The Use of Microperimetry to Detect Functional Progression in Non-Neovascular Age-Related Macular Degeneration: A

Evan N Wong1,2, Avenell L Chew1, William H Morgan1,3

  • 1Centre for Ophthalmology and Visual Science (Lions Eye Instiute), University of Western Australia.

Insights

Microperimetry effectively detects disease progression in non-neovascular age-related macular degeneration (AMD). Retinal sensitivity measurement via microperimetry shows promise, though standardized protocols are needed for wider clinical use.

Area of Science:

  • Ophthalmology
  • Retinal Imaging
  • Visual Function Assessment

Background:

  • Non-neovascular age-related macular degeneration (AMD) requires sensitive tools for monitoring disease progression.
  • Current methods for assessing AMD progression have limitations in detecting early functional changes.

Purpose of the Study:

  • To review the literature on microperimetry's ability to detect progression in non-neovascular AMD.
  • To compare microperimetry with other functional and structural measures for AMD progression detection.

Main Methods:

  • Literature search across multiple databases (MEDLINE, EMBASE, Cochrane Library, etc.) up to January 2016.
  • Inclusion of 6 studies involving 41 eyes with intermediate AMD and 80 eyes with geographic atrophy (GA).
  • Index test: retinal sensitivity by microperimetry; Comparators: visual acuities, fixation stability, retinal/choroidal thickness, GA area.

Main Results:

  • Retinal sensitivity measured by microperimetry consistently detected progression across cohorts.
  • Microperimetry demonstrated higher sensitivity than other functional measures for non-neovascular AMD progression.
  • Insufficient data precluded meta-analysis; analysis methods require further development.

Conclusions:

  • Microperimetry is a sensitive tool for detecting progression in non-neovascular AMD.
  • Standardization of testing protocols and progression analysis methods is crucial for clinical implementation.
  • Further research is needed to refine microperimetry analysis for AMD monitoring.

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