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Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter

BACKGROUND: Scotopic function is an important marker of many retinal diseases and is increasingly used as an outcome measure in clinical trials, such as those investigating gene therapy for Lebers congenital amaurosis. Scotopic visual function has traditionally been measured using an adapted perimet...

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Autores principales: Crossland, Michael D, Luong, Vy A, Rubin, Gary S, Fitzke, Fred W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042987/
https://www.ncbi.nlm.nih.gov/pubmed/21303544
http://dx.doi.org/10.1186/1471-2415-11-5
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author Crossland, Michael D
Luong, Vy A
Rubin, Gary S
Fitzke, Fred W
author_facet Crossland, Michael D
Luong, Vy A
Rubin, Gary S
Fitzke, Fred W
author_sort Crossland, Michael D
collection PubMed
description BACKGROUND: Scotopic function is an important marker of many retinal diseases and is increasingly used as an outcome measure in clinical trials, such as those investigating gene therapy for Lebers congenital amaurosis. Scotopic visual function has traditionally been measured using an adapted perimetry system such as the Humphrey field analyser (HFA). However this system does not control for fixation errors or poor fixation stability. Here we evaluate the use of an adapted microperimeter to measure visual function at defined retinal regions under scotopic conditions. METHODS: A MP-1 microperimeter (Nidek Technologies, Italy) was modified by adding a 1 log unit Neutral Density filter and a 530nm shortpass filter within the optical path of the instrument. Stray light was shielded. Fine matrix mapping perimetry was performed on five younger (<35 years) and five older (>65 years) subjects with no eye disease and good vision. All subjects were fully dark adapted before testing and pupils were dilated with 1% tropicamide. Tests was performed once on the modified MP-1 microperimeter and once using a modified HFA, in a counterbalanced order. RESULTS: A foveal scotopic scotoma with a sensitivity reduction of >1 log unit was found using each instrument. In addition, the MP-1 system showed the retinal location of the foveal scotoma. Mean test time was 25 minutes for the MP-1 and 32 minutes for the HFA. DISCUSSION: A modified MP-1 microperimeter can be used to measure scotopic retinal function, creating results which are comparable to the modified Humphrey field analyser. Advantages of the MP-1 system include the ability to track the retina through testing, retinal localisation of the scotoma and a faster test time.
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spelling pubmed-30429872011-02-23 Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter Crossland, Michael D Luong, Vy A Rubin, Gary S Fitzke, Fred W BMC Ophthalmol Technical Advance BACKGROUND: Scotopic function is an important marker of many retinal diseases and is increasingly used as an outcome measure in clinical trials, such as those investigating gene therapy for Lebers congenital amaurosis. Scotopic visual function has traditionally been measured using an adapted perimetry system such as the Humphrey field analyser (HFA). However this system does not control for fixation errors or poor fixation stability. Here we evaluate the use of an adapted microperimeter to measure visual function at defined retinal regions under scotopic conditions. METHODS: A MP-1 microperimeter (Nidek Technologies, Italy) was modified by adding a 1 log unit Neutral Density filter and a 530nm shortpass filter within the optical path of the instrument. Stray light was shielded. Fine matrix mapping perimetry was performed on five younger (<35 years) and five older (>65 years) subjects with no eye disease and good vision. All subjects were fully dark adapted before testing and pupils were dilated with 1% tropicamide. Tests was performed once on the modified MP-1 microperimeter and once using a modified HFA, in a counterbalanced order. RESULTS: A foveal scotopic scotoma with a sensitivity reduction of >1 log unit was found using each instrument. In addition, the MP-1 system showed the retinal location of the foveal scotoma. Mean test time was 25 minutes for the MP-1 and 32 minutes for the HFA. DISCUSSION: A modified MP-1 microperimeter can be used to measure scotopic retinal function, creating results which are comparable to the modified Humphrey field analyser. Advantages of the MP-1 system include the ability to track the retina through testing, retinal localisation of the scotoma and a faster test time. BioMed Central 2011-02-08 /pmc/articles/PMC3042987/ /pubmed/21303544 http://dx.doi.org/10.1186/1471-2415-11-5 Text en Copyright ©2011 Crossland et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Advance
Crossland, Michael D
Luong, Vy A
Rubin, Gary S
Fitzke, Fred W
Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
title Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
title_full Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
title_fullStr Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
title_full_unstemmed Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
title_short Retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
title_sort retinal specific measurement of dark-adapted visual function: validation of a modified microperimeter
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042987/
https://www.ncbi.nlm.nih.gov/pubmed/21303544
http://dx.doi.org/10.1186/1471-2415-11-5
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