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Dry eye disease ( DED), also known as keratoconjunctivitis sicca, is the condition of having dry eyes. The term dry eye syndrome was formerly used, but is now avoided following advances that have established it as a distinct disease entity.
Symptoms of dry eye include dryness in the eye, irritation, redness, discharge, blurred vision, and easily fatigued eyes. Symptoms range from mild and occasional to severe and continuous. Dry eye disease can lead to blurred vision, instability of the tear film, increased risk of damage to the ocular surface such as scarring of the cornea, and changes in the eye including the neurosensory system.
Dry eye occurs when either the eye does not produce enough tears or when the tears evaporate too quickly. This can be caused by age, contact lens use, meibomian gland dysfunction, pregnancy, Sjögren syndrome, vitamin A deficiency, omega-3 fatty acid deficiency, LASIK surgery, and certain medications such as , some blood pressure medication, hormone replacement therapy, and antidepressants. Chronic conjunctivitis such as from tobacco smoke exposure or infection may also lead to the condition. Diagnosis is mostly based on the symptoms, though several other tests may be used. Dry eye disease occasionally makes wearing contact lenses impossible.
Treatment depends on the underlying cause. Artificial tears are usually the first line of treatment. Wrap-around glasses that fit close to the face may decrease tear evaporation. Looking carefully at the medications a person is taking and, if safe, altering the medications, may also improve symptoms if these medications are the cause. Some topical medications, or , may be suggested to help treat the condition. The immunosuppressant Ciclosporin (ciclosporin) may be recommended to increase tear production and, for short-term use, topical corticosteroid medications are also sometimes helpful to reduce inflammation.
Dry eye syndrome is a common eye disease. It affects 5–34% of people to some degree depending on the population looked at. Among older people it affects up to 70%. In China it affects about 17% of people. The phrase "keratoconjunctivitis sicca" means "dryness of the cornea and conjunctiva" in Latin.
" A multifactorial disease of the ocular surface characterized by a loss of homeostasis of the tear film, and accompanied by ocular symptoms, in which tear film instability and hyperosmolarity, ocular surface inflammation and damage, and neurosensory abnormalities play etiological roles".
According to the TFOS DEWS III (2025), It was agreed that the definition did not require radical change, given the updated understanding of disease pathology and the tear film. However, the revised definition emphasized the intrinsic role of both the ocular surface tissues as well as the tear film in maintaining homeostasis leading to the following updated wording:
" Dry eye is a multifactorial, symptomatic disease characterized by a loss of homeostasis of the tear film and/or ocular surface, in which tear film instability and hyperosmolarity, ocular surface inflammation and damage, and neurosensory abnormalities are etiological factors".
The TFOS DEWS definitions have contributed to establishing a clear characterization of dry eye as a disease. Whereas it was formerly described as a syndrome because of the limited understanding of its etiology, subsequent advances in research have clarified its diagnostic features, natural history, and therapeutic responses, supporting its recognition as a distinct disease entity.
There may also be a stringy discharge from the eyes. Although it may seem contradictory, dry eye can cause the eyes to water due to irritation. One may experience excessive tearing such as if something got into the eye. These reflex tears will not necessarily make the eyes feel better since they are the watery tears that are produced in response to injury, irritation, or emotion which lack the lubricating qualities necessary to prevent dry eye.
Because blinking coats the eye with tears, symptoms are worsened by activities in which the rate of blinking is reduced due to prolonged use of the eyes. These activities include prolonged reading, computer usage (computer vision syndrome), driving, or watching television. Symptoms increase in windy, dusty, or smoky (including cigarette smoke) areas, in dry environments with high altitudes including airplanes, on days with low humidity, and in areas where an air conditioner (especially in a car), fan, heater, or even a hair dryer is being used. Symptoms reduce during cool, rainy, or foggy weather and in humid places, such as in the shower.
Most people who have dry eyes experience mild irritation with no long-term effects. However, if the condition is left untreated or becomes severe, it can produce complications that can cause eye damage, instability of the tear film, neurosensory changes, impaired vision, or (rarely) in the loss of vision.
In many cases, aqueous deficient dry eye may have no apparent cause (idiopathic). Other causes include congenital alacrima, xerophthalmia, lacrimal gland ablation, and sensory denervation. In rare cases, it may be a symptom of collagen vascular diseases, including relapsing polychondritis, rheumatoid arthritis, granulomatosis with polyangiitis, and systemic lupus erythematosus. Sjögren syndrome and other autoimmunity are associated with aqueous tear deficiency. Drugs such as isotretinoin, sedatives, diuretics, tricyclic antidepressants, , oral contraceptives, antihistamines, nasal decongestants, beta-blockers, phenothiazines, atropine, and pain relieving opiates such as morphine can cause or worsen this condition. Infiltration of the lacrimal glands by sarcoidosis or tumors, or post-radiation fibrosis of the lacrimal glands can also cause this condition. Recent attention has been paid to the composition of tears in normal or dry-eye individuals. Only a small fraction of the estimated 1543 proteins in tears are differentially deficient or upregulated in dry eye, one of which is lacritin. Topical lacritin promotes tearing in rabbit preclinical studies. Also, topical treatment of eyes of dry eye mice (Aire knockout mouse model of dry eye) restored tearing, and suppressed both corneal staining and the size of inflammatory foci in lacrimal glands.
Aging is one of the most common contributing factors to dry eye, as tear production declines with age. Several classes of medications, both prescription and over-the-counter (OTC), have been hypothesized to be one of the key contributros to dry eye, especially in the elderly. In particular, anticholinergic medications, which also cause dry mouth, are believed to promote dry eye. Dry eye may also be caused by thermal or chemical burns, or (in epidemic cases) by adenovirus. A number of studies have found that people with diabetes have an increased risk for the condition.
About half of all people who wear contact lenses complain of dry eyes. There are two potential connections between contact usage and dry eye. Traditionally, it was believed that soft contact lenses, which float on the tear film that covers the cornea, absorb the tears in the eyes. The connection between a loss in nerve sensitivity and tear production is also the subject of current research.
Dry eye also occurs or becomes worse after laser-assisted in situ keratomileusis (LASIK) and other refractive surgeries, in which the corneal nerves that stimulate tear secretion are cut during the creation of a corneal flap. Dry eye resulting from these procedures usually resolves after several months, but it can be permanent. Individuals considering refractive surgery should be aware of this potential complication.
An eye injury or other problem with the eyes or , such as bulging eyes or a drooping eyelid may lead to keratoconjunctivitis sicca. Eyelid disorders may disrupt the complex blinking motion necessary to distribute tears evenly.
Abnormalities of the mucin tear layer resulting from vitamin A deficiency, trachoma, diphtheric keratoconjunctivitis, mucocutaneous disorders, and certain topical medications are also implicated in keratoconjunctivitis sicca.
Individuals with keratoconjunctivitis sicca exhibit elevated levels of tear nerve growth factor (NGF). NGF on the ocular surface may play a significant role in the inflammation associated with dry eyes.
Seasonal variations in the manifestation of dry eye have also been reported.
The use of eye make-up products is another influencing factor. Although eye cosmetics have a long history and have been investigated for years, comprehensive reviews on their role in dry eye disease and in ocular surface and adnexal disease were first published in 2022 and 2023, respectively.
Based on the Women's Health Study criteria, DED prevalence increases with age, from about 2.7% at 20–29 years to 30% in women over 80. The rate rises notably after 40 in both sexes, with women showing higher prevalence beyond 50. One study also reported high rates among individuals aged 10–19, without sex differences.
Based on signs and symptoms, DED prevalence ranges from 4.7% in children aged 6–9 to 62.9% in women aged 20–29, although confidence intervals are wide. Rates remain relatively consistent across adult age groups, with a decline in symptoms after 70. Sex differences are small except in those ≥70, where women show higher prevalence.
Based on TFOS DEWS II criteria, DED prevalence ranges from 5.4% in children aged 6–9 to 44.2% overall. Rates are comparable to those based on signs and symptoms. Above 30 years, prevalence is higher in females, while males show a clearer age-related increase.
Based on claims data, DED prevalence ranges from 2.8% to 8.5%, generally lower than estimates from clinical criteria. These figures derive from diagnostic or treatment codes in insurance or ICD data. Insufficient information was available to assess age- or sex-specific trends.
Based on clinical diagnosis, DED prevalence ranges from 1.0% in men aged ≥80 to 15.3% in women aged 50–59. Rates remain relatively consistent across adult ages but are lower in those 10–15 and ≥80. Women show higher prevalence at all ages.
MGD prevalence ranges from 0% in individuals under 20 to 66.3% in men aged ≥80. Rates rise sharply after 40, with significantly higher prevalence in older men (≥70) than in women. Confidence intervals are wide across most age groups.
Clinically significant MGD (Grade ≥ 2) shows increasing prevalence with age, though sex differences remain unclear. No studies have reported rates in younger populations. Of 52 studies in the 2024 dataset, 33 were excluded due to missing or duplicate data. Overall prevalence estimates include international cohorts from 2015 and 2024 datasets. Only studies with age- and sex-stratified data were included in the meta-analysis.
Another contributing factor may be lacritin monomer deficiency. Lacritin monomer, the active form of lacritin, is selectively decreased in aqueous deficient dry eye, Sjögren syndrome dry eye, contact lens-related dry eye, and in blepharitis. The ocular surface microbiome, composed of a diverse community of microorganisms, has been implicated in the pathogenesis of dry eye disease, potentially influencing ocular surface inflammation and homeostasis.
Some tests allow patients to be classified into one of two categories, "aqueous-deficient" or "hyperevaporative". Diagnostic guidelines were published in 2007 by the Dry Eye Workshop, updated by the Dry Eye Workshop II in 2017. Dry Eye Workshop II A slit lamp examination can be performed to diagnose dry eyes and to document any damage to the eye. When realizing this test, the practitioner is testing the eyelid margin.
A Schirmer's test can measure the amount of moisture bathing the eye. This test is useful for determining the severity of the condition. A five-minute Schirmer's test with and without anesthesia using a Whatman #41 filter paper 5 mm wide by 35 mm long is performed. For this test, wetting under 5 mm with or without anesthesia is considered diagnostic for dry eyes.
If the results for the Schirmer's test are abnormal, a Schirmer II test can be performed to measure reflex secretion. In this test, the nasal mucosa is irritated with a cotton-tipped applicator, after which tear production is measured with a Whatman #41 filter paper. For this test, wetting under 15 mm after five minutes is considered abnormal.
A tear breakup time (TBUT) test measures the time it takes for tears to break up in the eye. The tear breakup time can be determined after placing a drop of fluorescein in the cul-de-sac.
A tear protein analysis test measures the lysozyme contained within tears. In tears, lysozyme accounts for approximately 20 to 40 percent of total protein content.
A lactoferrin analysis test provides good correlation with other tests.
The presence of the recently described molecule Ap4A, naturally occurring in tears, is abnormally high in different states of ocular dryness. This molecule can be quantified biochemically simply by taking a tear sample with a plain Schirmer test. Utilizing this technique it is possible to determine the concentrations of Ap4A in the tears of patients and in such a way diagnose objectively if the samples are indicative of dry eye.
The tear osmolarity test has been proposed as a test for dry eye disease. Tear osmolarity may be a more sensitive method of diagnosing and grading the severity of dry eye compared to corneal and conjunctival staining, tear break-up time, Schirmer test, and meibomian gland grading. Others have recently questioned the utility of tear osmolarity in monitoring dry eye treatment.
Conditions such as blepharitis can often co-exist and paying particular attention to cleaning the eyelids morning and night with mild soaps and warm compresses can improve both conditions.
In each eye, there are two Lacrimal punctum – little openings that drain tears into the tear ducts. There are methods to partially or completely close the tear ducts. This blocks the flow of tears into the nose, and thus more tears are available to the eyes. Drainage into either one or both puncta in each eye can be blocked.
Punctal plugs are inserted into the puncta to block tear drainage. It is not clear if punctal plugs are effective at reducing dry eye disease symptoms. Punctal plugs are thought to be "relatively safe", however, their use may result in epiphora (watery eyes), and more rarely, serious infection and swelling of the Lacrimal sac where the tears drain. They are reserved for people with moderate or severe dry eye when other medical treatment has not been adequate.
If punctal plugs are effective, thermal or electric cauterization of puncti can be performed. In thermal cauterization, a local anesthetic is used, and then a hot wire is applied. This shrinks the drainage area tissues and causes scarring, which closes the tear duct.
BlephEx is a medical device used blepharitis and dry eye disease. The handheld device is used by a doctor to exfoliate the eyelid at the lash line and remove the inflammatory biofilm that leads to chronic lid disease and discomfort.
For MGD, intense pulsed light (IPL) is a therapeutic modality that was originally developed for dermatological applications and later adopted in ophthalmology. IPL treatment has been shown to improve tear film stability, enhance meibomian gland function, and alleviate symptoms of ocular dryness. Based on the 2020 comprehensive review of IPL, the procedure shows considerable potential among reported studies in the literature, although large comparative studies with different treatment modalities are still lacking.
When dry eye symptoms are severe, they can interfere with quality of life. People sometimes feel their vision blurs with use, or severe irritation to the point that they have trouble keeping their eyes open or they may not be able to work or drive.
While persons with autoimmune diseases have a high likelihood of having dry eyes, most persons with dry eyes do not have an autoimmune disease. Instances of Sjögren syndrome and keratoconjunctivitis sicca associated with it are present much more commonly in women, with a ratio of 9:1. In addition, milder forms of keratoconjunctivitis sicca also are more common in women. This is partly because hormonal changes, such as those that occur in pregnancy, menstruation, and menopause, can decrease tear production.
In areas of the world where malnutrition is common, vitamin A deficiency is a common cause. This is rare in the United States.
Racial predilections do not exist for this disease.
A study based on 274 answers using the Ocular Surface Disease Index (OSDI) from medical school students aged between 20 and 25 years old found a prevalence of dry eye symptoms of 83.6%.
These advances are increasingly augmented by omics-based research, which provides a deeper molecular understanding of disease mechanisms and informs the development of precision therapies. The shift from hypothesis-driven to hypothesis-generating approaches allows comprehensive analysis of the genome, transcriptome, proteome, and other molecular layers in disease states. For example, metabolomics, a complementary omics discipline, can identify distinct metabolites and integrated metabolic profiles, guiding early diagnosis, monitoring, prognosis, and therapy selection. Integrating multi-omics data further facilitates the discovery of novel biomarkers and therapeutic targets, supporting personalized diagnostics and treatments. The first seminal reviews on tear metabolomics (2019) and systems biology (2025) in dry eye discussed these key aspects.
Tear replacers are a mainstay of treatment, preferably containing methylcellulose or carboxymethyl cellulose. Ciclosporin stimulates tear production and acts as a suppressant on the immune system processes that cause the disease. Topical and are sometimes used to treat secondary infections and inflammation. A surgery known as parotid duct transposition is used in some extreme cases where medical treatment has not helped. This redirects the duct from the parotid gland to the eye. Saliva replaces the tears. Dogs with cherry eye should have the condition corrected to help prevent this disease.
Dog breeds with a higher risk of dry eye compared to other breeds include American Cocker Spaniel, Bloodhound, Boston Terrier, Bulldog, Cavalier King Charles Spaniel, Lhasa Apso, Miniature Schnauzer, Pekingese, Pug, Samoyed, Shih Tzu, and West Highland White Terrier.
Definitions
In the Tear Film & Ocular Surface Society Dry Eye Workshop (TFOS DEWS) II report (2017), dry eye was defined by a multidisciplinary and transnational committee as:
Signs and symptoms
Typical symptoms of dry eye disease are dryness, burning and a sandy-gritty eye irritation that gets worse as the day goes on. Symptoms may also be described as itchy, stinging or tired eyes. Other symptoms are pain, redness, a pulling sensation, and pressure behind the eye. There may be a feeling that something, such as a speck of dirt, is in the eye. The resultant damage to the eye's surface increases discomfort and sensitivity to bright light. Both eyes usually are affected.
Classification
Any abnormality of any one of the three layers of tears produces an unstable tear film, resulting in symptoms of dry eyes. Dry eye can be classified in two ways. The Tear Film & Ocular Surface Society Dry Eye Workshop (TFOS DEWS) II report offers a clinically relevant classification, while the Madrid triple classification is based on etiology, anatomical pathology, and clinical severity. According to the TFOS DEWS II report, dry eye is broadly classified into two major types: (1) Aqueous-deficient dry eye (ADDE), which involves impaired lacrimal secretion, and (2) Evaporative dry eye (EDE), characterized by excessive tear loss from the ocular surface. However, many present with mixed forms of dry eye.
Increased evaporation
The most common cause of dry eye is increased evaporation of the tear film (evaporative dry eye; EDE), typically as a result of meibomian gland dysfunction (MGD). The meibomian glands are two sets of oil glands that line the upper and lower eyelids and secrete the oily outer layer of the tear film—the lipid layer (TFLL). These glands often become clogged due to inflammation caused by blepharitis and/or rosacea, preventing an even distribution of oil (meibum). The result is an unstable lipid layer that is believed to increase evaporation of the tear film. While the anti-evaporative function of the tear film as a whole is well established, scientific evidence specifically supporting the TFLL as the primary source of this resistance remains mixed. Another TFLL-associated mechanism is oxidative stress generated in the perturbed lipid layer due to altered meibum, based on a newly proposed function of the TFLL in corneal oxygenation by Mazyar Yazdani from Oslo University Hospital.
Decreased tear production
Keratoconjunctivitis sicca can be caused by inadequate tear production from lacrimal hyposecretion (aqueous-deficient dry eye; ADDE). The lacrimal gland does not produce sufficient tears to keep the entire conjunctiva and cornea covered by a complete layer. This usually occurs in people who are otherwise healthy. Increased age is associated with decreased tearing. This is the most common type found in postmenopausal women.
Risk factors
Excess screen time on computers, smartphones, tablets, or other digital devices can cause dry eye. "Humans normally blink about 15 times in one minute. However, studies show that we only blink about 5 to 7 times in a minute while using computers and other digital screen devices. Blinking is the eye's way of getting the moisture it needs on its surface."
Prevalence
The following summarizes DED and MGD prevalence from TFOS DEWS III (2025), highlighting findings from population-based studies and meta-analyses across different diagnostic approaches, stratified by age and sex.
Pathophysiology
Having dry eyes for a while can lead to tiny abrasions on the surface of the eyes. In advanced cases, the epithelium undergoes pathologic changes, namely squamous metaplasia and loss of . Some severe cases result in thickening of the corneal surface, corneal erosion, punctate keratopathy, epithelial defects, (sterile and infected), corneal neovascularization, corneal scarring, corneal thinning, and even corneal perforation.
Diagnosis
Symptom assessment is a key component of dry eye diagnosis – to the extent that many believe dry eye disease to be a symptom-based disease. Several questionnaires have been developed to determine a score that would allow for a diagnosis. The Ocular Surface Disease Index (OSDI) is the most frequently used questionnaire in clinical practice and research.
Prevention
Avoiding refractive surgery (LASIK and PRK), limiting contact lens use, limiting computer screen use, and avoiding environmental conditions can decrease symptoms. Complications can be prevented by use of wetting and lubricating drops and ointments.
Treatment
A variety of approaches can be taken to treat dry eye disease. Approaches include: avoidance of exacerbating factors (things that make it worse), tear stimulation and supplementation, increasing tear retention, eyelid cleansing, and treatment of eye inflammation.
Avoiding exacerbating factors and environmental control
Dry eyes can be worsened by smoky environments, dust, and indoor air conditioning, and by our natural tendency to reduce our blink rate when concentrating. Purposefully blinking, especially during computer use, and resting tired eyes are basic steps that can be taken to minimise discomfort. Rubbing one's eyes can irritate them further, so should be avoided. Dry, drafty environments and those with smoke and dust should be avoided. This includes avoiding hair dryers, heaters, air conditioners, or fans, especially when these devices are directed toward the eyes. Wearing glasses or directing gaze downward, for example, by lowering computer screens can be helpful to protect the eyes when aggravating environmental factors cannot be avoided. Using a humidifier, especially in the winter, can help by adding moisture to the dry indoor air.
Tear stimulation and supplementation
For mild and moderate cases, supplemental lubrication is the most important part of treatment. Application of artificial tears is sometimes suggested every few hours and may provide temporary relief. Most artificial tear fluids contain mucoadhesive polymers such as hyaluronic acid, cellulose derivatives or polyvinyl alcohol as . These polymers remain for a prolonged period of time on the ocular surface binding high amounts of water. By the covalent attachment of thiol groups to such polymers, their ocular residence time can be even improved, as thiolated polymers () form disulfide bonds with cysteine-rich subdomains of mucus glycoproteins on the ocular surface. Chitosan-N-acetylcysteine containing eye drops showed a significant reduction in symptoms of dry eye disease. There are many different types of artificial tear on the market, however, there is no strong evidence to suggest that certain artificial tear formulations are superior to others in treating dry eye.
Autologous serum eye drops
Eye drops that include autologous serum (serum taken from the same person's blood and used in an eye drop formulation) are sometimes suggested to help supplement natural tears. The composition of serum has similarities to natural tears and may mimic natural tears. Evidence supporting this approach shows that autologous serum may be superior to artificial tears at relieving symptoms in the short-term, however, there is no strong evidence that autologous serum eye drops are better than artificial tears or saline solution for long-term symptom relief.
Additional options
Lubricating tear ointments can be used during the day, but they generally are used at bedtime due to poor vision after application. They contain Petroleum jelly, mineral oil, and similar lubricants. They serve as a lubricant and an emollient. Application requires pulling down the lower eyelid and applying a small amount (0.25 in) inside. Depending on the severity of the condition, it may be applied from every hour to just at bedtime. It should never be used with contact lenses. Specially designed glasses that form a moisture chamber around the eye may be used to create additional humidity.
Medication
Inflammation occurring in response to tears film hypertonicity can be suppressed by mild topical or with topical immunosuppressants such as ciclosporin (Restasis, Vevye). Elevated levels of tear NGF can be decreased with 0.1% prednisolone.
Topical corticosteroids
Topical corticosteroids are commonly prescribed for those whose dry eye disease symptoms may be caused by inflammation and may lead to a small to moderate improvement in dry-eye symptoms when compared to lubricants or artificial tear drop treatment alone. It is not clear if topical corticosteroid treatment leads to an improvement in the quality of the tear film or the quantity of natural tears. There are also risks to consider with long-term use of topical corticosteroid treatment including an increased risk of ocular hypertension, risk of cataract development, and increased risk of eye infections. For people who may benefit from topical corticosteroid treatment for dry eye disease, the ideal treatment regime, formulation of the topical preparations, and balance between potential risks of this medication is unclear.
Ciclosporin (cyclosporin)
Topical ciclosporin (topical ciclosporin A, tCSA) 0.05% ophthalmic emulsion is an immunosuppressant that is commonly used to treat symptoms of dry eye disease. The drug decreases surface inflammation to increase tear production. Some people find relief and report increased tear production, however, evidence of effectiveness from clinical trials is not strong and although some people may find relief, effectiveness may be inconsistent in different people. Ciclosporin A treatment also comes with risks of adverse effects that are generally not serious but include a burning sensation. Ciclosporin should not be used while wearing contact lenses, during eye infections or in people with a history of herpes virus infections. Side effects include burning sensation (common), redness, discharge, watery eyes, eye pain, foreign body sensation, itching, stinging, and blurred vision. Long-term use of ciclosporin at high doses is associated with an increased risk of cancer.
Cheaper Generic drug alternatives are available in some countries.
Other medications
Conserving tears
There are methods that allow both natural and artificial tears to stay longer.
Other
There is evidence that long‐chain omega‐3 supplementation may be helpful, however, , fish- flax- and hemp-oil (omega-3) supplements do not appear to be effective in relieving symptoms.
Surgery
In severe cases of dry eyes, tarsorrhaphy may be performed where the eyelids are partially sewn together. This reduces the palpebral fissure (eyelid separation), ideally leading to a reduction in tear evaporation.
Prognosis
Keratoconjunctivitis sicca usually is a chronic problem. Its prognosis shows considerable variance, depending upon the severity of the condition. Most people have mild-to-moderate cases, and can be treated symptomatically with lubricants. This provides an adequate relief of symptoms.
Epidemiology
Keratoconjunctivitis sicca is relatively common within the United States, especially in patients aged 40 or older. 10–20% of adults experience Keratoconjunctivitis sicca. Approximately 1 to 4 million adults (age 65–84) in the US are affected.
Research
The field of dry eye research is rapidly evolving, moving beyond symptom management to target underlying causes such as inflammation and MGD. Current efforts focus on developing personalized treatments through genomic and proteomic profiling, advancing regenerative medicine, and improving drug delivery using biomaterials and nanotechnology. Diagnostic capabilities are also advancing, with enhanced imaging, tear film analysis, and biomarker studies, while artificial intelligence increasingly supports precision in diagnosis and treatment planning. Emerging therapies include gene and stem cell interventions, novel anti-inflammatory agents, and innovative approaches such as intranasal neurostimulation.
Synonyms
Other names for dry eye include dry eye syndrome, keratoconjunctivitis sicca, dysfunctional tear syndrome, lacrimal keratoconjunctivitis, evaporative tear deficiency, aqueous tear deficiency, and LASIK-induced neurotrophic epitheliopathy.
Veterinary uses
Among other animals, dry eye can occur in dogs, cats, and horses.
Dogs
Keratoconjunctivitis sicca is common in dogs. Most cases are caused by a genetics predisposition, but chronic conjunctivitis, canine distemper, and drugs such as sulfasalazine and co-trimoxazole also cause the disease. (1999). 9780683300765, Lippincott, Williams & Wilkins. ISBN 9780683300765 Symptoms include eye redness, a yellow or greenish discharge, corneal ulceration, cornea, and blood vessels on the cornea. Diagnosis is made by measuring tear production with a Schirmer tear test. Less than 15 mm of wetting by tears produced in a minute is abnormal.
(2025). 9780470960400, Wiley-Blackwell. ISBN 9780470960400
Cats
Keratoconjunctivitis sicca is uncommon in cats. (2025). 9780470960400, Wiley-Blackwell. ISBN 9780470960400 Most cases seem to be caused by chronic conjunctivitis, especially secondary to feline herpesvirus. Diagnosis, symptoms, and treatment are similar to those for dogs.
See also
External links
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