Variation associated with measurement of retinal vessel diameters at different points in the pulse cycle

Background/aims: To assess the variability in retinal vessel measurements at different points in the pulse cycle. Methods: A healthy white male aged 19 years had 30 digitised images taken at three distinct points in the pulse cycle over a one hour period. A pulse synchronised ear clip trigger device...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:British journal of ophthalmology 2004-01, Vol.88 (1), p.57-61
Hauptverfasser: Knudtson, M D, Klein, B E K, Klein, R, Wong, T Y, Hubbard, L D, Lee, K E, Meuer, S M, Bulla, C P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 61
container_issue 1
container_start_page 57
container_title British journal of ophthalmology
container_volume 88
creator Knudtson, M D
Klein, B E K
Klein, R
Wong, T Y
Hubbard, L D
Lee, K E
Meuer, S M
Bulla, C P
description Background/aims: To assess the variability in retinal vessel measurements at different points in the pulse cycle. Methods: A healthy white male aged 19 years had 30 digitised images taken at three distinct points in the pulse cycle over a one hour period. A pulse synchronised ear clip trigger device was used to capture images at the desired point in the pulse cycle. Two trained graders measured the retinal vessel diameter of one large arteriole, one large venule, one small arteriole, and one small venule 10 times in each of these 30 images. Results: Within an image, variability was similar between graders, pulse point, and vessel type. Across images taken at the same point in the pulse period, the change from the minimum to maximum measurement was between 6% and 17% for arterioles and between 2% and 11% for venules. In addition, measurements of small vessels had greater changes than large vessels and no point in the pulse period was more variable than another. Ignoring pulse cycle increased variability across images in the large venule, but not in the other vessel types. Mixed effect models were fit for each of the vessel types to determine the greatest source of variability. Controlling for pulse point and grader, the largest source of variability for all four vessels measured was across images, accounting for more than 50% of the total variability. Conclusion: Measurements of large retinal venules is generally less variable than measurements of other retinal vessels. After controlling for pulse point and grader, the largest source of variation is across images. Understanding the components of variability in measuring retinal vessels is important as these techniques are applied in epidemiological studies.
doi_str_mv 10.1136/bjo.88.1.57
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1771926</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A112801479</galeid><sourcerecordid>A112801479</sourcerecordid><originalsourceid>FETCH-LOGICAL-b581t-861d4ccb63ad19a3b8fb69513660ecdc7b766f2cae9076441e9b0aa25b33dbcb3</originalsourceid><addsrcrecordid>eNp9ksuP0zAQhyMEYsvCiTuyhOCCUuw4sZ0L0lKeUgGJR6-W7Uxal8QutrOw_z2uWm0BrZAP9ni--c1DUxQPCZ4TQtlzvfVzIeZk3vBbxYzUTJQV5u3tYoYx5iUhjJwV92LcZrNihN8tzjLUUs7rWbFZqWBVst4hFaM3-Q0d-mnTBo2g4hRgBJeQ71GAZJ0a0CXECAPqrBohQYhIpWz0PYQ9uPPWpYisQ2kDaDcNEZC5MgPcL-70KlsPjvd58e3N66-Ld-Xy09v3i4tlqRtBUikY6WpjNKOqI62iWvSatU3uk2EwneGaM9ZXRkGLOatrAq3GSlWNprTTRtPz4sVBdzfpETqTiwpqkLtgRxWupFdW_u1xdiPX_lISzklbsSzw9CgQ_I8JYpKjjQaGQTnwU5QC4zw8LDL4-B9w66eQRxT3WqLFlAieqfJArdUA0rre56xmDQ5ycu-gt_n7gpBKYFLzNvPzG_h8OhituTHg2SHABB9jgP66V4LlfkFkXhAphCSy2Zfz6M_xnNjjRmTgyRFQ0aihD8oZG09cU1NeE3rqy8YEv679KnyXjFPeyI-rhWzo5w-rL6-W8uVprHrc_rfC39Gy4PY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1778903187</pqid></control><display><type>article</type><title>Variation associated with measurement of retinal vessel diameters at different points in the pulse cycle</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Knudtson, M D ; Klein, B E K ; Klein, R ; Wong, T Y ; Hubbard, L D ; Lee, K E ; Meuer, S M ; Bulla, C P</creator><creatorcontrib>Knudtson, M D ; Klein, B E K ; Klein, R ; Wong, T Y ; Hubbard, L D ; Lee, K E ; Meuer, S M ; Bulla, C P</creatorcontrib><description>Background/aims: To assess the variability in retinal vessel measurements at different points in the pulse cycle. Methods: A healthy white male aged 19 years had 30 digitised images taken at three distinct points in the pulse cycle over a one hour period. A pulse synchronised ear clip trigger device was used to capture images at the desired point in the pulse cycle. Two trained graders measured the retinal vessel diameter of one large arteriole, one large venule, one small arteriole, and one small venule 10 times in each of these 30 images. Results: Within an image, variability was similar between graders, pulse point, and vessel type. Across images taken at the same point in the pulse period, the change from the minimum to maximum measurement was between 6% and 17% for arterioles and between 2% and 11% for venules. In addition, measurements of small vessels had greater changes than large vessels and no point in the pulse period was more variable than another. Ignoring pulse cycle increased variability across images in the large venule, but not in the other vessel types. Mixed effect models were fit for each of the vessel types to determine the greatest source of variability. Controlling for pulse point and grader, the largest source of variability for all four vessels measured was across images, accounting for more than 50% of the total variability. Conclusion: Measurements of large retinal venules is generally less variable than measurements of other retinal vessels. After controlling for pulse point and grader, the largest source of variation is across images. Understanding the components of variability in measuring retinal vessels is important as these techniques are applied in epidemiological studies.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjo.88.1.57</identifier><identifier>PMID: 14693774</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Adult ; Arterioles - anatomy &amp; histology ; Arterioles - physiology ; Bias ; Biological and medical sciences ; Blood pressure ; Cardiovascular disease ; Clinical Science - Scientific Reports ; Diabetes ; Diagnostic Techniques, Ophthalmological ; Humans ; Hypertension ; Image Processing, Computer-Assisted - methods ; Male ; Measurement techniques ; Medical sciences ; Ophthalmology ; Photography ; Pulse ; pulse cycle ; Reproducibility of Results ; Retina ; retinal vessel diameters ; Retinal Vessels - anatomy &amp; histology ; Retinal Vessels - physiology ; Retinopathies ; Studies ; variation ; Venules - anatomy &amp; histology ; Venules - physiology ; Womens health</subject><ispartof>British journal of ophthalmology, 2004-01, Vol.88 (1), p.57-61</ispartof><rights>Copyright 2004 British Journal of Ophthalmology</rights><rights>2004 INIST-CNRS</rights><rights>COPYRIGHT 2004 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2004 Copyright 2004 British Journal of Ophthalmology</rights><rights>Copyright © Copyright 2004 British Journal of Ophthalmology 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b581t-861d4ccb63ad19a3b8fb69513660ecdc7b766f2cae9076441e9b0aa25b33dbcb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1771926/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1771926/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15437413$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14693774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Knudtson, M D</creatorcontrib><creatorcontrib>Klein, B E K</creatorcontrib><creatorcontrib>Klein, R</creatorcontrib><creatorcontrib>Wong, T Y</creatorcontrib><creatorcontrib>Hubbard, L D</creatorcontrib><creatorcontrib>Lee, K E</creatorcontrib><creatorcontrib>Meuer, S M</creatorcontrib><creatorcontrib>Bulla, C P</creatorcontrib><title>Variation associated with measurement of retinal vessel diameters at different points in the pulse cycle</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><description>Background/aims: To assess the variability in retinal vessel measurements at different points in the pulse cycle. Methods: A healthy white male aged 19 years had 30 digitised images taken at three distinct points in the pulse cycle over a one hour period. A pulse synchronised ear clip trigger device was used to capture images at the desired point in the pulse cycle. Two trained graders measured the retinal vessel diameter of one large arteriole, one large venule, one small arteriole, and one small venule 10 times in each of these 30 images. Results: Within an image, variability was similar between graders, pulse point, and vessel type. Across images taken at the same point in the pulse period, the change from the minimum to maximum measurement was between 6% and 17% for arterioles and between 2% and 11% for venules. In addition, measurements of small vessels had greater changes than large vessels and no point in the pulse period was more variable than another. Ignoring pulse cycle increased variability across images in the large venule, but not in the other vessel types. Mixed effect models were fit for each of the vessel types to determine the greatest source of variability. Controlling for pulse point and grader, the largest source of variability for all four vessels measured was across images, accounting for more than 50% of the total variability. Conclusion: Measurements of large retinal venules is generally less variable than measurements of other retinal vessels. After controlling for pulse point and grader, the largest source of variation is across images. Understanding the components of variability in measuring retinal vessels is important as these techniques are applied in epidemiological studies.</description><subject>Adult</subject><subject>Arterioles - anatomy &amp; histology</subject><subject>Arterioles - physiology</subject><subject>Bias</subject><subject>Biological and medical sciences</subject><subject>Blood pressure</subject><subject>Cardiovascular disease</subject><subject>Clinical Science - Scientific Reports</subject><subject>Diabetes</subject><subject>Diagnostic Techniques, Ophthalmological</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Male</subject><subject>Measurement techniques</subject><subject>Medical sciences</subject><subject>Ophthalmology</subject><subject>Photography</subject><subject>Pulse</subject><subject>pulse cycle</subject><subject>Reproducibility of Results</subject><subject>Retina</subject><subject>retinal vessel diameters</subject><subject>Retinal Vessels - anatomy &amp; histology</subject><subject>Retinal Vessels - physiology</subject><subject>Retinopathies</subject><subject>Studies</subject><subject>variation</subject><subject>Venules - anatomy &amp; histology</subject><subject>Venules - physiology</subject><subject>Womens health</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9ksuP0zAQhyMEYsvCiTuyhOCCUuw4sZ0L0lKeUgGJR6-W7Uxal8QutrOw_z2uWm0BrZAP9ni--c1DUxQPCZ4TQtlzvfVzIeZk3vBbxYzUTJQV5u3tYoYx5iUhjJwV92LcZrNihN8tzjLUUs7rWbFZqWBVst4hFaM3-Q0d-mnTBo2g4hRgBJeQ71GAZJ0a0CXECAPqrBohQYhIpWz0PYQ9uPPWpYisQ2kDaDcNEZC5MgPcL-70KlsPjvd58e3N66-Ld-Xy09v3i4tlqRtBUikY6WpjNKOqI62iWvSatU3uk2EwneGaM9ZXRkGLOatrAq3GSlWNprTTRtPz4sVBdzfpETqTiwpqkLtgRxWupFdW_u1xdiPX_lISzklbsSzw9CgQ_I8JYpKjjQaGQTnwU5QC4zw8LDL4-B9w66eQRxT3WqLFlAieqfJArdUA0rre56xmDQ5ycu-gt_n7gpBKYFLzNvPzG_h8OhituTHg2SHABB9jgP66V4LlfkFkXhAphCSy2Zfz6M_xnNjjRmTgyRFQ0aihD8oZG09cU1NeE3rqy8YEv679KnyXjFPeyI-rhWzo5w-rL6-W8uVprHrc_rfC39Gy4PY</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Knudtson, M D</creator><creator>Klein, B E K</creator><creator>Klein, R</creator><creator>Wong, T Y</creator><creator>Hubbard, L D</creator><creator>Lee, K E</creator><creator>Meuer, S M</creator><creator>Bulla, C P</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>Copyright 2004 British Journal of Ophthalmology</general><scope>BSCLL</scope><scope>IQODW</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200401</creationdate><title>Variation associated with measurement of retinal vessel diameters at different points in the pulse cycle</title><author>Knudtson, M D ; Klein, B E K ; Klein, R ; Wong, T Y ; Hubbard, L D ; Lee, K E ; Meuer, S M ; Bulla, C P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b581t-861d4ccb63ad19a3b8fb69513660ecdc7b766f2cae9076441e9b0aa25b33dbcb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Arterioles - anatomy &amp; histology</topic><topic>Arterioles - physiology</topic><topic>Bias</topic><topic>Biological and medical sciences</topic><topic>Blood pressure</topic><topic>Cardiovascular disease</topic><topic>Clinical Science - Scientific Reports</topic><topic>Diabetes</topic><topic>Diagnostic Techniques, Ophthalmological</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Male</topic><topic>Measurement techniques</topic><topic>Medical sciences</topic><topic>Ophthalmology</topic><topic>Photography</topic><topic>Pulse</topic><topic>pulse cycle</topic><topic>Reproducibility of Results</topic><topic>Retina</topic><topic>retinal vessel diameters</topic><topic>Retinal Vessels - anatomy &amp; histology</topic><topic>Retinal Vessels - physiology</topic><topic>Retinopathies</topic><topic>Studies</topic><topic>variation</topic><topic>Venules - anatomy &amp; histology</topic><topic>Venules - physiology</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Knudtson, M D</creatorcontrib><creatorcontrib>Klein, B E K</creatorcontrib><creatorcontrib>Klein, R</creatorcontrib><creatorcontrib>Wong, T Y</creatorcontrib><creatorcontrib>Hubbard, L D</creatorcontrib><creatorcontrib>Lee, K E</creatorcontrib><creatorcontrib>Meuer, S M</creatorcontrib><creatorcontrib>Bulla, C P</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Knudtson, M D</au><au>Klein, B E K</au><au>Klein, R</au><au>Wong, T Y</au><au>Hubbard, L D</au><au>Lee, K E</au><au>Meuer, S M</au><au>Bulla, C P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Variation associated with measurement of retinal vessel diameters at different points in the pulse cycle</atitle><jtitle>British journal of ophthalmology</jtitle><addtitle>Br J Ophthalmol</addtitle><date>2004-01</date><risdate>2004</risdate><volume>88</volume><issue>1</issue><spage>57</spage><epage>61</epage><pages>57-61</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><coden>BJOPAL</coden><abstract>Background/aims: To assess the variability in retinal vessel measurements at different points in the pulse cycle. Methods: A healthy white male aged 19 years had 30 digitised images taken at three distinct points in the pulse cycle over a one hour period. A pulse synchronised ear clip trigger device was used to capture images at the desired point in the pulse cycle. Two trained graders measured the retinal vessel diameter of one large arteriole, one large venule, one small arteriole, and one small venule 10 times in each of these 30 images. Results: Within an image, variability was similar between graders, pulse point, and vessel type. Across images taken at the same point in the pulse period, the change from the minimum to maximum measurement was between 6% and 17% for arterioles and between 2% and 11% for venules. In addition, measurements of small vessels had greater changes than large vessels and no point in the pulse period was more variable than another. Ignoring pulse cycle increased variability across images in the large venule, but not in the other vessel types. Mixed effect models were fit for each of the vessel types to determine the greatest source of variability. Controlling for pulse point and grader, the largest source of variability for all four vessels measured was across images, accounting for more than 50% of the total variability. Conclusion: Measurements of large retinal venules is generally less variable than measurements of other retinal vessels. After controlling for pulse point and grader, the largest source of variation is across images. Understanding the components of variability in measuring retinal vessels is important as these techniques are applied in epidemiological studies.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>14693774</pmid><doi>10.1136/bjo.88.1.57</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0007-1161
ispartof British journal of ophthalmology, 2004-01, Vol.88 (1), p.57-61
issn 0007-1161
1468-2079
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1771926
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection
subjects Adult
Arterioles - anatomy & histology
Arterioles - physiology
Bias
Biological and medical sciences
Blood pressure
Cardiovascular disease
Clinical Science - Scientific Reports
Diabetes
Diagnostic Techniques, Ophthalmological
Humans
Hypertension
Image Processing, Computer-Assisted - methods
Male
Measurement techniques
Medical sciences
Ophthalmology
Photography
Pulse
pulse cycle
Reproducibility of Results
Retina
retinal vessel diameters
Retinal Vessels - anatomy & histology
Retinal Vessels - physiology
Retinopathies
Studies
variation
Venules - anatomy & histology
Venules - physiology
Womens health
title Variation associated with measurement of retinal vessel diameters at different points in the pulse cycle
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A50%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Variation%20associated%20with%20measurement%20of%20retinal%20vessel%20diameters%20at%20different%20points%20in%20the%20pulse%20cycle&rft.jtitle=British%20journal%20of%20ophthalmology&rft.au=Knudtson,%20M%20D&rft.date=2004-01&rft.volume=88&rft.issue=1&rft.spage=57&rft.epage=61&rft.pages=57-61&rft.issn=0007-1161&rft.eissn=1468-2079&rft.coden=BJOPAL&rft_id=info:doi/10.1136/bjo.88.1.57&rft_dat=%3Cgale_pubme%3EA112801479%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1778903187&rft_id=info:pmid/14693774&rft_galeid=A112801479&rfr_iscdi=true