EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP

Detalhes bibliográficos
Autor(a) principal: Martins, Amélia
Data de Publicação: 2016
Outros Autores: Farinha, Cláudia, Santos, Ana Rita, Figueira, João, Pires, Isabel, Cachulo, Maria Luz, Silva, Rufino
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.48560/rspo.7532
Resumo: PURPOSE: To assess the seven-year efficacy of intravitreal ranibizumab (IVR) in the treatment of myopic choroidal neovascularization (mCNV), and to estimate the progression of macular atrophy. MATERIAL AND METHODS: Retrospective study with cross-sectional evaluation. Medical records of high myopic patients with mCNV treated with IVR with minimum follow-up of 84months were analysed. A final cross-sectional evaluation included best corrected visual acuity (BCVA), colour fundus photography, spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging. RESULTS: Thirteen eyes of 13 patients with an average follow-up of 96.6±5.4 months were included. After a mean number of 8.5±4.5 IV injections of ranibizumab, BCVA at baseline and on the last visit was 48.4±16.7 letters (L) and 45.2±26.8 L, respectively (p=0.6).VA improved up to the third year (56.7±21.0 L) and decreased ever since. Regarding the last visit, 4 patients (30.8%) reached a significant visual gain (BCVA >5 L), 2 patients (15.4%) maintained visual acuity (range between -5 and 5L), and in 7 patients (53.8%) more than 5 L loss was reported. Concerning macular atrophy area, we noticed an increase, on average 4.6±3.2mm2, meaning a significant progression (p=0.002). The mean central macular thickness ranged from 304.9±116.5 µm at baseline to 360.5 ± 89.1 µm on the last visit (p> 0.05). CONCLUSIONS: Ranibizumab is an effective drug in the treatment of CNV, secondary to pathologic myopia, stabilizing or even improving BCVA. However it does not seem to prevent subsequent macular atrophy which could be related with progressive VA loss.
id RCAP_a7950ef8acfad8d5c2af80351926f567
oai_identifier_str oai:ojs.revistas.rcaap.pt:article/7532
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UPArtigos OriginaisPURPOSE: To assess the seven-year efficacy of intravitreal ranibizumab (IVR) in the treatment of myopic choroidal neovascularization (mCNV), and to estimate the progression of macular atrophy. MATERIAL AND METHODS: Retrospective study with cross-sectional evaluation. Medical records of high myopic patients with mCNV treated with IVR with minimum follow-up of 84months were analysed. A final cross-sectional evaluation included best corrected visual acuity (BCVA), colour fundus photography, spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging. RESULTS: Thirteen eyes of 13 patients with an average follow-up of 96.6±5.4 months were included. After a mean number of 8.5±4.5 IV injections of ranibizumab, BCVA at baseline and on the last visit was 48.4±16.7 letters (L) and 45.2±26.8 L, respectively (p=0.6).VA improved up to the third year (56.7±21.0 L) and decreased ever since. Regarding the last visit, 4 patients (30.8%) reached a significant visual gain (BCVA >5 L), 2 patients (15.4%) maintained visual acuity (range between -5 and 5L), and in 7 patients (53.8%) more than 5 L loss was reported. Concerning macular atrophy area, we noticed an increase, on average 4.6±3.2mm2, meaning a significant progression (p=0.002). The mean central macular thickness ranged from 304.9±116.5 µm at baseline to 360.5 ± 89.1 µm on the last visit (p> 0.05). CONCLUSIONS: Ranibizumab is an effective drug in the treatment of CNV, secondary to pathologic myopia, stabilizing or even improving BCVA. However it does not seem to prevent subsequent macular atrophy which could be related with progressive VA loss.Ajnet2016-07-19T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.48560/rspo.7532eng1646-69501646-6950Martins, AméliaFarinha, CláudiaSantos, Ana RitaFigueira, JoãoPires, IsabelCachulo, Maria LuzSilva, Rufinoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-22T17:05:55Zoai:ojs.revistas.rcaap.pt:article/7532Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:01:35.641337Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
title EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
spellingShingle EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
Martins, Amélia
Artigos Originais
title_short EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
title_full EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
title_fullStr EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
title_full_unstemmed EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
title_sort EFFICACY AND PROGRESSION OF MACULAR ATROPHY AFTER SEVEN YEARS OF TREATMENT WITH RANIBIZUMAB: THE MYOPIC SEVEN-UP
author Martins, Amélia
author_facet Martins, Amélia
Farinha, Cláudia
Santos, Ana Rita
Figueira, João
Pires, Isabel
Cachulo, Maria Luz
Silva, Rufino
author_role author
author2 Farinha, Cláudia
Santos, Ana Rita
Figueira, João
Pires, Isabel
Cachulo, Maria Luz
Silva, Rufino
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Martins, Amélia
Farinha, Cláudia
Santos, Ana Rita
Figueira, João
Pires, Isabel
Cachulo, Maria Luz
Silva, Rufino
dc.subject.por.fl_str_mv Artigos Originais
topic Artigos Originais
description PURPOSE: To assess the seven-year efficacy of intravitreal ranibizumab (IVR) in the treatment of myopic choroidal neovascularization (mCNV), and to estimate the progression of macular atrophy. MATERIAL AND METHODS: Retrospective study with cross-sectional evaluation. Medical records of high myopic patients with mCNV treated with IVR with minimum follow-up of 84months were analysed. A final cross-sectional evaluation included best corrected visual acuity (BCVA), colour fundus photography, spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging. RESULTS: Thirteen eyes of 13 patients with an average follow-up of 96.6±5.4 months were included. After a mean number of 8.5±4.5 IV injections of ranibizumab, BCVA at baseline and on the last visit was 48.4±16.7 letters (L) and 45.2±26.8 L, respectively (p=0.6).VA improved up to the third year (56.7±21.0 L) and decreased ever since. Regarding the last visit, 4 patients (30.8%) reached a significant visual gain (BCVA >5 L), 2 patients (15.4%) maintained visual acuity (range between -5 and 5L), and in 7 patients (53.8%) more than 5 L loss was reported. Concerning macular atrophy area, we noticed an increase, on average 4.6±3.2mm2, meaning a significant progression (p=0.002). The mean central macular thickness ranged from 304.9±116.5 µm at baseline to 360.5 ± 89.1 µm on the last visit (p> 0.05). CONCLUSIONS: Ranibizumab is an effective drug in the treatment of CNV, secondary to pathologic myopia, stabilizing or even improving BCVA. However it does not seem to prevent subsequent macular atrophy which could be related with progressive VA loss.
publishDate 2016
dc.date.none.fl_str_mv 2016-07-19T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.48560/rspo.7532
url https://doi.org/10.48560/rspo.7532
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1646-6950
1646-6950
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Ajnet
publisher.none.fl_str_mv Ajnet
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799130481154850816