Determinants of agreement between the confocal scanning laser tomograph and standardized assessment of glaucomatous progression
- PMID: 20557941
- PMCID: PMC2941775
- DOI: 10.1016/j.ophtha.2010.02.002
Determinants of agreement between the confocal scanning laser tomograph and standardized assessment of glaucomatous progression
Abstract
Purpose: To estimate the agreement of confocal scanning laser tomograph (CSLT), topographic change analysis (TCA) with assessment of stereophotographs, and standard automated perimetry (SAP) for detecting glaucomatous progression and to identify factors associated with agreement between methods.
Design: Observational cohort study.
Participants: We included 246 eyes of 167 glaucoma patients, glaucoma suspects, and ocular hypertensives.
Methods: We included CSLT series (n ≥ 4 tests; mean follow-up, 4 years), stereophotographs, and SAP results in the analysis. The number of progressors by guided progression analysis (GPA, "likely progression"), progressors by masked stereophotographs assessment and progressors by TCA as determined for 3 parameters related to the number of progressed superpixels within the disc margin was determined. Agreement between progression by each TCA parameter, stereophotographs and GPA was assessed using the Kappa test. Analysis of variance with post hoc analysis was applied to identify baseline factors including image quality (standard deviation of the mean topography), disc size and disease severity (pattern standard deviation [PSD] and cup area) associated with agreement/nonagreement between methods.
Main outcome measures: Agreement in assessing glaucomatous progression between the methods including factors associated with agreement/nonagreement between methods.
Results: Agreement between progression by TCA and progression by stereophotographs and/or GPA was generally poor regardless of the TCA parameter and specificity cutoffs applied. For the parameters with the strongest agreement, cluster size in disc (CSIZE(disc)) and cluster area in disc (CAREA(disc)), kappa values were 0.16 (63.9%, agreement on 134 nonprogressing eyes and 23 progressing eyes) and 0.15 (64.1%, agreement on 135 nonprogressing eyes and 22 progressing eyes) at 99% cutoff. Most of the factors evaluated were not significantly associated with agreement/nonagreement between methods (all P > 0.07). However, SAP PSD was greater in the progressors by stereophotography only group compared with the progressors by TCA only group (5.8 ± 4.7 and 2.6 ± 2.2, respectively [P = 0.003] for CSIZE(disc) at 95% specificity and 5.4 ± 4.6 and 2.5 ± 2.3, respectively [P = 0.002] for CAREA(disc) at 99% specificity).
Conclusions: Agreement for detection of longitudinal changes between TCA, stereophotography, and SAP GPA is poor. Progressors by stereophotography only tended to have more advanced disease at baseline than progressors by TCA only.
Copyright © 2010 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.
Figures



Similar articles
-
Performance of confocal scanning laser tomograph Topographic Change Analysis (TCA) for assessing glaucomatous progression.Invest Ophthalmol Vis Sci. 2009 Feb;50(2):691-701. doi: 10.1167/iovs.08-2136. Epub 2008 Oct 3. Invest Ophthalmol Vis Sci. 2009. PMID: 18836168 Free PMC article.
-
Agreement for detecting glaucoma progression with the GDx guided progression analysis, automated perimetry, and optic disc photography.Ophthalmology. 2010 Mar;117(3):462-70. doi: 10.1016/j.ophtha.2009.08.012. Epub 2009 Dec 24. Ophthalmology. 2010. PMID: 20036010 Free PMC article.
-
Clinicians agreement in establishing glaucomatous progression using the Heidelberg retina tomograph.Ophthalmology. 2009 Jan;116(1):14-24. doi: 10.1016/j.ophtha.2008.08.030. Epub 2008 Nov 17. Ophthalmology. 2009. PMID: 19010552 Free PMC article.
-
Imaging technologies for assessing neuroprotection in glaucomatous optic neuropathy.Eur J Ophthalmol. 1999 Jan-Mar;9 Suppl 1:S40-3. doi: 10.1177/112067219900901S14. Eur J Ophthalmol. 1999. PMID: 10230606 Review.
-
Assessment of the optic disc in glaucoma.J Glaucoma. 2001 Oct;10(5 Suppl 1):S59-61. doi: 10.1097/00061198-200110001-00021. J Glaucoma. 2001. PMID: 11890279 Review. No abstract available.
Cited by
-
Predictive value of retrobulbar blood flow velocities in glaucoma suspects.Invest Ophthalmol Vis Sci. 2012 Jun 22;53(7):3875-84. doi: 10.1167/iovs.11-8817. Invest Ophthalmol Vis Sci. 2012. PMID: 22589447 Free PMC article.
-
In vivo imaging methods to assess glaucomatous optic neuropathy.Exp Eye Res. 2015 Dec;141:139-53. doi: 10.1016/j.exer.2015.06.001. Epub 2015 Jun 3. Exp Eye Res. 2015. PMID: 26048475 Free PMC article. Review.
-
Comparison of Glaucoma Progression Detection by Optical Coherence Tomography and Visual Field.Am J Ophthalmol. 2017 Dec;184:63-74. doi: 10.1016/j.ajo.2017.09.020. Epub 2017 Sep 28. Am J Ophthalmol. 2017. PMID: 28964806 Free PMC article.
-
Optic nerve head morphology and visual field function in patients with AIDS and without infectious retinitis.Ocul Immunol Inflamm. 2012 Oct;20(5):342-8. doi: 10.3109/09273948.2012.694552. Epub 2012 Jun 14. Ocul Immunol Inflamm. 2012. PMID: 22697270 Free PMC article. Clinical Trial.
-
Frequency of Agreement Between Structural and Functional Glaucoma Testing: A Longitudinal Study of 3D OCT and Current Clinical Tests.Am J Ophthalmol. 2024 Oct;266:196-205. doi: 10.1016/j.ajo.2024.05.018. Epub 2024 May 27. Am J Ophthalmol. 2024. PMID: 38810864
References
-
- Tuulonen A, Airaksinen PJ. Initial glaucomatous optic disk and retinal nerve fiber layer abnormalities and their progression. Am J Ophthalmol. 1991;111:485–490. - PubMed
-
- Sommer A, Katz J, Quigley HA, et al. Clinically detectable nerve fiber atrophy precedes the onset of glaucomatous field loss. Arch Ophthalmol. 1991;109:77–83. - PubMed
-
- Heijl A, Leske MC, Bengtsson B, et al. Early Manifest Glaucoma Trial Group. Reduction of intraocular pressure and glaucoma progression: results from the Early Manifest Glaucoma Trial. Arch Ophthalmol. 2002;120:1268–1279. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous