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Article: Assessment of rates of structural change in glaucoma using imaging technologies

TitleAssessment of rates of structural change in glaucoma using imaging technologies
Authors
Keywordsrate of change
optical coherence tomography
glaucoma
scanning laser polarimetry
confocal scanning laser ophthalmoscopy
imaging technology
Issue Date2011
Citation
Eye, 2011, v. 25, n. 3, p. 269-277 How to Cite?
AbstractPurpose To review the ability of current imaging technologies to provide estimates of rates of structural change in glaucoma patients.Patients and methodsReview of literature.ResultsImaging technologies, such as confocal scanning laser ophthalmoscopy (CSLO), scanning laser polarimetry (SLP), and optical coherence tomography (OCT), provide quantifiable and reproducible measurements of the optic disc and parapapillary retinal nerve fibre layer (RNFL). Rates of change as quantified by the rim area (RA) (for CSLO) and RNFL thickness (for SLP and OCT) are related to glaucoma progression as detected by conventional methods (eg, visual fields and optic disc photography). Evidence shows that rates of RNFL and RA loss are significantly faster in progressing compared with non-progressing glaucoma patients.ConclusionMeasurements of rates of optic disc and RNFL change are becoming increasingly precise and individualized. Currently available imaging technologies have the ability to detect and quantify progression in glaucoma, and their measurements may be suitable end points in glaucoma clinical trials. © 2011 Macmillan Publishers Limited All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/298519
ISSN
2023 Impact Factor: 2.8
2023 SCImago Journal Rankings: 1.373
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMansouri, K.-
dc.contributor.authorLeite, M. T.-
dc.contributor.authorMedeiros, F. A.-
dc.contributor.authorLeung, C. K.-
dc.contributor.authorWeinreb, R. N.-
dc.date.accessioned2021-04-08T03:08:41Z-
dc.date.available2021-04-08T03:08:41Z-
dc.date.issued2011-
dc.identifier.citationEye, 2011, v. 25, n. 3, p. 269-277-
dc.identifier.issn0950-222X-
dc.identifier.urihttp://hdl.handle.net/10722/298519-
dc.description.abstractPurpose To review the ability of current imaging technologies to provide estimates of rates of structural change in glaucoma patients.Patients and methodsReview of literature.ResultsImaging technologies, such as confocal scanning laser ophthalmoscopy (CSLO), scanning laser polarimetry (SLP), and optical coherence tomography (OCT), provide quantifiable and reproducible measurements of the optic disc and parapapillary retinal nerve fibre layer (RNFL). Rates of change as quantified by the rim area (RA) (for CSLO) and RNFL thickness (for SLP and OCT) are related to glaucoma progression as detected by conventional methods (eg, visual fields and optic disc photography). Evidence shows that rates of RNFL and RA loss are significantly faster in progressing compared with non-progressing glaucoma patients.ConclusionMeasurements of rates of optic disc and RNFL change are becoming increasingly precise and individualized. Currently available imaging technologies have the ability to detect and quantify progression in glaucoma, and their measurements may be suitable end points in glaucoma clinical trials. © 2011 Macmillan Publishers Limited All rights reserved.-
dc.languageeng-
dc.relation.ispartofEye-
dc.subjectrate of change-
dc.subjectoptical coherence tomography-
dc.subjectglaucoma-
dc.subjectscanning laser polarimetry-
dc.subjectconfocal scanning laser ophthalmoscopy-
dc.subjectimaging technology-
dc.titleAssessment of rates of structural change in glaucoma using imaging technologies-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1038/eye.2010.202-
dc.identifier.pmid21212798-
dc.identifier.pmcidPMC3178322-
dc.identifier.scopuseid_2-s2.0-79952596593-
dc.identifier.volume25-
dc.identifier.issue3-
dc.identifier.spage269-
dc.identifier.epage277-
dc.identifier.eissn1476-5454-
dc.identifier.isiWOS:000288240500002-
dc.identifier.issnl0950-222X-

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