Massive submacular haemorrhage in polypoidal choroidal vasculopathy versus typical neovascular age‐related macular degeneration

Purpose To investigate the incidence rate of massive submacular haemorrhage (SMH) and risk factors in polypoidal choroidal vasculopathy (PCV) and typical neovascular age‐related macular degeneration (tnAMD). Methods A total of 465 patients who were diagnosed with either PCV (n = 245) or tnAMD (n = 2...

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Veröffentlicht in:Acta ophthalmologica (Oxford, England) England), 2021-08, Vol.99 (5), p.e706-e714
Hauptverfasser: Cho, Soo Chang, Cho, JoonHee, Park, Kyu Hyung, Woo, Se Joon
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Cho, JoonHee
Park, Kyu Hyung
Woo, Se Joon
description Purpose To investigate the incidence rate of massive submacular haemorrhage (SMH) and risk factors in polypoidal choroidal vasculopathy (PCV) and typical neovascular age‐related macular degeneration (tnAMD). Methods A total of 465 patients who were diagnosed with either PCV (n = 245) or tnAMD (n = 220) from 2003 to 2014 were enrolled. Cumulative incidence of massive SMH in PCV and that in tnAMD were compared. Risk factors of massive SMH were also analysed. Results Massive SMH occurred in 32 patients (13.1%) with PCV and 9 patients (4.1%) with tnAMD. Incidence rates of massive SMH 5 and 10 years after the first visit were 11.1% and 29.9% in PCV and 4.3% and 9.9% in tnAMD, respectively. Incidence rates of massive SMH in PCV were significantly higher than those in tnAMD (hazard ratio [HR], 2.66; p = 0.007). Cox regression analysis revealed that mean number of photodynamic therapies (PDTs) per year (HR, 4.24; p 
doi_str_mv 10.1111/aos.14676
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Methods A total of 465 patients who were diagnosed with either PCV (n = 245) or tnAMD (n = 220) from 2003 to 2014 were enrolled. Cumulative incidence of massive SMH in PCV and that in tnAMD were compared. Risk factors of massive SMH were also analysed. Results Massive SMH occurred in 32 patients (13.1%) with PCV and 9 patients (4.1%) with tnAMD. Incidence rates of massive SMH 5 and 10 years after the first visit were 11.1% and 29.9% in PCV and 4.3% and 9.9% in tnAMD, respectively. Incidence rates of massive SMH in PCV were significantly higher than those in tnAMD (hazard ratio [HR], 2.66; p = 0.007). Cox regression analysis revealed that mean number of photodynamic therapies (PDTs) per year (HR, 4.24; p &lt; 0.001), cluster type of polypoidal lesion (HR, 3.42; p = 0.003) in PCV, and mean number of anti‐VEGF injections per year (HR, 1.58; p &lt; 0.001) in tnAMD were significantly associated with risk of massive SMH. For patients with severe vision loss, proportion of incident massive SMH was significantly higher in PCV (29.5%) than in tnAMD (6.9%, p &lt; 0.001). Conclusion The incidence rate of massive SMH in eyes with PCV was about three times higher than that in eyes with tnAMD. Treatment methods that can reduce the incidence of massive SMH should be considered, especially for eyes with PCV.</description><identifier>ISSN: 1755-375X</identifier><identifier>EISSN: 1755-3768</identifier><identifier>DOI: 10.1111/aos.14676</identifier><identifier>PMID: 33289345</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Aged ; Choroid - blood supply ; Choroid Diseases - complications ; Choroid Diseases - diagnosis ; Female ; Fluorescein Angiography - methods ; Follow-Up Studies ; Fundus Oculi ; Hemorrhage ; Humans ; Incidence ; incidence rate ; Macular degeneration ; Male ; massive submacular haemorrhage ; Patients ; polypoidal choroidal vasculopathy ; Polyps - complications ; Polyps - diagnosis ; Republic of Korea - epidemiology ; Retinal Hemorrhage - diagnosis ; Retinal Hemorrhage - epidemiology ; Retinal Hemorrhage - etiology ; Retrospective Studies ; Risk factors ; Tomography, Optical Coherence - methods ; typical neovascular age‐related macular degeneration ; Vascular diseases ; Vascular endothelial growth factor ; Visual Acuity ; Wet Macular Degeneration - complications ; Wet Macular Degeneration - diagnosis</subject><ispartof>Acta ophthalmologica (Oxford, England), 2021-08, Vol.99 (5), p.e706-e714</ispartof><rights>2020 Acta Ophthalmologica Scandinavica Foundation. Published by John Wiley &amp; Sons Ltd</rights><rights>2020 Acta Ophthalmologica Scandinavica Foundation. 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Methods A total of 465 patients who were diagnosed with either PCV (n = 245) or tnAMD (n = 220) from 2003 to 2014 were enrolled. Cumulative incidence of massive SMH in PCV and that in tnAMD were compared. Risk factors of massive SMH were also analysed. Results Massive SMH occurred in 32 patients (13.1%) with PCV and 9 patients (4.1%) with tnAMD. Incidence rates of massive SMH 5 and 10 years after the first visit were 11.1% and 29.9% in PCV and 4.3% and 9.9% in tnAMD, respectively. Incidence rates of massive SMH in PCV were significantly higher than those in tnAMD (hazard ratio [HR], 2.66; p = 0.007). Cox regression analysis revealed that mean number of photodynamic therapies (PDTs) per year (HR, 4.24; p &lt; 0.001), cluster type of polypoidal lesion (HR, 3.42; p = 0.003) in PCV, and mean number of anti‐VEGF injections per year (HR, 1.58; p &lt; 0.001) in tnAMD were significantly associated with risk of massive SMH. For patients with severe vision loss, proportion of incident massive SMH was significantly higher in PCV (29.5%) than in tnAMD (6.9%, p &lt; 0.001). Conclusion The incidence rate of massive SMH in eyes with PCV was about three times higher than that in eyes with tnAMD. Treatment methods that can reduce the incidence of massive SMH should be considered, especially for eyes with PCV.</description><subject>Aged</subject><subject>Choroid - blood supply</subject><subject>Choroid Diseases - complications</subject><subject>Choroid Diseases - diagnosis</subject><subject>Female</subject><subject>Fluorescein Angiography - methods</subject><subject>Follow-Up Studies</subject><subject>Fundus Oculi</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Incidence</subject><subject>incidence rate</subject><subject>Macular degeneration</subject><subject>Male</subject><subject>massive submacular haemorrhage</subject><subject>Patients</subject><subject>polypoidal choroidal vasculopathy</subject><subject>Polyps - complications</subject><subject>Polyps - diagnosis</subject><subject>Republic of Korea - epidemiology</subject><subject>Retinal Hemorrhage - diagnosis</subject><subject>Retinal Hemorrhage - epidemiology</subject><subject>Retinal Hemorrhage - etiology</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Tomography, Optical Coherence - methods</subject><subject>typical neovascular age‐related macular degeneration</subject><subject>Vascular diseases</subject><subject>Vascular endothelial growth factor</subject><subject>Visual Acuity</subject><subject>Wet Macular Degeneration - complications</subject><subject>Wet Macular Degeneration - diagnosis</subject><issn>1755-375X</issn><issn>1755-3768</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1O3DAQx62qCJaFQ1-gitQLHBb8ETvOEaHyIYH2QCtxsybOLBuUjVM72So3eAOekSfBS4ADEnPxSPPTb0b-E_KD0SMW6xhcOGKpytQ3MmGZlDORKf39o5e3O2Q3hHtKFVMq3SY7QnCdi1ROyOM1hFCtMQl9sQLb1-CTJeDKeb-EO0yqJmldPbSuKqFO7NL5sVtDiLBroVsOyRp96EPSDW1l46xBN46jKzqeH5481tBhmbxvKPEOG_TQVa7ZI1sLqAPuv71T8vfs95_Ti9nV_Pzy9ORqZoXWaiYlLQqE3JZMFLrgWvK8zHJLATNmqUgXOVcFV6XOwaYLyjOVsRwYQ6k4k1JMycHobb3712PozKoKFusa4r19MDxVWgiqMx3RX5_Qe9f7Jl5nuFQigjLfCA9HynoXgseFaX21Aj8YRs0mFxNzMa-5RPbnmzF-M5Yf5HsQETgegf9VjcPXJnMyvxmVLyQOmsA</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Cho, Soo Chang</creator><creator>Cho, JoonHee</creator><creator>Park, Kyu Hyung</creator><creator>Woo, Se Joon</creator><general>Wiley Subscription Services, Inc</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>7TK</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5516-8121</orcidid><orcidid>https://orcid.org/0000-0003-3692-7169</orcidid></search><sort><creationdate>202108</creationdate><title>Massive submacular haemorrhage in polypoidal choroidal vasculopathy versus typical neovascular age‐related macular degeneration</title><author>Cho, Soo Chang ; Cho, JoonHee ; Park, Kyu Hyung ; Woo, Se Joon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3886-550bbea9cd13b8b28529d79c0ae71c034f926b26d89ac4f0276719a11e5621553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Choroid - blood supply</topic><topic>Choroid Diseases - complications</topic><topic>Choroid Diseases - diagnosis</topic><topic>Female</topic><topic>Fluorescein Angiography - methods</topic><topic>Follow-Up Studies</topic><topic>Fundus Oculi</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Incidence</topic><topic>incidence rate</topic><topic>Macular degeneration</topic><topic>Male</topic><topic>massive submacular haemorrhage</topic><topic>Patients</topic><topic>polypoidal choroidal vasculopathy</topic><topic>Polyps - complications</topic><topic>Polyps - diagnosis</topic><topic>Republic of Korea - epidemiology</topic><topic>Retinal Hemorrhage - diagnosis</topic><topic>Retinal Hemorrhage - epidemiology</topic><topic>Retinal Hemorrhage - etiology</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Tomography, Optical Coherence - methods</topic><topic>typical neovascular age‐related macular degeneration</topic><topic>Vascular diseases</topic><topic>Vascular endothelial growth factor</topic><topic>Visual Acuity</topic><topic>Wet Macular Degeneration - complications</topic><topic>Wet Macular Degeneration - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Soo Chang</creatorcontrib><creatorcontrib>Cho, JoonHee</creatorcontrib><creatorcontrib>Park, Kyu Hyung</creatorcontrib><creatorcontrib>Woo, Se Joon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Acta ophthalmologica (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Soo Chang</au><au>Cho, JoonHee</au><au>Park, Kyu Hyung</au><au>Woo, Se Joon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Massive submacular haemorrhage in polypoidal choroidal vasculopathy versus typical neovascular age‐related macular degeneration</atitle><jtitle>Acta ophthalmologica (Oxford, England)</jtitle><addtitle>Acta Ophthalmol</addtitle><date>2021-08</date><risdate>2021</risdate><volume>99</volume><issue>5</issue><spage>e706</spage><epage>e714</epage><pages>e706-e714</pages><issn>1755-375X</issn><eissn>1755-3768</eissn><abstract>Purpose To investigate the incidence rate of massive submacular haemorrhage (SMH) and risk factors in polypoidal choroidal vasculopathy (PCV) and typical neovascular age‐related macular degeneration (tnAMD). Methods A total of 465 patients who were diagnosed with either PCV (n = 245) or tnAMD (n = 220) from 2003 to 2014 were enrolled. Cumulative incidence of massive SMH in PCV and that in tnAMD were compared. Risk factors of massive SMH were also analysed. Results Massive SMH occurred in 32 patients (13.1%) with PCV and 9 patients (4.1%) with tnAMD. Incidence rates of massive SMH 5 and 10 years after the first visit were 11.1% and 29.9% in PCV and 4.3% and 9.9% in tnAMD, respectively. Incidence rates of massive SMH in PCV were significantly higher than those in tnAMD (hazard ratio [HR], 2.66; p = 0.007). Cox regression analysis revealed that mean number of photodynamic therapies (PDTs) per year (HR, 4.24; p &lt; 0.001), cluster type of polypoidal lesion (HR, 3.42; p = 0.003) in PCV, and mean number of anti‐VEGF injections per year (HR, 1.58; p &lt; 0.001) in tnAMD were significantly associated with risk of massive SMH. For patients with severe vision loss, proportion of incident massive SMH was significantly higher in PCV (29.5%) than in tnAMD (6.9%, p &lt; 0.001). Conclusion The incidence rate of massive SMH in eyes with PCV was about three times higher than that in eyes with tnAMD. Treatment methods that can reduce the incidence of massive SMH should be considered, especially for eyes with PCV.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33289345</pmid><doi>10.1111/aos.14676</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5516-8121</orcidid><orcidid>https://orcid.org/0000-0003-3692-7169</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Choroid - blood supply
Choroid Diseases - complications
Choroid Diseases - diagnosis
Female
Fluorescein Angiography - methods
Follow-Up Studies
Fundus Oculi
Hemorrhage
Humans
Incidence
incidence rate
Macular degeneration
Male
massive submacular haemorrhage
Patients
polypoidal choroidal vasculopathy
Polyps - complications
Polyps - diagnosis
Republic of Korea - epidemiology
Retinal Hemorrhage - diagnosis
Retinal Hemorrhage - epidemiology
Retinal Hemorrhage - etiology
Retrospective Studies
Risk factors
Tomography, Optical Coherence - methods
typical neovascular age‐related macular degeneration
Vascular diseases
Vascular endothelial growth factor
Visual Acuity
Wet Macular Degeneration - complications
Wet Macular Degeneration - diagnosis
title Massive submacular haemorrhage in polypoidal choroidal vasculopathy versus typical neovascular age‐related macular degeneration
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