Developing new automated alternation flicker using optic disc photography for the detection of glaucoma progression

PurposeTo evaluate a progression-detecting algorithm for a new automated matched alternation flicker (AMAF) in glaucoma patients.MethodsOpen-angle glaucoma patients with a baseline mean deviation of visual field (VF) test>−6 dB were included in this longitudinal and retrospective study. Functional progression was detected by two VF progression criteria and structural progression by both AMAF and conventional comparison methods using optic disc and retinal nerve fiber layer (RNFL) photography. Progression-detecting performances of AMAF and the conventional method were evaluated by an agreement between functional and structural progression criteria. RNFL thickness changes measured by optical coherence tomography (OCT) were compared between progressing and stable eyes determined by each method.ResultsAmong 103 eyes, 47 (45.6%), 21 (20.4%), and 32 (31.1%) eyes were evaluated as glaucoma progression using AMAF, the conventional method, and guided progression analysis (GPA) of the VF test, respectively. The AMAF showed better agreement than the conventional method, using GPA of the VF test (κ=0.337; P<0.001 and κ=0.124; P=0.191, respectively). The rates of RNFL thickness decay using OCT were significantly different between the progressing and stable eyes when progression was determined by AMAF (−3.49±2.86 μm per year vs −1.83±3.22 μm per year; P=0.007) but not by the conventional method (−3.24±2.42 μm per year vs −2.42±3.33 μm per year; P=0.290).ConclusionsThe AMAF was better than the conventional comparison method in discriminating structural changes during glaucoma progression, and showed a moderate agreement with functional progression criteria.

[1]  B. Bengtsson,et al.  FLICKER COMPARISON OF FUNDUS PHOTOGRAPHS , 1979, Acta ophthalmologica.

[2]  E. E. Hartmann,et al.  The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. , 2002, Archives of ophthalmology.

[3]  F. Medeiros,et al.  Rates of Retinal Nerve Fiber Layer Loss in Contralateral Eyes of Glaucoma Patients with Unilateral Progression by Conventional Methods. , 2015, Ophthalmology.

[4]  R. Harwerth,et al.  Linking structure and function in glaucoma , 2010, Progress in Retinal and Eye Research.

[5]  R. Ritch,et al.  Comparison of stereo disc photographs and alternation flicker using a novel matching technology for detecting glaucoma progression. , 2010, Ophthalmic surgery, lasers & imaging : the official journal of the International Society for Imaging in the Eye.

[6]  J. R. Landis,et al.  The measurement of observer agreement for categorical data. , 1977, Biometrics.

[7]  G. Holmström,et al.  Macular thickness assessed with spectral domain OCT in a population‐based study of children: normative data, repeatability and reproducibility and comparison with time domain OCT , 2015, Acta ophthalmologica.

[8]  Robert N Weinreb,et al.  Retinal nerve fiber layer imaging with spectral-domain optical coherence tomography: patterns of retinal nerve fiber layer progression. , 2012, Ophthalmology.

[9]  R. Ritch,et al.  Automated alternation flicker for the detection of optic disc haemorrhages , 2012, Acta ophthalmologica.

[10]  A Heijl,et al.  Early Manifest Glaucoma Trial: design and baseline data. , 1999, Ophthalmology.

[11]  W. Swanson,et al.  ‘Structure–function relationship’ in glaucoma: past thinking and current concepts , 2012, Clinical & experimental ophthalmology.

[12]  Luc Van Gool,et al.  SURF: Speeded Up Robust Features , 2006, ECCV.

[13]  A. Ambrosi,et al.  Retinal nerve fiber layer thickness reproducibility using seven different OCT instruments. , 2012, Investigative ophthalmology & visual science.

[14]  Robert N Weinreb,et al.  Evaluation of retinal nerve fiber layer progression in glaucoma: a comparison between spectral-domain and time-domain optical coherence tomography. , 2011, Ophthalmology.

[15]  R. Ritch,et al.  Detection of progressive glaucomatous optic neuropathy using automated alternation flicker with stereophotography. , 2011, Archives of ophthalmology.

[16]  Luc Van Gool,et al.  Speeded-Up Robust Features (SURF) , 2008, Comput. Vis. Image Underst..

[17]  J. Moreno-Montañés,et al.  Agreement among spectral-domain optical coherence tomography, standard automated perimetry, and stereophotography in the detection of glaucoma progression. , 2015, Investigative ophthalmology & visual science.

[18]  Agreement of New Automated Matched Alternation Flicker using Undilated Fundus Photography for the Detection of Glaucomatous Structural Change , 2017, Current eye research.

[19]  Douglas R. Anderson,et al.  Clinical Decisions In Glaucoma , 1993 .

[20]  F. Medeiros,et al.  Agreement for detecting glaucoma progression with the GDx guided progression analysis, automated perimetry, and optic disc photography. , 2010, Ophthalmology.

[21]  B. Bengtsson,et al.  Diagnosis of early glaucoma with flicker comparisons of serial disc photographs. , 1989, Investigative ophthalmology & visual science.

[22]  J. Ehrlich,et al.  Agreement of flicker chronoscopy for structural glaucomatous progression detection and factors associated with progression. , 2013, American journal of ophthalmology.

[23]  M. Cymbor,et al.  Concordance of flicker comparison versus side-by-side comparison in glaucoma. , 2009, Optometry.

[24]  J W Berger,et al.  Computerized stereochronoscopy and alternation flicker to detect optic nerve head contour change. , 2000, Ophthalmology.

[25]  R S Harwerth,et al.  Ganglion cell losses underlying visual field defects from experimental glaucoma. , 1999, Investigative ophthalmology & visual science.

[26]  B. Vanderbeek,et al.  Comparing the detection and agreement of parapapillary atrophy progression using digital optic disk photographs and alternation flicker , 2010, Graefe's Archive for Clinical and Experimental Ophthalmology.

[27]  Brenda W Gillespie,et al.  Visual field progression in the Collaborative Initial Glaucoma Treatment Study the impact of treatment and other baseline factors. , 2009, Ophthalmology.