Retinal Detachment
Retinal Detachment
Retinal Detachment
Retinal detachment is a separation of the light-sensitive membrane in the back of the eye (the retina) from its supporting layers.
Symptoms
Bright flashes of light, especially in peripheral vision Blurred vision Floaters in the eye Shadow or blindness in a part of the visual field of one eye
Electroretinogram (a record of the electrical currents in the retina produced by visual stimuli) Fluorescein angiography Intraocular pressure determination Ophthalmoscopy Refraction test Retinal photography Test to determine your ability to see colors properly (color defectiveness) Visual acuity Slit-lamp examination Ultrasound of the eye
Treatment
Most patients with a retinal detachment will need surgery, either immediately or after a short period of time. (However, surgery may not be needed if you do not have symptoms or have had the detachment for a while.) Types of surgery include:
Cryopexy (intense cold applied to the area with an ice probe) to help a scar form, which holds the retina to the underlying layer Laser surgery to seal the tears or holes in the retina Pneumatic retinopexy (placing a gas bubble in the eye) to help the retina float back into place
Laser surgery is performed after pneumatic retinopexy to permanently fix it in place. This is often done in a doctor's office. More extensive detachments may require surgery in an operating room. Such procedures include:
Scleral buckle to indent the wall of the eye Vitrectomy to remove gel or scar tissue pulling on the retina
Expectations (prognosis)
What happens will depend on the location and extent of the detachment and early treatment. If the macula has not detached, the results of treatment can be excellent. Most retinal detachments can be repaired, but not all of them.
Complications
The unsuccessful reattachment of the retina results in loss of vision.
Prevention
Use protective eye wear to prevent eye trauma. Control your blood sugar carefully if you have diabetes. See your eye care specialist at least yearly, especially if you have risk factors for retinal detachment.
Retinal detachment
Retinal detachment
Retinal detachment is a disorder of the eye in which the retina peels away from its underlying layer of support tissue. Initial detachment may be localized, but without rapid treatment the entire retina may detach, leading to vision loss and blindness. It is a medical emergency.[1]
The retina is a thin layer of light sensitive tissue on the back wall of the eye. The optical system of the eye focuses light on the retina much like light is focused on the film in a camera. The retina translates that focused image into neural impulses and sends them to the brain via theoptic nerve. Occasionally, posterior vitreous detachment, injury or trauma to the eye or head may cause a small tear in the retina. The tear allows vitreous fluid to seep through it under the retina, and peel it away like a bubble in wallpaper.
Types
Rhegmatogenous retinal detachment A rhegmatogenous retinal detachment occurs due to a break in the retina that allows fluid to pass from the vitreous space into the subretinal space between the sensory retina and the retinal pigment epithelium. Retinal breaks are divided into three types - holes, tears and dialyses. Holes form due to retinal atrophy especially within an area of lattice degeneration. Tears are due to vitreoretinal traction. Dialyses which are very peripheral and circumferential may be either tractional or atrophic, the atrophic form most often occurring as idiopathic dialysis of the young.
Exudative, serous, or secondary retinal detachment An exudative retinal detachment occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break. In evaluation of retinal detachment it is critical to exclude exudative detachment as surgery will make the situation worse, not better. Although rare, exudative retinal detachment can be caused by the growth of a tumor on the layers of tissue beneath the retina, namely the choroid. This cancer is called a choroidal melanoma.
Tractional retinal detachment A tractional retinal detachment occurs when fibrous or fibrovascular tissue, caused by an injury, inflammation or neovascularization, pulls the sensory retina from the retinal pigment epithelium.
A minority of retinal detachments result from trauma, including blunt blows to the orbit, penetrating trauma, and concussions to the head. A retrospective Indian study of more than 500 cases of rhegmatogenous detachments found that 11% were due to trauma, and that gradual onset was the norm, with over 50% presenting more than one month after the inciting injury. [2] [edit]Frequency
The incidence of retinal detachment in otherwise normal eyes is around 5 new cases in 100,000 persons per year.[3] Detachment is more frequent in middle-aged or elderly populations, with rates of around 20 in 100,000 per year.[4] The lifetime risk in normal individuals is about 1 in 300.[5]
Retinal detachment is more common in people with severe myopia (above 56 diopters), in whom the retina is more thinly stretched. In such patients, lifetime risk rises to 1 in 20.[6]About two-thirds of cases of retinal detachment occur in myopics. Myopic retinal detachment patients tend to be younger than non-myopic ones.
Retinal detachment is more frequent after surgery for cataracts. The estimated long-term prevalence of retinal detachment after cataract surgery is in the range of 5 to 16 per 1000 cataract operations, [7] but is much higher in patients who are highly myopic, with a prevalence of up to 7% being reported in one study.[8] One study found that the probability of experiencing retinal detachment within 10 years of cataract surgery may be about 5 times higher than in the absence of treatment.[9]
Tractional retinal detachments can also occur in patients with proliferative diabetic retinopathy [10] or those with proliferative retinopathy ofsickle cell disease.[11] In proliferative retinopathy, abnormal blood vessels (neovascularization) grow within the retina and extend into the vitreous. In advanced disease, the vessels can pull the retina away from the back wall of the eye, leading to tractional retinal detachment.
Although retinal detachment usually occurs in just one eye, there is a 15% chance of it developing in the other eye, and this risk increases to 2530% in patients who have had cataracts extracted from both eyes.[6]
[edit]Symptoms
A retinal detachment is commonly preceded by a posterior vitreous detachment which gives rise to these symptoms:
flashes of light (photopsia) very brief in the extreme peripheral (outside of center) part of vision a sudden dramatic increase in the number of floaters a ring of floaters or hairs just to the temporal side of the central vision a slight feeling of heaviness in the eye
Although most posterior vitreous detachments do not progress to retinal detachments, those that do produce the following symptoms:
a dense shadow that starts in the peripheral vision and slowly progresses towards the central vision the impression that a veil or curtain was drawn over the field of vision straight lines (scale, edge of the wall, road, etc.) that suddenly appear curved (positive Amsler grid test) central visual loss
(None of this is to be confused with the broken retina which is generally the tearing of muscle and nerve behind the eye)
1. 2. 3.
Find all retinal breaks Seal all retinal breaks Relieve present (and future) vitreoretinal traction
Cryopexy and Laser Photocoagulation Cryotherapy (freezing) or laser photocoagulation are occasionally used alone to wall off a small area of retinal detachment so that the detachment does not spread. Scleral buckle surgery Scleral buckle surgery is an established treatment in which the eye surgeon sews one or more silicone bands (bands, tyres) to the sclera (the white outer coat of the eyeball). The bands push the wall of the eye inward against the retinal hole, closing the break or reducing fluid flow through it and reducing the effect of vitreous traction thereby allowing the retina to re-attach. Cryotherapy (freezing) is applied around retinal breaks prior to placing the buckle. Often subretinal fluid is drained as part of the buckling procedure. The buckle remains in situ. The most common side effect of a scleral operation is myopic shift. That is, the operated eye will be more short sighted after the operation. Radial scleral buckle is indicated to U-shaped tears or Fishmouth tears and posterior breaks. Circumferential scleral buckle indicated to multiple breaks, anterior breaks and wide breaks. Encircling buckles indicated to breaks more than 2 quadrant of retinal area, lattice degeration located on more than 2 quadrant of retinal area, undetectable breaks, and proliferative vitreous retinopathy. Pneumatic retinopexy This operation is generally performed in the doctor's office under local anesthesia. It is another method of repairing a retinal detachment in which a gas bubble (SF6 or C3F8 gas) is injected into the eye after which laser or freezing treatment is applied to the retinal hole. The patient's head is then positioned so that the bubble rests against the retinal hole. Patients may have to keep their heads tilted for several days to keep the gas bubble in contact with the retinal hole. The surface tension of the air/water interface seals the hole in the retina, and allows the retinal pigment epithelium to pump the subretinal space dry and suck the retina back into place. This strict positioning requirement makes the treatment of the retinal holes and detachments that occurs in the lower part of the eyeball impractical. This procedure is usually combined with cryopexy or laser photocoagulation. Vitrectomy Vitrectomy is an increasingly used treatment for retinal detachment. It involves the removal of the vitreous gel and is usually combined with filling the eye with either a gas bubble (SF6 or C3F8 gas) or silicon oil. Advantages of using gas in this operation is that there is no myopic shift after the operation and gas is absorbed within a few weeks. Silicon oil
(PDMS), if filled needs to be removed after a period of 28 months depending on surgeon's preference. Silicon oil is more commonly used in cases associated with proliferative vitreo-retinopathy (PVR). A disadvantage is that a vitrectomy always leads to more rapid progression of a cataract in the operated eye. In many places vitrectomy is the most commonly performed operation for the treatment of retinal detachment.
Results of Surgery
85 percent of cases will be successfully treated with one operation with the remaining 15 percent requiring 2 or more operations. After treatment patients gradually regain their vision over a period of a few weeks, although the visual acuity may not be as good as it was prior to the detachment, particularly if the macula was involved in the area of the detachment. However, if left untreated, total blindness could occur in a matter of days.
a retinal exam. In the exam, drops are used to dilate the patient's pupils to make a more detailed exam easier. The symptoms of flashing lights and floaters may often be unassociated with a tear or detachment and can merely result from a separation of the vitreous gel from the retina. This condition is called a posterior vitreous detachment (PVD). Although a PVD occurs commonly, there are no tears associated with the condition most of the time. The flashing lights are caused by the vitreous gel pulling on the retina or a looseness of the vitreous, which allows the vitreous gel to bump against the retina. The lights are often described as resembling brief lightning streaks in the outside edges (periphery) of the eye. The floaters are caused by condensations (small solidifications) in the vitreous gel and frequently are described by patients as spots, strands, or little flies. Some patients even want to use a flyswatter to eliminate these pesky floaters. There is no safe treatment to make the floaters disappear. Floaters are usually not associated with tears of the retina. If the patient experiences a shadow or curtain that affects any part of the vision, this can indicate that a retinal tear has progressed to a detached retina. In this situation, one should immediately consult an eye doctor since time can be critical. The goal for the ophthalmologist is to make the diagnosis and treat the retinal tear or detachment before the central macular area of the retina detaches.
People taking certain kinds of eyedrops have an increased risk of developing a retinal detachment. Pilocarpine (Salagen), which for many years was a mainstay of therapy for glaucoma, has long been associated with retinal detachment. Moreover, by constricting the pupil, pilocarpine makes the diagnostic exam of the peripheral retina more difficult, possibly leading to a delay in the diagnosis.
Individuals with chronic inflammation of the eye (uveitis) are at increased risk of developing retinal detachment.
extracapsular cataract surgery, part of the capsule of the lens is left in place so that the vitreous gel is undisturbed. Phacoemulsification is a type of extracapsular cataract surgery that utilizes a very high speed ultrasonic instrument to break up and suck out the clouded lens of the eye. The capsule that is left in the eye may at a later time become cloudy, necessitating opening the capsule by using a laser. Opening the capsule increases the risk of retinal detachment. In intracapsular cataract surgery, the predominant surgical method used from 1965 to 1990, the entire lens was removed. The capsule at the back of the lens, therefore, was no longer present to hold the vitreous gel in place. Consequently, the vitreous gel moved forward, and the retina was subjected to increased pulling or traction on the retina from the vitreous, which led to tears of the retina. Today, if the capsule is broken, which can be a complication during extracapsular cataract surgery, the vitreous gel similarly can move forward and pull on the retina. This sequence can lead to a retinal tear and a detachment, especially during the first year after surgery.
A family history of a detached retina that is non-traumatic in nature seems to indicate a genetic (inherited) tendency for developing retinal detachments.
In as many as 5% of patients with a non-traumatic retinal detachment of one eye, a detachment subsequently occurs in the other eye. Accordingly, the second eye of a patient with a retinal detachment must be examined thoroughly and followed closely, both by the patient and the ophthalmologist. Diabetes can lead to a type of retinal detachment that is caused by pulling on the retina (traction) alone, without a tear. Because of abnormal blood vessels and scar tissue on the retinal surface in some people with diabetes, the retina can be lifted off (detached) from the back of the eye. In addition, the blood vessels may bleed into the vitreous gel. This detachment may involve either the periphery or central area of the retina.
A tear or hole of the retina that leads to a peripheral retinal detachment causes the loss of side (peripheral) vision. Almost all of those affected will progress to a full retinal detachment and loss of all vision if the problem is not repaired. The dark shadow or curtain obscuring a portion of the vision, either from the side, above, or below, almost invariably will advance to the loss of all useful vision. Spontaneous reattachment of the retina is rare. Early diagnosis and repair are urgent since visual improvement is much greater when the retina is repaired before the macula or central area is detached. The surgical repair of a retinal detachment is usually successful in reattaching the retina, although more than one procedure may be necessary. Once the retina is reattached, vision usually improves and then stabilizes. Successful reattachment does not always result in normal vision. The ability to read after successful surgery will depend on whether or not the macula (central part of the retina) was detached and the extent of time that it was detached.
of the defects, whether pulling on the retina (traction) or bleeding is involved, and the presence of any of the other risk factors discussed above. Three types of eye surgery are done for actual retinal detachment: scleral buckling, pneumatic retinopexy, and vitrectomy. Scleral buckling For many years, scleral buckling has been the standard treatment for detached retinas. The surgery is done in a hospital operating room with general or local anesthesia. Some patients stay in the hospital overnight (inpatient), while others go home the same day (outpatient). The surgeon identifies the holes or tears either through the operating microscope or a focusing headlight (indirect ophthalmoscope). The hole or tear is then sealed, either with diathermy (an electric current which heats tissue), a cryoprobe (freezing), or a laser. This results in scar tissue later forming around the retinal tear to keep it permanently sealed, so that fluid no longer can pass through and behind the retina. A scleral buckle, which is made of silicone, plastic, or sponge, is then sewn to the outer wall of the eye (thesclera). The buckle is like a tight cinch or belt around the eye. This application compresses the eye so that the hole or tear in the retina is pushed against the outer scleral wall of the eye, which has been indented by the buckle. The buckle may be left in place permanently. It usually is not visible because the buckle is located half way around the back of the eye (posteriorly) and is covered by the conjunctiva (the clear outer covering of the eye), which is carefully sewn (sutured) over it. Compressing the eye with the buckle also reduces any possible later pulling (traction) by the vitreous on the retina. A small slit in the sclera allows the surgeon to drain some of the fluid that has passed through and behind the retina. Removal of this fluid allows the retina to flatten in place against the back wall of the eye. A gas or air bubble may be placed into the vitreous cavity to help keep the hole or tear in proper position against the scleral buckle until the scarring has taken place. This procedure may require special positioning of the patient's head (such as looking down) so that the bubble can rise and better seal the break in the retina. The patient may have to walk, eat, and sleep with the head facing down for one to four weeks to achieve the desired result. Pneumatic retinopexy Pneumatic retinopexy is a newer method for repairing retinal detachments. It usually is performed on an outpatient basis under local anesthesia. Again, laser or cryotherapy is used to seal the hole or tear. The surgeon then injects a gas bubble directly inside the vitreous cavity of the eye to push the detached retina against the back outer wall of the eye (sclera). The gas bubble initially expands and then disappears over two to six weeks. Proper positioning of the head in the postoperative time period is crucial for success. Although this treatment is inappropriate for the repair of many retinal detachments, it is simpler and much less costly than scleral buckling. Furthermore, if pneumatic retinopexy is unsuccessful, scleral buckling still can be performed. Vitrectomy Certain complicated or severe retinal detachments may require a more complicated operation called a vitrectomy. These detachments include those that are caused by the growth of abnormal blood vessels on the retina or in the vitreous, as occurs in advanced diabetes. Vitrectomy also is used with giant retinal tears, vitreous hemorrhage (blood in the vitreous cavity that obscures the surgeon's view of the retina), extensive tractional retinal detachments (pulling from scar tissue), membranes (extra tissue) on the retina, or severe infections in the eye (endophthalmitis). Vitrectomy surgery is performed in the hospital under general or local anesthesia. Small openings are made through the sclera to allow positioning of a fiberoptic light, a cutting source (specialized scissors), and a delicate forceps. The vitreous gel of the eye is removed and replaced with a gas to refill the eye and reposition the retina. The gas eventually is absorbed and is replaced by the eye's own natural fluid. A scleral buckle is often also performed with the vitrectomy.
What are complications of surgery for a retinal detachment, and what is recovery like after retinal detachment surgery?
Discomfort, watering, redness, swelling, anditching of the affected eye are all common and may persist for some time after the operation. These symptoms are usually treated with eyedrops. Blurred vision may last for many months, and new glasses may need to be prescribed, especially because the scleral buckle may have changed the shape of the eye. The scleral buckle also can causedouble vision (diplopia) by affecting one of the muscles that controls the movements of the
eye. Other complications can include elevated pressure in the eye (glaucoma); bleeding into the vitreous, within the retina, or behind the retina; clouding of the lens of the eye (cataract); or drooping of the eyelid (ptosis). Additionally, infection can occur around the scleral buckle or even more widely in the eye (endophthalmitis). Occasionally, the buckle may need to be removed.
A retinal detachment is a separation of the retina from its attachments to the underlying tissue within the eye. Most retinal detachments are a result of a retinal break, hole, or tear. Most retinal breaks, holes, or tears are not the result of trauma but are due to preexisting factors such as high levels of myopia and prior ocular surgery. Flashing lights and floaters may be the initial symptoms of a retinal detachment or of a retinal tear that precedes the detachment itself. Early diagnosis and repair of retinal detachments are urgent since visual improvement is much greater when the retina is repaired before the macula or central area is detached. The surgical repair of a retinal detachment is usually successful in reattaching the retina.
Retinal Detachment
Results from separation of the sensory layer of the retina containing the rod and cones from the pigmented epithelial layer beneath. It may occur spontaneously because of degenerative changes in the retina (as in diabetic retinopathy) or vitreous humor, trauma, inflammation, tumor, or loss of a lens to a cataract. It is rare in children, the disorder most commonly occurs after age 40. Untreated retinal detachment results in loss of a portion of the visual field.
Assessment: 1. 2. Initially, the patient complains of flashes of light, floating spots or filaments in the vitreous, or blurred, sooty vision. Most of these phenomena result from traction between the retina and vitreous. If detachment progresses rapidly, the patient may report a veil-like curtain or shadow obscuring portions of the visual field. The veil appears to come from above, below, or from one side; the patient may initially mistake the obstruction for a drooping eyelid or elevated cheek. Straight-ahead vision may be unaffected in early stages but, as detachment progresses, there will be loss of central as well as peripheral vision. Diagnostic Evaluation: 1. Ophthalmoscopy or slit-lamp examination with full pupil dilation shows retina as gray or opaque in detached areas. The retina is normally transparent. Surgical Interventions: 1. Surgical intervention aims to reattach the retinal layer to the epithelial layer and has a 90% to 95% success rate. Techniques include: a. Photocoagulation, in which a laser or xenon are spot welds the retina to the pigment epithelium. b. Electrodiathermy, in which a tiny hole is made in the sclera to drain subretinal fluid, allowing the pigment epithelium to adhere to the retina. c. Cryosurgery or retinal cryopexy, another spot weld technique that uses a super cooled probe to adhere the pigment epithelium to the retina. d. Scleral buckling, in which the sclera is shortened to force the pigment epithelium closer to the retina; commonly accompanied by vitrectomy. Nursing Interventions: 1. Prepare the patient for surgery. Instruct the patient to remain quiet in prescribed (dependent) position, to keep the detached area of the retina in dependent position. Patch both eyes. Wash the patients face with antibacterial solution. Instruct the patient not to touch the eyes to avoid contamination. Administer preoperative medications as ordered. 2. Take measures to prevent postoperative complications. Caution the patient to avoid bumping head. Encourage the patient no to cough or sneeze or to perform other strain-inducing activities that will increase intraocular pressure. 3. Encourage ambulation and independence as tolerated. 4. Administer medication for pain, nausea, and vomiting as directed. 5. Provide quiet diversional activities, such as listening to a radio or audio books. 6. Teach proper technique in giving eye medications. 7. Advise patient to avoid rapid eye movements for several weeks as well as straining or bending the head below the waist. 8. Advise patient that driving is restricted until cleared by ophthalmologist. 9. Teach the patient to recognize and immediately report symptoms that indicate recurring detachment, such as floating spots, flashing lights, and progressive shadows. 10. Advise patient to follow up.
3.
I.
Definition
Retinal detachment is a separation of the retina from the choroid in the posterior eye. II. Risk Factors
Retinal layers separate from the choroid, creating a subretinal space. Vitreous fluid seeps between these layers, disrupting choroidal blood supply. Detachment may be partial, causing various degree of visual deficits, or total causing blindness in the affected eye. IV. Assessment/Clinical Manifestations/Signs and Symptoms
Recurrent flashes of light and floating spots Progressive blurring of vision in the affected eye, followed by visual field deficits, with the area of visual loss depending on the area of detachment. Anxiety, confusion, and fear of becoming blind Laboratory and diagnostic study findings Ophthalmoscopic examination may reveal an area of gray, opaque retina, possibly with folds, holes or tears. V. Medical Management
The treatment for a tear may be a cryopexy (freezing of the retinal area) or lase photocoagulation performed. Scleral bucking surgery is the most common method of treatment, requires that a piece of silicone, rubber or semihard plastic be placed against the outer surface of the eye and sutured into put. The piece pushes the sclera toward the middle of the eye, allowing the retina to settle back against the wall of the eye. Pneumatic retinopexy is used to reattach the retina, the physician uses a bubble of gas to push the two layers back together again. Vitrectomy is the possible procedure where the surgeon removes the vitreous fluid from the middle of the eye. The physician may then treat the retina with photocoagulation. At the end of the surgery, silicone oil or gas is injected into the ye to replace the vitreous fluid. VI. Nursing Diagnosis
Anxiety related to possible vision loss Disturbed sensory perception related to visual impairment Ineffective health maintenance related to knowledge deficit Risk for injury related to impaired vision Self-care deficit related to impaired vision VII. Nursing Management
Promote measures that limit mobility to prevent further injury. Position the client in bed preoperatively as prescribed (usually with the detached area dependent), and instruct the client to avoid lying face down, stooping, or bending. Enforce bed rest for 1 day postoperatively, with the client positioned supine or on the unoperated side unless otherwise directed. Promote measures that assist with the clients adaptation to the perceptual impairment. Preoperatively, patch both eyes if detachment threatens the macula. Administer sedation as prescribed, promote comfort and relaxation, and minimize eye strain. Administer prescribed medications, which may include adrenergic agonist agents (mydriatic) and anticholinergic (cycloplegic) agents.
Provide postoperative nursing care. Patch the affected eye for 1 to 4 hours Encourage visitors, socialization, sensory stimulation and diversionary activities. Administer mild analgesics for discomfort, and apply cool or warm compresses to edematous eyelids. Instruct the client on discharge instructions. Discuss allowed and restricted activities. Discuss prescribed positions. Instruct the client on the resumption of activity, including resuming activities of daily living gradually and as tolerated, commonly resuming light work in 3 weeks and normal activity in 6 weeks; avoiding heavy lifting, deep bending or stopping and avoiding bumping or otherwise injuring the head.