Literature DB >> 34708751

Clinical profile and magnitude of diabetic retinopathy: An electronic medical record-driven big data analytics from an eye care network in India.

Anthony Vipin Das1, Gumpili Sai Prashanthi1, Taraprasad Das2, Raja Narayanan3, Padmaja Kumari Rani2.   

Abstract

PURPOSE: This study aimed to describe the clinical profile and magnitude of diabetic retinopathy (DR) in patients presenting to a multitier eye hospital network in India.
METHODS: This cross-sectional hospital-based study included 263,419 individuals with diabetes mellitus (DM) presenting between February 2012 and February 2021 (9-year period). The data were collected using an electronic medical record (EMR). Patients with a clinical diagnosis of DR in at least one eye were included in the analysis. Severe nonproliferative DR/proliferative DR/diabetic macular edema (DME) were considered sight-threatening DR (STDR).
RESULTS: In the study period, 25% (n = 66,913) were new patients diagnosed with DR. The majority of patients were males (70%). The mean age of the patients was 57 ± 10 years. The risk factors for DR were increased age: 30 to 50 years (odds ratio [OR] = 2.42), and 51 to 70 years (OR = 3.02), increased duration of DM: 6 to 10 years (OR = 2.88) and >10 years (OR = 6.52), blindness (OR = 2.42), male gender (OR = 1.36), lower socioeconomic status (OR = 1.43), and rural habitation (OR = 1.09). STDR was seen in 58% (n = 38,538) of examined patients. Risk factors for STDR were increased age 31 to 50 years (OR = 3.51), increased duration of DM: 6 to 10 years (OR = 1.23) and >10 years (OR = 1.68), blindness (OR = 3.68), male gender (OR = 1.12), and higher socioeconomic status (OR = 1.09).
CONCLUSION: Every fourth person with DM was found to have DR, and every second person with DR had STDR in this study cohort. These real-world big data might provide greater insight into the current status of DR. Additional big data from similar EMR-based sources will help in planning and resource allocation.

Entities:  

Keywords:  Diabetic retinopathy; India; electronic medical records

Mesh:

Year:  2021        PMID: 34708751      PMCID: PMC8725066          DOI: 10.4103/ijo.IJO_1490_21

Source DB:  PubMed          Journal:  Indian J Ophthalmol        ISSN: 0301-4738            Impact factor:   2.969


Diabetes mellitus (DM) is a group of metabolic disorders characterized by high blood sugar over a prolonged time. India is ranked second behind China in the world today, with 77 million people with diabetes.[1] Additionally, 43.9 million people are undiagnosed with diabetes in India. Diabetic retinopathy (DR) is the most common microvascular complication of diabetes that can lead to irreversible blindness. It occurs both in type 1 and type 2 diabetes and is strongly related to glycemic control and the duration of diabetes.[2] Other risk factors that contribute to the development of diabetic retinopathy include hypertension, nephropathy, and dyslipidemia.[34] More than 90% of the patients with type 1 diabetes are at a lifetime risk of developing DR, and it is around 50% to 60% in people with type 2 diabetes.[5] The retinopathy progresses from the mild nonproliferative stage to the moderate and severe stage before the development of abnormal blood vessels in the proliferative stage, leading to complications such as persistent vitreous hemorrhage or tractional retinal detachment causing severe visual impairment.[6] Recent studies have shown a rising prevalence of diabetic macular edema (DME); it is twice more common than proliferative diabetic retinopathy (PDR) as a cause of visual impairment in people with type 2 DM.[6] Timely detection and treatment of sight-threatening diabetic retinopathy (STDR) are required to prevent avoidable blindness through patient education, appropriate referral, and policy implementation.[7] There is a lack of real-world data of estimated DR burden assessed through electronic medical record (EMR) big data analysis from India. In this communication, we have analyzed the clinical profile and magnitude of DR at a large multitier ophthalmology network in India using a large data set using EMR-driven analytics.

Methods

This cross-sectional observational hospital-based study included patients between February 2012 and February 2021 to an ophthalmology network spread across four adjacent states (Telangana, Andhra Pradesh, Odisha, and Karnataka) of India.[8] A standard consent form for electronic data privacy was filled by the patient or the parents/guardians of the patient (for minors) at the time of registration. None of the data used for analysis had identifiable parameters of the patient. The study adhered to the Declaration of Helsinki and was approved by the Institutional Ethics Committee. The clinical data of each patient who underwent a comprehensive ophthalmic examination using a standardized template were entered into a browser-based EMR system (eye Smart EMR) by trained ophthalmic personnel and supervised by an ophthalmologist.[9]

Subjects

In the study period, 2,735,194 new patients of all ages were examined in the tertiary and secondary centers of the network. It included 263,419 individuals with DM. The eyeSmart EMR was initially screened for patients with a final ophthalmic diagnosis of DR in one or both eyes made by an ophthalmologist. A total of 66,913 records of patients who had the clinical diagnosis of DR were identified and were complete with the record of visual acuity, symptoms, signs, and management plan. Clinical diagnosis of DM was based on the combination of self-reported DM/physician evaluation captured from the EMR database. Clinical diagnosis of DR was the final diagnosis made by retina specialists based on the combination of ophthalmic evaluation and investigations. DR diagnosis was made after fundus biomicroscopy, indirect ophthalmoscopy, and ancillary tests. The ancillary retinal tests included optical coherence tomography, angiography, and fluorescein angiography. Mild and moderate nonproliferative DR (NPDR) were considered as non–sight-threatening DR (N-STDR), and severe NPDR/proliferative DR (PDR)/diabetic macular edema (DME) were considered as sight-threatening DR (STDR).

Data retrieval and processing

The data of 124,153 eyes of 66,913 new patients included in this study were retrieved from the EMR database and segregated in a single excel sheet. The columns included the data on demographics, clinical presentation, visual acuity, ophthalmic diagnosis, and blood investigations and were exported for analysis. The excel sheet with the required data was then used for analysis using the appropriate statistical software. Standardized definitions were used for occupation and geographic categorization.[10] Patients with paying status were considered as belonging to higher socioeconomic strata and those with nonpaying status as belonging to low socioeconomic strata. The paying patients paid for their services, and the nonpaying patients did not pay for their services. Visual impairment (VI) was classified according to the World Health Organization guidelines.[11]

Statistical analysis

Descriptive statistics using mean ± standard deviation and median with interquartile range (IQR) were used to analyze the demographic data. Chi-square test (StataCorp, 2015, Stata Statistical Software: Release 14. TX, StataCorp LP) was used for univariate analysis to detect the significant differences in the distribution of demographic features between patients with DR and the overall population. Logistic regression was performed for the binary outcome, presence of STDR, with the listed predictors. The following predictors were included: age, gender, socioeconomic status, presenting visual acuity, cataract, age-related macular degeneration (AMD), glaucoma, venous occlusions, cataract surgery, an intravitreal injection given/not given, occupation, and urban–rural–metropolitan habitat. Odds ratios (ORs) and 95% confidence intervals were calculated using R software (Version 3.5.1). Statistical significance, in this case, was reached at an alpha level of 0.01.

Results

Hospital-based prevalence

In this cohort, 9.6% (263,419 of 2,735,194 new patients) of people were detected to have DM, and 25.4% (66,913 of 263,419 with DM) of people were detected to have DR. The study included 124,153 eyes of 66,913 patients with DR. The decade-wise age-adjusted prevalence of DM and DR is shown in Fig. 1. The age-adjusted prevalence of DR (17.4%) and DM (6.2%) was the highest among the 51 to 70 years age group.
Figure 1

Decade-wise age-adjusted prevalence of DM and DR

Decade-wise age-adjusted prevalence of DM and DR

Demography

The mean age of the patients with DR was 57 ± 10 years, and the median age was 57 (IQR: 51–64) years. There were 46,547 (70%) male and 20,366 (30%) female patients with DR. Table 1 shows a baseline comparison of demographic and ocular risk factors between Individuals with no DR and DR.
Table 1

Comparative of people with DM with No DR and DR

ParameterNo DR%DR% P
Total Patients196,50666,913
Age (years)57.14±11.9156.97±9.78
Male114,7277146,54729<0.001
Female81,7798020,36620<0.001
Paying170,0787557,26825<0.001
Nonpaying26,428739,64527<0.001
Urban103,0477631,86824<0.001
Rural68,9687325,92027<0.001
Metropolitan24,491739,12527<0.001
Duration of DM
 1-5 years71,536926,3198<0.001
 6-10 years34,144817,84419<0.001
 >10 years26,4686712,78433<0.001
Occupation
 Agriculture related14,237696,51331<0.001
 Office goers (Government/Private)45,1766425,82836<0.001
 Homemaker52,8317715,54823<0.001
 Manual Labor10,766773,27523<0.001
 Retired20,2656610,37934<0.001
 Student1,6958530315<0.001
Presenting Visual Acuity
 Mild or No Visual Impairment - 0119,6728127,52619<0.001
 Moderate Visual Impairment - 127,7676713,57133<0.001
 Severe Visual Impairment - 27,613624,67938<0.001
 Blindness - 327,8526813,31432<0.001
 Blindness - 46,895762237240.04
 Blindness - 53,46972131828<0.001
 Undetermined or Unspecified3,23843426857NA
NSTDR0028375100<0.001
STDR0038538100<0.001
Ocular Comorbidities
 Cataract68,264771999023<0.001
 Glaucoma8,82676278124<0.001
 AMD1,4088329717<0.001
 Venous Occlusions3,3478083720<0.001
 Cataract Surgery26,15082575918<0.001

DM=Diabetes mellitus; DR=Diabetic retinopathy; NSTDR=Non-sight-threatening diabetic retinopathy, STDR=Sight-threatening diabetic retinopathy, AMD=Age-related macular degeneration

Comparative of people with DM with No DR and DR DM=Diabetes mellitus; DR=Diabetic retinopathy; NSTDR=Non-sight-threatening diabetic retinopathy, STDR=Sight-threatening diabetic retinopathy, AMD=Age-related macular degeneration

Geography and socioeconomic status

In this cohort, 61.3% (n = 40,993) of people with DR were from urban districts and metropolitan regions. The overall prevalence of DR was equally distributed between the three regions: urban, metropolitan, and rural [Table 1]. A majority of patients (85.6%; n = 57,268) paid for the services (upper socioeconomic class), and the overall prevalence of DR was significantly higher (P < 0.00001) in this class of patients [Table 1].

State-wise distribution

Table 2 shows the state-wise distribution of patients with DR. The majority were from Andhra Pradesh (37.6%; n = 25,178), followed by Telangana (29.5%; n = 19,722) and Odisha (20%; n = 13,426).
Table 2

State-wise distribution of patients with diabetic retinopathy

State%Number
Andaman and Nicobar Islands0.01%4
Andhra Pradesh37.63%25,178
Arunachal Pradesh0.01%5
Assam0.61%407
Bihar0.25%166
Chhattisgarh0.77%517
Delhi0.05%36
Goa0.02%14
Gujarat0.07%45
Haryana0.02%15
Himachal Pradesh0.00%3
Jammu and Kashmir0.03%21
Jharkhand0.56%378
Karnataka1.63%1,093
Kerala0.04%24
Madhya Pradesh0.42%283
Maharashtra2.59%1,730
Manipur0.01%5
Meghalaya0.01%5
Mizoram0.00%2
Nagaland0.00%1
Odisha20.07%13,426
Pondicherry0.02%11
Punjab0.01%6
Rajasthan0.09%63
Sikkim0.01%4
Tamil Nadu0.07%47
Telangana29.47%19,722
Tripura0.23%152
Uttar Pradesh0.27%178
Uttarakhand0.02%13
West Bengal5.02%3,359
100.00%66,913
State-wise distribution of patients with diabetic retinopathy

Occupation

The overall prevalence of DR in the office goers (government/private related sector; 39%; n = 25,828) was significantly higher (P < 0.00001) than in other professions.

Laterality and type

The DR was bilateral in 85.5% (n = 57,240) and unilateral in 14.5% (n = 9,673) people; 59.6% (n = 39,925) of people had NPDR, 40.3% (n = 26,988) of people had PDR and 57.6% (n = 38,538) of people had STDR. Thus, in the entire cohort of people with DM, the prevalence of any DR, NPDR, PDR, and STDR was 2.44%, 1.45%, 0.98%, and 1.41%, respectively.

Presenting visual acuity

The majority, 61.5% (n = 41,184) of patients with any DR and 52.6% (n = 20,285) of patients with STDR, had mild to moderate visual impairment (20/20 to 20/200) on presentation. Blindness (<20/400 – No perception of light) was recorded in 25.2% (n = 16,869) of patients with any DR and 22.2% (n = 14,837) of patients with STDR. Logistic regression analysis of factors associated with presence of diabetic retinopathy AMD = Age-related macular degeneration

Risk factors associated with the presence of DR [Table 3]

The risk factors for DR increased with age: 30–50 years (OR = 2.42), 51–70 years (OR = 3.02); increased duration of DM: 6–10 years (OR = 2.88) and >10 years (OR = 6.52); blindness (OR = 2.42); male gender (OR = 1.36), office goers (OR = 1.47), lower socioeconomic class (nonpaying patients; OR = 1.43); and rural habitat (OR = 1.09). Comparison of patients with non-sight-threatening (N-STDR) and sight-threatening diabetic retinopathy (STDR) AMD = Age-related macular degeneration; PRP = Panretinal photocoagulation

Sight-threatening diabetic retinopathy [Table 4]

A subset analysis was performed in 38,538 patients with STDR. The average age was 57 ± 9 years, and it was more common in males (71%). The majority of them belonged to a higher socioeconomic class (paying patients 85%; and urban geography 48%). The regression analysis [Table 5] showed that the risk increased with age: 31–50 years (OR = 3.51), increased duration of DM: 6–10 years (OR = 1.23) and >10 years (OR = 1.68), blindness (OR = 3.68), male gender (OR 1.12), agriculture occupation (OR = 1.11), and higher socioeconomic (paying) status (OR = 1.09).
Table 5

Logistic regression analysis of factors associated with presence of STDR

Odds Ratio95% Confidence Interval P

Lower BoundUpper Bound
Age (Reference: 0-30 years)
 31-50 years3.512.784.43<0.001
 51-70 years3.302.624.15<0.001
 >70 years2.031.602.58<0.001
 Male1.121.051.200.001
Payer Status (Reference: Nonpaying)
 Paying1.091.031.150.002
District Status (Reference: Urban)
 Metropolitan0.920.870.970.002
 Rural0.970.931.010.126
Occupation (Reference: Office goers (Governement/Private sector)
 Agriculture Related1.111.041.180.002
 Homemaker1.010.941.090.741
 Manual Labor0.980.891.070.642
 Retired0.920.870.970.002
 Student0.520.370.720.002
Duration of Diabetes
 6-10 years1.231.141.32<0.001
 >10 years1.681.571.80<0.001
Visual Acuity (Reference: Mild or No Visual Impairment - 0)
 Moderate Visual Impairment - 12.862.733.00<0.001
 Severe Visual Impairment - 23.423.173.69<0.001
 Blindness3.683.513.86<0.001
Ocular Comorbidities
 Cataracts0.540.520.57<0.001
 Glaucoma0.730.660.80<0.001
 Venous Occlusions0.080.060.09<0.001
 AMD0.220.160.29<0.001
Interventions
 PRP3.883.684.09<0.001
 Intravitreal Injections5.004.645.39<0.001
 Vitreoretinal Surgery3.963.464.53<0.001
 Cataract Surgery0.600.560.64<0.001

NSTDR = Non-sight-threatening DR, STDR = Sight-threatening DR, PRP = Panretinal photocoagulation

Logistic regression analysis of factors associated with presence of STDR NSTDR = Non-sight-threatening DR, STDR = Sight-threatening DR, PRP = Panretinal photocoagulation

Ocular comorbidities

Cataract was the most common ocular comorbidity (29.8%, n = 19,990 people; 37,206 eyes). The others included glaucoma, AMD, and retinal vein occlusions [Table 1]. Regression analysis [Tables 3 and 5] revealed a reduced risk of DR and STDR associated with the aforementioned ocular comorbidities.
Table 3

Logistic regression analysis of factors associated with presence of diabetic retinopathy

Odds Ratio95% Confidence Interval P

Lower BoundUpper Bound
Age (Reference: 0-30 years)
 31-50 years2.422.172.71<0.001
 51-70 years3.022.703.37<0.001
 >70 years1.641.461.84<0.001
 Male1.361.311.40<0.001
Payer Status (Reference: Paying)
 Nonpaying1.431.381.47<0.001
District Status (Reference: Urban)
 Rural1.091.071.12<0.001
 Metropolitan1.010.981.040.424
Occupation (Reference: Agriculture Related)
 Office goers (Government/Private sector)1.471.421.52<0.001
 Homemaker0.960.911.000.065
 Manual Labor0.640.610.67<0.001
 Retired1.401.341.46<0.001
 Student1.050.891.230.557
Duration of Diabetes
 6-10 years2.882.772.99<0.001
 >10 years6.526.276.77<0.001
Visual Acuity (Reference: Mild or No Visual Impairment - 0)
 Moderate Visual Impairment - 12.602.532.67<0.001
 Severe Visual Impairment - 23.213.083.35<0.001
 Blindness2.422.362.48<0.001
Ocular comorbidities
 Venous Occlusions0.460.420.50<0.001
 Cataracts0.770.750.79<0.001
 AMD0.550.480.63<0.001
 Glaucoma0.780.750.82<0.001
 Cataract Surgery0.480.470.50<0.001

AMD = Age-related macular degeneration

Interventions

The most common intervention for people with DR was panretinal photocoagulation in 21% people (26,513 eyes), followed by intravitreal injections in 11% of people (13,987 eyes). The common intraocular surgeries were cataract surgery (8.6%; 5,759 people; 10,304 eyes) and vitreoretinal surgery (5.4%; 3,626 people; 7,027 eyes). Intravitreal bevacizumab more common intravitreal therapy (80%; n = 11,159 eyes); the others included intravitreal triamcinolone (IVTA) in 9% (n = 1,320) and ranibizumab in 5% (n = 670) eyes.

Blood and urine investigations

The blood investigations of the patients were analyzed where available, comparing the distribution in N-STDR and STDR. The average random blood sugar level was 235 ± 192 mg/dL, fasting blood sugar was 156 ± 68 mg/dL, postprandial blood sugar (PPBS) was 254 ± 91 mg/dL, blood urea was 74 ± 31 mg/dL, serum creatinine was 2.55 ± 0.07 mg/dL, and urine spot microalbumin was 137 ± 99 mg. A detailed listing of all the blood and urine investigations comparing N-STDR and DR are listed in the Supplementary Table.
Supplementary Table

Biochemical profile with sight-threatening diabetic retinopathy (STDR) and non-sight-threatening diabetic retinopathy (N-STDR)

Blood Investigations n MeanSDN-STDRSDSTDRSDUnits P
Random Blood Sugar8,40423519219296205101mg/dL<0.001
Blood Urea6,777743130163724mg/dL<0.001
Serum Creatinine7,0412.550.071.190.781.491.18mg/dL<0.001
Hemoglobin7,5148.092.2212.822.0012.012.10g/dL<0.001
MCH6,03228.36.4428.718.0428.155.64pg0.002
MCHC6,03233.472.4333.451.7233.482.68g/dL0.65
MCV6,03284.3321.2884.748.0584.1624.76fl0.34
RBC Count6,0324.390.974.571.044.320.94million cell<0.001
WBC count6,0328.264.848.174.118.305.11x109/L0.347
Urine Spot Microalbumin960137991119914397mg<0.001
HCT4,19436.986.238.905.8236.236.19%<0.001
MPV4,0248.261.158.131.038.321.20fl<0.001

MCH=Mean corpuscular hemoglobin; MCHC= Mean corpuscular hemoglobin concentration; MCV=Mean corpuscle volume; RBC=Red blood cell; WBC=White blood cell; HCT=Hematocrit; MPV=Mean platelet volume

Biochemical profile with sight-threatening diabetic retinopathy (STDR) and non-sight-threatening diabetic retinopathy (N-STDR) MCH=Mean corpuscular hemoglobin; MCHC= Mean corpuscular hemoglobin concentration; MCV=Mean corpuscle volume; RBC=Red blood cell; WBC=White blood cell; HCT=Hematocrit; MPV=Mean platelet volume

Discussion

This study sought to describe the clinical profile and magnitude of diabetic retinopathy in a large cohort of patients presenting to a multitier eye hospital network in India using EMR-driven big data analytics. The network treats patients who pay or do not pay for the service and is spread over both city and rural locations in four states in India. The primary purpose of the study was to determine the real-world relative proportion and demographic profile of DR in the clinical care setting. In this hospital-based study, the overall prevalence of DM was 10%. The overall prevalence of DR was 2.4% of all eye diseases diagnosed between 2012 and 2021 (a 9-year period). The overall prevalence of DR was 25% in people with DM. The retinopathy was predominantly bilateral (86%) and was more commonly seen in males (70%) in this study cohort. The prevalence of DR at 25% was higher than 21% reported in a nationwide opportunistic community screening,[12] and lower than 32.3% from another tertiary-based facilities study across India.[13] The methodologies of these studies are different, and unlike the two other studies of a limited period (6–12 months), the current study analyzed data for 9 years from four tertiary and 20 rural eye centers. The current study also showed a higher prevalence of DR in a rural community than reported in one south Indian state (Tamil Nadu).[14] The increasing prevalence of DR in a rural community is a matter of concern and calls for a suitable change in DR screening strategies. Male gender as a risk factor for DR (OR = 1.36) and STDR (OR = 1.12) seen in the present study could be biased due to possibly more males presenting to the hospital. But other investigators have also reported a higher risk of DR in the male gender.[131415] Our observation of a higher risk of DR with increased age and longer duration of DM is not new.[13141516] The higher risk of any DR in a lower socioeconomic class of people is possibly due to poverty (poor glycemic control) and ignorance (poor health-seeking behavior). It has been observed in other countries too.[1718] But incidentally, higher economic status had a higher risk of developing STDR. This knowledge will help customized DR risk reduction strategies. Office goers were found to be a risk factor (OR = 1.09) for the presence of DR and agriculture occupation as a risk factor (OR = 1.11) for the presence of STDR. These differences in occupational risk factors for DR and STDR are contrasting. Office goer occupation may suggest an underlying sedentary lifestyle for the development of DR, whereas the agricultural occupation as a risk factor for STDR suggests lack of treatment facilities in rural areas. In this study, more than 60% of people with any DR had a presenting visual acuity of mild to moderate visual impairment, but more than 25% of people also were blind at presentation [Table 1]. More people with STDR were blind than people with N-STDR (STDR: 32.5%, 12,538 of 38,538; N-STDR: 15.3%, 4,331 of 28,375). This knowledge is important to create awareness that individuals with diabetes require regular DR screening. Available blood parameters of study cohorts suggest deranged glycemic control (fasting and random blood sugars) in patients with DR and STDR. Poor glycemic control is a known risk factor associated with STDR.[1314] Deranged renal functions, evidenced from urine microalbuminuria, were more in individuals with STDR. Individuals with micro- and macroalbuminuria are more likely to have DR than those without albuminuria.[19] Glaucoma and AMD are known to protect people from severe DR and STDR partially.[2021] We also observed the same in our cohort. Cataract surgery showed a low association of DR and STDR in our study. This is not aligned with observations in other countries. A study in Taiwan has reported a link between cataract surgery and the development of NPDR, but no differences were observed in the progression of PDR/DME following cataract surgery.[22] An EMR-based real-world study from the United Kingdom reported that the rate of treatment requiring DME increases in severity for all grades of DR (higher risk with moderate and severe NPDR). It reported worsening of DME within a year of cataract surgery, with a peak at 3 to 6 months.[23]

Study limitations

The hospital data are the greatest limitations of this study. Therefore, the study results cannot be generalized to the population. We did not have uniform data of systemic risk parameters (e.g., blood pressure measurements) and biochemical risk factors for the entire study cohort.

Study strength

Big data obtained from EMR-based analytics of DR and STDR in the Indian population over 9 years is the biggest strength. The United States and the United Kingdom have the largest EMR registries covering various DR-related research issues.[2324] A similar large EMR database–reported analytics on DR is unavailable in India.

Conclusion

In conclusion, this study describes the epidemiology and clinical presentation of DR in 2.7 million new patients presenting to multitier ophthalmology hospital networks in India. The findings show that DR is a common disease affecting patients seeking eye care in India. Every fourth person among people with DM has DR and every second person among people with DR is a person with STDR in this hospital-based study cohort. The risk factors for DR found in this study, such as an increase in age, longer duration of DM, male gender, rural habitation, and lower socioeconomic status, can be considered while designing targeted DR screening programs. The magnitude and risk factors described in this decade-long study may help develop targeted guidelines for DR screening and referral in India.

Financial support and sponsorship

This study was supported by the Hyderabad Eye Research Foundation, Hyderabad, India.

Conflicts of interest

There are no conflicts of interest.
Table 4

Comparison of patients with non-sight-threatening (N-STDR) and sight-threatening diabetic retinopathy (STDR)

ParameterN-STDR%STDR% P
Total Patients28,3754238,53858
Age (years)57.93±10.2856.27±9.33
Male19,1094127,43859<0.00001
Female9,2664511,10055<0.00001
Paying24,5804332,688570.07
Nonpaying3,795395,85061<0.00001
Urban13,3404218,528580.1
Rural11,0254314,895570.72
Metropolitan4,010445,115560.01
Occupation
 Agriculture Related2,478384,03562<0.00001
 Office goers (Government/Private)10,4514015,37760<0.00001
 Homemaker6,912448,63656<0.00001
 Manual Labor1,324401,951600.02
 Retired4,958485,42152<0.00001
Duration of Diabetes
 1-5 years3,093493,22651<0.00001
 6-10 years3,623464,22154<0.00001
 >10 years5,305417,47959<0.00001
Presenting Visual Acuity
 Mild or No Visual Impairment - 016,3055911,22141<0.00001
 Moderate Visual Impairment - 14,507339,06467<0.00001
 Severe Visual Impairment - 21,263273,41673<0.00001
 Blindness - 33,329259,98575<0.00001
 Blindness - 4601271,63673<0.00001
 Blindness - 54013091770<0.00001
 Undetermined or Unspecified1,969462,29954<0.00001
Ocular comorbidities
 Cataract10,833549,15746<0.00001
 Glaucoma1,195431,586570.55
 AMD228776923<0.00001
 Venous Occlusions6097322827<0.00001
Interventions
 PRP2,5111811,48782<0.00001
 Intravitreal Injections1,146156,33785<0.00001
 Vitreoretinal Surgery29983,32792<0.00001
 Cataract Surgery2,715473,04453<0.00001

AMD = Age-related macular degeneration; PRP = Panretinal photocoagulation

  23 in total

1.  Racial, Ethnic, and Insurance-Based Disparities Upon Initiation of Anti-Vascular Endothelial Growth Factor Therapy for Diabetic Macular Edema in the US.

Authors:  Nisha A Malhotra; Tyler E Greenlee; Amogh I Iyer; Thais F Conti; Andrew X Chen; Rishi P Singh
Journal:  Ophthalmology       Date:  2021-03-11       Impact factor: 12.079

Review 2.  Diabetic retinopathy.

Authors:  Tien Y Wong; Chui Ming Gemmy Cheung; Michael Larsen; Sanjay Sharma; Rafael Simó
Journal:  Nat Rev Dis Primers       Date:  2016-03-17       Impact factor: 52.329

3.  Prevalence of diabetic retinopathy in the United States, 2005-2008.

Authors:  Xinzhi Zhang; Jinan B Saaddine; Chiu-Fang Chou; Mary Frances Cotch; Yiling J Cheng; Linda S Geiss; Edward W Gregg; Ann L Albright; Barbara E K Klein; Ronald Klein
Journal:  JAMA       Date:  2010-08-11       Impact factor: 56.272

4.  Prevalence of Visual Impairment and Associated Risk Factors in Subjects with Type II Diabetes Mellitus: Sankara Nethralaya Diabetic Retinopathy Epidemiology and Molecular Genetics Study (SN-DREAMS, Report 16).

Authors:  Padmaja Kumari Rani; Rajiv Raman; Laxmi Gella; Vaitheeswaran Kulothungan; Tarun Sharma
Journal:  Middle East Afr J Ophthalmol       Date:  2012-01

Review 5.  Diabetic Retinopathy: A Position Statement by the American Diabetes Association.

Authors:  Sharon D Solomon; Emily Chew; Elia J Duh; Lucia Sobrin; Jennifer K Sun; Brian L VanderBeek; Charles C Wykoff; Thomas W Gardner
Journal:  Diabetes Care       Date:  2017-03       Impact factor: 19.112

6.  Development of diabetic retinopathy after cataract surgery.

Authors:  Chi-Juei Jeng; Yi-Ting Hsieh; Chung-May Yang; Chang-Hao Yang; Cheng-Li Lin; I-Jong Wang
Journal:  PLoS One       Date:  2018-08-22       Impact factor: 3.240

7.  Diabetic retinopathy screening guidelines in India: All India Ophthalmological Society diabetic retinopathy task force and Vitreoretinal Society of India Consensus Statement.

Authors:  Rajiv Raman; Kim Ramasamy; Ramachandran Rajalakshmi; Sobha Sivaprasad; S Natarajan
Journal:  Indian J Ophthalmol       Date:  2021-03       Impact factor: 1.848

Review 8.  Integrated model of primary and secondary eye care for underserved rural areas: the L V Prasad Eye Institute experience.

Authors:  Gullapalli N Rao; Rohit C Khanna; Sashi Mohan Athota; Varda Rajshekar; Padmaja Kumari Rani
Journal:  Indian J Ophthalmol       Date:  2012 Sep-Oct       Impact factor: 1.848

9.  Prevalence of diabetic retinopathy in India: The All India Ophthalmological Society Diabetic Retinopathy Eye Screening Study 2014.

Authors:  Salil S Gadkari; Quresh B Maskati; Barun Kumar Nayak
Journal:  Indian J Ophthalmol       Date:  2016-01       Impact factor: 1.848

10.  Socioeconomic deprivation and development of diabetic retinopathy in patients with type 1 diabetes mellitus.

Authors:  Pablo Alvarez-Ramos; Soledad Jimenez-Carmona; Pedro Alemany-Marquez; Juan Antonio Cordoba-Doña; Manuel Aguilar-Diosdado
Journal:  BMJ Open Diabetes Res Care       Date:  2020-11
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1.  The All India Ophthalmological Society - Academic and Research Committee pan-India diabetic retinopathy project "Fixing the missing link": Prevalence data from Madhya Pradesh and Chhattisgarh.

Authors:  Partha Biswas; Sneha Batra; Amit C Porwal; R Krishna Prasad; Prashant Bawankule; Rohit Saxena; Satyajit Sinha; Prajjwal Ghosh
Journal:  Indian J Ophthalmol       Date:  2022-05       Impact factor: 2.969

  1 in total

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