, acute zonal occult outer retinopathy, multifocal choroiditis, and panuveitis, Birdshot retino-choroiditis) [54]
- Both early and the late stage of retinitis pigmentosa
Causes of floaters other than posterior vitreous detachment include the following:
- Vitreous hemorrhage due to any cause including retinal tear or retinal detachment, proliferative diabetic retinopathy
- Vitreous exudates in posterior uveitis, endophthalmitis
- Vitreous pigments
- Vitreous amyloidosis
- Intravitreal injection of drugs
Clinically
Early Stages:
- Usually asymptomatic
- Often undetected clinically until separation from optic disc margins
Symptoms:
- Flashes of light (photopsia)
- Quick, temporal quadrant, induced by head or eye movement, noticeable in dim environments
- Floaters (myodesopsia)
- Small, mobile vitreous particles against a bright background
- patient usually has normal vision
- no visual field defects
- Blurring of vision (67% of patients) due to vitreous hemorrhage from retinal breaks or ample floaters crowding the visual field
- no relative afferent pupillary defect
Treatment
- Follow-up and Examination:
- Acute symptomatic PVD without vitreous hemorrhage and peripheral retinal breaks:
- Follow-up at 2-4 weeks for precise peripheral retinal examination with scleral indentation
- Conservative management for patients with floaters:
- Reassurance that adaptation to visual symptoms will develop over time or floaters may resolve
- Floaters may persist beyond six months to one year in many cases
- Acute symptomatic PVD without vitreous hemorrhage and peripheral retinal breaks:
- Vitreous Hemorrhage:
- Typically mild, with a blob of hemorrhage just in front of the posterior pole
- May include intraretinal hemorrhage near the optic disc
- Circular circumferential attachment of the vitreous to the retina around the equator
- Some preretinal bleed may settle inferiorly behind the posterior vitreous face
- Associated breaks usually lie in the superior retina
- Management for Obscured Fundal View due to Vitreous Hemorrhage:
- Propped up position and bed rest
- Bilateral eye patching as an option
- Ultrasonography to rule out the presence of retinal breaks and other retinal conditions
- Interventional Options for Persistent, Clinically Significant Floaters:
- For highly symptomatic floaters impacting quality of life:
- Various interventional options may be considered based on the specific clinical scenario and patient needs.
- For highly symptomatic floaters impacting quality of life:
Complications
- higher risk of retinal detachment if it is associated with vitreous haemorrhage
- about 70% of these patients have been found to have at least one retinal tear
Aspect | Vitreous Detachment (PVD) | Retinal Detachment (RD) |
---|---|---|
Definition | Separation of vitreous gel from the retina due to aging-related changes. | Separation of neurosensory retina from underlying retinal pigment epithelium (RPE) and choroid. |
Cause | Natural process of vitreous liquefaction and shrinkage. | Usually results from a tear or hole in the retina. |
Clinical Features | Floaters, flashes of light (photopsia), transient visual disturbances. | Sudden onset of floaters, flashes of light, shadow or curtain in vision. |
Complications | Risk of retinal tears leading to detachment. | Permanent vision loss if untreated, proliferative vitreoretinopathy (PVR) in severe cases. |
Management | Observation, monitoring for retinal tears, surgical intervention if indicated. | Urgent surgical repair (e.g., vitrectomy, scleral buckling) to reattach the retina. |