Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Prevalence and associated factors of refractive error among adults in South Ethiopia, a community-based cross-sectional study

  • Marshet Gete Abebe ,

    Contributed equally to this work with: Marshet Gete Abebe, Abiy Maru Alemayehu, Minychil Bantihun Munaw, Mikias Mered Tilahun, Henok Biruk Alemayehu

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Software, Writing – original draft

    Affiliation Department of Ophthalmology and Optometry, Hawassa University, Comprehensive Specialized Hospital, Hawassa, Ethiopia

  • Abiy Maru Alemayehu ,

    Contributed equally to this work with: Marshet Gete Abebe, Abiy Maru Alemayehu, Minychil Bantihun Munaw, Mikias Mered Tilahun, Henok Biruk Alemayehu

    Roles Data curation, Software, Supervision, Visualization

    Affiliation Department of Optometry, School of Medicine, University of Gondar, Comprehensive Specialized Hospital, Gondar, Ethiopia

  • Minychil Bantihun Munaw ,

    Contributed equally to this work with: Marshet Gete Abebe, Abiy Maru Alemayehu, Minychil Bantihun Munaw, Mikias Mered Tilahun, Henok Biruk Alemayehu

    Roles Data curation, Software, Validation, Writing – review & editing

    Affiliation Department of Optometry, School of Medicine, University of Gondar, Comprehensive Specialized Hospital, Gondar, Ethiopia

  • Mikias Mered Tilahun ,

    Contributed equally to this work with: Marshet Gete Abebe, Abiy Maru Alemayehu, Minychil Bantihun Munaw, Mikias Mered Tilahun, Henok Biruk Alemayehu

    Roles Conceptualization, Validation, Visualization, Writing – review & editing

    Affiliation Department of Optometry, School of Medicine, University of Gondar, Comprehensive Specialized Hospital, Gondar, Ethiopia

  • Henok Biruk Alemayehu

    Contributed equally to this work with: Marshet Gete Abebe, Abiy Maru Alemayehu, Minychil Bantihun Munaw, Mikias Mered Tilahun, Henok Biruk Alemayehu

    Roles Data curation, Formal analysis, Methodology, Software, Visualization, Writing – review & editing

    Henokbiruk37@gmail.com

    Affiliation Department of Ophthalmology and Optometry, Hawassa University, Comprehensive Specialized Hospital, Hawassa, Ethiopia

Abstract

Introduction

The increasing prevalence of refractive error has become a serious health issue that needs serious attention. However, there are few studies regarding the prevalence and associated factors of refractive error at the community level in Ethiopia as well as in the study area. Therefore, providing updated data is crucial to reduce the burdens of refractive error in the community.

Objective

To assess the prevalence and associated factors of refractive error among adults in Hawassa City, South Ethiopia, 2023.

Method

A community-based cross-sectional study was conducted on 951 adults using a multistage sampling technique from May 8 to June 8, 2023, in Hawassa City, South Ethiopia. A pretested, structured questionnaire combined with an ocular examination and a refraction procedure was used to collect data. The collected data from the Kobo Toolbox was exported to a statistical package for social sciences for analysis. Binary and multivariable logistic regression analyses were performed. A P-value of less than 0.05 was considered statistically significant in the multivariable analysis.

Result

A total of 894 study participants were involved in this study with a 94.1% response rate. The prevalence of refractive error was 12.3% (95% CI: 10.2, 14.5%). Regular use of electronic devices (adjusted odds ratio = 3.64, 95% CI: 2.25, 5.91), being diabetic (adjusted odds ratio = 4.02, 95% CI: 2.16, 7.48), positive family history of refractive error (adjusted odds ratio = 2.71, 95% CI 1.59, 4.61) and positive history of cataract surgery (adjusted odds ratio = 5.17, 95% CI 2.19, 12.4) were significantly associated with refractive error.

Conclusion and recommendation

The overall magnitude of refractive error in our study area was high. Regular use of electronic devices, being diabetic, positive family history of refractive error, and a positive history of cataract surgery were associated with refractive error.

Introduction

Refractive error (RE) is a condition where the optical system of the eye fails to focus parallel rays of light on the retina. The RE occurs when there is an imbalance between the axial length and the refractive power of the eye [1]. Symptoms of RE include blurring of vision, headaches, eyestrain, and problems with focusing and seeing details at any distance. Globally, the prevalence of RE was 12% [2]. The prevalence of RE ranges from 6% to 72% in developed countries [3, 4]. In Sub-Saharan Africa, the prevalence of RE was approximately 46% [5, 6]. Hospital-based studies conducted in Gondar, Borumeda, and Arba Minch, Ethiopia showed that the prevalence of RE was 76.3%, 18.3%, and 27.5% respectively [79].

Globally, 2.2 billion people suffer from visual impairment (VI), and RE accounts for 88.4 million cases [10]. RE is the most common cause of visual impairment worldwide. Around 50% of the world’s vision impairment and blindness caused by RE are found in Asia [11]. According to Ethiopian national surveys, RE accounts for 33.4% of low vision and is the second leading cause of VI after cataracts [12]. RE can undermine individual performance, reduce social participation, and reduce employability. RE can also increase the economic burden on the country. Approximately US$202 billion is attributed to VI due to uncorrected RE [13]. Those above conditions result in a reduced quality of life for individuals with RE [11]. Among the top 20 causes of disability-adjusted life years, RE is one of the four non-fatal disorders [14].

Some of the factors, such as age, educational level, history of cataract surgery, family history of RE, and history of diabetes mellitus were associated with the development of RE, as reported by studies [15, 16]. Although RE cannot be completely prevented, it can be treated easily. RE can be treated with spectacle, contact lens, or refractive surgery [17].

To address the issue, multi-tiered points of delivery for refractive care services and optical dispensing units were established, together with highly qualified optometry personnel [18]. Ethiopia launched the Vision 2020 global initiative to develop a comprehensive and sustainable eye care system that will eliminate the major causes of avoidable blindness [19].

The increasing prevalence of RE in both developed and developing nations remains an urgent public health problem that needs serious attention [10, 11]. Although RE is prevalent across the world, there is limited evidence on the burden and predictors of RE among adults at the community level in Ethiopia. Hence, conducting the prevalence and associated factors gives updated information that contributes to reducing the burden of RE. In addition, this study can be used as baseline information for policymakers, the Ministry of Health, and other researchers to allocate resources for eye care service delivery.

Method and materials

Study design

A community-based cross-sectional study was conducted.

Study area and period

The study was conducted in Hawassa City, South Ethiopia from May 8, 2023, to June 8, 2023. Hawassa is the capital city of the Southern Nations, Nationalities, and Peoples Region as well as the Sidama Regional State. It is located 273 kilometers (170 miles) south of Addis Ababa. According to the Ethiopian National Housing and Census Statistical Agency, the population of Hawassa city administration is expected to be 403,025 people, and out of this, 266,331 people live in the urban with an estimated household of 63,412 [20]. There are 20 kebeles (The smallest administrative unit of Ethiopia, contained within a woreda) in the city. Five government health centers and four hospitals are found in Hawassa City. In general, there are four private eye clinics and one comprehensive, specialized hospital that provides a comprehensive eye care service that serves more than 16 million people in the catchment area. In addition, there is one general hospital that provides eye care services.

Source and study population

All adults who lived in Hawassa City were the source population and all adults aged ≥18 years who lived for at least 6 months in households of selected kebeles in Hawassa City were the study population.

Inclusion and exclusion criteria

All adults aged ≥18 years who lived for at least 6 months in households of selected kebeles in Hawassa city were included in the study and adults aged ≥18 years with ocular comorbidities (like corneal opacity, and active eye infection) that obscure retinoscopy reflex during the refraction, adults aged ≥18 years with an absolute blind eye, adults aged ≥18 years who were unable to respond due to serious illness, and mental illness were excluded from the study.

Sample size and sampling procedure

Sample size determination.

A single population proportion formula was used by considering the following assumptions:

Where;

n = sample size

Z = Value of z statistic at 95% confidence interval = 1.96

α (level of significance) = 5%

P = proportion of RE from a study in Eritrea 6.4% [21]

d = allowable maximum margin of error 2%

Design effect = 1.5 and Non response rate = 10%

The final sample size was 951

Sampling technique and procedure.

In Hawassa city, there are 20 kebeles. A multistage sampling technique was employed to select a representative sample from the city. The list of the total of kebeles was obtained from the Hawassa city administration. The four kebeles were chosen by lottery using simple random sampling. The selected four kebeles contained 12,363 of the city’s total households (63,412). The appropriate household was then picked by systematic random sampling with a K interval after the sample size was proportionally assigned based on the household size of each selected kebele Fig 1. The K interval was calculated by dividing the number of total households in the selected kebele by the total sample size (i.e., 12,363 / 951; K = 13).

thumbnail
Fig 1. Schematic presentation of sampling technique and procedures for prevalence and associated factors of refractive error among adults in Hawassa City, South Ethiopia, 2023.

https://doi.org/10.1371/journal.pone.0298960.g001

Then, at random, we chose a number between 1 and 13 to choose the first family to be included in the sample, and every 13th household was included after that. For families with more than one person eligible for the study, a lottery approach was used to choose study participants. When the eligible individual was not present at the time of data collection, the residence was revisited twice. When there were no eligible persons who met the inclusion criteria in the selected household, a household listed immediately was evaluated.

Operational definitions

RE was defined as a spherical equivalent of > +0.50 or < -0.50 diopter in either eye on subjective refraction. Myopia was defined as a spherical equivalent of < -0.50 D. High myopia was defined as a spherical equivalent of > -6.00 D [22]. Hyperopia was defined as a spherical equivalent of > +0.50 D. Astigmatism was defined as cylinder power > 0.50 D, without taking the direction of the axis into account [23]. Smoking was defined as those who smoked one stick of cigarette within the last month [24]. Sleeping Duration was defined as a longer duration when an individual sleeps for 6 hours or more and a short duration when an individual sleeps for less than 6 hours [25]. History of cataract surgery was defined as the examiner, facing the patient, shining the light source on the patient’s eye to see Purkinje’s reflexes like small shining bubbles. Regular use of electronic devices was defined as using mobile phones or computers, and other electronic devices at least once a day for at least two hours [26]. Family history of RE was defined as a family member (mother, father, brother, and sister) of RE diagnosed by professionals or any spectacle use [27]. History of diabetes mellitus and hypertension was defined if the individual has/had a diagnosed diabetic mellitus/ hypertension or undergoing anti-diabetes mellitus/antihypertensive treatment [28].

Data collection tools, procedures, and quality control

Data collection tools, procedures.

In this study, data were collected in three sections which were face-to-face interviews, ocular examinations, and refraction procedures. The data were collected by five qualified and well-trained Optometrists. A brief explanation of the purpose of the study was provided then verbal informed consent was obtained before collecting the information. An electronic data collection tool called Kobo Toolbox version 2022.4.4 was used to collect the data. A pre-tested and semi-structured interviewer-administered questionnaire adapted from previous studies [9, 29, 30] was used to conduct the data collection. The questionnaires consist of several questions to assess socio-demographic characteristics, behavioral factors, systemic co-morbidity, and clinical factors (S1 File). One supervisor (MSc in Clinical Optometry) from Hawassa University supervises the data collector every day during the data collection time.

Ophthalmic examination.

Following the interview, all study participants received an ophthalmic examination and refraction. Optometrists performed ophthalmic examinations, which began with a VA test. Monocular and binocular unaided VA, and VA after refractive correction were measured using reduced Snellen acuity charts measured at 3 meters under normal illumination. When participants could not see a letter at 3 meters their VA was tested by reducing the testing distance and when the participant could not see letters at 1 meter, VA was determined by counting fingers, hand motion, light perception, and no light perception. Following the recording of the VA, a torch was used to inspect for the presence of any corneal opacity, cataracts, or pseudophakia/aphakia.

Finally, the optometrist set up a semi-dark room within the participant’s home for the static retinoscopy technique and retinoscopy was performed for each study participant. Objective refraction was performed using streak retinoscopy. The objective retinoscopy result was then refined using monocular subjective refraction. Subjective refraction was then recorded for each eye. Finally, the spherical equivalent was calculated for the result of subjective refraction. Study participants with a spherical equivalent of > +0.50 or < -0.50 diopter in either eye were categorized as having RE. Finally, for individuals with refractive problems, a spectacle prescription was supplied to the participant.

Data quality control

To ensure the consistency of the data, the questionnaire was translated from English to Amharic and back again. A pre-tested Amharic version of semi-structured questions was used to ensure the reliability of the questionnaires. Before collecting data, a pretest of 48 participants (5% of the sample size) was conducted in Yirgalem, Sidama, to ensure that the questionnaire was clear, acceptable, and understandable.

To increase the quality of the data, the data collectors and one supervisor received one day of training before the actual data collection day. Training on how to utilize the Kobo Toolbox, examination procedures, and interviewing techniques was given. The supervisor closely monitored the data collection activities in the field and ensured that the collected data was complete and consistent.

Data processing and analysis

The data collected in the Kobo Toolbox was checked for completeness and consistency. The data were exported to Microsoft Excel, cleaned, and coded with SPSS 26, and then further analysis was conducted by using SPSS. Descriptive statistics like percentage and frequency were used to summarize demographic data and categorical variables. A binary logistic regression was used to identify factors related to RE. In the bivariable analysis, variables having a P-value of less than 0.2 were entered on the multivariable logistic regression (S2 File).

The variance inflation factor (VIF) and tolerance test have been used to determine whether the independent variables were multi-collinear, and a value less than 1.05 with a tolerance less than 0.955 was found. The model’s fitness was evaluated using the Hosmer and Lemeshow goodness of fits, and the P-value was 0.76. To demonstrate the relationship between the independent and dependent variables, an adjusted odds ratio with a 95% confidence interval was computed. A P-value of less than 0.05 was considered statistically significant.

Result

Socio-demographic characteristics of study participants

A total of 894 participants were involved in the study, the remaining 57 individuals were non-respondents making a response rate 94.1%. 3 cases with corneal opacity and 2 cases with infection were excluded during the study. The median age of the participant was 37 years, with an interquartile range (IQR) (28–50). Out of 894 study participants, 466 (52.1%) were male, (23.0%) were private employees and 478(53.5%) had college/university educational status (Table 1).

thumbnail
Table 1. Socio-demographic characteristics of study participants among adults in Hawassa City, South Ethiopia, 2023 (n = 894).

https://doi.org/10.1371/journal.pone.0298960.t001

Systemic comorbidities, clinical and behavioral characteristics of study participants

This study reported that 69(7.7%), 58(6.5%), and 124(13.9%) of the study participants had a history of diabetic mellitus, hypertension, and a family history of RE respectively. Besides, regular use of electronic devices was found among 201(22.5%) of the study participants (Table 2).

thumbnail
Table 2. Systemic comorbidities, clinical and behavioral characteristics of study participants among adults in Hawassa City, South Ethiopia, 2023 (n = 894).

https://doi.org/10.1371/journal.pone.0298960.t002

Prevalence of RE

Among the total of 894 participants, 110 (12.3%) [95% CI: 10.2, 14.5%] had a RE. The prevalence of uncorrected RE was 11.1%. This study revealed that from the total RE 43.8% of them had myopia and 2.7% had high myopia (Fig 2).

thumbnail
Fig 2. Types of refractive error among adults in Hawassa City, South Ethiopia, 2023 (n = 110).

https://doi.org/10.1371/journal.pone.0298960.g002

Factors associated with RE

Bivariable and multivariable binary logistic regression was performed to identify the associated factors with RE. In bivariable binary logistic regression analysis, older age, being male, regular use of electronic devices, longer sleeping duration, positive history of diabetes mellitus, family history of RE, having cataract, and history of cataract surgery were associated with RE.

Those variables in the bivariable analysis that had a P-value less than 0.2 were entered into a multivariable binary logistic regression. A family history of RE, regular use of electronic devices, a positive history of diabetes mellitus, and a history of cataract surgery were associated with RE in multivariable logistic regression with a P-value of less than 0.05.

The odds of having RE among participants aged 51–80 years were two times more likely compared with participants aged 18–28 years (AOR = 2.08, 95% CI: 1.01–4.31).

Regular use of electronic devices was also significantly associated with RE. The odds of having RE among participants with regular use of electronic devices were 3.64 times higher compared to participants who had no regular use of electronic devices (AOR = 3.64, 95% CI: 2.25–5.91).

The odds of having RE among participants who had a positive history of diabetes mellitus were 4.02 times higher than those who had no history of diabetes mellitus (AOR = 4.02, 95% CI: 2.16–7.48).

The odds of having RE among Participants who had a family history of RE were 2.71 times more likely than participants who had no family history of RE (AOR = 2.71, 95% CI: 1.59–4.61). The odds of having RE among participants who had a history of cataract surgery were 5.17 times higher compared to participants who had no history of cataract surgery (AOR = 5.17, 95% CI: 2.19–12.4) (Table 3).

thumbnail
Table 3. Bivariable and multivariable binary logistic regression analysis for factors associated with RE among adults in Hawassa City, South Ethiopia, 2023 (n = 894).

https://doi.org/10.1371/journal.pone.0298960.t003

Discussion

The prevalence and associated factors of RE were assessed in this community-based cross-sectional study among adults in Hawssa City, South Ethiopia.

The finding of this study revealed that the prevalence of RE was 12.3% (95% CI: 10.2–14.5%). This result was in line with the study conducted in Bogota, Colombia 12.5% [29]. Both studies used similar study designs, which may account for this similarity.

On the other hand, the finding of this study was lower than studies conducted in Gondar Northwest Ethiopia 35.6% [31], Borumed Ethiopia 18.3% [7], and London United Kingdom 54% [32]. In this case, the discrepancy may be due to the socio-demographic characteristics of the study population and the study setting. As an example, the study done in Gondar was conducted among pregnant women. During pregnancy, corneal curvature and central corneal thickness increase substantially, while intraocular pressure decreases. Those physiological changes contribute to RE, which may lead to an increase in the prevalence of RE [33]. Furthermore, the study in Borumed, Ethiopia, was hospital-based. Given that most patients go to the hospital for vision difficulties, this could overestimate the magnitude of RE. Furthermore, a study in London, United Kingdom, was conducted among older persons, as age causes structural changes in the ocular system, which increase the magnitude of RE [34].

The current study’s results were greater than those obtained in Eritrea 6.4% [35], Kenya 7.4% [36], and Durban South Africa [37]. This difference may be due to variations in the method they employed and cut-off points for RE. The study in Eritrea employed a definition of RE with a VA of 6/12 or worse, which excluded participants who had RE with a VA better than 6/12, which may reduce the prevalence of RE. A study done in Durban, South Africa only included 15- to 24-year-olds, but this study included all persons 18 years and above. Several ocular diseases (diabetic retinopathy, glaucoma, and cataracts) and structural changes (retinal degeneration) in the ocular system are common among older adults and thus lead to RE. Since ocular growth stabilizes at older ages, RE risk factors will likely differ from those of younger ages due to ocular growth stability and slight changes in biometrics [34]. Because of age-related ocular disorders that increase the prevalence of RE, the above condition causes an increase in RE. Furthermore, the result of a study conducted in Bangladesh 4.7% [38] was lower than in this study; this discrepancy might be caused by the difference in the study population.

The odds of having RE among participants who had a history of diabetes mellitus were 4.02 times higher compared to participants who had no diabetes mellitus. This result is comparable with the studies conducted in Borumed, Ethiopia, and Yunnan, China [7, 39]. Clinical research has demonstrated that transient RE shifts are related to blood glucose levels. Increasing glucose may decrease the osmotic pressure of aqueous humor, leading to a flow of water from the aqueous humor into the lens, resulting in functional and morphologic changes in the lens. As a result of changes in lens refractive index, diabetics are more likely to develop RE [40, 41].

The odds of having RE among participants who underwent cataract surgery were 5.17 times higher than those participants who had no history of cataract surgery. This result was supported by the study conducted in South India [42]. Cataract surgery induces RE in different ways, which can be in preoperative (errors in biometry parameters, Pre-existing systemic & ocular comorbidities, Pre-existing uncorrected corneal astigmatism >1.00 DC), intraoperative (surgical variations of incision size, incision location, Use of sutures), or postoperative (shift in IOL position) conditions [4345].

The odds of having RE in participants who had a family history of RE was 2.71 times higher than in participants who had no family history of RE. This result is comparable with the studies conducted in Arba Minch, Ethiopia, and East China [9, 30]. Studies have found considerable relationships between first-degree relatives’ RE. Research has shown that RE aggregates significantly within families. It has been reported that the heritability of RE ranges from 50% to 90% within various populations [46, 47].

The odds of having RE among participants who have regular use of electronic devices were 3.64 times higher than participants who have no regular use of electronic devices. This result was consistent with a study conducted in Gondar, Northwest Ethiopia, and Rohtak India [48, 49]. Staring at the computer for an extended period causes prolonged accommodation and muscle fatigue, which might result in a transient shift in the refractive status of the eye [50]. In addition, staring at the computer for an extended time will cause dry eye, which will affect the refractive power of the cornea [51].

Strengths and limitations of the study

Both objective and subjective full refraction procedure was performed to determine the refractive status of the eye. As the study is community-based it is more representative than institution-based studies.

A cross-sectional study design does not reveal a cause-and-effect relationship between dependent and independent variables. Recall bias was another issue due to the nature of the questionnaire to assess family history of RE and smoking.

Conclusion

As a conclusion, the prevalence of RE in this study area was 12.3%. A family history of RE, regular use of electronic devices, a positive history of diabetes mellitus, and a history of cataract surgery were significantly associated with RE. Since most of these associated factors are modifiable (regular use of electronic devices, a positive history of diabetes mellitus, and a history of cataract surgery), eye care professionals should primarily focus on the prevention of these modifiable causes. To mitigate the burden of RE, it is recommended that eye care professionals prioritize early screening of individuals with diabetes. From a perspective of minimizing post-operative RE following cataract surgery, there is a need to enhance preoperative evaluation and intraoperative care.

Supporting information

S1 File. English version of questionnaire.

https://doi.org/10.1371/journal.pone.0298960.s001

(DOCX)

S2 File. Data used for analysis including data on refractive error and associated factors.

https://doi.org/10.1371/journal.pone.0298960.s002

(SAV)

Acknowledgments

The authors would like to acknowledge study participants for their participation in the study and also, we would like to acknowledge data collectors (optometrists).

Ethical consideration

The University of Gondar, College of Medicine and Health Sciences, School of Medicine, and the Ethical Review Committee provided us with ethical approval, approval ID 06/01/622/2015EC, and the regional administrative office gave us a letter of support. All study participants provided verbal informed consent after they were provided with an information sheet receiving a full explanation of the study’s objective and being informed that they have the right to question and withdraw from the study at any moment during data collection. this was approved by the IRB.

There was no reward or risk for the study participants who were chosen. By avoiding any personal identifiers in the data-gathering tools and using password-protected data on a computer, confidentiality was maintained. In addition, the collected data on the data collector’s phone was discarded after sending the daily collected information to the principal investigator to maintain confidentiality.

References

  1. 1. Alem KD, Gebru EA. A cross-sectional analysis of refractive error prevalence and associated factors among elementary school children in Hawassa, Ethiopia. J Int Med Res. 2021;49(3):300060521998894. pmid:33752506
  2. 2. Hashemi H, Fotouhi A, Yekta A, Pakzad R, Ostadimoghaddam H, Khabazkhoob M. Global and regional estimates of prevalence of refractive errors: Systematic review and meta-analysis. J Curr Ophthalmol. 2018;30(1):3–22. pmid:29564404
  3. 3. Jonas JB, Bourne RR, White RA, Flaxman SR, Keeffe J, Leasher J, et al. Visual impairment and blindness due to macular diseases globally: a systematic review and meta-analysis. Am J Ophthalmol. 2014;158(4):808–15. pmid:24973605
  4. 4. Collaborators G RL. Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: the Right to Sight: an analysis for the Global Burden of Disease Study. Lancet Glob Health. 2021;9(2):144–60.
  5. 5. Naidoo K, Gichuhi S, Basáñez M-G, Flaxman SR, Jonas JB, Keeffe J, et al. Prevalence and causes of vision loss in sub-Saharan Africa: 1990–2010. British Journal of Ophthalmology. 2014;98(5):612–8. pmid:24568870
  6. 6. Flaxman SR, Bourne RR, Resnikoff S, Ackland P, Braithwaite T, Cicinelli MV, et al. Global causes of blindness and distance vision impairment 1990–2020: a systematic review and meta-analysis. Lancet Glob Health. 2017;5(12):1221–34. pmid:29032195
  7. 7. Besufikad B, Hailemichael W, Tilahun L, Yimam W, Anteneh S. Refractive errors and associated factors among patients visiting BoruMeda Hospital’s secondary eye Unit in Dessie Town, South Wollo Zone, Ethiopia. BMC ophthalmology. 2022;22(1):1–5.
  8. 8. Shiferaw Alemu D, Desalegn Gudeta A, Tsega Ferede A, Woretaw Alemu H. Prevalence and degrees of myopia and hyperopia at Gondar university hospital tertiary eye care and training center, Northwest Ethiopia. Clinical optometry. 2016:85–91. pmid:30214353
  9. 9. Worku S, Getachew T, Nagarchi K, Shewangizaw M. The Magnitude of Refractive Error and Its Associated Factors Among Patients Visiting Ophthalmology Clinics in Southern Ethiopia, 2022. Clin Ophthalmol. 2023;17:1801–11. pmid:37383841
  10. 10. World Health Organization. Blindness and vision impairment 2022 [cited 2023 March]. Available from: https://www.who.int/news-room/fact-sheets/detail/blindness-and-visual-impairment.
  11. 11. Lou L, Yao C, Jin Y, Perez V, Ye J. Global patterns in health burden of uncorrected refractive error. Invest Ophthalmol Vis Sci. 2016;57(14):6271–7. pmid:27893092
  12. 12. Berhane Y, Worku A, Bejiga A, Adamu L, Alemayehu W, Bedri A, et al. National survey on blindness, low vision and trachoma in Ethiopia: Methods and study clusters profile. Ethiop J Health Dev. 2007;21(3):185–203.
  13. 13. Fricke T, Holden B, Wilson D, Schlenther G, Naidoo K, Resnikoff S, et al. Global cost of correcting vision impairment from uncorrected refractive error. Bulletin of the World Health Organization. 2012;90:728–38. pmid:23109740
  14. 14. Mohammadi S, Farzadfar F, Pour PM, Ashrafi E, Lashay A, Mohajer B, et al. Prevalence and burden of refractive errors at national and sub-national levels in Iran. J Ophthalmic Vis Res. 2022;17(1):78. pmid:35194499
  15. 15. Ye H, Qian Y, Zhang Q, Liu X, Cai X, Yu W, et al. Prevalence and risk factors of uncorrected refractive error among an elderly Chinese population in urban China: A cross-sectional study. BMJ Open. 2018;8(3):bmjopen–2017-021325.
  16. 16. Naël V, Moreau G, Monfermé S, Cougnard-Grégoire A, Scherlen A-C, Arleo A, et al. Prevalence and associated factors of uncorrected refractive error in older adults in a population-based study in France. JAMA ophthalmology. 2019;137(1):3–11. pmid:30326038
  17. 17. Cochrane GM, du Toit R, Le Mesurier RT. Management of refractive errors. BMJ. 2010;340. pmid:20385718
  18. 18. Honavar SG. The burden of uncorrected refractive error. Indian J Ophthalmol. 2019;67(5):577. pmid:31007210
  19. 19. Soboka JG, Teshome TT, Salamanca O, Calise A. Evaluating eye health care services progress towards VISION 2020 goals in Gurage Zone, Ethiopia. BMC Health Serv Res. 2022;22(1):1–9.
  20. 20. Agency CS. National Population and Housing Census of Ethiopia: Population Projection of Ethiopia for All Regions, at Wereda Level from 2014–2017. Ethiopian Central Statistics Agency. 2018.
  21. 21. Chan VF, Mebrahtu G, Ramson P, Wepo M, Naidoo KS. Prevalence of refractive error and spectacle coverage in Zoba Ma’ekel Eritrea: a rapid assessment of refractive error. Ophthalmic Epidemiol. 2013;20(3):131–7. pmid:23713915
  22. 22. Cumberland PM, Bountziouka V, Hammond CJ, Hysi PG, Rahi JS, Eye UB, et al. Temporal trends in frequency, type and severity of myopia and associations with key environmental risk factors in the UK: Findings from the UK Biobank Study. Plos one. 2022;17(1):e0260993. pmid:35045072
  23. 23. Cheng F, Shan L, Song W, Fan P, Zhang L, Wang X, et al. Prevalence and risk factor for refractive error in rural Chinese adults in Kailu, Inner Mongolia. Opht and Physiol Optics. 2021;41(1):13–20. pmid:33104269
  24. 24. Nikaj S, Chaloupka FJ. The effect of prices on cigarette use among youths in the global youth tobacco survey. Nicotine Tob Res. 2014;16(Suppl_1):S16–S23. pmid:23709614
  25. 25. Na K-S, Park Y-G, Han K, Mok JW, Joo C-K. Prevalence of and risk factors for age-related and anterior polar cataracts in a Korean population. PLoS One. 2014;9(6):96461.
  26. 26. Sewunet SA, Aredo KK, Gedefew M. Uncorrected refractive error and associated factors among primary school children in Debre Markos District, Northwest Ethiopia. BMC Ophthalmol. 2014;14:1–6.
  27. 27. Berhane MA, Demilew KZ, Assem AS. Myopia: an increasing problem for medical students at the University of Gondar. Clinical Ophthalmol. 2022:1529–39. pmid:35615078
  28. 28. Raman R, Pal SS, Adams JSK, Rani PK, Vaitheeswaran K, Sharma T. Prevalence and risk factors for cataract in diabetes: Sankara Nethralaya Diabetic Retinopathy Epidemiology and Molecular Genetics Study, report no. 17. Invest Ophthalmol Vis Sci. 2010;51(12):6253–61. pmid:20610838
  29. 29. Luque LC, Naidoo K, Chan VF, Silva JC, Naduvilath TJ, Peña F, et al. Prevalence of refractive error, presbyopia, and spectacle coverage in Bogotá, Colombia: a rapid assessment of refractive error. Optometry and Vision Science. 2019;96(8):579–86.
  30. 30. Xu C, Pan C, Zhao C, Bi M, Ma Q, Cheng J, et al. Prevalence and risk factors for myopia in older adult east Chinese population. BMC Ophthalmol. 2017;17:1–11.
  31. 31. Diress M, Yeshaw Y, Bantihun M, Dagnew B, Ambelu A, Seid MA, et al. Refractive error and its associated factors among pregnant women attending antenatal care unit at the University of Gondar Comprehensive Specialized Hospital, Northwest Ethiopia. PLoS One. 2021;16(2):0246174. pmid:33577552
  32. 32. Cumberland PM, Bao Y, Hysi PG, Foster PJ, Hammond CJ, Rahi JS, et al. Frequency and distribution of refractive error in adult life: methodology and findings of the UK Biobank Study. PLoS One. 2015;10(10):0139780. pmid:26430771
  33. 33. Agrawal N, Agarwal LT, Lavaju P, Chaudhary SK. Physiological ocular changes in various trimesters of pregnancy. Nepal J Ophthalmol. 2018;10(1):16–22. pmid:31056572
  34. 34. Hashemi A, Khabazkhoob M, Hashemi H. High prevalence of refractive errors in an elderly population; a public health issue. BMC Ophthalmology. 2023;23(1):38. pmid:36707798
  35. 35. Chan VF, Mebrahtu G, Ramson P, Wepo M, Naidoo KS. Prevalence of refractive error and spectacle coverage in Zoba Ma’ekel Eritrea: a rapid assessment of refractive error. Ophthalmic epidemiology. 2013;20(3):131–7. pmid:23713915
  36. 36. Bastawrous A, Mathenge W, Foster A, Kuper H. Prevalence and predictors of refractive error and spectacle coverage in Nakuru, Kenya: a cross-sectional, population-based study. Int Ophthalmol. 2013;33:541–8. pmid:23440405
  37. 37. Naidoo KS, Chinanayi FS, Ramson P, Mashige KP. Rapid assessment of refractive error in the eThekwini Municipality of KwaZulu‐Natal, Durban, South Africa. Clin Exp Optom. 2016;99(4):360–5. pmid:27161520
  38. 38. Muhit M, Minto H, Parvin A, Jadoon MZ, Islam J, Yasmin S, et al. Prevalence of refractive error, presbyopia, and unmet need of spectacle coverage in a northern district of Bangladesh: Rapid Assessment of Refractive Error study. Ophthalmic Epidemiol. 2018;25(2):126–32. pmid:28976783
  39. 39. Wang M, Cui J, Shan G, Peng X, Pan L, Yan Z, et al. Prevalence and risk factors of refractive error: a cross-sectional Study in Han and Yi adults in Yunnan, China. BMC Ophthalmol. 2019;19(1):33. pmid:30683073
  40. 40. Song E, Qian Dj, Wang S, Xu C, Pan Cw. Refractive error in Chinese with type 2 diabetes and its association with glycaemic control. Clin Exp Optom. 2018;101(2):213–9. pmid:28975669
  41. 41. Kaštelan S, Gverović-Antunica A, Pelčić G, Gotovac M, Marković I, Kasun B, editors. Refractive changes associated with diabetes mellitus. Seminars in Ophthalmology; 2018: Taylor & Francis. pmid:30199309
  42. 42. Marmamula S, Barrenkala NR, Challa R, Kumbam TR, Modepalli SB, Yellapragada R, et al. Uncorrected refractive errors for distance among the residents in’homes for the aged’in South India–The Hyderabad Ocular Morbidity in Elderly Study (HOMES). Ophthalmic Physiol Opt. 2020;40(3):343–9. pmid:32207179
  43. 43. Lundström M, Dickman M, Henry Y, Manning S, Rosen P, Tassignon MJ, et al. Risk factors for refractive error after cataract surgery: Analysis of 282 811 cataract extractions reported to the European Registry of Quality Outcomes for cataract and refractive surgery. J Cataract Refract Surg. 2018;44(4):447–52.
  44. 44. Khoramnia R, Auffarth G, Łabuz G, Pettit G, Suryakumar R. Refractive outcomes after cataract surgery. Diagnostics. 2022;12(2):243. pmid:35204334
  45. 45. Aristodemou P, Sparrow JM, Kaye S. Evaluating refractive outcomes after cataract surgery. Ophthalmology. 2019;126(1):13–8. pmid:30153943
  46. 46. Peet JA, Cotch M-F, Wojciechowski R, Bailey-Wilson JE, Stambolian D. Heritability and familial aggregation of refractive error in the Old Order Amish. Invest Ophthalmol Vis Sci. 2007;48(9):4002–6. pmid:17724179
  47. 47. Wojciechowski R, Congdon N, Bowie H, Munoz B, Gilbert D, West SK. Heritability of refractive error and familial aggregation of myopia in an elderly American population. Invest Ophthalmol Vis Sci. 2005;46(5):1588–92. pmid:15851555
  48. 48. Diress M, Yeshaw Y, Bantihun M, Dagnew B, Ambelu A, Seid MA, et al. Refractive error and its associated factors among pregnant women attending antenatal care unit at the University of Gondar Comprehensive Specialized Hospital, Northwest Ethiopia. Plos one. 2021;16(2):e0246174. pmid:33577552
  49. 49. Kumar N, Jangra B, Jangra MS, Pawar N. Risk factors associated with refractive error among medical students. Int J Community Med Public Health. 2018;5(2):634–8.
  50. 50. Kim S-H, Suh Y-W, Choi Y-M, Han J-Y, Nam G-T, You E-J, et al. Effect of watching 3-dimensional television on refractive error in children. Korean Journal of Ophthalmology. 2015;29(1):53–7. pmid:25646061
  51. 51. Alemayehu A, Alemayehu MM. Pathophysiologic mechanisms of computer vision syndrome and its prevention. World J Ophthalmol Vis Res. 2019;2(5):1–7.