Background/aims To assess accuracy of telemedical retinopathy of prematurity (ROP) diagnosis by trained non-expert graders compared with expert graders.
Methods Eye examinations (n=248) from 67 consecutive infants were captured using wide-angle retinal photography (RetCam-II, Clarity Medical Systems, Pleasanton, California, USA). Non-expert graders attended two 1-h training sessions on image-based ROP diagnosis. Using a web-based telemedicine system, 14 non-expert and three expert graders provided a diagnosis for each eye: no ROP, mild ROP, type 2 pre-threshold ROP or treatment-requiring ROP. All diagnoses were compared with a reference standard of dilated indirect ophthalmoscopy by an experienced paediatric ophthalmologist.
Results For detection of type 2 or worse ROP, the mean (range) sensitivities and specificities were 0.95 (0.94–0.97) and 0.93 (0.91–0.96) for experts, 0.87 (0.71–0.97) and 0.73 (0.39–0.95) for resident non-experts, and 0.73 (0.41–0.88) and 0.91 (0.84–0.96) for student non-experts, respectively. For detection of treatment-requiring ROP, the mean (range) sensitivities and specificities were 1.00 (1.00–1.00) and 0.93 (0.88–0.96) for experts, 0.88 (0.50–1.00) and 0.84 (0.71–0.98) for resident non-experts, and 0.82 (0.42–1.00) and 0.92 (0.83–0.97) for student non-experts, respectively.
Conclusions Mean sensitivity and specificity of trained non-experts were lower than that of experts, although several non-experts had high accuracy. Development of methods for training non-expert graders may help support telemedical ROP evaluation.
- Child health (paediatrics), diagnostic tests/investigation
- medical informatics
- paediatric ophthalmology
- retinopathy of prematurity
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Funding This study was supported by the Starr Foundation, New York (SLW), the Doris Duke Charitable Foundation, New York (SLW), a Career Development Award from Research to Prevent Blindness, New York (MFC) and grant EY13972 from the National Institutes of Health, Bethesda, MD (MFC). MFC is an unpaid member of the Scientific Advisory Board for Clarity Medical Systems (Pleasanton, California, USA). The authors have no commercial, proprietary, or financial interest in any of the products or companies described in this article.
Competing interests MFC is an unpaid member of the Scientific Advisory Board for Clarity Medical Systems (Pleasanton, California, USA). The authors have no commercial, proprietary, or financial interest in any of the products or companies described in this article.
Ethics approval This study was approved by the Institutional Review Board at Columbia University Medical Center, and included waiver of consent for use of de-identified retinal images.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
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