It’s time to act with a few rational and relatively modest proposals.
Substantial research shows significant racial and class disparities in diabetes care and outcomes. For instance, non-Hispanic Black Americans with type 2 diabetes are at a doubly higher risk of dying from a diabetes complication, a 2.5 times higher risk of being hospitalized for a diabetes complication, and are over 3 times more likely to suffer end-stage renal disease than their White counterparts.1 Low income increased mortality risk by more than 80% in both White and Black Americans with type 2 diabetes in an analysis of more than 60,000 patients enrolled in the Southern Community Cohort Study.2 Rates of lower extremity amputation associated with diabetes are also 2 to 4 times higher among Americans of color and those with annual household incomes of less than $40,000.3 Moreover, data shows that many of these same patients are far less likely to be prescribed cardiorenal-protective drugs such as glucagon-like peptide-1 receptor analogs or sodium glucose transporter type-2 inhibitors, even after controlling for household income,4 as well as technologies that significantly improve metabolic control of diabetes, such as newer insulins and continuous glucose-monitoring devices.5
Rates of sight-threatening diabetic retinopathy (STDR) are similarly higher in Black and Hispanic Americans,6 with recent evidence showing that, irrespective of income, glycated hemoglobin (HbA1c) blood pressure, dyslipidemia and diabetes duration, Black Americans are 40% more likely to develop diabetic macular edema (DME), the leading cause of vision loss associated with diabetes.7 To put a finer point on the significance of this finding, being Black in the United States poses an equivalent elevated risk for DME as does a 3-point higher HbA1c value. Another cross-sectional studyrevealed that patients with diabetes who are Black, Hispanic and/or have a limited income encounter specific barriers with respect to receiving timely eye examinations, including lack of child care, inability to take time off from work, accessibility of providers, lack of transportation, lower awareness of good diabetes self-management practices due to limited or no formal diabetes education, and a perception that their providers are more judgmental, less willing to answer questions, and less concerned about their welfare.8
These realities are both ethically reprehensible and indefensible from a public health perspective. But what can be done? Standing on the shoulders of smart clinicians, researchers and public health advocates, I would like to offer a few modest proposals, as follows:
This includes involvement from primary care providers’ offices, community clinics, pharmacies, and wherever else eye care providers see patients. DR used to be the leading cause of severe, irreversible vision loss in adults of working age in the UK, but that is no longer true with the implementation of a nationwide telescreening program over the past decade.9 The details of such programs are debatable (e.g. frequency, density of access points, image field of view, certification of image-readers, and use of artificial intelligence, to name a few) and disparities remain in the UK among under-served, limited income, minority and/or rural populations. However, this single strategy is anticipated to make a real difference both now and in the future by reducing significant visual impairment due to DR in the UK from 4.7% in 2013 to 3.1% in 2050 and saving the National Health Service hundreds of millions of British pounds over the coming decades.10 Despite decades of trying to achieve higher rates of dilated eye examinations among patients with diabetes in the US, 40% to 60% of them are not receiving dilated eye exams at recommended intervals.11 Additionally, DR and/or DME remain the leading causes of severe vision loss in Americans of working age.11 The current US model simply is not working as well as it should.
The CDC and National Eye Institute have instituted several patient engagement programs, including the Don’t Lose Sight of Diabetic Eye Disease and Promoting Eye Health campaigns. However, these programs have had limited impact to date,12 most likely due to problems with health care literacy as well as (largely digital) access to materials.13 In addressing this digital divide, using easily understood language and fostering delivery of diabetes education via trusted community-based resources have proven effective. Studies also show that providing patient education alongside meaningful financial incentives ($300 to $600) to underserved patient populations to achieve weight loss, medication and appointment adherence, and improved metabolic control results in better outcomes and is cost-effective.14-16 The only randomized trial that assessed eye screening attendance in patients with a 2-year history of nonattendance used paltry sums ($12 at the visit or a raffle system with low odds of receiving $1200) and found that both incentives resulted in less eye screening attendance than usual patient communications.17 There is good reason to believe that a combination of patient communications with meaningful financial incentives would improve eye assessment and examination rates for people with diabetes and reduce rates of vision loss.
Health professional schools must reexamine admission criteria to help meet the needs of diverse, underserved and at-risk patient populations. Rather than only prioritizing applicant grades and standardized test scores, alternative admissions metrics could be deployed that also emphasize empathy and communications skills.18 Specifically recruiting high school students and college undergraduates from communities under-represented within the eye care workforce could help forge higher levels of patient trust, adherence, and improved clinical outcomes; this is something that can be addressed by both health professions schools’ admissions committees as well as community practitioners. The notion that optometrists could and should participate in growing a cadre of highly knowledgeable and culturally competent diabetes care providers is obvious.
A combination of these modest tactics, perhaps in tandem with a few more radical strategies (eg, reduction of diabetogenic environmental exposures that unequally affect different populations—think micro-plastics, air pollution, food deserts/swamps, poverty and racism, universal access to health care, and science-based and public health-centered regulation of food ingredients and advertising) would undoubtedly reduce both vision loss and multiple complications associated with diabetes and other cardio-metabolic diseases.