Abstract
Background
Dry eye is a multifactorial disease defined less than 30 years ago. It is a relatively common disorder, affected by a number of well-known risk factors. Dry eye can be challenging to diagnose because of the possible discrepancy between patients’ symptoms and clinical signs, and its overlap with other ocular surface diseases. Literature-wise, dry eye is usually associated with age and therefore investigated within older populations. Recently, studies focusing on young adult and student populations have demonstrated a higher prevalence of dry eye than previously expected.
Aim
The study aims to determine the frequency of dry eye symptoms in the student population, and the impact of students’ activities and habits as potential risk factors.
Methodology
Our study involved 397 students from the medical school at the University of Belgrade, Serbia. Students were asked to complete an online survey that addressed general information, health, habits, and routine in everyday use of electronic devices. In addition, students completed a standard Ocular Surface Disease Index questionnaire.
Results
The prevalence of dry eye was 60.5% (240/397) in our study population. Contact lens wear (p<0.001), allergies (p = 0.049) and increased number of hours per day using VD devices for studying purposes (p = 0.014) were associtated with a higher risk of dry eye disease. Risk factors that did not significantly impact dry eye were the use of oral contraceptives, smoking, systemic diseases, year of study and sex.
Conclusion
In our study, the prevalence of dry eye disease was similar or slightly higher than in previous studies among young adults. In addition, contact lenses, allergies and visual display devices were associated with the development of the dry eye.
Introduction
Dry eye disease (DED) is a common tear film disorder that has been documented worldwide in all age groups and ethnicities. It was recognized as a disorder less than 30 years ago, with progress being made in understanding the basis and impact of this disease. It is one of the most common reasons for patient referral to an ophthalmologist [1].
Dry eye is a multifactorial disease of the ocular surface. It is 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 [2]. Symptoms of DED include eye dryness, ocular pain, a burning sensation, visual problems, eye fatigue, sensitivity to light and itchy eyes [3–5]. The definition of the DED through symptoms encompasses all stages of the disease, including the initial stages when evident signs of disease are still nonexistent. Therefore, assessing individual patients through questionnaires would give a better insight into morbidity. In addition to the Ocular Surface Disease Index (OSDI), a reliable and validated method for measuring the severity of DED and its influence on visual function [6], numerous other tools are used to evaluate the symptoms and their impact on every day life (Impact of dry eye on everyday life questionnaire, Dry Eye-Related Quality-Of-Life Score, Dry Eye Questionnaire, and the Standard Patient Evaluation of Eye Dryness Questionnaire). Friedman reported that mild to severe DED impacts the quality of life to a similar degree as mild to severe angina when examined using utility assessment questionnaires [7].
The prevalence of DED ranges from approximately 5% to 50% [8]. It differs according to the definition, classification, diagnostic criteria, and population of interest. DED has been shown to be more prevalent among women and the elderly [9, 10]. However, several recent studies investigated DED in the young adult population, and reported a prevalence up to 70.8% [11–15]. These findings indicate the possibility of a higher prevalence of DED in this age group than previously thought. Most of these studies were conducted in Asia, South America, and Africa; to the best of our knowledge, there are not many studies on this topic amongst the European population.
In addition to age and female sex, significant risk factors include Asian race, Meibomian gland dysfunction, connective tissue diseases, Sjögren’s syndrome, computer use, contact lens wear, androgen deficiency, environmental factors, hormone replacement therapy, hematopoietic stem cell transplantation, use of medications (antihistamines, antidepressants, anxiolytics, isotretinoin), and allergies [8]. Aside from these, already established factors, there is also the recently reported problem of increased daily use of visual display (VD) devices, especially in young adults [16]. Nowadays, young generations are exposed to VD devices from a very young age. Moreover, this habit could be even more pronounced after the Covid-19 pandemic, where most young adults had to study and socialize online more than in previous years. Therefore, it is of great significance to determine the prevalence of DED and its risk factors in the young adult population for better prevention and diagnosis of DED.
The aim of this study was to determine the prevalence of DED and its risk factors among medical students at the University of Belgrade, Serbia.
Materials and methods
In total, 397 students attending the School of Medicine, University of Belgrade, Serbia, participated in this cross-sectional study. The median age of this population was 22.5 years (range, 18–34 years). The survey was conducted in August and September 2019. Students were asked to complete an anonymous electronic survey which comprised of questions divided into three sections. The link to the questionnaire was attached to the school’s website. This study was performed in accordance with The Declaration of Helsinki. Informed consent was obtained from all participants by ticking the relevant box before beginning the survey.
In the first part of the questionnaire, students were asked to give general information: sex, age, and the year of study that they were attending, followed by questions about their health (allergies and systemic diseases) and habits (contact lens wear, smoking, use of contraceptive pills) (S1 Fig). The second part comprised questions concerning their studying habits and everyday use of computers, mobile phones, tablets, and similar digital devices, as well as their use during their free time (S1 Fig). The questions were as follows: (1) How many hours per day do you study? (2) How many hours per day do you study using hard copy sources of literature? (3) How many hours per day do you study from computers, laptops, and other digital devices? (4) How many hours per day do you use a mobile phone, computer, laptop, or tablet when you are not studying? For every question, students were asked to choose the answer: a) I do not use, b) 0–3 h per day, c) 3–6 h per day, and d) more than 6 h per day.
The third part was the standard OSDI questionnaire (S2 Fig). The total OSDI score was calculated for every student based on the formula: the sum of scores for all answered questions multiplied by 25, divided by the total number of answered questions. Values of the OSDI score range between 0 and 100, where a higher score indicates a more severe DED (S2 Fig). In this study, the cut-off for symptomatic DED was an OSDI score greater than or equal to 13.
After analyzing the descriptive statistics, we established the OSDI score for each student using the OSDI formula. According to our cut-off value, we divided them into two groups. Students who had a score greater than or equal to 13 were recognized as having symptomatic DED, and those who scored less than 13 did not have DED. We compared these two groups according to each factor included in the first part of the questionnaire (S1 Fig). Finally, the number of hours of electronic device use across different purposes was compared in the symptomatic and asymptomatic students.
Statistical analysis
SPSS software (version 20.0, IBM, Armonk, NY, USA) was used for statistical analysis. Frequency, mean, and standard deviation were used for descriptive statistics. For the comparison of categorical variables between groups chi-square test was used. A logistic regression was performed to ascertain the effects of different risk factors on the likelihood that participants have DED. The odds ratio (OR) and 95% confidence intervals (CI) were calculated. The level of significance for all statistical analyses was set at p<0.05.
Results
A total of 397 participants were included in this study, with an average age of 22.6 years ± 2.3 (range:18–34 years). The majority of the population were women and were not contact lens users (Table 1). Further characteristics are displayed in Table 1.
Table 1. Epidemiological characteristics in the medical students population.
N | Percentage % | ||
---|---|---|---|
Sex | Male | 96 | 24.2% |
Female | 301 | 75.8% | |
Contact lens use | Yes | 82 | 20.7% |
No | 315 | 79.3% | |
Allergies | Yes | 130 | 32.7% |
No | 267 | 67.3% | |
Systemic diseases | Yes | 15 | 3.8% |
No | 382 | 96.2% | |
Smoking | Yes | 90 | 22.7% |
No | 307 | 77.3% | |
Contraceptive pills | Yes | 27 | 6.8% |
No | 370 | 93.2% |
The OSDI score for each student was determined through the OSDI questionnaire. The average OSDI score for the examined population was 20.6 ± 16.5. After analyzing the data, 60.5% of the participants had a symptomatic DED (240 students). The majority of students (45.4%, n = 109) had a mild form of DED, while 20.8% (n = 50) had a moderate presentation, and 33.8% (n = 81) had a severe form. The prevalence of symptomatic DED among female and male respondents was 62.8% and 53.1%, respectively (Table 2). The differences in prevalence between sexes and age were not statistically significant (p = 0.092 and p = 0.283, respectively). Contact lens users were significantly more often affected by DED symptoms (p<0.001). Other possible factors that were analyzed had no significant relationship with DED (see Table 2).
Table 2. General information of the students with and without DED symptoms.
Dry eye (OSDI≥ 13) | ||||||
---|---|---|---|---|---|---|
No N = 157 | Yes N = 240 | |||||
N | % | N | % | P-value | ||
Sex | Male | 45 | 46.9% | 51 | 53.1% | 0.092 |
Female | 112 | 37.2% | 189 | 62.8% | ||
Year of study | First | 29 | 49.2% | 30 | 50.8% | 0.367 |
Second | 30 | 41.1% | 43 | 58.9% | ||
Third | 32 | 42.7% | 43 | 57.3% | ||
Fourth | 11 | 29.7% | 26 | 70.3% | ||
Fifth | 14 | 31.8% | 30 | 68.2% | ||
Sixth | 41 | 37.6% | 68 | 62.4% | ||
Contact lens use | Yes | 16 | 19.5% | 66 | 80.5% | <0.001 |
No | 141 | 44.8% | 174 | 55.2% | ||
Allergies | Yes | 43 | 33.1% | 87 | 66.9% | 0.066 |
No | 114 | 42.7% | 153 | 57.3% | ||
Systemic diseases | Yes | 6 | 40.0% | 9 | 60.0% | 0.971 |
No | 151 | 39.5% | 231 | 60.5% | ||
Smoking | Yes | 30 | 33.3% | 60 | 66.7% | 0.170 |
No | 127 | 41.4% | 180 | 58.6% | ||
Contraceptive pills | Yes | 11 | 40.7% | 16 | 59.3% | 0.895 |
No | 146 | 39.5% | 224 | 60.5% |
A Chi-square test was performed, p<0.05 was considered as statistically significant.
Students’ recreational and studying habits are presented in Table 3.
Table 3. Habits of the students with and without DED symptoms.
Dry eye (OSDI≥13) | ||||||
---|---|---|---|---|---|---|
No | Yes | |||||
N | % | N | % | P-value | ||
Total number of hours spent studying per day | 0-3h | 28 | 17.8% | 26 | 10.8% | 0.137 |
3-6h | 75 | 47.8% | 123 | 51.2% | ||
>6h | 54 | 34.4% | 91 | 37.9% | ||
Number of hours per day spent studying books and hard copy literature | Not using | 2 | 1.3% | 2 | 0.8% | 0.195 |
0-3h | 34 | 21.7% | 36 | 15.0% | ||
3-6h | 70 | 44.6% | 131 | 54.6% | ||
>6h | 51 | 32.5% | 71 | 29.6% | ||
Number of hours per day spent studying using computers, laptops, and other VD devices | Not using | 69 | 43.9% | 73 | 30.4% | 0.007 |
0-3h | 85 | 54.1% | 148 | 61.7% | ||
3-6h | 2 | 1.3% | 15 | 6.3% | ||
>6h | 1 | 0.6% | 4 | 1.7% | ||
Number of hours per day spent using mobile phones, computers, laptops, and other VD devices in their free time | Not using | 0 | 0.0% | 0 | 0.0% | 0.911 |
0-3h | 75 | 47.8% | 111 | 46.3% | ||
3-6h | 57 | 36.3% | 87 | 36.3% | ||
>6h | 25 | 15.9% | 42 | 17.5% |
A Chi square test was performed, p<0.05 was considered as statistically significant.
For further insight, univariate analysis was performed using logistic regression (Table 4). Results showed that contact lens wear was associated with a higher risk of DED (p<0.001). Initially allergies were marginally associated with DED using chi square test (p = 0.066) (Table 2). Additional logistic regression analysis demonstrated that students with allergies were more likely to have DED (p = 0.049) (Table 4). Regarding students’ studying and free time habits, the total number of hours per day spent studying did not significantly impact DED prevalence (p = 0.083) (Table 4). Also, increasing number of hours studying using hard copy literature and longer recreational VD devices use were not associated with increased likelihood of exhibiting DED (p = 0.308 and p = 0.626, respectively). The results do indicate that the time used to study using VD devices is associated with DED symptoms and that the more time was used studying with VD devices, the higher the prevalence of DED symptoms was (p = 0.014).
Table 4. Logistic regression analysis.
OR | 95% CI for OR | P-value | |
---|---|---|---|
Sex | 1.624 | 0.37–1.04 | 0.071 |
Year of study | 1.100 | 0.97–1.24 | 0.123 |
Contact lens wear | 3.832 | 2.06–7.11 | <0.001 |
Allergies | 1.637 | 1.00–2.67 | 0.049 |
Systemic disease | 0.975 | 0.32–2.99 | 0.964 |
Smoking | 1.498 | 0.89–2.53 | 0.132 |
Contraceptive pills | 0.813 | 0.34–1.95 | 0.642 |
Total number of hours spent studying per day | 1.753 | 0.93–3.31 | 0.083 |
Number of h/day spent studying books and hard copy literature | 0.737 | 0.41–1.33 | 0.308 |
Number of h/day spent studying using computers, laptops, and other VD devices | 1.616 | 1.10–2.37 | 0.014 |
Number of h/day spent using mobile phones, computers, laptops, and other VD devices in their free time | 1.075 | 0.80–1.44 | 0.626 |
OR- Odds ratio; CI- Confidence Interval
Discussion
The prevalence of symptomatic DED in this study was 60.5%, which was slightly higher than those reported in other studies including symptomatic DED with or without clinical signs in the older population [8]. Most previous studies included a population aged 40 years and older. Studies focusing on younger people, observed a relatively similar DED prevalence using the OSDI questionnaire: 50.6% among Korean university students [17], 48.1% among students in Ghana [18], 62.6% among medical students and workers at a medical university and hospitals in Dubai [19], 59.64% among undergraduate students in Brazil [20] and 50,5% among Ethiopian postgraduate students [21]. Other studies that involved student population included clinical assesment and showed a lower DED prevalence [22–24]. A recent study in Thailand observed a DED prevalence of 70.8% among medical students at Chiang Mai University. This study recognized the impact of VD devices and the psychological stress on DED among students during Covid-19 pandemic [11]. Similar studies conducted during Covid-19 pandemic reported DED prevalence from 51,8% to 71,7%, using different criteria [12–15].
In many epidemiological studies, female sex is a risk factor for DED [24–29]. The prevalence of DED in our study was higher among women than in men, but the difference did not reach statistical significance. The lack of statistical correlation between being female and DED in our study could be explained by the younger average age of the participants. The Tear Film and Ocular Surface Society, Dry Eye Workshop II indicated that the difference between sexes in symptomatic patients becomes a statistically significant risk factor only in older populations (50 years old and above) [9]. However, the Karachi Ocular Surface Study of 2433 non-clinical individuals showed no significant relationship between being female and having DED, even after excluding the younger population and analyzing only individuals aged 45 years and older [30].
We found that people using contact lenses more frequently had DED (p<0.001). Many studies among adults have shown a correlation between DED and contact lens use [10, 25]. Several studies among young adults reported similar results [11, 22, 24, 31–33]. DED occurs up to four times more frequently in the population of contact lens users than in the general population [10, 25, 31]. Contact lens use is also linked to a higher prevalence of more severe forms of symptomatic DED [34]. Contact lenses mechanically stimulate the cornea, leading to lower corneal sensitivity, relative hypoxia, and damage to nerve endings following prolonged contact lens wear. These factors affect tear film quality, integrity, and metabolic functions, reducing basal tear secretion [35]. In one study of 1844 contact lens users in Japan, symptoms of DED associated with contact lens use were present in 78.6% of the cohort. Only one-third of these cases were previously diagnosed by an ophthalmologist or an eye care provider. These findings emphasize the importance of DED screening and prevention even among young contact lens users [36].
Our logistic regression analysis results indicated that students with allergies were more likely to have DED (p = 0.049). Allergic conjunctivitis and other eye surface diseases may be associated with symptoms similar to DED, but they are considered separate clinical entities in certain studies [1, 37]. There is evidence that allergic diseases, such as vernal and atopic keratoconjunctivitis and allergic conjunctivitis, correlate with a higher risk of DED. However, this has not been proven in population studies [38–40]. These diseases should be distinguished from primary DED due to their different risk factors and therapies. The significant overlap of DED with other chronic disorders of the ocular surface, including allergies, has raised the question of whether those disorders are risk factors or contribute to the development of DED. Better understanding and recognition of the role and influence of allergies and other inflammatory diseases in developing DED could provide answers to this question in the future.
Smoking was not found to be a risk factor among the respondents of this study. In addition, studies in Singapore and Palestine found no statistically significant correlation between smoking and DED [5, 29]. However, one study in Turkey that included female smokers [41] and a meta-analysis conducted over the past ten years concerning the general population [42] indicated that smoking could be a risk factor. Therefore, further research is needed to understand and establish the role of smoking in the onset of DED.
The presence of systemic diseases and the use of contraceptive pills did not affect DED symptoms in our study. Unfortunately, we could not acquire data about the specific type of systemic disease present. Only a small fraction of students reported having a systemic disease (3.8%) or using contraceptive pills (6.8%).
The majority of the students who met the criteria for DED reported studying for 3–6 h per day. However, the total number of hours per day spent studying did not significantly impact DED prevalence (p = 0.083). One of the disadvantages of diagnosing this disorder through a questionnaire is recall bias among the participants. There is a chance that students could underestimate or overestimate their time spent on specific activities.
Our results showed an association between longer VD device use for studying and likelihood of developing DED (p = 0.014). Several studies have found a high prevalence of DED symptoms in people exposed to VD screens for work, especially among younger professionals [43–45]. A study conducted in Dubai indicated a significant association between screen time of >6 h per day and DED [19]. A recent study taken among high school students in East Java, Indonesia investigated the impact of mobile devices on evaporative DED and reported that the risk of developing evaporative DED could be induced even with a minimal use of these devices [46]. However, a study conducted in Saudi Arabia did not find a significant impact of longer electronic device use on increased computer vision syndrome symptoms among health sciences students [47]. Our results could be affected by the small sample of students who studied for more than 3 h per day using electronic sources and the possibility that the students used more than one type of literature medium (e.g., both electronic and paper). During Covid-19 pandemic several studies reported significant associtation between VD screen usage and DED among students who studied online, as well as female sex and contact lens wear [12, 13, 48]. Studies taken in Spain and Poland showed intensified DED symptoms among student population who studied online [49, 50]. In addition, one study investigated the effect of face mask usage on DED during Covid-19 pandemic. They indicated female sex, basic science years, allergy reporting, and spending more than 6h looking at screens being significantly associated with symptomatic DED, however facemask wear was not associated with DED [14]. It is still inconclusive whether the time spent studying using VD devices can exclusively increase the frequency of DED symptoms. Further research is required to determine the association between the duration of VD screen use and the development of DED symptoms. This is a potential risk factor, especially with the increasing use of VD devices for professional or personal purposes.
One strength of this study was its reasonably large sample size. The electronic survey is a more efficient and convenient means of data collection for the younger generation. In addition, information was obtained from symptomatic and asymptomatic individuals who may not seek early medical consultation. The main limitation of this study was a possible selection bias since students with DED symptoms may have been more motivated to participate in this survey than others, resulting in a higher DED prevalence. Also, another previously mentioned limitation of this type of study is recall bias.
Conclusion
This study reported that 60.5% of the students had DED symptoms. The significant risk factors for DED were contact lens wear and allergies. Longer use of electronic devices for studying purposes was associated with a higher risk of DED. Our study is in line with a growing pool of evidence that DED symptoms are present more often and earlier in life than what was previously thought. However, additional research on the younger generation is needed to define the prevalence, incidence, and risk factors of DED, especially knowing that DED affects the quality of everyday life. Educating the youth about DED and its symptoms could potentially help with diagnosing and preventing this disease. Further research is needed to obtain a more detailed analysis of the impact of screen use on DED among the younger population and in other age groups as well.
Supporting information
Acknowledgments
We would like to thank Editage (www.editage.com) for English language editing.
Data Availability
We have provided URL link and DOI for our publicly available data: 1) Dataset used for statistical analysis URL link: https://figshare.com/s/bf6fad23836e87f79a00 and DOI: https://doi.org/10.6084/m9.figshare.21235578 2) Supporting information (in addition to already attached PDF files) S1 Fig URL: https://figshare.com/s/2b18dbd7002f497fc9a3 and DOI: https://doi.org/10.6084/m9.figshare.21235599. S2 Fig URL: https://figshare.com/s/9ee6608a6925d2868673 and DOI: https://doi.org/10.6084/m9.figshare.21235626.
Funding Statement
The author(s) received no specific funding for this work.
References
- 1.Moss SE, Klein R, Klein BE. Prevalence of and risk factors for dry eye syndrome. Arch Ophthalmol. 2000;118:1264–1268. doi: 10.1001/archopht.118.9.1264 [DOI] [PubMed] [Google Scholar]
- 2.Craig JP, Nichols KK, Akpek EK, Caffery B, Dua HS, Joo CK, et al. TFOS DEWS II Definition and Classification Report. Ocul Surf. 2017;15: 276–283. doi: 10.1016/j.jtos.2017.05.008 [DOI] [PubMed] [Google Scholar]
- 3.McGinnigle S, Naroo SA, Eperjesi F. Evaluation of dry Eye. Surv Ophthalmol. 2012;57:293–316. doi: 10.1016/j.survophthal.2011.11.003 [DOI] [PubMed] [Google Scholar]
- 4.Lee AJ, Lee J, Saw SM, Gazzard G, Koh D, Widjaja D, et al. Prevalence and risk factors associated with dry eye symptoms: a population based study in Indonesia. Br J Ophthalmol. 2002;86:1347–1351. doi: 10.1136/bjo.86.12.1347 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Tan LL, Morgan P, Cai ZQ, Straughan RA. Prevalence of and risk factors for symptomatic dry eye disease in Singapore. Clin Exp Optom. 2015;98:45–53. doi: 10.1111/cxo.12210 [DOI] [PubMed] [Google Scholar]
- 6.Schiffman RM, Christianson MD, Jacobsen G, Hirsch JD, Reis BL. Reliability and validity of the ocular surface disease index. Arch Ophthalmol. 2000;118:615–621. doi: 10.1001/archopht.118.5.615 [DOI] [PubMed] [Google Scholar]
- 7.Friedman NJ. Impact of dry eye disease and treatment on quality of life. Curr Opin Ophthalmol. 2010;21:310–316. doi: 10.1097/ICU.0b013e32833a8c15 [DOI] [PubMed] [Google Scholar]
- 8.Stapleton F, Alves M, Bunya VY, Jalbert I, Lekhanont K, Malet F, et al. TFOS DEWS II epidemiology report. Ocul Surf. 2017;15:334–365. doi: 10.1016/j.jtos.2017.05.003 [DOI] [PubMed] [Google Scholar]
- 9.The Epidemiology of dry eye disease: report of the epidemiology subcommittee of the international dry eye workShop (2007). Ocul Surf. 2007;5:93–107. doi: 10.1016/s1542-0124(12)70082-4 [DOI] [PubMed] [Google Scholar]
- 10.Viso E, Rodriguez-Ares MT, Gude F. Prevalence of and associated factors for dry eye in a Spanish adult population (The Salnes Eye Study). Ophthal Epidemiol. 2009;16:15–21. doi: 10.1080/09286580802228509 [DOI] [PubMed] [Google Scholar]
- 11.Tangmonkongvoragul C, Chokesuwattanaskul S, Khankaeo C, Punyasevee R, Nakkara L, Moolsan S, et al. Prevalence of symptomatic dry eye disease with associated risk factors among medical students at Chiang Mai University due to increased screen time and stress during COVID-19 pandemic. PLOS ONE. 2022;17:0265733. doi: 10.1371/journal.pone.0265733 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.García-Ayuso D, Di Pierdomenico J, Moya-Rodríguez E, Valiente-Soriano FJ, Galindo-Romero C, Sobrado-Calvo P. Assessment of dry eye symptoms among university students during the COVID-19 pandemic. Clin Exp Optom. 2022;105:507–513. doi: 10.1080/08164622.2021.1945411 [DOI] [PubMed] [Google Scholar]
- 13.Lin F, Cai Y, Fei X, Wang Y, Zhou M, Liu Y. Prevalence of dry eye disease among Chinese high school students during the COVID-19 outbreak. BMC Ophthalmol. 2022;22:190. doi: 10.1186/s12886-022-02408-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Al-Dolat W, Abu-Ismail L, Khamees A, Alqudah N, Abukawan MM, Alrawashdeh HM, et al. Is wearing a face mask associated with symptomatic dry eye disease among medical students during the COVID-19 era? An online survey. BMC Ophthalmol. 2022;22:159. doi: 10.1186/s12886-022-02377-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Condori-Meza IB, Dávila-Cabanillas LA, Challapa-Mamani MR, Pinedo-Soria A, Torres RR, Yalle J, et al. Problematic internet use associated with symptomatic dry eye disease in medical students from Peru. Clin Ophthalmol. 2021;15:4357–4365. doi: 10.2147/OPTH.S334156 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Jamir L, Duggal M, Nehra R, Singh P, Grover S. Epidemiology of technology addiction among school students in rural India. Asian J Psychiatr. 2019;40:30–38. doi: 10.1016/j.ajp.2019.01.009 [DOI] [PubMed] [Google Scholar]
- 17.Yun CM, Kang SY, Kim H, Song J. Prevalence of dry eye disease among University students. J Korean Ophthalmol Soc. 2012;53:505–509. doi: 10.3341/jkos.2012.53.4.505 [DOI] [Google Scholar]
- 18.Asiedu K, Kyei S, Boampong F, Ocansey S. Symptomatic dry eye and its associated factors: a study of University undergraduate students in Ghana. Eye Contact Lens. 2017;43:262–266. doi: 10.1097/ICL.0000000000000256 [DOI] [PubMed] [Google Scholar]
- 19.Alkabbani S, Jeyaseelan L, Rao AP, Thakur SP, Warhekar PT. The prevalence, severity, and risk factors for dry eye disease in Dubai—a cross sectional study. BMC Ophthalmol. 2021;21:219. doi: 10.1186/s12886-021-01978-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Yang I, Wakamatsu T, Sacho IBI, Fazzi JH, de Aquino AC, Ayub G, et al. Prevalence and associated risk factors for dry eye disease among Brazilian undergraduate students. PLOS ONE. 2021;16:0259399. doi: 10.1371/journal.pone.0259399 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Zeleke TC, Adimassu NF, Alemayehu AM, Dawud TW, Mersha GA. Symptomatic dry eye disease and associated factors among postgraduate students in Ethiopia. PLOS ONE. 2022;17:0272808. doi: 10.1371/journal.pone.0272808 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Supiyaphun C, Jongkhajornpong P, Rattanasiri S, Lekhanont K. Prevalence and risk factors of dry eye disease among university students in Bangkok, Thailand. PLOS ONE. 2021;16:0258217. doi: 10.1371/journal.pone.0258217 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Li S, He J, Chen Q, Zhu J, Zou H, Xu X. Ocular surface health in Shanghai University students: a cross-sectional study. BMC Ophthalmol. 2018;18:245. doi: 10.1186/s12886-018-0825-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Hyon JY, Yang HK, Han SB. Dry eye symptoms may have association with psychological stress in medical students. Eye Contact Lens. 2019;45:310–314. doi: 10.1097/ICL.0000000000000567 [DOI] [PubMed] [Google Scholar]
- 25.Uchino M, Nishiwaki Y, Michikawa T, Shirakawa K, Kuwahara E, Yamada M, et al. Prevalence and risk factors of dry eye disease in Japan: Koumi Study. Ophthalmology. 2011;118:2361–2367. doi: 10.1016/j.ophtha.2011.05.029 [DOI] [PubMed] [Google Scholar]
- 26.Ahn JM, Lee SH, Rim TH, Park RJ, Yang HS, Kim TI, et al. Prevalence of and risk factors associated with dry eye: the Korea National Health and Nutrition Examination survey 2010–2011. Am J Ophthalmol. 2014;158:1205–1214.e7. doi: 10.1016/j.ajo.2014.08.021 [DOI] [PubMed] [Google Scholar]
- 27.Um SB, Kim NH, Lee HK, Song JS, Kim HC. Spatial epidemiology of dry eye disease: findings from South Korea. Int J Health Geogr. 2014;13:31. doi: 10.1186/1476-072X-13-31 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Moss SE, Klein R, Klein BE. Long-term incidence of dry eye in an older population. Optom Vis Sci. 2008;85:668–674. doi: 10.1097/OPX.0b013e318181a947 [DOI] [PubMed] [Google Scholar]
- 29.Shanti Y, Shehada R, Bakkar MM, Qaddumi J. Prevalence and associated risk factors of dry eye disease in 16 northern West Bank towns in Palestine: a cross-sectional study. BMC Ophthalmol. 2020;20:26. doi: 10.1186/s12886-019-1290-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Hashmani N, Mustafa FG, Tariq MA, Ali SF, Bukhari F, Memon AS, et al. Distribution and correlation of Ocular Surface Disease Index scores in a Non-clinical population: the Karachi Ocular Surface Disease Study. Cureus. 2020;12:e9193. doi: 10.7759/cureus.9193 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Paulsen AJ, Cruickshanks KJ, Fischer ME, Huang GH, Klein BE, Klein R, et al. Dry Eye in the Beaver Dam Offspring Study: prevalence, risk factors, and health-related quality of life. Am J Ophthalmol. 2014;157:799–806. doi: 10.1016/j.ajo.2013.12.023 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Zhang Y, Chen H, Wu X. Prevalence and risk factors associated with dry eye syndrome among senior high school students in a county of Shandong Province, China. Ophthalmic Epidemiol. 2012;19:226–30. doi: 10.3109/09286586.2012.670742 [DOI] [PubMed] [Google Scholar]
- 33.Garza-León M, López-Chavez E, De La Parra-Colín P. Prevalence of ocular surface disease symptoms in high school students in Monterrey, Mexico. J Pediatr Ophthalmol Strabismus. 2021;58:287–291. doi: 10.3928/01913913-20210308-01 [DOI] [PubMed] [Google Scholar]
- 34.Uchino M, Dogru M, Uchino Y, Fukagawa K, Shimmura S, Takebayashi T, et al. Japan Ministry of Health Study on prevalence of dry eye disease among Japanese high school students. Am J Ophthalmol.Ophthalmol. 2008;146:925–9.e2. doi: 10.1016/j.ajo.2008.06.030 [DOI] [PubMed] [Google Scholar]
- 35.Yang WJ, Yang YN, Cao J, Man ZH, Yuan J, Xiao X, et al. Risk factors for dry eye syndrome: A Retrospective Case-Control Study. Optom Vis Sci. 2015;92:199–205. doi: 10.1097/OPX.0000000000000541 [DOI] [PubMed] [Google Scholar]
- 36.Inomata T, Nakamura M, Iwagami M, Midorikawa-Inomata A, Sung J, Fujimoto K, et al. Stratification of individual symptoms of contact lens–associated dry eye using the iPhone app DryEyeRhythm: crowdsourcedcross-sectional study. J Med Internet Res. 2020;22:18996. doi: 10.2196/18996 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.McCarty CA, Bansal AK, Livingston PM, Stanislavsky YL, Taylor HR. The epidemiology of dry eye in Melbourne, Australia. Ophthalmology. 1998;105:1114–1119. doi: 10.1016/S0161-6420(98)96016-X [DOI] [PubMed] [Google Scholar]
- 38.Hu Y, Matsumoto Y, Dogru M, Okada N, Igarashi A, Fukagawa K, et al. The differences of tear function and ocular surface findings in patients with atopic keratoconjunctivitis and vernal keratoconjunctivitis. Allergy. 2007;62:917–925. doi: 10.1111/j.1398-9995.2007.01414.x [DOI] [PubMed] [Google Scholar]
- 39.Villani E, Dello Strologo M, Pichi F, Luccarelli SV, De Cillà S, Serafino M, et al. Dry eye in vernal keratoconjunctivitis: across-sectional comparative study. Medicine. 2015;94:1648. doi: 10.1097/MD.0000000000001648 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Chen L, Pi L, Fang J, Chen X, Ke N, Liu Q. High incidence of dry eye in young children with allergic conjunctivitis in Southwest China. Acta Ophthalmol. 2016;94:727–730. doi: 10.1111/aos.13093 [DOI] [PubMed] [Google Scholar]
- 41.Erginturk Acar D, Acar U, Ozen Tunay Z, Ozdemir O, Germen H. The effects of smoking on dry eye parameters in healthy women. Cutan Ocul Toxicol. 2017;36:1–4. doi: 10.3109/15569527.2015.1136828 [DOI] [PubMed] [Google Scholar]
- 42.Xu L, Zhang W, Zhu XY, Suo T, Fan XQ, Fu Y. Smoking and the risk of dry eye: a meta-analysis. Int J Ophthalmol. 2016;9:1480–1486. doi: 10.18240/ijo.2016.10.19 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Uchino M, Schaumberg DA, Dogru M, Uchino Y, Fukagawa K, Shimmura S, et al. Prevalence of dry eye disease among Japanese visual display terminal users. Ophthalmology. 2008;115:1982–1988. doi: 10.1016/j.ophtha.2008.06.022 [DOI] [PubMed] [Google Scholar]
- 44.Uchino M, Yokoi N, Uchino Y, Dogru M, Kawashima M, Komuro A, et al. Prevalence of dry eye disease and its risk factors in visual display terminal users: the Osaka study. Am J Ophthalmol. 2013;156:759–766. doi: 10.1016/j.ajo.2013.05.040 [DOI] [PubMed] [Google Scholar]
- 45.Kaido M, Kawashima M, Yokoi N, Fukui M, Ichihashi Y, Kato H, et al. Advanced dry eye screening for visual display terminal workers using functional visual acuity measurement: the Moriguchi study. Br J Ophthalmol. 2015;99:1488–1492. doi: 10.1136/bjophthalmol-2015-306640 [DOI] [PubMed] [Google Scholar]
- 46.Loebis R, Subakti Zulkarnain B, Zahra N. Correlation between the exposure time to mobile devices and the prevalence of evaporative dry eyes as one of the symptoms of computer vision syndrome among senior high school students in East Java, Indonesia. J Basic Clin Physiol Pharmacol. 2021;32:541–545. doi: 10.1515/jbcpp-2020-0478 [DOI] [PubMed] [Google Scholar]
- 47.Altalhi A, Khayyat W, Khojah O, Alsalmi M, Almarzouki H. Computer vision syndrome among health sciences students in Saudi Arabia: prevalence and risk factors. Cureus. 2020;12:7060. doi: 10.7759/cureus.7060 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Cartes C, Segovia C, Salinas-Toro D, Goya C, Alonso MJ, Lopez-Solis R, et al. Dry eye and visual display terminal-related symptoms among university students during the Coronavirus disease pandemic. Ophthalmic Epidemiol. 2022;29:245–251. doi: 10.1080/09286586.2021.1943457 [DOI] [PubMed] [Google Scholar]
- 49.Talens-Estarelles C, García-Marqués JV, Cervino A, García-Lázaro S. Online vs In-person education: evaluating the potential influence of teaching modality on dry eye symptoms and risk factors during the COVID-19 pandemic. Eye Contact Lens. 2021;47:565–572. doi: 10.1097/ICL.0000000000000816 [DOI] [PubMed] [Google Scholar]
- 50.Sterczewska A, Wojtyniak A, Mrukwa-Kominek E. Ocular complaints from students during COVID-19 pandemic. Adv Clin Exp Med. 2022;31:197–202. doi: 10.17219/acem/144199 [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
We have provided URL link and DOI for our publicly available data: 1) Dataset used for statistical analysis URL link: https://figshare.com/s/bf6fad23836e87f79a00 and DOI: https://doi.org/10.6084/m9.figshare.21235578 2) Supporting information (in addition to already attached PDF files) S1 Fig URL: https://figshare.com/s/2b18dbd7002f497fc9a3 and DOI: https://doi.org/10.6084/m9.figshare.21235599. S2 Fig URL: https://figshare.com/s/9ee6608a6925d2868673 and DOI: https://doi.org/10.6084/m9.figshare.21235626.