Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group

To determine the feasibility, safety, and clinical effect of primary intravitreal bevacizumab (Avastin) in patients with cystoid macular edema (CME) after cataract surgery. Five institutions in Venezuela, Costa Rica, Puerto Rico, Peru, and Brazil. Twenty-eight eyes of 25 patients treated with at lea...

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Tipo de recurso:
Fecha de publicación:
2007
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/25914
Acceso en línea:
https://doi.org/10.1016/j.jcrs.2007.07.046
https://repository.urosario.edu.co/handle/10336/25914
Palabra clave:
Aged
Aged
80 and over
Angiogenesis Inhibitors
Antibodies
Monoclonal
Antibodies
Monoclonal
Humanized
Bevacizumab
Cataract Extraction
Feasibility Studies
Female
Humans
Injections
Macular Edema
Male
Middle Aged
Pilot Projects
Postoperative Complications
Pseudophakia
Retreatment
Retrospective Studies
South America
Tomography
Optical Coherence
Vascular Endothelial Growth Factor A
Visual Acuity
Vitreous Body
Rights
License
Restringido (Acceso a grupos específicos)
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oai_identifier_str oai:repository.urosario.edu.co:10336/25914
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 739ecf4c-3887-4668-bcea-2114906b5010-15e73b0b0-f241-40ab-a7bf-65cf76736d48-17fe3703f-ddb2-4ce2-b045-4212aa98c927-1e69e8b13-e9f7-4381-a9a8-95e96943618f-1e9382a84-7532-4238-a6e9-d0b1e9cc130f-1390567f2-51a9-42ab-b5cb-bca59742d357-1c4f0daa5-b76d-47f4-bec5-e92a853049b8-13f599f3a-6436-4792-b37a-3147425aba25-1e982d410-c073-4210-be50-890548540cfa6002020-08-06T16:20:12Z2020-08-06T16:20:12Z2007-12To determine the feasibility, safety, and clinical effect of primary intravitreal bevacizumab (Avastin) in patients with cystoid macular edema (CME) after cataract surgery. Five institutions in Venezuela, Costa Rica, Puerto Rico, Peru, and Brazil. Twenty-eight eyes of 25 patients treated with at least 1 intravitreal injection of 1.25 mg or 2.50 mg of Avastin participated in this interventional retrospective multicenter study at 5 institutions from 5 countries. Baseline and follow-up visits included Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity testing, optical coherence tomography (OCT) imaging, and ophthalmoscopic examination. The mean follow-up was 32 weeks (range 24 to 52 weeks). Twenty eyes (71.4%) had improved best corrected visual acuity (BCVA) (R2 ETDRS lines), and no eye had worse visual acuity (R2 ETDRS lines). The BCVA remained stable in 8 eyes (28.6%). The mean baseline BCVA was 20/160 (logMAR Z 0.92) and the mean final BCVA, 20/63 (logMAR Z 0.50); the difference was statistically significant (P<.0001). The mean central macular thickness at baseline (466.3 mm; range 208 to 784 mm) decreased significantly (264.5 mm; range 176 to 513 mm) by the end of follow-up (P<.0001). Eight eyes (28.6%) required a second injection and 4 (14.3%), a third injection. The mean interval between injections was 13 weeks (range 5 to 26 weeks). No ocular or systemic adverse events were observed. Short-term results suggest that primary intravitreal Avastin is well tolerated in patients with pseudophakic CME. Treated eyes had a significant improvement in BCVA and decrease in macular thickness by OCT.application/pdfhttps://doi.org/10.1016/j.jcrs.2007.07.046ISSN: 0886-3350https://repository.urosario.edu.co/handle/10336/25914engLippincott Williams & Wilkins (LWW)2105No. 122098Journal of Cataract & Refractive SurgeryVol. 33Journal of Cataract & Refractive Surgery, ISSN: 0886-3350, Vol.33, No.12 (December, 2007); pp.2098-2105https://journals.lww.com/jcrs/FullText/2007/12000/Primary_intravitreal_bevacizumab_for_the.35.aspxRestringido (Acceso a grupos específicos)http://purl.org/coar/access_right/c_16ecJournal of Cataract & Refractive Surgeryinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAgedAged80 and overAngiogenesis InhibitorsAntibodiesMonoclonalAntibodiesMonoclonalHumanizedBevacizumabCataract ExtractionFeasibility StudiesFemaleHumansInjectionsMacular EdemaMaleMiddle AgedPilot ProjectsPostoperative ComplicationsPseudophakiaRetreatmentRetrospective StudiesSouth AmericaTomographyOptical CoherenceVascular Endothelial Growth Factor AVisual AcuityVitreous BodyPrimary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study GroupPilot study of the Pan-American Collaborative Retina Study GrouparticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Arevalo, J. FernandoGarcia-Amaris, Rafael A.Roca, Jose A.Sanchez, Juan G.Wu, LihtehBerrocal, Maria H.Maia, MauricioGroup, Pan-American Collaborative Retina StudyPan-American Collaborative Retina Study Group (PACORES)10336/25914oai:repository.urosario.edu.co:10336/259142022-05-02 07:37:21.802519https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
dc.title.TranslatedTitle.eng.fl_str_mv Pilot study of the Pan-American Collaborative Retina Study Group
title Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
spellingShingle Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
Aged
Aged
80 and over
Angiogenesis Inhibitors
Antibodies
Monoclonal
Antibodies
Monoclonal
Humanized
Bevacizumab
Cataract Extraction
Feasibility Studies
Female
Humans
Injections
Macular Edema
Male
Middle Aged
Pilot Projects
Postoperative Complications
Pseudophakia
Retreatment
Retrospective Studies
South America
Tomography
Optical Coherence
Vascular Endothelial Growth Factor A
Visual Acuity
Vitreous Body
title_short Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
title_full Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
title_fullStr Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
title_full_unstemmed Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
title_sort Primary intravitreal bevacizumab for the management of pseudophakic cystoid macular edema Pilot study of the Pan-American Collaborative Retina Study Group
dc.subject.keyword.spa.fl_str_mv Aged
Aged
80 and over
Angiogenesis Inhibitors
Antibodies
Monoclonal
Antibodies
Monoclonal
Humanized
Bevacizumab
Cataract Extraction
Feasibility Studies
Female
Humans
Injections
Macular Edema
Male
Middle Aged
Pilot Projects
Postoperative Complications
Pseudophakia
Retreatment
Retrospective Studies
South America
Tomography
Optical Coherence
Vascular Endothelial Growth Factor A
Visual Acuity
Vitreous Body
topic Aged
Aged
80 and over
Angiogenesis Inhibitors
Antibodies
Monoclonal
Antibodies
Monoclonal
Humanized
Bevacizumab
Cataract Extraction
Feasibility Studies
Female
Humans
Injections
Macular Edema
Male
Middle Aged
Pilot Projects
Postoperative Complications
Pseudophakia
Retreatment
Retrospective Studies
South America
Tomography
Optical Coherence
Vascular Endothelial Growth Factor A
Visual Acuity
Vitreous Body
description To determine the feasibility, safety, and clinical effect of primary intravitreal bevacizumab (Avastin) in patients with cystoid macular edema (CME) after cataract surgery. Five institutions in Venezuela, Costa Rica, Puerto Rico, Peru, and Brazil. Twenty-eight eyes of 25 patients treated with at least 1 intravitreal injection of 1.25 mg or 2.50 mg of Avastin participated in this interventional retrospective multicenter study at 5 institutions from 5 countries. Baseline and follow-up visits included Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity testing, optical coherence tomography (OCT) imaging, and ophthalmoscopic examination. The mean follow-up was 32 weeks (range 24 to 52 weeks). Twenty eyes (71.4%) had improved best corrected visual acuity (BCVA) (R2 ETDRS lines), and no eye had worse visual acuity (R2 ETDRS lines). The BCVA remained stable in 8 eyes (28.6%). The mean baseline BCVA was 20/160 (logMAR Z 0.92) and the mean final BCVA, 20/63 (logMAR Z 0.50); the difference was statistically significant (P<.0001). The mean central macular thickness at baseline (466.3 mm; range 208 to 784 mm) decreased significantly (264.5 mm; range 176 to 513 mm) by the end of follow-up (P<.0001). Eight eyes (28.6%) required a second injection and 4 (14.3%), a third injection. The mean interval between injections was 13 weeks (range 5 to 26 weeks). No ocular or systemic adverse events were observed. Short-term results suggest that primary intravitreal Avastin is well tolerated in patients with pseudophakic CME. Treated eyes had a significant improvement in BCVA and decrease in macular thickness by OCT.
publishDate 2007
dc.date.created.spa.fl_str_mv 2007-12
dc.date.accessioned.none.fl_str_mv 2020-08-06T16:20:12Z
dc.date.available.none.fl_str_mv 2020-08-06T16:20:12Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.jcrs.2007.07.046
dc.identifier.issn.none.fl_str_mv ISSN: 0886-3350
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/25914
url https://doi.org/10.1016/j.jcrs.2007.07.046
https://repository.urosario.edu.co/handle/10336/25914
identifier_str_mv ISSN: 0886-3350
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 2105
dc.relation.citationIssue.none.fl_str_mv No. 12
dc.relation.citationStartPage.none.fl_str_mv 2098
dc.relation.citationTitle.none.fl_str_mv Journal of Cataract & Refractive Surgery
dc.relation.citationVolume.none.fl_str_mv Vol. 33
dc.relation.ispartof.spa.fl_str_mv Journal of Cataract & Refractive Surgery, ISSN: 0886-3350, Vol.33, No.12 (December, 2007); pp.2098-2105
dc.relation.uri.spa.fl_str_mv https://journals.lww.com/jcrs/FullText/2007/12000/Primary_intravitreal_bevacizumab_for_the.35.aspx
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.rights.acceso.spa.fl_str_mv Restringido (Acceso a grupos específicos)
rights_invalid_str_mv Restringido (Acceso a grupos específicos)
http://purl.org/coar/access_right/c_16ec
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Lippincott Williams & Wilkins (LWW)
dc.source.spa.fl_str_mv Journal of Cataract & Refractive Surgery
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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