ETDRS Chart - Type: Chart 2 Series: 2000 Series Distance: 2M
Product information
- Quantity Unit Each
- Product Code 2137
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Description
The ETDRS Chart, or Early Treatment Diabetic Retinopathy Study Chart, is a highly specialized tool designed for precise measurement of visual acuity. Widely recognized in clinical trials and ophthalmic examinations, it serves as a gold standard, particularly beneficial for patients with diabetic retinopathy and other eye conditions.
Design and Layout
- Sloan Letters: Each line of the chart comprises five Sloan letters, chosen for their consistent difficulty. These letters are arranged to prevent the formation of words or acronyms, ensuring unbiased results.
- Geometric Progression: The chart features a geometric progression in letter size, known as logMAR, from line to line. This design includes standardized spacing between letters and rows, typically across 14 lines.
Material and Dimensions
- Size: Approximately 64.8 cm wide by 62.2 cm high.
- Material: Constructed from non-reflective, white polystyrene, providing high-contrast optotypes.
- Illumination Compatibility: Designed for use with trans-illuminated or retro-illuminated cabinets, offering uniform background luminance.
Testing Protocol
- Distance: Standard testing is conducted at 4 meters, with protocols for reduced distances for low vision patients.
- Letter Sizes: Ranges from 58.18 mm to 2.92 mm in height, corresponding to Snellen visual acuity fractions from 20/200 to 20/10.
Scoring System
- Visual Acuity Score (VAS): Scoring is based on letter count or logMAR, with each letter contributing 0.02 log units.
- Reproducibility: Allows for consistent, quantitative results across different sites and subjects, easily convertible to Snellen notation.
Versions and Formats
- Multiple Versions: Includes variations like Chart R, Chart 1, and Chart 2 to prevent memorization and accommodate different testing needs.
- Formats: Available in printed, backlit, and computerized formats.
Clinical Relevance
The ETDRS Chart is essential for best-corrected visual acuity (BCVA) measurement, required by regulatory bodies such as the FDA for clinical trial assessments. Its design, based on the Bailey-Lovie principles, enables detection of clinically significant changes in visual acuity, making it invaluable for vision studies worldwide.