In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods Study
Retinal sensitivity is frequently listed as an end point in clinical trials, often with long working practices. The purpose of this methods study was to provide a new workflow and reduced test time for in-depth characterization of retinal sensitivity. A workflow for the MP3-S microperimeter with det...
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Veröffentlicht in: | Translational vision science & technology 2024-04, Vol.13 (4), p.14-14 |
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description | Retinal sensitivity is frequently listed as an end point in clinical trials, often with long working practices. The purpose of this methods study was to provide a new workflow and reduced test time for in-depth characterization of retinal sensitivity.
A workflow for the MP3-S microperimeter with detailed functional characterization of the retina under photopic, mesopic, and scotopic conditions was evaluated. Grids of 32 and 28 test positions for photopic/mesopic and scotopic, respectively, were tested in 12 healthy individuals and compared with an established 68-point grid for test time, mean sensitivity (MS), and bivariate contour ellipse area (BCEA).
The mean test time (range; ±SD) was 10.5 minutes (8.4-14.9; ±2.0) in the 68-point grid and 4.3 minutes (3.8-5.0; ±0.4) in the 32-point grid, which was significantly different (P < 0.0001). The mean of difference in test time (±SD; 95% confidence interval) was 6.1 minutes (±2.0; 4.6-7.6). MS and BCEA were significantly correlated between grids (r = 0.89 and 0.74; P = 0.0005 and 0.014, respectively). Mean test time of subjects who underwent the full protocol (n = 4) was 2.15 hours.
The protocol suggested herein appears highly feasible with in-depth characterization of retinal function under different testing conditions and in a short test time.
The protocol described herein allows for characterization of the retina under different testing conditions and in a short test time, which is relevant due to its potential for patient prognostication and follow-up in clinical settings and also given its increasing role as a clinical trial end point. |
doi_str_mv | 10.1167/tvst.13.4.14 |
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A workflow for the MP3-S microperimeter with detailed functional characterization of the retina under photopic, mesopic, and scotopic conditions was evaluated. Grids of 32 and 28 test positions for photopic/mesopic and scotopic, respectively, were tested in 12 healthy individuals and compared with an established 68-point grid for test time, mean sensitivity (MS), and bivariate contour ellipse area (BCEA).
The mean test time (range; ±SD) was 10.5 minutes (8.4-14.9; ±2.0) in the 68-point grid and 4.3 minutes (3.8-5.0; ±0.4) in the 32-point grid, which was significantly different (P < 0.0001). The mean of difference in test time (±SD; 95% confidence interval) was 6.1 minutes (±2.0; 4.6-7.6). MS and BCEA were significantly correlated between grids (r = 0.89 and 0.74; P = 0.0005 and 0.014, respectively). Mean test time of subjects who underwent the full protocol (n = 4) was 2.15 hours.
The protocol suggested herein appears highly feasible with in-depth characterization of retinal function under different testing conditions and in a short test time.
The protocol described herein allows for characterization of the retina under different testing conditions and in a short test time, which is relevant due to its potential for patient prognostication and follow-up in clinical settings and also given its increasing role as a clinical trial end point.</description><identifier>ISSN: 2164-2591</identifier><identifier>EISSN: 2164-2591</identifier><identifier>DOI: 10.1167/tvst.13.4.14</identifier><identifier>PMID: 38591946</identifier><language>eng</language><publisher>United States: The Association for Research in Vision and Ophthalmology</publisher><subject>Clinical Trials as Topic ; Endpoint Determination ; Humans ; Methods ; Retina - physiology ; Workflow</subject><ispartof>Translational vision science & technology, 2024-04, Vol.13 (4), p.14-14</ispartof><rights>Copyright 2024 The Authors 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c342t-5444cc73aa8d1530bef20a153a559cf9d36759c6f6b2a88c7893bcebadf8f9423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11008759/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11008759/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38591946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Guimaraes, Thales A C</creatorcontrib><creatorcontrib>de Guimaraes, Isabela M C</creatorcontrib><creatorcontrib>Ali, Naser</creatorcontrib><creatorcontrib>Kalitzeos, Angelos</creatorcontrib><creatorcontrib>Michaelides, Michel</creatorcontrib><title>In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods Study</title><title>Translational vision science & technology</title><addtitle>Transl Vis Sci Technol</addtitle><description>Retinal sensitivity is frequently listed as an end point in clinical trials, often with long working practices. The purpose of this methods study was to provide a new workflow and reduced test time for in-depth characterization of retinal sensitivity.
A workflow for the MP3-S microperimeter with detailed functional characterization of the retina under photopic, mesopic, and scotopic conditions was evaluated. Grids of 32 and 28 test positions for photopic/mesopic and scotopic, respectively, were tested in 12 healthy individuals and compared with an established 68-point grid for test time, mean sensitivity (MS), and bivariate contour ellipse area (BCEA).
The mean test time (range; ±SD) was 10.5 minutes (8.4-14.9; ±2.0) in the 68-point grid and 4.3 minutes (3.8-5.0; ±0.4) in the 32-point grid, which was significantly different (P < 0.0001). The mean of difference in test time (±SD; 95% confidence interval) was 6.1 minutes (±2.0; 4.6-7.6). MS and BCEA were significantly correlated between grids (r = 0.89 and 0.74; P = 0.0005 and 0.014, respectively). Mean test time of subjects who underwent the full protocol (n = 4) was 2.15 hours.
The protocol suggested herein appears highly feasible with in-depth characterization of retinal function under different testing conditions and in a short test time.
The protocol described herein allows for characterization of the retina under different testing conditions and in a short test time, which is relevant due to its potential for patient prognostication and follow-up in clinical settings and also given its increasing role as a clinical trial end point.</description><subject>Clinical Trials as Topic</subject><subject>Endpoint Determination</subject><subject>Humans</subject><subject>Methods</subject><subject>Retina - physiology</subject><subject>Workflow</subject><issn>2164-2591</issn><issn>2164-2591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUctOwzAQtBCIVqU3zshHDqTYsfPigqryqtQKRIs4cLAcZ0OM0iTEbqX8Pa5aUNnLjnZHs7MahM4pGVEaRtd2Y-yIshEfUX6E-j4NuecHCT0-wD00NOaLuArjgPPwFPVY7OYJD_voY1p5d9DYAr-C1ZUs8QIqo63eaNvhsTFgzAoqi9-149gC8PyF4WXXAF7guVZt3UCrV2ChvcFjPAdb1JnBC7vOujN0ksvSwHDfB-jt4X45efJmz4_TyXjmKcZ96zlPXKmISRlnNGAkhdwn0iEZBInKk4yFkQNhHqa-jGMVxQlLFaQyy-M84T4boNudbrNOV5ApZ7eVpWicL9l2opZa_N9UuhCf9UZQSkjstJ3C5V6hrb_XYKxYaaOgLGUF9doIRlhAIh6w7bGrHdW9bkwL-d8dSsQ2E7HNRFAmuKDc0S8Ovf2RfxNgPxYFiSo</recordid><startdate>20240409</startdate><enddate>20240409</enddate><creator>de Guimaraes, Thales A C</creator><creator>de Guimaraes, Isabela M C</creator><creator>Ali, Naser</creator><creator>Kalitzeos, Angelos</creator><creator>Michaelides, Michel</creator><general>The Association for Research in Vision and Ophthalmology</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><scope>5PM</scope></search><sort><creationdate>20240409</creationdate><title>In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods Study</title><author>de Guimaraes, Thales A C ; de Guimaraes, Isabela M C ; Ali, Naser ; Kalitzeos, Angelos ; Michaelides, Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-5444cc73aa8d1530bef20a153a559cf9d36759c6f6b2a88c7893bcebadf8f9423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Clinical Trials as Topic</topic><topic>Endpoint Determination</topic><topic>Humans</topic><topic>Methods</topic><topic>Retina - physiology</topic><topic>Workflow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Guimaraes, Thales A C</creatorcontrib><creatorcontrib>de Guimaraes, Isabela M C</creatorcontrib><creatorcontrib>Ali, Naser</creatorcontrib><creatorcontrib>Kalitzeos, Angelos</creatorcontrib><creatorcontrib>Michaelides, Michel</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Translational vision science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Guimaraes, Thales A C</au><au>de Guimaraes, Isabela M C</au><au>Ali, Naser</au><au>Kalitzeos, Angelos</au><au>Michaelides, Michel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods Study</atitle><jtitle>Translational vision science & technology</jtitle><addtitle>Transl Vis Sci Technol</addtitle><date>2024-04-09</date><risdate>2024</risdate><volume>13</volume><issue>4</issue><spage>14</spage><epage>14</epage><pages>14-14</pages><issn>2164-2591</issn><eissn>2164-2591</eissn><abstract>Retinal sensitivity is frequently listed as an end point in clinical trials, often with long working practices. The purpose of this methods study was to provide a new workflow and reduced test time for in-depth characterization of retinal sensitivity.
A workflow for the MP3-S microperimeter with detailed functional characterization of the retina under photopic, mesopic, and scotopic conditions was evaluated. Grids of 32 and 28 test positions for photopic/mesopic and scotopic, respectively, were tested in 12 healthy individuals and compared with an established 68-point grid for test time, mean sensitivity (MS), and bivariate contour ellipse area (BCEA).
The mean test time (range; ±SD) was 10.5 minutes (8.4-14.9; ±2.0) in the 68-point grid and 4.3 minutes (3.8-5.0; ±0.4) in the 32-point grid, which was significantly different (P < 0.0001). The mean of difference in test time (±SD; 95% confidence interval) was 6.1 minutes (±2.0; 4.6-7.6). MS and BCEA were significantly correlated between grids (r = 0.89 and 0.74; P = 0.0005 and 0.014, respectively). Mean test time of subjects who underwent the full protocol (n = 4) was 2.15 hours.
The protocol suggested herein appears highly feasible with in-depth characterization of retinal function under different testing conditions and in a short test time.
The protocol described herein allows for characterization of the retina under different testing conditions and in a short test time, which is relevant due to its potential for patient prognostication and follow-up in clinical settings and also given its increasing role as a clinical trial end point.</abstract><cop>United States</cop><pub>The Association for Research in Vision and Ophthalmology</pub><pmid>38591946</pmid><doi>10.1167/tvst.13.4.14</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Clinical Trials as Topic Endpoint Determination Humans Methods Retina - physiology Workflow |
title | In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods Study |
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