Management of type 2 diabetes: A handbook for general practice

Complications

Diabetes-related eye disease

Complictions | Diabetes-related eye disease 


Recommendation 

Grade 

References 

Recommended as of:

Individuals with type 2 diabetes should be screened and evaluated for retinopathy by an optometrist or ophthalmologist at the time of diagnosis. 

B

1

14/11/2024

Follow-up screening interval for people with retinopathy should be tailored to the severity of retinopathy. B 1 14/11/2024
The recommended interval for those with no or minimal retinopathy is 1–2 years. B 1 14/11/2024
Examine higher-risk patients who do not have diabetic retinopathy (DR) at least annually (high risk defined as: longer duration of diabetes; suboptimal glycaemic management, blood pressure or blood lipid control; people from cross-cultural and linguistically diverse background). Consensus 2 14/11/2024
Conduct annual DR screening for Aboriginal or Torres Strait Islander people with diabetes. Consensus 2 14/11/2024
To delay onset and progression of DR, people with type 2 diabetes should be offered pharmacologic and non-pharmacological management options to achieve optimal control* of:
  • blood glucose
  • blood pressure
  • lipid levels.
*management
A 1 14/11/2024
Fenofibrate, in addition to statin therapy, may be used in people with type 2 diabetes to slow the progression of established retinopathy. A, Level 1A 3 14/11/2024
Promptly refer* individuals with any level of diabetic macular oedema, moderate or worse non-proliferative DR (a precursor of proliferative diabetic retinopathy [PDR]), or any PDR to an ophthalmologist who is knowledgeable and experienced in the management of DR.
*Refer to Clinical context for timing of referral.
A 1 14/11/2024
Counsel individuals of childbearing potential with type 2 diabetes who are planning pregnancy or who are pregnant on the risk of development and/or progression of DR. B 1 14/11/2024
Individuals with type 2 diabetes should receive an eye exam before pregnancy and in the first trimester and should be monitored every trimester and for one year postpartum as indicated by the degree of retinopathy*.
*Back to the usual timeframes for the general population.
B 1 14/11/2024

Clinical context

Diabetes-related retinopathy (DR) occurs as a result of microvascular disease of the retina. It affects up to one in three people with diabetes, and can cause visual impairment and blindness.4 DR also impairs quality of life and the ability to manage diabetes.5

Three distinct forms of DR are:

  • macular oedema, which includes diffuse or focal vascular leakage within the macula
  • DR caused by microvascular changes:
    • non-proliferative DR (NPDR), which includes microaneurysms, intra-retinal haemorrhage, malformation and torturous vessels; may be asymptomatic
    • PDR, which involves abnormal vessel growth on the optic disc or retina.

Sight-threatening DR includes:

  • severe NPDR
  • PDR
  • foveal-threatening diabetic macular oedema.

NPDR affects 19.3% of people with diabetes, whereas 2.1% of people with diabetes may have PDR and 3.3% may have macular oedema.6 PDR and macular oedema are associated with an elevated risk of cardiovascular disease.7

In practice

Risk factors for the onset or progression of DR include:

  • existing DR
  • poor glycaemic management
  • raised blood pressure
  • duration of diabetes >10 years (DR may be present at the time of diagnosis of type 2 diabetes)
  • microalbuminuria
  • dyslipidaemia
  • anaemia
  • pregnancy.

Visual impairment due to diabetes can be avoided for the vast majority of people through recommended screening and the management of risk factors. This involves regular review of fundi, early detection and optimisation of therapy. DR may progress to advanced stages without affecting vision, hence the importance of regular DR screening examinations. A meta-analysis has suggested some increased risk of DR with the use of sulfonylureas.8

Monitoring for diabetic eye disease involves assessment of:

  • changes in visual acuity (with correction)
  • lens disease (eg cataracts; see below)
  • fundal disease (eg fundoscopy with dilation or retinal camera, or refer to an optometrist or ophthalmologist).

Screening methods and intervals for retinopathy are presented in Box 1.

Consider the timing of referral to an ophthalmologist; for instance, non-centre-involving macular oedema and moderate NPDR are less urgent (within 12 weeks) than PDR (within 1 week).

Strategies for delaying the onset and progression of DR include:

  • Lifestyle advice to optimise healthy nutrition and activity levels9
  • optimising blood glucose10-12

Refer to the section ‘Glucose monitoring ’ for suggested glycated haemoglobin (HbA1c) targets. Note that intensive glucose management in people with DR that is more severe than moderate NPDR on the International Clinical Diabetic Retinopathy Disease Severity Scale may not be beneficial.13,14 Rapid and marked reductions in HbA1c as a result of improved glycaemic management initiated during pregnancy, bariatric surgery or intensified insulin treatment have previously been associated with transitory worsening of DR and should be avoided. Eye examinations should occur at shorter intervals.

  • managing blood pressure15
  • adding fenofibrate

Indicated for the reduction of DR progression in people with type 2 diabetes who have existing DR. Fenofibrate does not replace managing blood pressure, blood glucose and blood lipids as strategies to delay the progression of DR.16,17

  • ophthalmological specialist care:
    • laser therapy
    • intraocular anti-vascular endothelial growth factor (VEGF) agents (for further information, refer to the Pharmaceutical Benefits Scheme)
    • vitreoretinal surgery.

KeepSight, managed by Diabetes Australia, is a free online reminder system for people with diabetes about their next diabetes eye examination.

The National Diabetes Services Scheme (NDSS) and Diabetes Australia send alerts and reminders to people with diabetes registered on the NDSS to have their eyes checked.

A report on diabetes-related eye disease, titled ‘Out of sight’ has been published.6

The article by Yuen et al includes clinical references to support person centred care in diabetes associated eye disease.9

Box 1. Screening for retinopathy in type 2 diabetes

When to initiate screening1
  • At diagnosis (non-pregnant with type 2 diabetes)
    • Educate people with diabetes about the link to sight-threatening eye disease, highlighting the importance of regular eye screening to protect their vision.
  • At diagnosis (pregnancy with diabetes)
    • Examination in first trimester. Routine referral to ophthalmologist. Pregnant women who develop gestational diabetes do not require screening for diabetic retinopathy2

Screening methods1

  • Visual acuity should be tested for each eye in turn (with occlusion of the fellow eye)
  • Retinal photography, with or without pupil dilation (mydriasis), with disc-centred and macular-centred images of both eyes, with interpretation by a trained reader
  • Direct ophthalmoscopy or indirect slit-lamp fundoscopy through dilated pupil, performed by an examiner proficient in the use of these methods

Research on the optimal number of fields to be photographed is still unclear

If retinopathy is present1,3

  • Grade retinopathy severity, refer to ophthalmologist as appropriate and establish appropriate monitoring intervals (≤1 year)
  • Sight-threatening retinopathy may be treated with laser, pharmacological or surgical therapy by an ophthalmologist*
  • Review glycaemic, blood pressure and lipid management, and adjust therapy to reach targets as per guidelines
  • Screen for other diabetes complications, especially cardiovascular disease, including peripheral arterial disease and chronic kidney disease

If retinopathy is not present

  • Rescreen every year:2
    • people with duration of diabetes >15 years
    • suboptimal glycaemic management (HbA1c >8% or 64 mmol/mol)
    • systemic disease (poorly managed hypertension, lipids; other diabetes complications; foot ulcers)
    • Aboriginal and Torres Strait Islander people
    • people from a non-English-speaking background
  • Uncertainties over the presence of retinopathy or maculopathy (eg unclear retinal photographs) may warrant referral to an ophthalmologist.
  • Rescreen every two years:2
    • all other people with type 2 diabetes
  • Review glycaemic, blood pressure and lipid management, and adjust therapy to reach targets as per guidelines
  • Screen for other diabetes complications

For more information, refer to The Royal Australian and New Zealand College of Ophthalmologists (RANZCO) screening and referral algorithm for diabetic retinopathy.2

*Treatment options include fenofibrate, laser therapy, intra-ocular anti-VEGF agents and vitreoretinal surgery. Evidence highlights the importance of regular, life-long participation in retinopathy screening.

Role of retinal photography

Retinal photography is technically simple and is now usually performed within the Australian community by general practitioners, optometrists and ophthalmologists. Training is required to ensure quality of image interpretation.

Some Aboriginal Community Controlled Health Services are providing their own retinal photography services with support through telemedicine to promote access to screening.

People whose retinal images suggest they may be at increased risk of having, or at some point developing, sight-threatening retinopathy should be referred for assessment by an ophthalmologist.

Retinal photography may serve as a screening tool for retinopathy; however, it is not a substitute for a comprehensive eye exam.5

Note, a Medicare Benefits Schedule item number for retinal photography with a non-mydriatic retinal camera is available for general practice use.

Refractive errors

Refractive errors occur as the lens shape alters with changes in blood glucose concentrations and results in blurred vision. Correction of refractive errors should be postponed until blood glucose levels are stabilised. Detection is done with a pinhole test; blurred vision due purely to refractive error corrects with the pinhole test.

Cataracts

Cataracts occur prematurely in people with diabetes. People with cataracts may present with blurred vision and glare intolerance, and may find night vision a particular problem. Over time, interpretation of colours becomes more difficult.

Clinically, the light reflex is reduced, and the fundus may be difficult to see.

Surgical treatment is recommended when reduced acuity is affecting lifestyle and independence.

Maculopathy

Macular oedema is difficult for the non-expert to detect via ophthalmoscopy. Any unexplained vision loss in a person with diabetes should warrant prompt review by an optometrist or ophthalmologist.

Glaucoma

The incidence of glaucoma in people with diabetes is approximately twice that of the general population. All people with type 2 diabetes should be monitored for glaucoma by an optometrist or an ophthalmologist.18

Ischaemic optic neuropathy

Ischaemic optic neuropathy is a cause of sudden vision loss and has a poor prognosis for sight.

Sudden blindness

Sudden loss of vision is an emergency and may be caused by:

  • central retinal artery occlusion
  • retinal detachment
  • vitreous haemorrhage.

These conditions can occur independently of diabetes. Urgent contact with an ophthalmologist or timely assessment by a specialist team is indicated.

Semaglutide has been associated with an increased risk of non-arteritic anterior ischemic optic neuropathy in an observational study. These conditions can occur independently of diabetes. Urgent contact with an ophthalmologist or timely assessment by a specialist team would be indicated.19

  1. American Diabetes Association Professional Practice Committee et al. 12. Retinopathy, neuropathy, and foot care: Standards of care in diabetes – 2024. Diabetes Care 2024;47(Suppl 1):S231–43. doi: 10.2337/dc24-S012.
  2. The Royal Australian and New Zealand College of Ophthalmologists (RANZCO). RANZCO screening and referral pathway for diabetic retinopathy. RANZCO, 2019.
  3. Diabetes Canada Clinical Practice Guidelines Expert Committee. Diabetes Canada 2018 clinical practice guidelines for the prevention and management of diabetes in Canada. Can J Diabetes 2018;42(Suppl 1):S1–326.
  4. Smith-Morris C, Bresnick GH, Cuadros J, Bouskill KE, Pedersen ER. Diabetic retinopathy and the cascade into vision loss. Med Anthropol 2020;39(2):109–22. doi: 10.1080/01459740.2018.1425839.
  5. Khoo K, Man REK, Rees G, Gupta P, Lamoureux EL, Fenwick EK. The relationship between diabetic retinopathy and psychosocial functioning: A systematic review. Qual Life Res 2019;28(8):2017–39. doi: 10.1007/s11136-019-02165-1.
  6. Dirani M. Out of sight: A report into diabetic eye disease in Australia. Baker IDI Heart and Diabetes Institute and the Centre for Eye Research Australia, 2013.
  7. Xie J, Ikram MK, Cotch MF, et al. Association of diabetic macular edema and proliferative diabetic retinopathy with cardiovascular disease: A systematic review and meta-analysis. JAMA Ophthalmol Tang H, Li G, Zhao Y, et al. Comparisons of diabetic retinopathy events associated with glucose-lowering drugs in patients with type 2 diabetes mellitus: A network meta-analysis. Diabetes Obes Metab 2018;20(5):1262–79. doi: 10.1111/dom.13232.
  8. Yuen YS, Gilhotra JS, Dalton M, et al. Diabetic macular oedema guidelines: An Australian perspective. J Ophthalmol 2023;2023(1):6329819. doi: 10.1155/2023/6329819.
  9. The Diabetes Control and Complications (DCCT) Research Group. Effect of intensive therapy on the development and progression of diabetic nephropathy in the Diabetes Control and Complications Trial. Kidney Int 1995;47(6):1703–20. doi: 10.1038/ki.1995.236.
  10. UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 1998;352(9131):837–53. doi: 10.1016/S0140-6736(98)07019-6.
  11. Chew EY, Davis MD, Danis RP, et al. The effects of medical management on the progression of diabetic retinopathy in persons with type 2 diabetes: The Action to Control Cardiovascular Risk in Diabetes (ACCORD) Eye Study. Ophthalmology 2014;121(12):2443–51. doi: 10.1016/j.ophtha.2014.07.019.
  12. Vilsbøll T, Bain SC, Leiter LA, et al. Semaglutide, reduction in glycated haemoglobin and the risk of diabetic retinopathy. Diabetes Obes Metab 2018;20(4):889–97. doi: 10.1111/dom.13172.
  13. Liu Y, Li J, Ma J, Tong N. The threshold of the severity of diabetic retinopathy below which intensive glycemic control is beneficial in diabetic patients: Estimation using data from large randomized clinical trials. J Diabetes Res 2020;2020:1. doi: 10.1155/2020/5498528.
  14. UK Prospective Diabetes Study Group. Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. BMJ 1998;317(7160):703–13. doi: 10.1136/bmj.317.7160.703.
  15. Abbott Australasia. Product information Lipidil®. Therapeutic Goods Administration, 2014 [Accessed 13 September 2024].
  16. Sharma N, Ooi JL, Ong J, Newman D. The use of fenofibrate in the management of patients with diabetic retinopathy: An evidence-based review. Aust Fam Physician 2015;44(6):367–70.
  17. National Health and Medical Research Council (NHMRC). Guidelines for the screening, prognosis, diagnosis, management and prevention of glaucoma. NHMRC, 2010.
  18. Hathaway JT, Shah MP, Hathaway DB, et al. Risk of nonarteritic anterior ischemic optic neuropathy in patients prescribed semaglutide. JAMA Ophthalmol 2024;142(8):732–39. doi: 10.1001/jamaophthalmol.2024.2296.
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