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Research Article | Volume 4 Issue 1 (None, 2018) | Pages 48 - 53
Prevalence and Risk Factors of Dry Eye Disease A Cross-Sectional Study in a Tertiary Care Teaching Hospital
1
Associate Professor, Department of Ophthalmology, Venkateshwara Institute of Medical Sciences, Gajraula
Under a Creative Commons license
Open Access
Received
April 2, 2018
Revised
April 11, 2018
Accepted
April 20, 2018
Published
May 7, 2018
Abstract
Background: Dry eye disease (DED) is one of the most prevalent eye conditions affecting millions of people. It is also known as tear film dysfunction and one of the most common ocular disorders affecting the general population. It can cause disabilities ranging from mild irritation to severe debilitation due to loss of homeostasis of the tear film. Tear film is a 3-layered structure of mucin, aqueous and lipid layer. Material & methods: The study was conducted from 20/01/2017 to 31/12/2017 for one year. The entire rural population of specific area (block wise) having 272500 persons were contacted. 76196 persons were found symptomatic and were subjected to standard Shirmer’s test without anesthesia in field area. The data was recorded separately for age and sex groups. The DED determination was done on the basis of positive Shirmer’s test reading less than 10 mm. There were three age groups 0 to 25 years, 25 to 50 years and more than 50 years. Male and female were recorded separately. Results: Prevalence of DED in females 0-25 year group 5.5%, 25-50 years 15.1% and more than 50 years 57.01%. Males had 0-25 years group 4.1%, 25-50 years 15.9% while more than 50 years 65.1%. Overall prevalence for 0-25 years 4.77%, 25-50 years 15.5% and more than 50 years was 60.87%. The DED prevalence in rural population was determined 19.2% which is in the same order with previous studies. Conclusion: However more resources required conducting other diagnostic test for DED in field settings, then the prevalence may be more in rural population as accepted theoretically.
INTRODUCTION
Dry eye disease (DED) is one of the most prevalent eye conditions affecting millions of people. It is also known as tear film dysfunction and one of the most common ocular disorders affecting the general population. It can cause disabilities ranging from mild irritation to severe debilitation due to loss of homeostasis of the tear film. Tear film is a 3-layered structure of mucin, aqueous and lipid layer. The muco-aqueous layer reduces friction and hydrates the ocular surface, while the lipid layer decreases surface tension and minimizes evaporation. Each blink drives capillary movement, upward drift of the lipid and muco-aqueous layers, which contributes to proper tear distribution across the corneal and conjunctival surfaces (1,2,3). In ancient Indian medical literature the DED named as Shushkakshipaka described as Sarvagata Netraroga in Ayurveda text Sushruta Samhita 600 BCE by the great Indian surgeon Sushruta in Shalakya Tantra (4,5). However, in the modern medicinal system the phrase "Dry Eye" was first used in 1950 by Andrew de Roetth a dacryologist (6) and was considered mainly due to reduction in water secretion in tears (7). The Prevalence ranges from 5% to 35%, depending on the geographic region (8, 9, 18, 19) DED defined as“ disorders of tear film due to reduced tear production and or excessive tear evaporation associated with symptoms of ocular discomfort” (10) DED is a multi-factorial disorder and manifests as loss of the tear film stability (9, 10, 11). The etiology is nonspecific except reduced tear production. Various etio-pathological explanations have been given but being multi factorial none is able to explain fully. Researchers all over the world are working on it as the magnitude of DED is very high. The dry eye disease global market research report projected that the DED industry will be over 7 billion dollars by (12,14).The symptoms included discomfort, burning sensation, tearing, stinging, Itching, gritty feeling, foreign-body sensation, frequent blinking, redness, blurry or fluctuating vision, light sensitivity, ocular pain, heavy eyelids, eye fatigue and finally vision loss (16). Assessment of large-scale DED prevalence and incidence has been hindered by inconsistencies in the definition and diagnostic criteria among prior studies. When the diagnosis is based on symptoms (with or without signs), meta-analysis yields prevalence values ranging from 5% to 35%; when signs alone are used, and the prevalence is as high as 75% in certain cohorts (13,14,15,17,18,19,27). There is a paucity of research from rural area, so the possible effects of regional differences have gone largely unstudied. Ophthalmic fraternity can never forget the contribution of HenrikSjögren who explained Sjögren’s Syndrome in 1933 (20). The diagnosis of dry eye disease was revolutionized by German ophthalmologist Schirmer by a simple test known as Schirmer’s test in 1903(21). Presently there is no single gold standard diagnostic marker of DED available (19). The prevalence of dry eye ranges from 5% to35% globally, depending on the geographic region (19, 20, 21, 27). Prevalence in India is 32% as 9.9% (496/5000) had mild DED; 61.2% (3060/5000) Moderate DED; and 28.9% (1444/5000) severe DED in an urban hospital (21). There is a major difference between rural and urban environment in terms of living and working conditions thus the present study was done in rural population of northern India. The prevalence of dry eye was higher in East Asian countries (22). Dry eye prevalence was maximum in those above 70 years of age (36.1%) followed by the age group 31-40 years (20%). It was more common in rural residents 19.6% than in urban 17.5% and highest among farmers/labourer 25.3% (23). The prevalence was studied mainly in urban area in India and no major study was conducted in rural area exclusively.
MATERIAL AND METHODS
The Present Study was conducted in rural population distributed in 627 villages with sex ratio 866 (24, 25). We organized 155 camps in rural area during the study period of one year (Jan 2017 to Dec 2017). The population of these villages varies from 500 to 5000 and total population covered during screening was 2, 72,500, approx.40% of total rural population under study.125 screening camps were organized under National Program for Control of Blindness and Visually Impaired (NPCB & VI) (26) and 30 camps under arrangement of Venkateshwara Institute as social service medical camps. All willing persons residing in rural area of all age groups were included in this study during 155 camps. A simple questionnaire related to DED symptoms was given to patients during screening to answer as:- 1. Do you have discomfort in eyes? 2. Do you have burning in eyes? 3. Are you having gritty feeling in eyes? 4. Are you having foreign body sensation in eyes? 5. Do you have tearing in eyes? 6. Do you feel dryness in eyes? 7. Is there itching in your eyes? 8. Is there redness in eyes? 9. Is there discomfort in eyes on exposure to bright light/ sun light? 10. Do you have blurred vision in Eyes? These questions were related to DED and Individuals were also enquired about vision and other symptoms of eyes as this was organized under NPCB & VI program. Responses were recorded and documented. Persons with positive symptoms were subjected to ophthalmic examination and Schirmer’s test (28). We used Whatman filter paper no 41 (measuring 5 mm × 35 mm) which was placed in the lower fornix at the lateral one-third of the lower lid margin. The extent of wetting of the strip was measured after 5 minutes andless than 10 mm of wetting was taken as dry eye (28). Schirmer’s test was done without anesthesia. All 76,196 Individuals with positive answers were recorded in the format of symptoms with age and gender distribution.
RESULTS
Table 1: Population profile Urban Rural Male Female Total Total Population 1,28,621 6,81,745 4,34,280 3,76,086 8,10,366 Screened population - 2,72,500 1,38,975 1,33,525 2,72,500 Table 2: Age and sex distribution of study population Age Group in yrs 0-25 25-50 More than 50 yrs Grand total Male 65,400 49,050 24,525 1,38,975 Female 59,950 46,325 27,250 1,33,525 Total 1,25,350 95,375 51,775 2,72,500 Table 3: Distribution of Symptoms Symptomatic Cases Male Female 76,196 40,376 35,820 Out of 2, 72,500 patients screened, 76,196 (28 %) were symptomatic. Out of which 40,376 (52.98 %) were males and 35,820(47.06 %) were females. Table 4: Clinical symptoms of dry eye disease in study population Symptoms Male Female Total Discomfort / unwell feeling 40376 35820 76196 Burning 35576 30650 66226 Gritty feeling 34600 26465 61065 Foreign body sensation 20764 19650 40414 Tearing 19250 17650 36900 Dryness 11800 9093 20893 Itching 9880 8660 18640 Redness 4670 3450 8120 Discomfort in eyes on exposure to bright light. 3560 2580 6410 Blurring of vision 8070 6890 14960 Discomfort/ un-well feeling were present in all the cases. Burning sensation followed by gritty feeling were the two more common symptoms and noted in 86.91% and 80.14% patients respectively. Table 5: Schirmer’s test readings in study population Reading Male 0-25 yrs Male 26 -50 yrs Male> 50 yrs Female 0-25 yrs Female 26 – 50 yrs Female>50 yrs Grand Total 0-5 mm 177 1671 6258 102 1653 5710 15571 5-10 mm 2504 6134 9718 3208 5350 8830 35744 >10 mm 6516 5010 3835 4300 2105 3115 24881 Total 9197 12815 19811 7610 9108 17655 76196 Out of 76196 suspected dry eye disease screened patients, 51315 (67.34%) were having dry eye out of which 26462 (51.56%) were male and 24853 (48.44%) were female. Table 6: Age and gender distribution of dry eye disease cases Schirmer’s reading Male 0-25 yrs Male 26 -50 yrs Male> 50 yrs Female 0-25 yrs Female 26 – 50 yrs Female>50 yrs 0-5 mm 177 1671 6258 102 1653 5710 5-10 mm 2504 6134 9718 3208 5350 8830 Total 2681 7805 15976 3310 7003 14540 Dry eye disease was more common in patients above the age group of more than 50 years with gender predisposition of 60.87% and 57.01% cases in males and females respectively. The disease prevalence was least in the age group of less than 25 years in both males and females.
DISCUSSION
The DED is most prevalent ocular disorder with multi factorial patho-physiology. The DED refers to disorders of the tear film due to reduced tear production and or excessive tear evaporation associated with symptoms of ocular discomfort (10). There has been excellent development in the diagnosis and management of DED in last century. Various diagnostic tests have been developed and now being used for the same. The gold standard tests are tear film breakup time (29), ocular redness measurement using the validated bulbar redness (30,31), Schirmer’s Test (28,32), fluorescein dye clearance test (33), tear fluid osmolarity test (34,35), measurement of MMP-9 in tear fluid (36) and meibomian gland imaging (37). Schirmer’s test is the most convenient for outdoor procedure and the same was adopted in present study. There are many studies based on urban population in India and abroad but none is based on rural population. A K Bansal, P M Living stonetal conducted a study in Australia and diagnosed DED 10.8% by rose bengal, 16.3% by Schirmer's test, 8.6% by tear film breakup time, 1.5% by fluorescein staining. It shows the importance to Schirmer's test due to highest sensitivity& positivity (38). However, Lin P Yet al in their study of Taiwan population observed that amongst 37.7 % symptomatic persons the 62.5% had low Schirmer's test result (39). In India, a clinical study done by Gupta N et al observed that the overall prevalence of dry eye based on OSDI was 29.25 %( 40), and Schirmer’s test was an effective tool in diagnosing dry eye. The global prevalence of DED varies from 5 to 35% (1, 2). Indian studies done in urban population shown overall prevalence 26% (42). The present study was done as population based observational study in rural area based on the questionnaire and Schirmer's test result. A hospital-based population study in West Bengal, Eastern India by Samar K Basak et al (42) showed that dry eye diseases were significantly higher in women than in men i.e., 51.9% versus 48.1% (p < 0.01).J S Titiyalet al, observed that the prevalence of DED in North India is 32%, with the age group of 21-40 years (43). However in our study of rural population, male predominance with age more than 50 years was noted which could be due to exposure and outdoor work in sun light. In our study the screening was done for 2, 72,500 rural populations of all age groups and 76196 persons were found symptomatic, accounting for 28% population. The DED determination was done on the basis of Schirmer’s test reading less than 10 mm. There were three age groups 0 to 25 years, 25 to 50 years and more than 50 years. Male and female were recorded separately. Prevalence of DED in females 0-25year group 5.5%, 25-50 years 15.1% and more than 50 years 57.01%. Males had 0-25 years group 4.1%, 25-50 years 15.9% while more than 50 years 65.1%. Overall prevalence for 0-25 years 4.77%, 25-50 years 15.5% and more than 50 years was 60.87%. The DED prevalence in rural population was determined 19.2%. The prevalence rate found in present study falls within the results of various studies done earlier. During analysis we also found that DED is not significantly more in rural population and there is no major difference in female versus male population. The field work and data collection requires much more resources and has got limitations of investigational tools thus the questionnaire method and single diagnostic method (Schirmer’s test) was adopted. However more diagnostic tests for DED required due to environmental differences in urban and rural setting (44, 45) , then the prevalence may be more in rural population as accepted theoretically.
CONCLUSION
The dry eye disease screening was conducted for 2, 72,500 rural populations of all age groups and 76,196 persons were symptomatic accounting for 28% screened population. The dry eye disease was more commonly seen in males than females. In both the groups, the disease was more common in the age group of more than 50 years. Due to life style and environmental changes, now the dry eye disease is also seen commonly in rural population and screening of rural population is advocated to prevent the burden of the disease.
REFERENCES
1. Albert and jacobiec’s principles and practice of ophthalmology (AJPPO) 4th edition; volume1. Pg. 380 2. American Academy of Ophthalmology. https://www.aao.org/eyehealth/anatomy/tear-film-3 3. https://eyewiki.org/Dry_Eye_Syndrome 4. Sushrut Samhita : ShalakyaTantra 5. Journal List >Int J >Ayurveda Res v.2 (1); Jan-Mar 2011 PMC3157110 6. The Ocular SurfaceVolume 2, Issue 4, October 2004, Pages 225-227 7. Hoopes Vision Research Center Nathan R. Brott; Marco Zeppieri; YasmyneRonquillo 8. FarrandKF,Fridman M, Stillman IO, Schaumberg DA. Prevalence of diagnosed dry eye disease in the United States among adults aged 18 years and older. Am J Ophthalmol.2017; 182:90-8 9. Statistical reports. Eye bank association of America website available http://www .restoresight.org/general/faqs.htm. 10. Albert and jacobiec’s principles and practice of ophthalmology(AJPPO) 4thEdn; volume1, pg 378 11. Albert and jacobiec’s principles and practice of ophthalmology (AJPPO) 4th Edn;volume1, pg385 12. Polaris Market Research. https://www.polarismarketresearch.com › Healthca 13. The Ocular Surface Volume 2, Issue 4, October 2004, Pages 225-227 14. Albert and Jacobiec’s principles and practice of Ophthalmology (AJPPO) 4thEdn; volume1, pg379 15. Kallarackal GU, Ansari EA, Amos N, Martin JC, Lane C, Camilleri JP, et al. A comparative study to assess the clinical use of fluorescein meniscus time (FMT) with tear break up time (TBUT) and Schirmer's tests (ST) in the diagnosis of dry eyes. Eye (Lond) 2002;16:594–600. [PubMed] [Google Scholar] 16. Albert and Jacobiec’s principles and practice of Ophthalmology (AJPPO) 4thEdn; volume1, pg.388-389 17. Schiffman RM, Christianson MD, Jacobsen G, Hirsch JD, Reis BL. Reliability and validity of the ocular surface disease index. Arch Ophthalmol. 2000;118:615–21. 18. The epidemiology of dry eye disease: Report of the Epidemiology Subcommittee of the International Dry Eye Workshop (2007) Ocul Surf. 2007;5:93–107. 19. Indian Journal of Ophthalmology 69(5):p 1061-1066, May 2011. | DOI: 10.4103/ ijo.IJO_1796_20 20. https://en.wikipedia.org/wiki/henrik Sj%C3%B6gren 21. Schirmer Test by Nathan R. Brott; Marco Zeppieri; YasmyneRonquillo. 22. Ophthalmic Res (2002)65 (6): 647-658. https://doi.org/10.1159/000525696 23. Prevalence and risk factors of dry eye disease in North India: Ocular surface disease index-based cross-sectional hospital study.Jeewan Singh Titiyal , Ruchita Clara Falera , Manpreet Kaur, Vijay Sharma, NamrataSharma.Indian J Ophthalmol. 2018 Feb; 66(2): 207–211. 24. Consensusindia2011.com 25. https://www.censusindia2011.com/uttar-pradesh/\-population. html 26. https://npcbvi.mohfw.gov.in/Home 27. Principles and Practice of Ophthalmology by Albert and Jakobiec,s 4th Edition Page 379 28. Principles and Practice of Ophthalmology by Albert and Jakobiec,s 4th Edition Page 392 29. Menger LS, Bron AJ, Tonge SR, Gibert DJ. Effect of fluoroscein instillation on the pre-corneal tear film instability. Vurr Eye.1985; 4(1):9-12 30. Schulze MM, Jones DA, Simpson TL. The development of validated bulbar redness grading scales. Optom Vis Sci. 2007; 84(10):976-83. 31. Wu S, Hong J, Tian L, Cui X, Sun X, Xu J. Assesment of bulbar redness with a newly developed keratograph. Optom Vis Sci. 2015;92(8):892-9. 32. Schirmer Test; Nathan R. Brott; Marco Zeppieri: yasmyneRonquillo; https://www. ncbi. nlm.nih.gov/books/NBK55159 33. Gilbard JP, Rossi SR. Tear film and ocular surface changes in arabbit model of neurotrophic keratitis. Ophthalmology. 1990;97(3):308-12. 34. Lemp MA, Bron AJ, Boudouin C, et all. Tear Osmolarity in the diagnosis and management of dry eye disease. Am J Ophthalmol.2011;151(5):792-8.e791. 35. Balik J, The lactrimal fluid in keratoconjunctivitissicca; a quantitative and qualitative investigation. Am J Ophthalmol. 1952;35(6):1773-82 36. Sambursky R, Davitt WF 3rd, Friedberg M Tauber S. Prospective, multicenter, clinical evaluation of point- of- care matrix metalloproteinase-9 test for confirming dry eye disease. Cornea.2014; 33(8):812-8 37. YeotikarNS,Zhu H, Markoulli M, Nicholas KK, Naduvilath T, Papas FB. Functional and morpholoigical changes of meibomian glands in an asymptomatic adult population. Invest Ophthalmol Vis Sci.2016;57(10):3996-4007. 38. The epidemiology of dry eye in Melbourne Australia; Ophthalmology: 1998 Jun: 105(6):1114-9. Doi: 10. 1016/S0161-6420(98)96016-X 39. Lin PY, Tsai SY, Cheng CY, Liu JH, Chou P, Hsu WM, et al. Prevalence of dry eye among an elderly Chinese population in Taiwan: The Shihpai eye study. Ophthalmology. 2003; 110:1096–101. 40. Gupta N, Prasad I, Jain R, D'Souza P. Estimating the prevalence of dry eye among Indian patients attending a tertiary ophthalmology clinic. Ann Trop Med Parasitol. 2010;104:247–55. 41. Indian J Ophthalmol. 2018 Feb: 66(2): 207-211.doi: 10.4103/ijo.IJO. 17 42. Basak SK, Pal PP, Basak S, Bandyopadhyay A, Choudhury S, Sar S, et al. Prevalence of dry eye diseases in hospital-based population in West Bengal, Eastern India. J Indian Med Assoc. 2012; 110:789–94. 43. Prevalence and risk factors of dry eye disease in North India: Ocular surface disease index-based cross-sectional hospital study.Jeewan Singh Titiyal , Ruchita Clara Falera , Manpreet Kaur, Vijay Sharma, NamrataSharma.Indian J Ophthalmol. 2018 Feb; 66(2): 207–211. 44. https://www.envisioneyeaustin.com/ultraviolet-light-and-its-effects 45. https://www.webmd.com/eye-health/dry-eye-irretants
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