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Twelve-Month Efficacy of Intravitreal Bevacizumab Injection for Chronic, Atypical, or Recurrent Central Serous Chorioretinopathy
DC Field | Value | Language |
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dc.contributor.author | Chung, YR | - |
dc.contributor.author | Kim, JW | - |
dc.contributor.author | Song, JH | - |
dc.contributor.author | Park, A | - |
dc.contributor.author | Kim, MH | - |
dc.date.accessioned | 2022-01-14T05:16:30Z | - |
dc.date.available | 2022-01-14T05:16:30Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 0275-004X | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/19957 | - |
dc.description.abstract | PURPOSE: To evaluate intravitreal bevacizumab (IVB) injection efficacy for the treatment of chronic, atypical, or recurrent central serous chorioretinopathy (CSC).
METHODS: Clinical data from 77 eyes of 71 patients with chronic, atypical, or recurrent CSC treated with IVB were retrospectively analyzed. After initial 6-weekly IVB administration until no subretinal fluid remained at the fovea, additional as-needed IVBs were administered, based on optical coherence tomography findings. Best-corrected visual acuity and central retinal thickness (CRT) were analyzed at baseline and 3, 6, 9, and 12 months after initial IVB. RESULTS: The significant improvement of baseline logarithm of minimum angle of resolution best-corrected visual acuity and CRT at 3 months (both P < 0.001) was maintained throughout the 12-month follow-up period. Best-corrected visual acuity improved significantly in patients with chronic and recurrent CSC, at all time points (all P < 0.05), but not in patients with atypical CSC. The CRT reduction was significant in all subgroups during the follow-up period (all P < 0.05). Definite leakage on initial fluorescein angiography correlated with improved reduction in CRT (P = 0.039). CONCLUSION: As-needed optical coherence tomography-based IVB was effective for reducing CRT in patients with chronic, atypical, or recurrent CSC, and for vision improvement in chronic and recurrent CSC over the 1-year follow-up period. | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Angiogenesis Inhibitors | - |
dc.subject.MESH | Bevacizumab | - |
dc.subject.MESH | Central Serous Chorioretinopathy | - |
dc.subject.MESH | Choroid | - |
dc.subject.MESH | Chronic Disease | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fluorescein Angiography | - |
dc.subject.MESH | Follow-Up Studies | - |
dc.subject.MESH | Fundus Oculi | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Intravitreal Injections | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Receptors, Vascular Endothelial Growth Factor | - |
dc.subject.MESH | Recurrence | - |
dc.subject.MESH | Retina | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Time Factors | - |
dc.subject.MESH | Tomography, Optical Coherence | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Visual Acuity | - |
dc.title | Twelve-Month Efficacy of Intravitreal Bevacizumab Injection for Chronic, Atypical, or Recurrent Central Serous Chorioretinopathy | - |
dc.type | Article | - |
dc.identifier.pmid | 29077604 | - |
dc.subject.keyword | central retinal thickness | - |
dc.subject.keyword | central serous chorioretinopathy | - |
dc.subject.keyword | intravitreal bevacizumab | - |
dc.subject.keyword | optical coherence tomography | - |
dc.subject.keyword | visual acuity | - |
dc.contributor.affiliatedAuthor | Chung, YR | - |
dc.contributor.affiliatedAuthor | Song, JH | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1097/IAE.0000000000001917 | - |
dc.citation.title | Retina (Philadelphia, Pa.) | - |
dc.citation.volume | 39 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2019 | - |
dc.citation.startPage | 134 | - |
dc.citation.endPage | 142 | - |
dc.identifier.bibliographicCitation | Retina (Philadelphia, Pa.), 39(1). : 134-142, 2019 | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.identifier.eissn | 1539-2864 | - |
dc.relation.journalid | J00275004X | - |
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