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Retinal Detachment

Retinal detachment affects approximately 30,000 Americans yearly, and without prompt treatment commonly leads to complete vision loss. Early detection and treatment by an ophthalmologist is critical to preventing severe vision loss and blindness.

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What is Retinal Detachment?

The cause of retinal detachment is the leakage of vitreous liquid beneath the retina. Age and other factors can cause a thinning of the retina, causing small holes to develop and leak vitreous liquid, through these holes or underneath the retina. As the liquid leaks and collects, the surrounding areas of the retina can peel away from the choroid, the underlying layer. When these areas detach from the retina, vision loss results.

The choroid is a very thin layer of blood vessels that serves to supply nutrients and oxygen to the retina. Ensuring that this layer is attached to the retina is critical to maintaining vision.

Key to retinal detachment is the vitreous fluid found in the vitreous cavity of the eye. The vitreous fluid, typically jelly-like, changes over time, partly liquefying and shrinking. This can cause the vitreous to separate from the retina's surface. Most aging eyes experience this condition to some degree and typically it does not cause significant problems. It often causes the appearance of floaters or flashes in the field of vision, resulting from the shadows that the fluid creates on the retina.

The presence of intense, sudden floaters can signal a serious problem. The sagging vitreous can pull enough such that the retina tears, typically along the periphery of the retina. These tears can cause retinal detachment.

Vitreous liquid seeps underneath the retina from the open areas of the tears. As the fluid collects, the surrounding areas of the retina peel away from the choroid. The peeling areas expand over time, and loose their ability to see. Critical in preventing the complete detachment of the retina is early detection and treatment. Some retinal tears and holes remain attached to the choroid, and swift treatment can prevent further injury to the eye.

Are you at risk?

The risk of retinal detachment increase with age. With age, the vitreous changes, becoming increasingly fluid like. Individuals who have experienced retinal detachment in one eye are at increased risk of developing a detached retina in the other eye. Those with a family history of retinal detachment are also at increased risk.

Other risk factors include:

1) Nearsightedness
2) Causian
3) Male
4) Eye surgery
5) Weakness in the peripheral areas of the retina

Diagnosing Retinal Detachment

One or two tools are typically used to diagnose retinal attachment. Using an ophthalmoscope, an eye doctor can closely examine the inside of the eyes in detail, and can often see any small tears or holes in the retina.

In situations where the vitreous cavity interferes with complete view of the retina, a doctor will typically employ ultrasonography to help get a complete picture. Ultrasonography is painless, and uses sound waves to image the retina on a monitor. This enables a doctor to clearly see the state of the retina and all other structures inside the eye.

Retinal detachment can be a very serious eye condition and can cause blindness. Early detection and treatment of retinal tears is critical to preventing complete detachment of the retina.

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Resources: Read about the different types of retinal detachment. Understand the difference between retinal tears and retinal detachment.

 

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