July 2018
Volume 59, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2018
A Novel Classification of High Myopia into Anterior and Posterior Pathologic Subtypes
Author Affiliations & Notes
  • Cassie Ann Ludwig
    Byers Eye Institute, Stanford University, Palo Alto, California, United States
  • Ryan A Shields
    Byers Eye Institute, Stanford University, Palo Alto, California, United States
  • Tiffany Ann Chen
    Byers Eye Institute, Stanford University, Palo Alto, California, United States
  • Matthew A Powers
    Byers Eye Institute, Stanford University, Palo Alto, California, United States
  • Darius M. Moshfeghi
    Byers Eye Institute, Stanford University, Palo Alto, California, United States
  • Footnotes
    Commercial Relationships   Cassie Ludwig, None; Ryan Shields, None; Tiffany Chen, None; Matthew Powers, None; Darius Moshfeghi, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2018, Vol.59, 3371. doi:
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      Cassie Ann Ludwig, Ryan A Shields, Tiffany Ann Chen, Matthew A Powers, Darius M. Moshfeghi; A Novel Classification of High Myopia into Anterior and Posterior Pathologic Subtypes. Invest. Ophthalmol. Vis. Sci. 2018;59(9):3371.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : High myopia and pathologic myopia are common causes of visual morbidity. Myopic pathology can affect all regions of the retina, though there is currently no classification system to distinguish anterior (peripheral) and posterior (macular) pathology. We hypothesize that these classifications are characterized by distinct demographic and refractive features, highlighting the disparity in types of pathologic myopia.

Methods : The Stanford University Medical Center Clinical Data Warehouse was used to identify patients with high myopia by ICD-9 and ICD-10 codes. Predetermined ICD diagnoses were then used to classify patients with high myopia into isolated high myopia (IHM), anterior pathologic myopia (APM), posterior pathologic myopia (PPM), and combined pathologic myopia (CPM). A cohort of this population was then manually reviewed to gather refractive data and confirm the accuracy of ICD coding.

Results : 3,274 patients were identified with high myopia. Overall, 22.1% individuals met criteria for APM, 10.7% for PPM, 17.0% for CPM and 50.2% for IHM. We identified a significantly higher frequency of females with PPM compared to APM (62.3% vs. 48.3%; OR, 1.73; 95% CI, 1.34 to 2.25), Asian patients with PPM as compared to APM (42.9% vs. 33.3%; OR, 1.50; 95% CI, 1.16 to 1.95), and younger patients with APM compared to PPM (median 45.3 vs 63.4 years). The refractive error was significantly more myopic in the CPM (median -9.8D; IQR -13.5, -6.8) and PPM (median -10.5D; IQR -16.6, -6.8) subgroups as compared to the APM (median -8.1D; IQR -10.4, -6.9) and IHM (median -8.2D; -10.4, -6.3) subgroups (p = 0.003).

Conclusions : High myopia may be divided into four distinct subgroups based on presence and location of pathology, which is associated with differences in age, gender, race, and refractive error.

This is an abstract that was submitted for the 2018 ARVO Annual Meeting, held in Honolulu, Hawaii, April 29 - May 3, 2018.

 

FIGURE 1. Classification of High Myopia into Isolated, Anterior Pathologic, Posterior Pathologic and Combined Pathologic Subtypes. A retrospective chart review was performed on a subsample of patients in the full cohort to assess the consistency of diagnoses and to compare refractive error between the subgroups.

FIGURE 1. Classification of High Myopia into Isolated, Anterior Pathologic, Posterior Pathologic and Combined Pathologic Subtypes. A retrospective chart review was performed on a subsample of patients in the full cohort to assess the consistency of diagnoses and to compare refractive error between the subgroups.

 

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