Baseline factors predicting the risk of conversion from ocular hypertension to primary open-angle glaucoma during a 10-year follow-up
Purpose To evaluate the ability of baseline clinical, morphological, and functional factors to predict the conversion to primary open-angle glaucoma (POAG) in ocular hypertensive (OHT) patients. Methods This single-center prospective longitudinal observational study included 116 eyes of 116 OHT pati...
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description | Purpose
To evaluate the ability of baseline clinical, morphological, and functional factors to predict the conversion to primary open-angle glaucoma (POAG) in ocular hypertensive (OHT) patients.
Methods
This single-center prospective longitudinal observational study included 116 eyes of 116 OHT patients followed for a 10-year period. All patients had intraocular pressure (IOP) ≥24 mm Hg in one eye and >21 mm Hg in the other eye, normal visual fields (VFs) and normal optic disc (OD) appearance in both eyes at baseline. All OHT patients were untreated at baseline with subsequent treatment upon need according to clinical judgement. Only one eye per subject was randomly selected. Patient age, gender, IOP, central corneal thickness (CCT), and ibopamine test results were collected at baseline. All patients underwent standard automated perimetry, short-wavelength automated perimetry (SWAP), frequency-doubling technology, confocal scanning laser ophthalmoscopy (CSLO), and scanning laser polarimetry (SLP) at baseline and every 6 months thereafter. Main outcome measure was the conversion to POAG, defined as the development of reproducible VF and/or OD abnormalities attributable to glaucoma. Cox proportional hazards models were used to identify the baseline factors predictive of POAG conversion.
Results
During the 10-year follow-up, 25% of eyes converted to POAG. In multivariate Cox models, baseline factors that were significant predictors of POAG development included: older age (hazard ratio (HR) 1.0, 99% confidence intervals (CIs) 1.0–1.2, per 1 year older); SWAP Glaucoma Hemifield test ‘outside normal limits’ (HR 4.3, 99% CIs 1.2–17.9); greater SLP ‘Inter-eye Symmetry’ (HR 1.1, 99% CIs 0.4–3.0, per 1 unit lower); lower CSLO Rim Volume (HR 1.1, 99% CIs 0.3–3.2, per 0.1 mm
3
lower); and greater CSLO cup-to-disc ratio (HR 6.0, 99% CIs 3.6–16.8, per 0.1 unit greater).
Conclusions
The baseline parameters that proved to be useful in assessing the likelihood of an OHT patient to develop POAG included age, functional variables provided by SWAP, and structural variables provided by SLP and CSLO. In this cohort of patients, baseline IOP, CCT, and ibopamine provocative test results were not significant predictors of POAG conversion. |
doi_str_mv | 10.1038/eye.2016.86 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4906466</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4082451841</sourcerecordid><originalsourceid>FETCH-LOGICAL-c516t-a89bb4465053f3a8052d4c65502924f4b7547e5941ff00dcb04e72361ead68473</originalsourceid><addsrcrecordid>eNptkU2L1TAUhoMoznV05V4CbgTtNUnz1Y2gg18w4EbBXUjTk3s7pklN2pH7A_zftt7rMIqrLN7nPDnJi9BjSraU1PolHGDLCJVbLe-gDeVKVoILfhdtSCNIxRj7eoYelHJFyBIqch-dMUUVrzXdoJ9vbIHQR8DeuinlgscMXe-mPu7wtAec-_INJ49diteQS58i9jkNOLk52Iz3hxHyBPF3MKVluh9sPuA0Qqxs3AXAu2BnlwaLuzmvVospqQ6wDPsUQvpRzeNDdM_bUODR6TxHX969_Xzxobr89P7jxevLygkqp8rqpm05l4KI2tdWE8E67qQQhDWMe94qwRWIhlPvCelcSzgoVksKtpOaq_ocvTp6x7kdoHMQp2yDOS1tku3N30ns92aXrg1viORSLoJnJ0FO32cokxn64iAEGyHNxVDVCC2lFHRBn_6DXqU5x-V5K8U103WzCp8fKZdTKRn8zTKUmLVes9Rr1nqNXuknt_e_Yf_0uQAvjkAZ17-GfOvS__h-AZrCsXc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1794828396</pqid></control><display><type>article</type><title>Baseline factors predicting the risk of conversion from ocular hypertension to primary open-angle glaucoma during a 10-year follow-up</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Salvetat, M L ; Zeppieri, M ; Tosoni, C ; Brusini, P</creator><creatorcontrib>Salvetat, M L ; Zeppieri, M ; Tosoni, C ; Brusini, P ; Medscape</creatorcontrib><description>Purpose
To evaluate the ability of baseline clinical, morphological, and functional factors to predict the conversion to primary open-angle glaucoma (POAG) in ocular hypertensive (OHT) patients.
Methods
This single-center prospective longitudinal observational study included 116 eyes of 116 OHT patients followed for a 10-year period. All patients had intraocular pressure (IOP) ≥24 mm Hg in one eye and >21 mm Hg in the other eye, normal visual fields (VFs) and normal optic disc (OD) appearance in both eyes at baseline. All OHT patients were untreated at baseline with subsequent treatment upon need according to clinical judgement. Only one eye per subject was randomly selected. Patient age, gender, IOP, central corneal thickness (CCT), and ibopamine test results were collected at baseline. All patients underwent standard automated perimetry, short-wavelength automated perimetry (SWAP), frequency-doubling technology, confocal scanning laser ophthalmoscopy (CSLO), and scanning laser polarimetry (SLP) at baseline and every 6 months thereafter. Main outcome measure was the conversion to POAG, defined as the development of reproducible VF and/or OD abnormalities attributable to glaucoma. Cox proportional hazards models were used to identify the baseline factors predictive of POAG conversion.
Results
During the 10-year follow-up, 25% of eyes converted to POAG. In multivariate Cox models, baseline factors that were significant predictors of POAG development included: older age (hazard ratio (HR) 1.0, 99% confidence intervals (CIs) 1.0–1.2, per 1 year older); SWAP Glaucoma Hemifield test ‘outside normal limits’ (HR 4.3, 99% CIs 1.2–17.9); greater SLP ‘Inter-eye Symmetry’ (HR 1.1, 99% CIs 0.4–3.0, per 1 unit lower); lower CSLO Rim Volume (HR 1.1, 99% CIs 0.3–3.2, per 0.1 mm
3
lower); and greater CSLO cup-to-disc ratio (HR 6.0, 99% CIs 3.6–16.8, per 0.1 unit greater).
Conclusions
The baseline parameters that proved to be useful in assessing the likelihood of an OHT patient to develop POAG included age, functional variables provided by SWAP, and structural variables provided by SLP and CSLO. In this cohort of patients, baseline IOP, CCT, and ibopamine provocative test results were not significant predictors of POAG conversion.</description><identifier>ISSN: 0950-222X</identifier><identifier>EISSN: 1476-5454</identifier><identifier>DOI: 10.1038/eye.2016.86</identifier><identifier>PMID: 27174381</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/1647 ; 692/699/3161/3169/3170 ; 706/648 ; Aged ; Clinical Study ; Deoxyepinephrine - administration & dosage ; Deoxyepinephrine - analogs & derivatives ; Disease Progression ; Female ; Follow-Up Studies ; Glaucoma ; Glaucoma, Open-Angle - diagnosis ; Humans ; Intraocular Pressure - physiology ; Laboratory Medicine ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Mydriatics - administration & dosage ; Ocular Hypertension - diagnosis ; Ophthalmology ; Ophthalmoscopy ; Pharmaceutical Sciences/Technology ; Prospective Studies ; Risk Factors ; Surgery ; Surgical Oncology ; Tonometry, Ocular ; Visual Field Tests ; Visual Fields - physiology</subject><ispartof>Eye (London), 2016-06, Vol.30 (6), p.784-795</ispartof><rights>Royal College of Ophthalmologists 2016</rights><rights>Copyright Nature Publishing Group Jun 2016</rights><rights>Copyright © 2016 Royal College of Ophthalmologists 2016 Royal College of Ophthalmologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-a89bb4465053f3a8052d4c65502924f4b7547e5941ff00dcb04e72361ead68473</citedby><cites>FETCH-LOGICAL-c516t-a89bb4465053f3a8052d4c65502924f4b7547e5941ff00dcb04e72361ead68473</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/PMC4906466/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906466/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27174381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salvetat, M L</creatorcontrib><creatorcontrib>Zeppieri, M</creatorcontrib><creatorcontrib>Tosoni, C</creatorcontrib><creatorcontrib>Brusini, P</creatorcontrib><creatorcontrib>Medscape</creatorcontrib><title>Baseline factors predicting the risk of conversion from ocular hypertension to primary open-angle glaucoma during a 10-year follow-up</title><title>Eye (London)</title><addtitle>Eye</addtitle><addtitle>Eye (Lond)</addtitle><description>Purpose
To evaluate the ability of baseline clinical, morphological, and functional factors to predict the conversion to primary open-angle glaucoma (POAG) in ocular hypertensive (OHT) patients.
Methods
This single-center prospective longitudinal observational study included 116 eyes of 116 OHT patients followed for a 10-year period. All patients had intraocular pressure (IOP) ≥24 mm Hg in one eye and >21 mm Hg in the other eye, normal visual fields (VFs) and normal optic disc (OD) appearance in both eyes at baseline. All OHT patients were untreated at baseline with subsequent treatment upon need according to clinical judgement. Only one eye per subject was randomly selected. Patient age, gender, IOP, central corneal thickness (CCT), and ibopamine test results were collected at baseline. All patients underwent standard automated perimetry, short-wavelength automated perimetry (SWAP), frequency-doubling technology, confocal scanning laser ophthalmoscopy (CSLO), and scanning laser polarimetry (SLP) at baseline and every 6 months thereafter. Main outcome measure was the conversion to POAG, defined as the development of reproducible VF and/or OD abnormalities attributable to glaucoma. Cox proportional hazards models were used to identify the baseline factors predictive of POAG conversion.
Results
During the 10-year follow-up, 25% of eyes converted to POAG. In multivariate Cox models, baseline factors that were significant predictors of POAG development included: older age (hazard ratio (HR) 1.0, 99% confidence intervals (CIs) 1.0–1.2, per 1 year older); SWAP Glaucoma Hemifield test ‘outside normal limits’ (HR 4.3, 99% CIs 1.2–17.9); greater SLP ‘Inter-eye Symmetry’ (HR 1.1, 99% CIs 0.4–3.0, per 1 unit lower); lower CSLO Rim Volume (HR 1.1, 99% CIs 0.3–3.2, per 0.1 mm
3
lower); and greater CSLO cup-to-disc ratio (HR 6.0, 99% CIs 3.6–16.8, per 0.1 unit greater).
Conclusions
The baseline parameters that proved to be useful in assessing the likelihood of an OHT patient to develop POAG included age, functional variables provided by SWAP, and structural variables provided by SLP and CSLO. In this cohort of patients, baseline IOP, CCT, and ibopamine provocative test results were not significant predictors of POAG conversion.</description><subject>631/1647</subject><subject>692/699/3161/3169/3170</subject><subject>706/648</subject><subject>Aged</subject><subject>Clinical Study</subject><subject>Deoxyepinephrine - administration & dosage</subject><subject>Deoxyepinephrine - analogs & derivatives</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glaucoma</subject><subject>Glaucoma, Open-Angle - diagnosis</subject><subject>Humans</subject><subject>Intraocular Pressure - physiology</subject><subject>Laboratory Medicine</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Mydriatics - administration & dosage</subject><subject>Ocular Hypertension - diagnosis</subject><subject>Ophthalmology</subject><subject>Ophthalmoscopy</subject><subject>Pharmaceutical Sciences/Technology</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Tonometry, Ocular</subject><subject>Visual Field Tests</subject><subject>Visual Fields - physiology</subject><issn>0950-222X</issn><issn>1476-5454</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkU2L1TAUhoMoznV05V4CbgTtNUnz1Y2gg18w4EbBXUjTk3s7pklN2pH7A_zftt7rMIqrLN7nPDnJi9BjSraU1PolHGDLCJVbLe-gDeVKVoILfhdtSCNIxRj7eoYelHJFyBIqch-dMUUVrzXdoJ9vbIHQR8DeuinlgscMXe-mPu7wtAec-_INJ49diteQS58i9jkNOLk52Iz3hxHyBPF3MKVluh9sPuA0Qqxs3AXAu2BnlwaLuzmvVospqQ6wDPsUQvpRzeNDdM_bUODR6TxHX969_Xzxobr89P7jxevLygkqp8rqpm05l4KI2tdWE8E67qQQhDWMe94qwRWIhlPvCelcSzgoVksKtpOaq_ocvTp6x7kdoHMQp2yDOS1tku3N30ns92aXrg1viORSLoJnJ0FO32cokxn64iAEGyHNxVDVCC2lFHRBn_6DXqU5x-V5K8U103WzCp8fKZdTKRn8zTKUmLVes9Rr1nqNXuknt_e_Yf_0uQAvjkAZ17-GfOvS__h-AZrCsXc</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Salvetat, M L</creator><creator>Zeppieri, M</creator><creator>Tosoni, C</creator><creator>Brusini, P</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160601</creationdate><title>Baseline factors predicting the risk of conversion from ocular hypertension to primary open-angle glaucoma during a 10-year follow-up</title><author>Salvetat, M L ; Zeppieri, M ; Tosoni, C ; Brusini, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-a89bb4465053f3a8052d4c65502924f4b7547e5941ff00dcb04e72361ead68473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>631/1647</topic><topic>692/699/3161/3169/3170</topic><topic>706/648</topic><topic>Aged</topic><topic>Clinical Study</topic><topic>Deoxyepinephrine - administration & dosage</topic><topic>Deoxyepinephrine - analogs & derivatives</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glaucoma</topic><topic>Glaucoma, Open-Angle - diagnosis</topic><topic>Humans</topic><topic>Intraocular Pressure - physiology</topic><topic>Laboratory Medicine</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Mydriatics - administration & dosage</topic><topic>Ocular Hypertension - diagnosis</topic><topic>Ophthalmology</topic><topic>Ophthalmoscopy</topic><topic>Pharmaceutical Sciences/Technology</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Tonometry, Ocular</topic><topic>Visual Field Tests</topic><topic>Visual Fields - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salvetat, M L</creatorcontrib><creatorcontrib>Zeppieri, M</creatorcontrib><creatorcontrib>Tosoni, C</creatorcontrib><creatorcontrib>Brusini, P</creatorcontrib><creatorcontrib>Medscape</creatorcontrib><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>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Eye (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salvetat, M L</au><au>Zeppieri, M</au><au>Tosoni, C</au><au>Brusini, P</au><aucorp>Medscape</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Baseline factors predicting the risk of conversion from ocular hypertension to primary open-angle glaucoma during a 10-year follow-up</atitle><jtitle>Eye (London)</jtitle><stitle>Eye</stitle><addtitle>Eye (Lond)</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>30</volume><issue>6</issue><spage>784</spage><epage>795</epage><pages>784-795</pages><issn>0950-222X</issn><eissn>1476-5454</eissn><abstract>Purpose
To evaluate the ability of baseline clinical, morphological, and functional factors to predict the conversion to primary open-angle glaucoma (POAG) in ocular hypertensive (OHT) patients.
Methods
This single-center prospective longitudinal observational study included 116 eyes of 116 OHT patients followed for a 10-year period. All patients had intraocular pressure (IOP) ≥24 mm Hg in one eye and >21 mm Hg in the other eye, normal visual fields (VFs) and normal optic disc (OD) appearance in both eyes at baseline. All OHT patients were untreated at baseline with subsequent treatment upon need according to clinical judgement. Only one eye per subject was randomly selected. Patient age, gender, IOP, central corneal thickness (CCT), and ibopamine test results were collected at baseline. All patients underwent standard automated perimetry, short-wavelength automated perimetry (SWAP), frequency-doubling technology, confocal scanning laser ophthalmoscopy (CSLO), and scanning laser polarimetry (SLP) at baseline and every 6 months thereafter. Main outcome measure was the conversion to POAG, defined as the development of reproducible VF and/or OD abnormalities attributable to glaucoma. Cox proportional hazards models were used to identify the baseline factors predictive of POAG conversion.
Results
During the 10-year follow-up, 25% of eyes converted to POAG. In multivariate Cox models, baseline factors that were significant predictors of POAG development included: older age (hazard ratio (HR) 1.0, 99% confidence intervals (CIs) 1.0–1.2, per 1 year older); SWAP Glaucoma Hemifield test ‘outside normal limits’ (HR 4.3, 99% CIs 1.2–17.9); greater SLP ‘Inter-eye Symmetry’ (HR 1.1, 99% CIs 0.4–3.0, per 1 unit lower); lower CSLO Rim Volume (HR 1.1, 99% CIs 0.3–3.2, per 0.1 mm
3
lower); and greater CSLO cup-to-disc ratio (HR 6.0, 99% CIs 3.6–16.8, per 0.1 unit greater).
Conclusions
The baseline parameters that proved to be useful in assessing the likelihood of an OHT patient to develop POAG included age, functional variables provided by SWAP, and structural variables provided by SLP and CSLO. In this cohort of patients, baseline IOP, CCT, and ibopamine provocative test results were not significant predictors of POAG conversion.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27174381</pmid><doi>10.1038/eye.2016.86</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/1647 692/699/3161/3169/3170 706/648 Aged Clinical Study Deoxyepinephrine - administration & dosage Deoxyepinephrine - analogs & derivatives Disease Progression Female Follow-Up Studies Glaucoma Glaucoma, Open-Angle - diagnosis Humans Intraocular Pressure - physiology Laboratory Medicine Male Medicine Medicine & Public Health Middle Aged Mydriatics - administration & dosage Ocular Hypertension - diagnosis Ophthalmology Ophthalmoscopy Pharmaceutical Sciences/Technology Prospective Studies Risk Factors Surgery Surgical Oncology Tonometry, Ocular Visual Field Tests Visual Fields - physiology |
title | Baseline factors predicting the risk of conversion from ocular hypertension to primary open-angle glaucoma during a 10-year follow-up |
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