Abstract
BackgroundMyopic maculopathy (MM) is one of the major causes of visual impairment and irreversible blindness in eyes with pathologic myopia (PM). However, the classification of each type of lesion associated with MM has not been determined. Recently, a new MM classification system, known as the ATN grading and classification system, was proposed; it is based on the fundus photographs and optical coherence tomography (OCT) images and includes three variable components: atrophy (A), traction (T), and neovascularization (N). This study aimed to perform an independent evaluation of interobserver and intraobserver agreement for the recently developed ATN grading system for MM.MethodsThis was a retrospective study. Fundus photographs and OCT images of 125 patients (226 eyes) with various MMs were evaluated and classified using the ATN grading of the new MM classification system by four blinded and independent evaluators (2 attending ophthalmologists and 2 ophthalmic residents). All cases were randomly re-evaluated by the same observers after an interval of 6 weeks. The kappa coefficient (κ) and 95% confidence interval (CI) were used to determine the interobserver and intraobserver agreement.ResultsThe interobserver agreement was substantial when considering the maculopathy type (A, T, and N). The weighted Fleiss κ values for each MM type (A, T, and N) were 0.651 (95% CI: 0.602–0.700), 0.734 (95% CI: 0.689–0.779), and 0.702 (95% CI: 0.649–0.755), respectively. The interobserver agreement when considering the subtypes was good or excellent, except for stages A1, A2, and N1, in which the weighted κ value was less than 0.6, with moderate agreement. The intraobserver agreement of types and subtypes was excellent, with κ > 0.8. No significant differences were observed between the attending ophthalmologists and residents for interobserver reliability or intraobserver reproducibility.ConclusionsThe ATN classification allows an adequate agreement among ophthalmologists with different qualifications and by the same observer on separate occasions. Future prospective studies should further evaluate whether this classification can be better implemented in clinical decision-making and disease progression assessments.
Highlights
Myopic maculopathy (MM) is one of the major causes of visual impairment and irreversible blindness in eyes with pathologic myopia (PM)
Myopia has been one of the global public health problems leading to visual impairment and blinding complications, especially in East Asia [1]
MM is clinically important, the classification of each type of lesion associated with MM has not been determined, and the current classification systems for MM cannot entirely explain the various changes that occur in the patient’s macula
Summary
Myopic maculopathy (MM) is one of the major causes of visual impairment and irreversible blindness in eyes with pathologic myopia (PM). Myopic maculopathy (MM) is one of the major causes of visual impairment and irreversible blindness in eyes with PM and is predicted to impact approximately 55.7 million people and up to 18.5 million people worldwide in 2050, respectively [6, 7]. The META-PM classification of MM established by the International Pathologic Myopia Study Group in 2015 is currently still accepted worldwide; it is just based on color fundus photography [8], and other myopic macular lesions, such as myopic traction maculopathy (MTM) and dome shaped macula (DSM) were not included in this classification system [9, 10]. Fundus images may look different due to the different background pigmentations of ethnic groups and the use of different examinations, which could affect a reliable diagnosis of fundus lesions
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