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Published on: July 5, 2022
Feasibility of retinal screening in a pediatric population with type 1 diabetes mellitus
Insights
A nonmydriatic camera effectively screens young children with type 1 diabetes for diabetic retinopathy. This imaging method is feasible for early detection of diabetic eye disease in pediatric patients.
Area of Science:
- Ophthalmology
- Pediatrics
- Endocrinology
Background:
- Diabetic retinopathy is a leading cause of vision loss in children with type 1 diabetes.
- Early detection and management are crucial to prevent vision impairment.
- Traditional screening methods often require pupil dilation, which can be challenging in young children.
Purpose of the Study:
- To assess the feasibility of using a nonmydriatic camera for screening diabetic retinopathy in children with type 1 diabetes mellitus (DM1) as young as 2 years old.
- To evaluate the quality and clinical value of images obtained with nonmydriatic technology in this pediatric population.
Main Methods:
- A prospective pilot study involved 104 children with DM1 (aged 2-17 years).
- Screening included visual acuity assessment and nonmydriatic color fundus imaging using a Canon CX-1 camera.
- Images were graded for quality and signs of diabetic retinopathy by two independent clinicians, with inter-observer agreement assessed using the Kappa coefficient.
Main Results:
- High-quality images (grades 4-5) were obtained in 86% of eyes, with 99.5% of eyes yielding images of clinical value (grade ≥ 2).
- One child (1%) was diagnosed with nonproliferative diabetic retinopathy, and two (1.9%) had incidental findings.
- Inter-observer agreement for image quality was high (0.896).
Conclusions:
- Nonmydriatic fundus imaging is a feasible method for screening diabetic retinopathy in children with type 1 diabetes, even as young as 2 years old.
- This technology can supplement standard dilated eye examinations for specific pediatric patient groups.
- The study demonstrates the potential of nonmydriatic cameras for early detection of diabetic eye disease in children.
Purpose:
To study the feasibility of using a nonmydriatic camera to screen children with type 1 diabetes mellitus (DM1) as young as 2 years for diabetic retinopathy.
Methods:
Prospective pilot imaging study involving children with DM1 aged 2 to 17 years. The screening consisted of: (1) intake form; (2) measurement of blood pressure, pulse, and oximetry; (3) assessment of visual acuity (SIMAV, Padova, Italy); and (4) nonmydriatic color imaging (Canon CX-1 45° 15.1 megapixel camera; Canon Corp., Tokyo, Japan). Images were assessed for signs of diabetic retinopathy and graded for quality on a scale of 1 to 5 by two clinicians. Kappa coefficient was calculated to determine inter-observer agreement.
Results:
One hundred four of 106 (98%) children underwent imaging (mean age: 11.1 years, 51% male, 88% white). One (1%) child had nonproliferative diabetic retinopathy and 2 (1.9%) had incidental findings. Only 62% of children had an eye examination within the past year, with children with DM1 for more than 5 years significantly more likely to have done so (P = .03). Children who had an eye examination within the past year were significantly older than their counterparts (P = .01). Images of high quality (grades 4 and 5) were acquired in 178 (86%) eyes, and images of some clinical value (grades ≥ 2) were obtained in 207 (99.5%) eyes. Inter-observer agreement for image quality was 0.896.
Conclusions:
The feasibility of using a nonmydriatic camera to screen children as young as 2 years for changes related to diabetic eye disease was demonstrated. Nonmydriatic imaging may supplement standard dilated clinical ophthalmology examinations for select patient populations.
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