Flicker defined form, standard perimetry and Heidelberg retinal tomography: Structure-function relationships
Abstract Objective To compare flicker defined form (FDF) perimetry using the Heidelberg edge perimeter (HEP) with standard automated perimetry (SAP) on the Humphrey visual field (HVF) analyzer and to compare their relationship to structural measurements acquired with the Heidelberg retina tomograph....
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Veröffentlicht in: | Canadian journal of ophthalmology 2015-08, Vol.50 (4), p.290-296 |
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creator | Ichhpujani, Parul, MD Lo, David C., MD, MBA Cvintal, Victor, MD Waisbourd, Michael, MD Averbuch, Adam, BS Leiby, Benjamin E., PhD Myers, Jonathan S., MD Spaeth, George L., MD Katz, L. Jay, MD |
description | Abstract Objective To compare flicker defined form (FDF) perimetry using the Heidelberg edge perimeter (HEP) with standard automated perimetry (SAP) on the Humphrey visual field (HVF) analyzer and to compare their relationship to structural measurements acquired with the Heidelberg retina tomograph. Design Prospective, observational study. Participants Thirty-one glaucomatous eyes with varying severity and 13 normal control eyes were included in this analysis. Methods All subjects underwent FDF testing on the HEP using the 24-2 protocol by the adaptive staircase thresholding algorithm standard strategy and SAP on the HVF analyzer 750 II using the SITA-Standard 24-2 test. Heidelberg retina tomography (HRT) testing was obtained for each patient. Spearman correlation coefficient, mean deviation (MD), and pattern standard deviation measurements by both machines were compared. Results FDF and SAP MD were significantly correlated ( r = 0.81, p < 0.001). FDF and SAP MD were significantly correlated with HRT cup/disc ratio (FDF MD: p < 0.001; SAP MD: p = 0.003), disc area (FDF MD: p = 0.005; SAP MD: p = 0.059), rim volume (FDF MD: p < 0.001; SAP MD: p < 0.001), and retinal nerve fibre layer (FDF MD: p < 0.001; SAP MD: p < 0.001). Conclusions This pilot study shows that the MD parameter of FDF correlated with SAP results. FDF and SAP had significant correlations with HRT parameters in glaucomatous and healthy eyes. The potential utility of FDF in the clinical management of glaucoma requires further investigation. |
doi_str_mv | 10.1016/j.jcjo.2015.05.010 |
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Jay, MD</creator><creatorcontrib>Ichhpujani, Parul, MD ; Lo, David C., MD, MBA ; Cvintal, Victor, MD ; Waisbourd, Michael, MD ; Averbuch, Adam, BS ; Leiby, Benjamin E., PhD ; Myers, Jonathan S., MD ; Spaeth, George L., MD ; Katz, L. Jay, MD</creatorcontrib><description><![CDATA[Abstract Objective To compare flicker defined form (FDF) perimetry using the Heidelberg edge perimeter (HEP) with standard automated perimetry (SAP) on the Humphrey visual field (HVF) analyzer and to compare their relationship to structural measurements acquired with the Heidelberg retina tomograph. Design Prospective, observational study. Participants Thirty-one glaucomatous eyes with varying severity and 13 normal control eyes were included in this analysis. Methods All subjects underwent FDF testing on the HEP using the 24-2 protocol by the adaptive staircase thresholding algorithm standard strategy and SAP on the HVF analyzer 750 II using the SITA-Standard 24-2 test. Heidelberg retina tomography (HRT) testing was obtained for each patient. Spearman correlation coefficient, mean deviation (MD), and pattern standard deviation measurements by both machines were compared. Results FDF and SAP MD were significantly correlated ( r = 0.81, p < 0.001). FDF and SAP MD were significantly correlated with HRT cup/disc ratio (FDF MD: p < 0.001; SAP MD: p = 0.003), disc area (FDF MD: p = 0.005; SAP MD: p = 0.059), rim volume (FDF MD: p < 0.001; SAP MD: p < 0.001), and retinal nerve fibre layer (FDF MD: p < 0.001; SAP MD: p < 0.001). Conclusions This pilot study shows that the MD parameter of FDF correlated with SAP results. FDF and SAP had significant correlations with HRT parameters in glaucomatous and healthy eyes. The potential utility of FDF in the clinical management of glaucoma requires further investigation.]]></description><identifier>ISSN: 0008-4182</identifier><identifier>EISSN: 1715-3360</identifier><identifier>DOI: 10.1016/j.jcjo.2015.05.010</identifier><identifier>PMID: 26257223</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Adult ; Aged ; Algorithms ; Area Under Curve ; Axons - pathology ; Female ; Glaucoma - classification ; Glaucoma - diagnosis ; Humans ; Internal Medicine ; Male ; Middle Aged ; Ophthalmology ; Optic Disk - pathology ; Optic Nerve Diseases - diagnosis ; Pilot Projects ; Prospective Studies ; Retinal Ganglion Cells - pathology ; Tomography ; Visual Field Tests - methods ; Visual Fields - physiology</subject><ispartof>Canadian journal of ophthalmology, 2015-08, Vol.50 (4), p.290-296</ispartof><rights>Canadian Ophthalmological Society</rights><rights>2015 Canadian Ophthalmological Society</rights><rights>Copyright © 2015 Canadian Ophthalmological Society. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-55894e6e0197e9c041911ebd831124516c981b77095164a26410021ecbc6fe9c3</citedby><cites>FETCH-LOGICAL-c411t-55894e6e0197e9c041911ebd831124516c981b77095164a26410021ecbc6fe9c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jcjo.2015.05.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26257223$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ichhpujani, Parul, MD</creatorcontrib><creatorcontrib>Lo, David C., MD, MBA</creatorcontrib><creatorcontrib>Cvintal, Victor, MD</creatorcontrib><creatorcontrib>Waisbourd, Michael, MD</creatorcontrib><creatorcontrib>Averbuch, Adam, BS</creatorcontrib><creatorcontrib>Leiby, Benjamin E., PhD</creatorcontrib><creatorcontrib>Myers, Jonathan S., MD</creatorcontrib><creatorcontrib>Spaeth, George L., MD</creatorcontrib><creatorcontrib>Katz, L. Jay, MD</creatorcontrib><title>Flicker defined form, standard perimetry and Heidelberg retinal tomography: Structure-function relationships</title><title>Canadian journal of ophthalmology</title><addtitle>Can J Ophthalmol</addtitle><description><![CDATA[Abstract Objective To compare flicker defined form (FDF) perimetry using the Heidelberg edge perimeter (HEP) with standard automated perimetry (SAP) on the Humphrey visual field (HVF) analyzer and to compare their relationship to structural measurements acquired with the Heidelberg retina tomograph. Design Prospective, observational study. Participants Thirty-one glaucomatous eyes with varying severity and 13 normal control eyes were included in this analysis. Methods All subjects underwent FDF testing on the HEP using the 24-2 protocol by the adaptive staircase thresholding algorithm standard strategy and SAP on the HVF analyzer 750 II using the SITA-Standard 24-2 test. Heidelberg retina tomography (HRT) testing was obtained for each patient. Spearman correlation coefficient, mean deviation (MD), and pattern standard deviation measurements by both machines were compared. Results FDF and SAP MD were significantly correlated ( r = 0.81, p < 0.001). FDF and SAP MD were significantly correlated with HRT cup/disc ratio (FDF MD: p < 0.001; SAP MD: p = 0.003), disc area (FDF MD: p = 0.005; SAP MD: p = 0.059), rim volume (FDF MD: p < 0.001; SAP MD: p < 0.001), and retinal nerve fibre layer (FDF MD: p < 0.001; SAP MD: p < 0.001). Conclusions This pilot study shows that the MD parameter of FDF correlated with SAP results. FDF and SAP had significant correlations with HRT parameters in glaucomatous and healthy eyes. The potential utility of FDF in the clinical management of glaucoma requires further investigation.]]></description><subject>Adult</subject><subject>Aged</subject><subject>Algorithms</subject><subject>Area Under Curve</subject><subject>Axons - pathology</subject><subject>Female</subject><subject>Glaucoma - classification</subject><subject>Glaucoma - diagnosis</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Ophthalmology</subject><subject>Optic Disk - pathology</subject><subject>Optic Nerve Diseases - diagnosis</subject><subject>Pilot Projects</subject><subject>Prospective Studies</subject><subject>Retinal Ganglion Cells - pathology</subject><subject>Tomography</subject><subject>Visual Field Tests - methods</subject><subject>Visual Fields - physiology</subject><issn>0008-4182</issn><issn>1715-3360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9rFTEUxYNY7LP6BVzILF04r_cm81ekIMVaodBF6zpkMnfaTDOTMckI79ub4VUXLoQLuYRzDpzfZewdwh4Bq_NxP-rR7TlguYc0CC_YDmsscyEqeMl2ANDkBTb8lL0OYQQQoi6qV-yUV7ysORc7Zq-s0U_ks54GM1OfDc5PH7MQ1dwr32cLeTNR9IcsfWTXZHqyHfmHzFM0s7JZdJN78Gp5PHzK7qJfdVw95cM662jcnGRWbUt4NEt4w04GZQO9fX7P2I-rr_eX1_nN7bfvl19ucl0gxrwsm7agigDbmloNBbaI1PWNQORFiZVuG-zqGtq0F4pXBQJwJN3pakgGccY-HHMX736uFKKcTNBkrZrJrUFiDYKLthFNkvKjVHsXgqdBLqmw8geJIDfKcpQbZblRlpAGIZneP-ev3UT9X8sfrEnw-Sig1PKXIS-DNjRr6o0nHWXvzP_zL_6xa2tmo5V9ogOF0a0-oU89ZOAS5N125-3MWCYOAirxG_qwo0E</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Ichhpujani, Parul, MD</creator><creator>Lo, David C., MD, MBA</creator><creator>Cvintal, Victor, MD</creator><creator>Waisbourd, Michael, MD</creator><creator>Averbuch, Adam, BS</creator><creator>Leiby, Benjamin E., PhD</creator><creator>Myers, Jonathan S., MD</creator><creator>Spaeth, George L., MD</creator><creator>Katz, L. Jay, MD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150801</creationdate><title>Flicker defined form, standard perimetry and Heidelberg retinal tomography: Structure-function relationships</title><author>Ichhpujani, Parul, MD ; Lo, David C., MD, MBA ; Cvintal, Victor, MD ; Waisbourd, Michael, MD ; Averbuch, Adam, BS ; Leiby, Benjamin E., PhD ; Myers, Jonathan S., MD ; Spaeth, George L., MD ; Katz, L. Jay, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-55894e6e0197e9c041911ebd831124516c981b77095164a26410021ecbc6fe9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Algorithms</topic><topic>Area Under Curve</topic><topic>Axons - pathology</topic><topic>Female</topic><topic>Glaucoma - classification</topic><topic>Glaucoma - diagnosis</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Ophthalmology</topic><topic>Optic Disk - pathology</topic><topic>Optic Nerve Diseases - diagnosis</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>Retinal Ganglion Cells - pathology</topic><topic>Tomography</topic><topic>Visual Field Tests - methods</topic><topic>Visual Fields - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ichhpujani, Parul, MD</creatorcontrib><creatorcontrib>Lo, David C., MD, MBA</creatorcontrib><creatorcontrib>Cvintal, Victor, MD</creatorcontrib><creatorcontrib>Waisbourd, Michael, MD</creatorcontrib><creatorcontrib>Averbuch, Adam, BS</creatorcontrib><creatorcontrib>Leiby, Benjamin E., PhD</creatorcontrib><creatorcontrib>Myers, Jonathan S., MD</creatorcontrib><creatorcontrib>Spaeth, George L., MD</creatorcontrib><creatorcontrib>Katz, L. Jay, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Canadian journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ichhpujani, Parul, MD</au><au>Lo, David C., MD, MBA</au><au>Cvintal, Victor, MD</au><au>Waisbourd, Michael, MD</au><au>Averbuch, Adam, BS</au><au>Leiby, Benjamin E., PhD</au><au>Myers, Jonathan S., MD</au><au>Spaeth, George L., MD</au><au>Katz, L. Jay, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flicker defined form, standard perimetry and Heidelberg retinal tomography: Structure-function relationships</atitle><jtitle>Canadian journal of ophthalmology</jtitle><addtitle>Can J Ophthalmol</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>50</volume><issue>4</issue><spage>290</spage><epage>296</epage><pages>290-296</pages><issn>0008-4182</issn><eissn>1715-3360</eissn><abstract><![CDATA[Abstract Objective To compare flicker defined form (FDF) perimetry using the Heidelberg edge perimeter (HEP) with standard automated perimetry (SAP) on the Humphrey visual field (HVF) analyzer and to compare their relationship to structural measurements acquired with the Heidelberg retina tomograph. Design Prospective, observational study. Participants Thirty-one glaucomatous eyes with varying severity and 13 normal control eyes were included in this analysis. Methods All subjects underwent FDF testing on the HEP using the 24-2 protocol by the adaptive staircase thresholding algorithm standard strategy and SAP on the HVF analyzer 750 II using the SITA-Standard 24-2 test. Heidelberg retina tomography (HRT) testing was obtained for each patient. Spearman correlation coefficient, mean deviation (MD), and pattern standard deviation measurements by both machines were compared. Results FDF and SAP MD were significantly correlated ( r = 0.81, p < 0.001). FDF and SAP MD were significantly correlated with HRT cup/disc ratio (FDF MD: p < 0.001; SAP MD: p = 0.003), disc area (FDF MD: p = 0.005; SAP MD: p = 0.059), rim volume (FDF MD: p < 0.001; SAP MD: p < 0.001), and retinal nerve fibre layer (FDF MD: p < 0.001; SAP MD: p < 0.001). Conclusions This pilot study shows that the MD parameter of FDF correlated with SAP results. FDF and SAP had significant correlations with HRT parameters in glaucomatous and healthy eyes. The potential utility of FDF in the clinical management of glaucoma requires further investigation.]]></abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>26257223</pmid><doi>10.1016/j.jcjo.2015.05.010</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Algorithms Area Under Curve Axons - pathology Female Glaucoma - classification Glaucoma - diagnosis Humans Internal Medicine Male Middle Aged Ophthalmology Optic Disk - pathology Optic Nerve Diseases - diagnosis Pilot Projects Prospective Studies Retinal Ganglion Cells - pathology Tomography Visual Field Tests - methods Visual Fields - physiology |
title | Flicker defined form, standard perimetry and Heidelberg retinal tomography: Structure-function relationships |
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